Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1785 |
|---|---|
| ensemblid | ENSG00000079805.19 |
| hgncid | 2974 |
| symbol | DNM2 |
| name | dynamin 2 |
| refseq_nuc | NM_001005361.3 |
| refseq_prot | NP_001005361.1 |
| ensembl_nuc | ENST00000389253.9 |
| ensembl_prot | ENSP00000373905.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 10718079 |
| end | 10831903 |
| strand | + |
| ver | v1.2 |
| region | chr19:10718079-10831903 |
| region5000 | chr19:10713079-10836903 |
| regionname0 | DNM2_chr19_10718079_10831903 |
| regionname5000 | DNM2_chr19_10713079_10836903 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 870 | 276 | 59 | 56 | 114 | 9 | 36 | 86 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0002 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0003 | 0/0 | 694 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2613 | 139 | 40 | 34 | 35 | 5 | 23 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0002 | 0/0 | 2613 | 125 | 17 | 20 | 72 | 3 | 13 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0003 | 0/0 | 2613 | 5 | 0 | 0 | 5 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0004 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0005 | 0/0 | 2613 | 2 | 1 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0006 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0007 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0008 | 0/0 | 2648 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0009 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| c0010 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1021 | 172 | 27 | 43 | 64 | 8 | 28 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0002 | 0/0 | 1021 | 84 | 18 | 11 | 45 | 2 | 8 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0003 | 0/0 | 1021 | 9 | 8 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0004 | 0/0 | 1021 | 2 | 0 | 0 | 2 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0005 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0006 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0007 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0008 | 0/0 | 1021 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0009 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0010 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0011 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0012 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| t0013 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2613 | 139 | 40 | 34 | 35 | 5 | 23 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002 | 0/0 | 2613 | 125 | 17 | 20 | 72 | 3 | 13 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0003 | 0/0 | 2613 | 5 | 0 | 0 | 5 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0004 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0005 | 0/0 | 2613 | 2 | 1 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0007 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0009 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0010 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0002c0006 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0003c0008 | 0/0 | 2648 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3633 | 119 | 26 | 32 | 32 | 5 | 22 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0001t0002 | 0/0 | 3633 | 7 | 4 | 0 | 2 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0001t0003 | 0/0 | 3633 | 9 | 8 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0001t0005 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0001t0008 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0001t0009 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0001 | 0/0 | 3633 | 44 | 0 | 9 | 27 | 2 | 6 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0002 | 0/0 | 3633 | 72 | 12 | 11 | 41 | 1 | 7 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0004 | 0/0 | 3633 | 2 | 0 | 0 | 2 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0006 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0007 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0010 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0011 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0012 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0002t0013 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0003t0001 | 0/0 | 3633 | 5 | 0 | 0 | 5 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0004t0001 | 0/0 | 3633 | 2 | 0 | 2 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0005t0001 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0005t0002 | 0/0 | 3633 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0007t0002 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0009t0002 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0001c0010t0002 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0002c0006t0002 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| a0003c0008t0001 | 0/0 | 3668 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | copy fasta | chr19 | 10713079 | 10836903 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0002t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0004t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0005t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0005t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0007t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0009t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0001c0010t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0002c0006t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| a0003c0008t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0124 | EUR | GBR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0105 | EUR | GBR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00140 | hp2 | a0001 | c0005 | t0002 | g0141 | EUR | GBR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | CHS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0269 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0087 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0266 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0008 | EUR | IBS | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0042 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0274 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02155 | hp1 | a0001 | c0010 | t0002 | g0077 | EAS | CDX | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02622 | hp2 | a0001 | c0002 | t0012 | g0149 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0163 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02965 | hp1 | a0001 | c0002 | t0006 | g0161 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0143 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03130 | hp2 | a0002 | c0006 | t0002 | g0056 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | YRI | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18522 | hp2 | a0001 | c0002 | t0010 | g0092 | AFR | YRI | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CHB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0183 | EAS | CHB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | YRI | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | YRI | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18947 | hp1 | a0001 | c0002 | t0011 | g0079 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18979 | hp2 | a0001 | c0002 | t0007 | g0045 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19007 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19009 | hp1 | a0001 | c0007 | t0002 | g0076 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0165 | AFR | LWK | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | LWK | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | LWK | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0068 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19088 | hp1 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA20129 | hp1 | a0001 | c0009 | t0002 | g0018 | AFR | ASW | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA20129 | hp2 | a0001 | c0002 | t0013 | g0263 | AFR | ASW | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA20805 | hp1 | a0003 | c0008 | t0001 | g0267 | EUR | TSI | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0272 | AFR | USA | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0223 | REF | REF | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | DNM2_chr19_10713079_10836903 | DNM2 | chr19 | 10713079 | 10836903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10759766
|
G | A | 1 | a0002 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.190G>A | p.Val64Ile | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/21 | 354/3633 | 190/2613 | 64/870 | chr19 | 10759766 | ||
| chr19:10823837
|
G | A | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1831G>A | p.Glu611Lys | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 1995/3633 | 1831/2613 | 611/870 | chr19 | 10823837 | ||
| chr19:10823838
|
A | C | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1832A>C | p.Glu611Ala | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 1996/3633 | 1832/2613 | 611/870 | chr19 | 10823838 | ||
| chr19:10823840
|
G | C | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1834G>C | p.Asp612His | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 1998/3633 | 1834/2613 | 612/870 | chr19 | 10823840 | ||
| chr19:10823842
|
C | A | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1836C>A | p.Asp612Glu | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 2000/3633 | 1836/2613 | 612/870 | chr19 | 10823842 | ||
| chr19:10823847
|
A | C | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1841A>C | p.Asp614Ala | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 2005/3633 | 1841/2613 | 614/870 | chr19 | 10823847 | ||
| chr19:10823850
|
G | C | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1844G>C | p.Ser615Thr | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 2008/3633 | 1844/2613 | 615/870 | chr19 | 10823850 | ||
| chr19:10823861
|
T | C | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1855T>C | p.Ser619Pro | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 2019/3633 | 1855/2613 | 619/870 | chr19 | 10823861 | ||
| chr19:10823862
|
C | CCCCACAC others(28): Show |
1 | a0003 | 1 | NA20805.hp1 | frameshift_variant | HIGH | c.1856_1857insCCCACA others(29): Show |
p.Phe620fs | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 2021/3633 | 1857/2613 | 619/870 | chr19 | 10823862 | ||
| chr19:10823886
|
C | A | 1 | a0003 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1880C>A | p.Pro627His | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/21 | 2044/3633 | 1880/2613 | 627/870 | chr19 | 10823886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10783060
|
G | A | 1 | a0001c0007 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.789G>A | p.Pro263Pro | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/21 | 953/3633 | 789/2613 | 263/870 | chr19 | 10783060 | ||
| chr19:10786572
|
C | G | 1 | a0001c0010 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.858C>G | p.Thr286Thr | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/21 | 1022/3633 | 858/2613 | 286/870 | chr19 | 10786572 | ||
| chr19:10793804
|
C | T | 1 | a0001c0005 | 2 | HG00140.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.1077C>T | p.Gly359Gly | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/21 | 1241/3633 | 1077/2613 | 359/870 | chr19 | 10793804 | ||
| chr19:10829116
|
T | C | 6 | a0001c0002a0001c0005a0001c0007others(3): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
synonymous_variant | LOW | c.2139T>C | p.Ala713Ala | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 19/21 | 2303/3633 | 2139/2613 | 713/870 | chr19 | 10829116 | ||
| chr19:10829137
|
C | T | 1 | a0001c0003 | 5 | NA18747.hp2 NA18948.hp2 NA18964.hp2 others(2): Show |
synonymous_variant | LOW | c.2160C>T | p.Asp720Asp | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 19/21 | 2324/3633 | 2160/2613 | 720/870 | chr19 | 10829137 | ||
| chr19:10830319
|
G | A | 1 | a0001c0009 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2484G>A | p.Pro828Pro | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/21 | 2648/3633 | 2484/2613 | 828/870 | chr19 | 10830319 | ||
| chr19:10830346
|
G | A | 1 | a0001c0004 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.2511G>A | p.Arg837Arg | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/21 | 2675/3633 | 2511/2613 | 837/870 | chr19 | 10830346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10718097
|
C | T | 1 | a0001c0002t0013 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-146C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/21 | 146 | chr19 | 10718097 | |||||
| chr19:10831057
|
G | A | 1 | a0001c0002t0004 | 2 | NA19081.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 10 | chr19 | 10831057 | |||||
| chr19:10831082
|
C | G | 1 | a0001c0002t0006 | 2 | HG02965.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*35C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 35 | chr19 | 10831082 | |||||
| chr19:10831153
|
T | C | 1 | a0001c0002t0007 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 106 | chr19 | 10831153 | |||||
| chr19:10831315
|
A | T | 15 | a0001c0001t0002a0001c0001t0005a0001c0002t0002others(12): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*268A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 268 | chr19 | 10831315 | |||||
| chr19:10831368
|
A | G | 1 | a0001c0002t0012 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 321 | chr19 | 10831368 | |||||
| chr19:10831432
|
C | T | 1 | a0001c0001t0003 | 9 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*385C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 385 | chr19 | 10831432 | |||||
| chr19:10831433
|
G | C | 1 | a0001c0001t0005 | 2 | HG02280.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*386G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 386 | chr19 | 10831433 | |||||
| chr19:10831524
|
G | A | 1 | a0001c0001t0008 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 477 | chr19 | 10831524 | |||||
| chr19:10831643
|
T | C | 1 | a0001c0001t0009 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*596T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 596 | chr19 | 10831643 | |||||
| chr19:10831648
|
C | T | 1 | a0001c0002t0011 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*601C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 601 | chr19 | 10831648 | |||||
| chr19:10831887
|
G | A | 1 | a0001c0002t0010 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*840G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 21/21 | 840 | chr19 | 10831887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10718525
|
C | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+122C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718525 | ||||||
| chr19:10718598
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161+195C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718598 | ||||||
| chr19:10718631
|
C | G | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+228C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718631 | ||||||
| chr19:10718647
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.161+244G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718647 | ||||||
| chr19:10718651
|
G | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161+248G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718651 | ||||||
| chr19:10718807
|
T | C | 20 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(17): Show | 20 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.161+404T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718807 | ||||||
| chr19:10718962
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+559C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10718962 | ||||||
| chr19:10719003
|
A | C | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.161+600A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10719003 | ||||||
| chr19:10719196
|
C | G | 3 | a0001c0002t0002g0259a0001c0002t0002g0260a0001c0002t0002g0261 | 3 | NA18975.hp1 NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.161+793C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10719196 | ||||||
| chr19:10719237
|
A | C | 1 | a0001c0001t0001g0258 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.161+834A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10719237 | ||||||
| chr19:10719605
|
G | T | 81 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(78): Show | 81 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.161+1202G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10719605 | ||||||
| chr19:10720087
|
C | T | 1 | a0001c0002t0002g0198 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.161+1684C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720087 | ||||||
| chr19:10720092
|
G | A | 51 | a0001c0001t0003g0088a0001c0001t0008g0087a0001c0002t0002g0042others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.161+1689G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720092 | ||||||
| chr19:10720134
|
T | C | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161+1731T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720134 | ||||||
| chr19:10720137
|
C | G | 1 | a0001c0001t0001g0257 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.161+1734C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720137 | ||||||
| chr19:10720147
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.161+1744G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720147 | ||||||
| chr19:10720212
|
A | T | 122 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(119): Show | 122 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.161+1809A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720212 | ||||||
| chr19:10720213
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.161+1810T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720213 | ||||||
| chr19:10720216
|
A | AT | 52 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.161+1827dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10720216 | |||||
| chr19:10720216
|
A | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+1813A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720216 | ||||||
| chr19:10720217
|
T | A | 1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+1814T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720217 | ||||||
| chr19:10720218
|
T | A | 2 | a0001c0001t0002g0091a0001c0002t0013g0263 | 2 | HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.161+1815T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720218 | ||||||
| chr19:10720219
|
T | TA | 26 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0005g0020others(23): Show | 26 | HG00423.hp2 HG00558.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.161+1816_161+1817i others(3): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720219 | ||||||
| chr19:10720220
|
T | A | 15 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+1817T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720220 | ||||||
| chr19:10720312
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161+1909A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720312 | ||||||
| chr19:10720314
|
G | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+1911G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720314 | ||||||
| chr19:10720522
|
C | G | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+2119C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720522 | ||||||
| chr19:10720679
|
G | A | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161+2276G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720679 | ||||||
| chr19:10720684
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+2281T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720684 | ||||||
| chr19:10720762
|
A | G | 2 | a0001c0001t0003g0088a0001c0002t0013g0263 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.161+2359A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720762 | ||||||
| chr19:10720799
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.161+2396G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720799 | ||||||
| chr19:10720997
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+2594T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10720997 | ||||||
| chr19:10721111
|
C | T | 3 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276 | 3 | HG02896.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161+2708C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721111 | ||||||
| chr19:10721125
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+2722G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721125 | ||||||
| chr19:10721305
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155 | 3 | HG02559.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.161+2902C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721305 | ||||||
| chr19:10721365
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+2962C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721365 | ||||||
| chr19:10721374
|
C | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+2971C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721374 | ||||||
| chr19:10721408
|
C | T | 2 | a0001c0002t0001g0147a0001c0002t0001g0148 | 2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.161+3005C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721408 | ||||||
| chr19:10721491
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.161+3088A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721491 | ||||||
| chr19:10721514
|
G | C | 13 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+3111G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721514 | ||||||
| chr19:10721515
|
G | A | 13 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+3112G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721515 | ||||||
| chr19:10721536
|
G | A | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161+3133G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721536 | ||||||
| chr19:10721549
|
T | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+3146T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721549 | ||||||
| chr19:10721629
|
G | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+3226G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721629 | ||||||
| chr19:10721672
|
G | C | 1 | a0001c0002t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.161+3269G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721672 | ||||||
| chr19:10721689
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161+3286G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721689 | ||||||
| chr19:10721794
|
G | A | 3 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003 | 3 | HG03239.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.161+3391G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721794 | ||||||
| chr19:10721830
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+3427C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721830 | ||||||
| chr19:10721884
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.161+3481G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10721884 | ||||||
| chr19:10722455
|
G | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+4052G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722455 | ||||||
| chr19:10722456
|
C | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+4053C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722456 | ||||||
| chr19:10722493
|
C | T | 6 | a0001c0001t0001g0253a0001c0002t0002g0270a0001c0002t0002g0271others(3): Show | 6 | HG00741.hp1 HG01934.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+4090C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722493 | ||||||
| chr19:10722501
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+4098C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722501 | ||||||
| chr19:10722627
|
G | A | 13 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+4224G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722627 | ||||||
| chr19:10722633
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+4230G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722633 | ||||||
| chr19:10722640
|
G | T | 2 | a0001c0002t0002g0046a0001c0002t0002g0047 | 2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.161+4237G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722640 | ||||||
| chr19:10722656
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161+4253T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722656 | ||||||
| chr19:10722856
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+4453G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722856 | ||||||
| chr19:10722919
|
G | A | 1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+4516G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10722919 | ||||||
| chr19:10723035
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.161+4632C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10723035 | ||||||
| chr19:10723132
|
A | AT | 38 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0040others(35): Show | 38 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.161+4748dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10723132 | |||||
| chr19:10723132
|
AT | A | 58 | a0001c0001t0001g0022a0001c0001t0001g0095a0001c0001t0001g0153others(55): Show | 58 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.161+4748delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10723132 | |||||
| chr19:10723175
|
C | T | 13 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+4772C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10723175 | ||||||
| chr19:10723277
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+4874G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10723277 | ||||||
| chr19:10723339
|
G | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+4936G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10723339 | ||||||
| chr19:10723428
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.161+5025C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10723428 | ||||||
| chr19:10723456
|
T | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.161+5053T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10723456 | ||||||
| chr19:10724083
|
C | CA | 9 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0156others(6): Show | 9 | HG01243.hp2 HG02074.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+5695dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10724083 | |||||
| chr19:10724083
|
CA | C | 7 | a0001c0001t0001g0256a0001c0001t0003g0189a0001c0001t0003g0190others(4): Show | 7 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+5695delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10724083 | |||||
| chr19:10724095
|
A | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+5692A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724095 | ||||||
| chr19:10724096
|
A | AAAAGGAG others(11): Show |
2 | a0001c0002t0002g0052a0001c0002t0002g0259 | 2 | HG00438.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.161+5695_161+5696i others(20): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10724096 | |||||
| chr19:10724096
|
A | AAAGGAGA others(10): Show |
88 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(85): Show | 88 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.161+5697_161+5698i others(19): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10724096 | |||||
| chr19:10724096
|
A | AAGGAGAA others(9): Show |
2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161+5694_161+5695i others(18): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10724096 | |||||
| chr19:10724128
|
A | C | 2 | a0001c0001t0001g0251a0001c0002t0001g0250 | 2 | HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.161+5725A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724128 | ||||||
| chr19:10724217
|
T | G | 1 | a0001c0002t0002g0005 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161+5814T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724217 | ||||||
| chr19:10724237
|
A | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+5834A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724237 | ||||||
| chr19:10724302
|
C | T | 1 | a0001c0002t0001g0099 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.161+5899C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724302 | ||||||
| chr19:10724351
|
G | A | 3 | a0001c0001t0002g0160a0001c0002t0001g0162a0001c0002t0002g0163 | 3 | HG02602.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.161+5948G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724351 | ||||||
| chr19:10724367
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.161+5964T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724367 | ||||||
| chr19:10724384
|
A | G | 1 | a0001c0002t0002g0083 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.161+5981A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724384 | ||||||
| chr19:10724536
|
C | T | 48 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0044others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.161+6133C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724536 | ||||||
| chr19:10724592
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.161+6189G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724592 | ||||||
| chr19:10724662
|
C | G | 125 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.161+6259C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724662 | ||||||
| chr19:10724729
|
C | T | 205 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(202): Show | 205 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.161+6326C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724729 | ||||||
| chr19:10724914
|
T | C | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+6511T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724914 | ||||||
| chr19:10724928
|
G | GA | 17 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(14): Show | 17 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+6526dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10724928 | |||||
| chr19:10724936
|
G | A | 32 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.161+6533G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724936 | ||||||
| chr19:10724944
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.161+6541G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724944 | ||||||
| chr19:10724963
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161+6560C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10724963 | ||||||
| chr19:10725267
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+6864G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725267 | ||||||
| chr19:10725290
|
A | G | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161+6887A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725290 | ||||||
| chr19:10725315
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161+6912G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725315 | ||||||
| chr19:10725386
|
C | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+6983C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725386 | ||||||
| chr19:10725445
|
C | CA | 16 | a0001c0001t0001g0210a0001c0001t0001g0264a0001c0001t0001g0268others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+7058dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10725445 | |||||
| chr19:10725445
|
CA | C | 22 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0258others(19): Show | 22 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.161+7058delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10725445 | |||||
| chr19:10725463
|
G | A | 1 | a0001c0002t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.161+7060G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725463 | ||||||
| chr19:10725604
|
G | C | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+7201G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725604 | ||||||
| chr19:10725653
|
A | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+7250A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725653 | ||||||
| chr19:10725714
|
C | A | 3 | a0001c0001t0001g0212a0001c0002t0002g0211a0001c0002t0002g0213 | 3 | HG02698.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.161+7311C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725714 | ||||||
| chr19:10725792
|
C | T | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161+7389C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725792 | ||||||
| chr19:10725869
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+7466T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725869 | ||||||
| chr19:10725925
|
A | C | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+7522A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725925 | ||||||
| chr19:10725929
|
A | C | 1 | a0001c0002t0002g0050 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.161+7526A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725929 | ||||||
| chr19:10725937
|
T | G | 1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161+7534T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725937 | ||||||
| chr19:10725957
|
A | C | 3 | a0001c0002t0002g0096a0001c0002t0002g0140a0001c0005t0002g0141 | 3 | HG00140.hp2 NA18942.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.161+7554A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10725957 | ||||||
| chr19:10726173
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7770C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726173 | ||||||
| chr19:10726175
|
T | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7772T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726175 | ||||||
| chr19:10726181
|
T | TGCAGTCC | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7781_161+7782i others(9): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10726181 | |||||
| chr19:10726185
|
C | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7782C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726185 | ||||||
| chr19:10726189
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7786A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726189 | ||||||
| chr19:10726213
|
T | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7810T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726213 | ||||||
| chr19:10726215
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7812C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726215 | ||||||
| chr19:10726218
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0016a0001c0002t0001g0003a0001c0002t0002g0017 | 3 | HG02135.hp1 HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.161+7827_161+7828i others(25): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10726218 | |||||
| chr19:10726218
|
C | CAAAAAAA others(17): Show |
10 | a0001c0001t0001g0010a0001c0002t0001g0001a0001c0002t0001g0002others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.161+7827_161+7828i others(26): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10726218 | |||||
| chr19:10726218
|
C | CAAAAAAA others(18): Show |
3 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009 | 3 | HG01516.hp2 HG01981.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.161+7827_161+7828i others(27): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10726218 | |||||
| chr19:10726218
|
C | CAAAAAAA others(20): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0007 | 2 | HG00423.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.161+7827_161+7828i others(29): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10726218 | |||||
| chr19:10726230
|
AT | A | 195 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(192): Show | 195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.161+7840delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10726230 | |||||
| chr19:10726231
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7828T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726231 | ||||||
| chr19:10726232
|
T | A | 2 | a0001c0002t0002g0008a0001c0002t0002g0009 | 2 | HG01516.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.161+7829T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726232 | ||||||
| chr19:10726348
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+7945G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726348 | ||||||
| chr19:10726354
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.161+7951C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726354 | ||||||
| chr19:10726368
|
C | G | 5 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0138others(2): Show | 5 | HG00323.hp1 HG01109.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+7965C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726368 | ||||||
| chr19:10726578
|
G | A | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+8175G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726578 | ||||||
| chr19:10726756
|
C | G | 1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161+8353C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726756 | ||||||
| chr19:10726769
|
C | T | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+8366C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726769 | ||||||
| chr19:10726849
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+8446C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726849 | ||||||
| chr19:10726926
|
C | T | 3 | a0001c0001t0002g0091a0001c0002t0002g0090a0001c0002t0010g0092 | 3 | HG02717.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161+8523C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10726926 | ||||||
| chr19:10727001
|
G | A | 126 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(123): Show | 126 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.161+8598G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727001 | ||||||
| chr19:10727032
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+8629C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727032 | ||||||
| chr19:10727059
|
G | T | 1 | a0001c0002t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.161+8656G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727059 | ||||||
| chr19:10727115
|
A | T | 1 | a0001c0001t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161+8712A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727115 | ||||||
| chr19:10727171
|
C | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+8768C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727171 | ||||||
| chr19:10727328
|
G | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+8925G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727328 | ||||||
| chr19:10727345
|
GTTTTC | G | 13 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+8957_161+8961d others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10727345 | |||||
| chr19:10727621
|
CG | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+9220delG | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10727621 | |||||
| chr19:10727645
|
C | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+9242C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727645 | ||||||
| chr19:10727667
|
G | T | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161+9264G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727667 | ||||||
| chr19:10727671
|
A | C | 1 | a0001c0002t0002g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.161+9268A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727671 | ||||||
| chr19:10727705
|
C | T | 16 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+9302C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727705 | ||||||
| chr19:10727755
|
G | A | 1 | a0001c0002t0002g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.161+9352G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727755 | ||||||
| chr19:10727810
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+9407G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10727810 | ||||||
| chr19:10728215
|
C | T | 1 | a0001c0002t0012g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+9812C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728215 | ||||||
| chr19:10728330
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.161+9927C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728330 | ||||||
| chr19:10728413
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+10010T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728413 | ||||||
| chr19:10728519
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+10116C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728519 | ||||||
| chr19:10728680
|
G | T | 2 | a0001c0004t0001g0014a0001c0004t0001g0015 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.161+10277G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728680 | ||||||
| chr19:10728710
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.161+10307G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728710 | ||||||
| chr19:10728771
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+10368G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728771 | ||||||
| chr19:10728818
|
T | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+10415T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10728818 | ||||||
| chr19:10728944
|
C | CA | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+10554dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10728944 | |||||
| chr19:10729045
|
A | G | 56 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(53): Show | 56 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.161+10642A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729045 | ||||||
| chr19:10729058
|
TAAAAATA others(120): Show |
T | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+10665_161+1079 others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729058 | |||||
| chr19:10729122
|
A | G | 243 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.161+10719A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729122 | ||||||
| chr19:10729164
|
C | CA | 46 | a0001c0001t0001g0039a0001c0001t0001g0095a0001c0001t0001g0101others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.161+10787dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729164 | |||||
| chr19:10729164
|
C | CAA | 92 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.161+10786_161+1078 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729164 | |||||
| chr19:10729164
|
C | CAAA | 65 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0156others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.161+10785_161+1078 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729164 | |||||
| chr19:10729164
|
C | CAAAA | 15 | a0001c0001t0001g0153a0001c0001t0001g0214a0001c0001t0001g0215others(12): Show | 15 | HG02015.hp1 HG02074.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+10784_161+1078 others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729164 | |||||
| chr19:10729164
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0200a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01175.hp1 HG01884.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+10778_161+1078 others(14): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729164 | |||||
| chr19:10729164
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0003g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.161+10771_161+1078 others(21): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729164 | |||||
| chr19:10729187
|
A | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+10784A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729187 | ||||||
| chr19:10729189
|
A | AAAT | 6 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0002t0002g0044others(3): Show | 6 | HG03209.hp2 NA18962.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+10787_161+1078 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10729189 | |||||
| chr19:10729189
|
A | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+10786A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729189 | ||||||
| chr19:10729191
|
T | A | 3 | a0001c0001t0001g0027a0001c0002t0001g0026a0001c0002t0002g0140 | 3 | HG00621.hp2 NA19030.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.161+10788T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729191 | ||||||
| chr19:10729241
|
C | T | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.161+10838C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729241 | ||||||
| chr19:10729257
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.161+10854G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729257 | ||||||
| chr19:10729259
|
G | T | 56 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(53): Show | 56 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.161+10856G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729259 | ||||||
| chr19:10729307
|
G | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+10904G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729307 | ||||||
| chr19:10729426
|
G | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+11023G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729426 | ||||||
| chr19:10729525
|
A | G | 123 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(120): Show | 123 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.161+11122A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729525 | ||||||
| chr19:10729582
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+11179G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729582 | ||||||
| chr19:10729637
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0174 | 2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+11234G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729637 | ||||||
| chr19:10729752
|
T | C | 220 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(217): Show | 220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.161+11349T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729752 | ||||||
| chr19:10729866
|
T | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+11463T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729866 | ||||||
| chr19:10729867
|
A | T | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+11464A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10729867 | ||||||
| chr19:10730031
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.161+11628G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730031 | ||||||
| chr19:10730373
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+11970T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730373 | ||||||
| chr19:10730410
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.161+12007T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730410 | ||||||
| chr19:10730478
|
C | CA | 88 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(85): Show | 88 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.161+12087dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10730478 | |||||
| chr19:10730512
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.161+12109G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730512 | ||||||
| chr19:10730516
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.161+12113A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730516 | ||||||
| chr19:10730523
|
T | C | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+12120T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730523 | ||||||
| chr19:10730706
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+12303G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730706 | ||||||
| chr19:10730796
|
T | C | 222 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(219): Show | 222 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.161+12393T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730796 | ||||||
| chr19:10730835
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161+12432G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730835 | ||||||
| chr19:10730908
|
C | T | 56 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(53): Show | 56 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.161+12505C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730908 | ||||||
| chr19:10730935
|
G | A | 2 | a0001c0002t0002g0063a0002c0006t0002g0056 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.161+12532G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10730935 | ||||||
| chr19:10731039
|
C | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+12636C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731039 | ||||||
| chr19:10731073
|
C | T | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161+12670C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731073 | ||||||
| chr19:10731091
|
A | C | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+12688A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731091 | ||||||
| chr19:10731176
|
C | T | 1 | a0001c0002t0002g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.161+12773C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731176 | ||||||
| chr19:10731178
|
G | A | 1 | a0001c0002t0002g0259 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.161+12775G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731178 | ||||||
| chr19:10731271
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+12868G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731271 | ||||||
| chr19:10731354
|
C | CT | 5 | a0001c0001t0001g0208a0001c0001t0001g0242a0001c0002t0002g0055others(2): Show | 5 | HG00408.hp1 HG01243.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+12968dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10731354 | |||||
| chr19:10731354
|
C | CTT | 50 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(47): Show | 50 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.161+12967_161+1296 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10731354 | |||||
| chr19:10731354
|
CT | C | 21 | a0001c0001t0001g0116a0001c0001t0001g0205a0001c0001t0001g0226others(18): Show | 21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.161+12968delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10731354 | |||||
| chr19:10731354
|
CTTT | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+12966_161+1296 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10731354 | |||||
| chr19:10731387
|
A | G | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+12984A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731387 | ||||||
| chr19:10731397
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161+12994G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731397 | ||||||
| chr19:10731403
|
G | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+13000G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731403 | ||||||
| chr19:10731518
|
A | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+13115A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731518 | ||||||
| chr19:10731534
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+13131A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731534 | ||||||
| chr19:10731585
|
C | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+13182C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731585 | ||||||
| chr19:10731709
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+13306G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731709 | ||||||
| chr19:10731791
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161+13388G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731791 | ||||||
| chr19:10731952
|
G | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+13549G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731952 | ||||||
| chr19:10731953
|
A | AT | 13 | a0001c0001t0001g0158a0001c0001t0002g0160a0001c0001t0002g0277others(10): Show | 13 | HG02280.hp1 HG02602.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.161+13568dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10731953 | |||||
| chr19:10731957
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+13554T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731957 | ||||||
| chr19:10731986
|
C | T | 3 | a0001c0002t0001g0104a0001c0002t0001g0132a0001c0002t0001g0133 | 3 | HG00438.hp2 NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.161+13583C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10731986 | ||||||
| chr19:10732040
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+13637C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732040 | ||||||
| chr19:10732048
|
A | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+13645A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732048 | ||||||
| chr19:10732057
|
C | G | 14 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+13654C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732057 | ||||||
| chr19:10732060
|
T | A | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+13657T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732060 | ||||||
| chr19:10732100
|
G | A | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.161+13697G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732100 | ||||||
| chr19:10732195
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.161+13792C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732195 | ||||||
| chr19:10732243
|
G | A | 2 | a0001c0001t0001g0251a0001c0002t0001g0250 | 2 | HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.161+13840G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732243 | ||||||
| chr19:10732244
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+13841C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732244 | ||||||
| chr19:10732299
|
G | GA | 31 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0039others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.161+13915dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10732299 | |||||
| chr19:10732299
|
GA | G | 8 | a0001c0001t0001g0159a0001c0001t0001g0202a0001c0001t0001g0251others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+13915delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10732299 | |||||
| chr19:10732299
|
GAAA | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+13913_161+1391 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10732299 | |||||
| chr19:10732299
|
GAAAA | G | 15 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0275others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+13912_161+1391 others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10732299 | |||||
| chr19:10732322
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.161+13919G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732322 | ||||||
| chr19:10732335
|
T | A | 55 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.161+13932T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732335 | ||||||
| chr19:10732375
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+13972C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732375 | ||||||
| chr19:10732380
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0002g0152 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.161+13977C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732380 | ||||||
| chr19:10732427
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.161+14024C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732427 | ||||||
| chr19:10732470
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.161+14067A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732470 | ||||||
| chr19:10732488
|
T | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276 | 3 | HG02896.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161+14085T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732488 | ||||||
| chr19:10732493
|
G | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+14090G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732493 | ||||||
| chr19:10732507
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.161+14104A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732507 | ||||||
| chr19:10732532
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.161+14129G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732532 | ||||||
| chr19:10732557
|
G | C | 2 | a0001c0001t0001g0251a0001c0002t0001g0250 | 2 | HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.161+14154G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732557 | ||||||
| chr19:10732571
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.161+14168G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732571 | ||||||
| chr19:10732652
|
G | C | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.161+14249G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732652 | ||||||
| chr19:10732707
|
TTA | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(17): Show | 20 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.161+14320_161+1432 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10732707 | |||||
| chr19:10732711
|
A | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+14308A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732711 | ||||||
| chr19:10732846
|
A | G | 19 | a0001c0002t0002g0043a0001c0002t0002g0052a0001c0002t0002g0054others(16): Show | 19 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.161+14443A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10732846 | ||||||
| chr19:10733008
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+14605C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733008 | ||||||
| chr19:10733161
|
A | G | 80 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(77): Show | 80 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.161+14758A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733161 | ||||||
| chr19:10733191
|
G | GT | 69 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0101others(66): Show | 69 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.161+14805dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10733191 | |||||
| chr19:10733191
|
G | GTT | 17 | a0001c0002t0001g0002a0001c0002t0002g0008a0001c0002t0002g0017others(14): Show | 17 | HG00438.hp1 HG01516.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+14804_161+1480 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10733191 | |||||
| chr19:10733191
|
GT | G | 124 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(121): Show | 124 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.161+14805delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10733191 | |||||
| chr19:10733432
|
A | ATCTGCCT others(9): Show |
1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+15032_161+1504 others(20): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10733432 | |||||
| chr19:10733515
|
G | A | 4 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276others(1): Show | 4 | HG02896.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+15112G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733515 | ||||||
| chr19:10733522
|
A | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.161+15119A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733522 | ||||||
| chr19:10733693
|
A | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0244others(2): Show | 5 | HG01884.hp1 HG01952.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+15290A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733693 | ||||||
| chr19:10733718
|
T | C | 3 | a0001c0002t0002g0053a0001c0002t0002g0083a0001c0002t0002g0086 | 3 | NA18963.hp2 NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.161+15315T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733718 | ||||||
| chr19:10733836
|
A | G | 1 | a0001c0007t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.161+15433A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10733836 | ||||||
| chr19:10734014
|
T | A | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+15611T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734014 | ||||||
| chr19:10734015
|
A | T | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.161+15612A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734015 | ||||||
| chr19:10734019
|
A | T | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.161+15616A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734019 | ||||||
| chr19:10734235
|
C | T | 14 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01099.hp1 NA18747.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+15832C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734235 | ||||||
| chr19:10734273
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.161+15870G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734273 | ||||||
| chr19:10734291
|
T | C | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+15888T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734291 | ||||||
| chr19:10734342
|
C | CAA | 75 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0040others(72): Show | 75 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.161+15954_161+1595 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734342 | |||||
| chr19:10734476
|
GA | G | 81 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(78): Show | 81 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.161+16086delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734476 | |||||
| chr19:10734598
|
C | T | 74 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.161+16195C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734598 | ||||||
| chr19:10734613
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(14): Show | 17 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+16210C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734613 | ||||||
| chr19:10734638
|
C | CA | 54 | a0001c0001t0001g0118a0001c0001t0001g0138a0001c0001t0001g0145others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.161+16258dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734638 | |||||
| chr19:10734638
|
C | CAA | 24 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.161+16257_161+1625 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734638 | |||||
| chr19:10734638
|
C | CAAA | 6 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0002g0011others(3): Show | 6 | HG02071.hp1 HG03492.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+16256_161+1625 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734638 | |||||
| chr19:10734638
|
CA | C | 126 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(123): Show | 126 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.161+16258delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734638 | |||||
| chr19:10734669
|
C | A | 1 | a0001c0002t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.161+16266C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734669 | ||||||
| chr19:10734714
|
TA | T | 5 | a0001c0002t0001g0104a0001c0002t0002g0059a0001c0002t0002g0081others(2): Show | 5 | HG01069.hp2 NA18986.hp1 NA19084.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+16320delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10734714 | |||||
| chr19:10734721
|
A | T | 1 | a0001c0002t0002g0069 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.161+16318A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734721 | ||||||
| chr19:10734722
|
A | T | 59 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0264others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.161+16319A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734722 | ||||||
| chr19:10734723
|
A | T | 81 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(78): Show | 81 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.161+16320A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734723 | ||||||
| chr19:10734741
|
G | A | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+16338G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734741 | ||||||
| chr19:10734825
|
G | A | 1 | a0001c0002t0002g0011 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.161+16422G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734825 | ||||||
| chr19:10734926
|
T | C | 1 | a0001c0002t0002g0078 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.161+16523T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734926 | ||||||
| chr19:10734948
|
G | A | 20 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(17): Show | 20 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.161+16545G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10734948 | ||||||
| chr19:10735019
|
G | C | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161+16616G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735019 | ||||||
| chr19:10735079
|
T | C | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+16676T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735079 | ||||||
| chr19:10735140
|
T | G | 80 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(77): Show | 80 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.161+16737T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735140 | ||||||
| chr19:10735182
|
T | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+16779T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735182 | ||||||
| chr19:10735201
|
C | T | 1 | a0001c0002t0012g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+16798C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735201 | ||||||
| chr19:10735277
|
A | T | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+16874A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735277 | ||||||
| chr19:10735316
|
G | A | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+16913G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735316 | ||||||
| chr19:10735617
|
G | A | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+17214G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735617 | ||||||
| chr19:10735635
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.161+17232G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735635 | ||||||
| chr19:10735670
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0193 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.161+17267C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735670 | ||||||
| chr19:10735708
|
G | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+17305G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735708 | ||||||
| chr19:10735789
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+17386C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735789 | ||||||
| chr19:10735802
|
C | T | 3 | a0001c0001t0001g0212a0001c0002t0002g0211a0001c0002t0002g0213 | 3 | HG02698.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.161+17399C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735802 | ||||||
| chr19:10735866
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0254 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.161+17463T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735866 | ||||||
| chr19:10735916
|
G | C | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.161+17513G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735916 | ||||||
| chr19:10735945
|
T | G | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+17542T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10735945 | ||||||
| chr19:10736140
|
C | T | 74 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.161+17737C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736140 | ||||||
| chr19:10736264
|
C | CA | 81 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(78): Show | 81 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.161+17876dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10736264 | |||||
| chr19:10736300
|
G | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+17897G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736300 | ||||||
| chr19:10736403
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.161+18000C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736403 | ||||||
| chr19:10736411
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+18008C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736411 | ||||||
| chr19:10736514
|
G | C | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+18111G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736514 | ||||||
| chr19:10736622
|
G | T | 220 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(217): Show | 220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.161+18219G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736622 | ||||||
| chr19:10736707
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.161+18304A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736707 | ||||||
| chr19:10736941
|
G | A | 1 | a0001c0002t0002g0085 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.161+18538G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736941 | ||||||
| chr19:10736990
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.161+18587A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10736990 | ||||||
| chr19:10737032
|
C | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+18629C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737032 | ||||||
| chr19:10737201
|
A | C | 1 | a0001c0007t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.161+18798A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737201 | ||||||
| chr19:10737205
|
G | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0244others(2): Show | 5 | HG01884.hp1 HG01952.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+18802G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737205 | ||||||
| chr19:10737291
|
T | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161+18888T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737291 | ||||||
| chr19:10737548
|
C | T | 12 | a0001c0001t0001g0268a0001c0002t0002g0144a0001c0002t0002g0265others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.161+19145C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737548 | ||||||
| chr19:10737579
|
G | A | 1 | a0001c0007t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.161+19176G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737579 | ||||||
| chr19:10737631
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.161+19228G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737631 | ||||||
| chr19:10737685
|
A | T | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+19282A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737685 | ||||||
| chr19:10737811
|
C | A | 1 | a0001c0002t0002g0163 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.161+19408C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737811 | ||||||
| chr19:10737846
|
G | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161+19443G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10737846 | ||||||
| chr19:10738132
|
C | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161+19729C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738132 | ||||||
| chr19:10738364
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+19961C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738364 | ||||||
| chr19:10738372
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.161+19969T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738372 | ||||||
| chr19:10738518
|
C | T | 124 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(121): Show | 124 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.161+20115C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738518 | ||||||
| chr19:10738626
|
T | C | 276 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.161+20223T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738626 | ||||||
| chr19:10738659
|
G | C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.161+20256G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738659 | ||||||
| chr19:10738737
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.161+20334G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738737 | ||||||
| chr19:10738812
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0275 | 2 | HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161+20409G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738812 | ||||||
| chr19:10738830
|
G | A | 76 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(73): Show | 76 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.161+20427G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738830 | ||||||
| chr19:10738839
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.161+20436C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738839 | ||||||
| chr19:10738870
|
C | CA | 43 | a0001c0001t0001g0010a0001c0001t0001g0150a0001c0001t0001g0151others(40): Show | 43 | HG00642.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.161+20483dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10738870 | |||||
| chr19:10738942
|
G | T | 1 | a0001c0002t0002g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.161+20539G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738942 | ||||||
| chr19:10738950
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161+20547C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10738950 | ||||||
| chr19:10739018
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.161+20615A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739018 | ||||||
| chr19:10739024
|
G | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+20621G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739024 | ||||||
| chr19:10739027
|
G | T | 73 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.161+20624G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739027 | ||||||
| chr19:10739057
|
C | G | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+20654C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739057 | ||||||
| chr19:10739177
|
A | G | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162-20561A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739177 | ||||||
| chr19:10739429
|
C | G | 140 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(137): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.162-20309C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739429 | ||||||
| chr19:10739432
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-20306G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739432 | ||||||
| chr19:10739559
|
G | T | 1 | a0001c0002t0012g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.162-20179G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739559 | ||||||
| chr19:10739573
|
G | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0007 | 2 | HG00423.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.162-20165G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739573 | ||||||
| chr19:10739625
|
G | A | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.162-20113G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739625 | ||||||
| chr19:10739711
|
C | G | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162-20027C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739711 | ||||||
| chr19:10739765
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155 | 3 | HG02559.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.162-19973G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739765 | ||||||
| chr19:10739785
|
G | A | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.162-19953G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739785 | ||||||
| chr19:10739859
|
CTCA | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0055others(4): Show | 7 | HG02896.hp1 HG03471.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-19878_162-1987 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739859 | ||||||
| chr19:10739859
|
CTCAA | C | 55 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.162-19878_162-1987 others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739859 | ||||||
| chr19:10739859
|
CTCAAA | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0002others(12): Show | 15 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.162-19878_162-1987 others(9): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10739859 | ||||||
| chr19:10739861
|
C | CA | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0041others(27): Show | 30 | HG00408.hp1 HG00642.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.162-19851dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10739861 | |||||
| chr19:10739861
|
CA | C | 9 | a0001c0001t0001g0138a0001c0001t0001g0220a0001c0001t0001g0227others(6): Show | 9 | HG01081.hp1 HG01358.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-19851delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10739861 | |||||
| chr19:10740032
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.162-19706C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740032 | ||||||
| chr19:10740381
|
G | GT | 11 | a0001c0001t0001g0039a0001c0001t0001g0193a0001c0001t0001g0201others(8): Show | 11 | HG01255.hp1 HG02155.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.162-19345dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10740381 | |||||
| chr19:10740389
|
T | TG | 72 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(69): Show | 72 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162-19349_162-1934 others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740389 | ||||||
| chr19:10740399
|
G | A | 1 | a0001c0002t0001g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.162-19339G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740399 | ||||||
| chr19:10740407
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.162-19331G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740407 | ||||||
| chr19:10740415
|
G | A | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.162-19323G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740415 | ||||||
| chr19:10740444
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.162-19294T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740444 | ||||||
| chr19:10740461
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162-19277C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740461 | ||||||
| chr19:10740520
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162-19218C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740520 | ||||||
| chr19:10740556
|
G | A | 79 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.162-19182G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740556 | ||||||
| chr19:10740672
|
C | T | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-19066C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740672 | ||||||
| chr19:10740736
|
C | G | 1 | a0001c0002t0002g0044 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.162-19002C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10740736 | ||||||
| chr19:10741073
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162-18665A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741073 | ||||||
| chr19:10741356
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0173 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.162-18382C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741356 | ||||||
| chr19:10741551
|
C | CT | 21 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0188others(18): Show | 21 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.162-18171dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10741551 | |||||
| chr19:10741574
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0242a0001c0001t0001g0257 | 3 | HG00408.hp1 NA18941.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.162-18164G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741574 | ||||||
| chr19:10741588
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155 | 3 | HG02559.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.162-18150C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741588 | ||||||
| chr19:10741589
|
G | A | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.162-18149G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741589 | ||||||
| chr19:10741662
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.162-18076G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741662 | ||||||
| chr19:10741693
|
G | A | 55 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0088others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.162-18045G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741693 | ||||||
| chr19:10741710
|
C | T | 5 | a0001c0001t0001g0268a0001c0002t0002g0265a0001c0002t0002g0266others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-18028C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741710 | ||||||
| chr19:10741715
|
A | G | 1 | a0001c0002t0002g0019 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.162-18023A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741715 | ||||||
| chr19:10741741
|
C | T | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-17997C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741741 | ||||||
| chr19:10741798
|
G | A | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-17940G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741798 | ||||||
| chr19:10741803
|
T | C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-17935T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741803 | ||||||
| chr19:10741858
|
C | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0240 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.162-17880C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10741858 | ||||||
| chr19:10741888
|
CCCTTCCT others(5): Show |
C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-17826_162-1781 others(16): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10741888 | |||||
| chr19:10741912
|
A | ACCTTCCT others(5): Show |
1 | a0001c0001t0001g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162-17822_162-1781 others(16): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10741912 | |||||
| chr19:10742032
|
T | A | 5 | a0001c0001t0001g0268a0001c0002t0002g0265a0001c0002t0002g0266others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-17706T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10742032 | ||||||
| chr19:10742270
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155 | 3 | HG02559.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.162-17468A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10742270 | ||||||
| chr19:10742359
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162-17379C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10742359 | ||||||
| chr19:10742488
|
T | A | 5 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0002g0277others(2): Show | 5 | HG02896.hp1 HG03471.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-17250T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10742488 | ||||||
| chr19:10742620
|
G | A | 120 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(117): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.162-17118G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10742620 | ||||||
| chr19:10742848
|
G | GGAAGAAG others(5): Show |
1 | a0001c0003t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.162-16888_162-1687 others(16): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10742848 | |||||
| chr19:10742913
|
C | CT | 12 | a0001c0001t0001g0038a0001c0001t0001g0108a0001c0001t0001g0145others(9): Show | 12 | HG00741.hp1 HG01261.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-16807dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10742913 | |||||
| chr19:10742913
|
CT | C | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.162-16807delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10742913 | |||||
| chr19:10743075
|
G | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-16663G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743075 | ||||||
| chr19:10743149
|
G | A | 48 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0044others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.162-16589G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743149 | ||||||
| chr19:10743201
|
C | T | 54 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.162-16537C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743201 | ||||||
| chr19:10743227
|
G | A | 1 | a0001c0002t0002g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.162-16511G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743227 | ||||||
| chr19:10743301
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0193 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.162-16437C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743301 | ||||||
| chr19:10743410
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.162-16328C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743410 | ||||||
| chr19:10743473
|
G | A | 1 | a0001c0002t0001g0132 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.162-16265G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743473 | ||||||
| chr19:10743606
|
C | G | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.162-16132C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743606 | ||||||
| chr19:10743665
|
C | T | 10 | a0001c0001t0001g0268a0001c0002t0002g0265a0001c0002t0002g0266others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-16073C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743665 | ||||||
| chr19:10743669
|
G | T | 10 | a0001c0001t0001g0268a0001c0002t0002g0265a0001c0002t0002g0266others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-16069G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743669 | ||||||
| chr19:10743759
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.162-15979G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743759 | ||||||
| chr19:10743809
|
C | CA | 47 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0123others(44): Show | 47 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.162-15901dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10743809 | |||||
| chr19:10743809
|
CA | C | 109 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(106): Show | 109 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.162-15901delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10743809 | |||||
| chr19:10743843
|
C | A | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-15895C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743843 | ||||||
| chr19:10743860
|
G | A | 49 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0044others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.162-15878G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743860 | ||||||
| chr19:10743985
|
AG | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0002g0277others(61): Show | 64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.162-15752delG | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743985 | ||||||
| chr19:10743986
|
G | A | 12 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0275others(9): Show | 12 | HG00639.hp1 HG01928.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.162-15752G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10743986 | ||||||
| chr19:10744090
|
G | A | 73 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.162-15648G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744090 | ||||||
| chr19:10744156
|
T | TA | 61 | a0001c0001t0001g0113a0001c0001t0001g0153a0001c0001t0001g0154others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.162-15568dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10744156 | |||||
| chr19:10744238
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.162-15500T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744238 | ||||||
| chr19:10744239
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.162-15499G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744239 | ||||||
| chr19:10744492
|
C | T | 1 | a0001c0001t0003g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162-15246C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744492 | ||||||
| chr19:10744496
|
T | C | 2 | a0001c0001t0002g0091a0001c0002t0002g0090 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.162-15242T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744496 | ||||||
| chr19:10744625
|
C | A | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-15113C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744625 | ||||||
| chr19:10744744
|
G | A | 3 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273 | 3 | HG02615.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162-14994G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744744 | ||||||
| chr19:10744816
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(14): Show | 17 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.162-14922T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744816 | ||||||
| chr19:10744879
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162-14859C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10744879 | ||||||
| chr19:10745052
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.162-14686C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745052 | ||||||
| chr19:10745060
|
A | G | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-14678A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745060 | ||||||
| chr19:10745105
|
A | C | 139 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.162-14633A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745105 | ||||||
| chr19:10745142
|
G | GA | 9 | a0001c0001t0001g0145a0001c0001t0001g0158a0001c0001t0001g0209others(6): Show | 9 | HG01928.hp1 HG01978.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.162-14588dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10745142 | |||||
| chr19:10745174
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0002g0152 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.162-14564C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745174 | ||||||
| chr19:10745412
|
G | T | 4 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276others(1): Show | 4 | HG02896.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-14326G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745412 | ||||||
| chr19:10745449
|
A | G | 1 | a0001c0002t0002g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.162-14289A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745449 | ||||||
| chr19:10745463
|
G | T | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-14275G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745463 | ||||||
| chr19:10745556
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.162-14182G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745556 | ||||||
| chr19:10745584
|
C | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.162-14154C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745584 | ||||||
| chr19:10745597
|
T | C | 220 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(217): Show | 220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.162-14141T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745597 | ||||||
| chr19:10745742
|
C | T | 139 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.162-13996C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745742 | ||||||
| chr19:10745802
|
A | T | 53 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.162-13936A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745802 | ||||||
| chr19:10745983
|
C | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-13755C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10745983 | ||||||
| chr19:10746057
|
C | G | 3 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276 | 3 | HG02896.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162-13681C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746057 | ||||||
| chr19:10746069
|
G | A | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162-13669G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746069 | ||||||
| chr19:10746167
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.162-13571G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746167 | ||||||
| chr19:10746301
|
G | T | 1 | a0001c0002t0002g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.162-13437G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746301 | ||||||
| chr19:10746373
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.162-13365C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746373 | ||||||
| chr19:10746569
|
A | G | 1 | a0001c0002t0002g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.162-13169A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746569 | ||||||
| chr19:10746618
|
C | G | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-13120C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746618 | ||||||
| chr19:10746645
|
C | T | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-13093C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746645 | ||||||
| chr19:10746662
|
T | C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-13076T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746662 | ||||||
| chr19:10746725
|
TTG | T | 53 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.162-13011_162-1301 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10746725 | |||||
| chr19:10746727
|
G | GT | 105 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(102): Show | 105 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.162-13005dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10746727 | |||||
| chr19:10746727
|
G | GTT | 19 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0159others(16): Show | 19 | HG00642.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.162-13006_162-1300 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10746727 | |||||
| chr19:10746727
|
G | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0039others(2): Show | 5 | HG02615.hp1 HG04204.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-13011G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746727 | ||||||
| chr19:10746727
|
GTTTTTTG others(3): Show |
G | 1 | a0001c0002t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162-13004_162-1299 others(14): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10746727 | |||||
| chr19:10746731
|
T | G | 51 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(48): Show | 51 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.162-13007T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746731 | ||||||
| chr19:10746731
|
TTTG | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(19): Show | 22 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-13004_162-1300 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10746731 | |||||
| chr19:10746734
|
G | T | 139 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.162-13004G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746734 | ||||||
| chr19:10746734
|
GT | G | 53 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.162-12990delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10746734 | |||||
| chr19:10746735
|
T | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0264others(19): Show | 22 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-13003T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746735 | ||||||
| chr19:10746737
|
T | G | 2 | a0001c0002t0002g0065a0001c0002t0012g0149 | 2 | HG02622.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.162-13001T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746737 | ||||||
| chr19:10746738
|
T | G | 53 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.162-13000T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746738 | ||||||
| chr19:10746741
|
T | G | 2 | a0001c0002t0002g0042a0001c0002t0002g0057 | 2 | HG01928.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.162-12997T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746741 | ||||||
| chr19:10746760
|
A | G | 1 | a0001c0002t0002g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.162-12978A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746760 | ||||||
| chr19:10746860
|
T | C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-12878T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746860 | ||||||
| chr19:10746891
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.162-12847C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10746891 | ||||||
| chr19:10747038
|
A | AT | 9 | a0001c0001t0001g0221a0001c0001t0001g0253a0001c0001t0002g0091others(6): Show | 9 | HG00741.hp1 HG01261.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-12684dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10747038 | |||||
| chr19:10747038
|
AT | A | 5 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0002t0001g0089others(2): Show | 5 | HG02015.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-12684delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10747038 | |||||
| chr19:10747310
|
C | G | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-12428C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10747310 | ||||||
| chr19:10747349
|
C | T | 1 | a0001c0002t0002g0130 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-12389C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10747349 | ||||||
| chr19:10747923
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162-11815A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10747923 | ||||||
| chr19:10748468
|
G | A | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0169others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-11270G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10748468 | ||||||
| chr19:10748474
|
T | C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-11264T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10748474 | ||||||
| chr19:10748832
|
G | A | 52 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0003g0155others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.162-10906G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10748832 | ||||||
| chr19:10749127
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.162-10611G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749127 | ||||||
| chr19:10749140
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162-10598G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749140 | ||||||
| chr19:10749315
|
A | G | 1 | a0001c0002t0001g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.162-10423A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749315 | ||||||
| chr19:10749439
|
C | G | 3 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276 | 3 | HG02896.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162-10299C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749439 | ||||||
| chr19:10749539
|
T | A | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-10199T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749539 | ||||||
| chr19:10749539
|
T | C | 146 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.162-10199T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749539 | ||||||
| chr19:10749610
|
C | T | 5 | a0001c0002t0002g0058a0001c0002t0002g0065a0001c0002t0002g0066others(2): Show | 5 | HG00639.hp1 HG02293.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-10128C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749610 | ||||||
| chr19:10749729
|
C | A | 18 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0207others(15): Show | 18 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.162-10009C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749729 | ||||||
| chr19:10749810
|
G | A | 12 | a0001c0001t0001g0268a0001c0002t0002g0144a0001c0002t0002g0265others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-9928G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749810 | ||||||
| chr19:10749833
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.162-9905T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749833 | ||||||
| chr19:10749925
|
C | T | 2 | a0001c0002t0006g0161a0001c0002t0006g0165 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.162-9813C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749925 | ||||||
| chr19:10749978
|
G | A | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-9760G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10749978 | ||||||
| chr19:10750055
|
G | A | 3 | a0001c0001t0001g0215a0001c0002t0001g0218a0001c0002t0001g0247 | 3 | HG02074.hp1 HG02135.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.162-9683G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750055 | ||||||
| chr19:10750244
|
C | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-9494C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750244 | ||||||
| chr19:10750453
|
T | C | 1 | a0001c0002t0002g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.162-9285T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750453 | ||||||
| chr19:10750461
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.162-9277A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750461 | ||||||
| chr19:10750479
|
T | TA | 6 | a0001c0001t0001g0032a0001c0001t0003g0088a0001c0002t0002g0052others(3): Show | 6 | HG00438.hp1 HG00597.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-9247dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10750479 | |||||
| chr19:10750658
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.162-9080C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750658 | ||||||
| chr19:10750668
|
T | C | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-9070T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750668 | ||||||
| chr19:10750692
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-9046C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750692 | ||||||
| chr19:10750705
|
T | C | 223 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(220): Show | 223 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.162-9033T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750705 | ||||||
| chr19:10750762
|
C | T | 4 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276others(1): Show | 4 | HG02896.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-8976C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750762 | ||||||
| chr19:10750847
|
G | A | 1 | a0001c0002t0002g0019 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.162-8891G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750847 | ||||||
| chr19:10750858
|
G | A | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162-8880G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10750858 | ||||||
| chr19:10750900
|
CA | C | 76 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(73): Show | 76 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.162-8825delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10750900 | |||||
| chr19:10751004
|
CTG | C | 6 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-8727_162-8726d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10751004 | |||||
| chr19:10751124
|
G | C | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-8614G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751124 | ||||||
| chr19:10751315
|
G | T | 1 | a0001c0007t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.162-8423G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751315 | ||||||
| chr19:10751360
|
G | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.162-8378G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751360 | ||||||
| chr19:10751816
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.162-7922G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751816 | ||||||
| chr19:10751825
|
C | G | 15 | a0001c0002t0001g0099a0001c0002t0001g0104a0001c0002t0001g0107others(12): Show | 15 | HG00438.hp2 HG00673.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.162-7913C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751825 | ||||||
| chr19:10751940
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162-7798A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751940 | ||||||
| chr19:10751967
|
T | C | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-7771T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10751967 | ||||||
| chr19:10752242
|
G | T | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.162-7496G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10752242 | ||||||
| chr19:10752247
|
T | G | 14 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01099.hp1 NA18747.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.162-7491T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10752247 | ||||||
| chr19:10752440
|
C | T | 1 | a0001c0001t0008g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.162-7298C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10752440 | ||||||
| chr19:10753089
|
A | C | 49 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0044others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.162-6649A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753089 | ||||||
| chr19:10753164
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.162-6574T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753164 | ||||||
| chr19:10753200
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.162-6538A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753200 | ||||||
| chr19:10753388
|
TC | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(74): Show | 77 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.162-6344delC | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10753388 | |||||
| chr19:10753407
|
T | TC | 19 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0036others(16): Show | 19 | HG00438.hp2 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.162-6322dupC | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10753407 | |||||
| chr19:10753407
|
TC | T | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.162-6322delC | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10753407 | |||||
| chr19:10753521
|
CACTT | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0002t0001g0001others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.162-6215_162-6212d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10753521 | |||||
| chr19:10753548
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.162-6190A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753548 | ||||||
| chr19:10753713
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-6025A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753713 | ||||||
| chr19:10753936
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162-5802C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753936 | ||||||
| chr19:10753975
|
G | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0002t0002g0276 | 3 | HG02896.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162-5763G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10753975 | ||||||
| chr19:10754102
|
G | A | 78 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0153others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.162-5636G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754102 | ||||||
| chr19:10754250
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.162-5488C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754250 | ||||||
| chr19:10754259
|
C | CT | 11 | a0001c0001t0001g0031a0001c0001t0001g0145a0001c0001t0001g0220others(8): Show | 11 | HG00140.hp2 HG01175.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.162-5464dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10754259 | |||||
| chr19:10754259
|
CT | C | 9 | a0001c0001t0001g0151a0001c0001t0001g0191a0001c0001t0001g0214others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.162-5464delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10754259 | |||||
| chr19:10754280
|
G | T | 136 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(133): Show | 136 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.162-5458G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754280 | ||||||
| chr19:10754365
|
G | A | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.162-5373G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754365 | ||||||
| chr19:10754498
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.162-5240G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754498 | ||||||
| chr19:10754628
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-5110T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754628 | ||||||
| chr19:10754647
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.162-5091C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754647 | ||||||
| chr19:10754714
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.162-5024C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754714 | ||||||
| chr19:10754780
|
CAG | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0153a0001c0001t0001g0154others(73): Show | 76 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.162-4957_162-4956d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754780 | ||||||
| chr19:10754840
|
C | T | 53 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.162-4898C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754840 | ||||||
| chr19:10754999
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.162-4739C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10754999 | ||||||
| chr19:10755047
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.162-4691C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755047 | ||||||
| chr19:10755171
|
A | C | 1 | a0001c0002t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.162-4567A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755171 | ||||||
| chr19:10755221
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.162-4517A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755221 | ||||||
| chr19:10755232
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162-4506C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755232 | ||||||
| chr19:10755254
|
T | A | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.162-4484T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755254 | ||||||
| chr19:10755271
|
A | G | 4 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0013g0263others(1): Show | 4 | HG02738.hp1 HG03942.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-4467A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755271 | ||||||
| chr19:10755439
|
G | A | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0002t0010g0092 | 3 | HG02257.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.162-4299G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755439 | ||||||
| chr19:10755466
|
C | CT | 132 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(129): Show | 132 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.162-4258dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10755466 | |||||
| chr19:10755466
|
C | CTT | 9 | a0001c0001t0001g0175a0001c0001t0003g0164a0001c0001t0003g0189others(6): Show | 9 | HG01099.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.162-4259_162-4258d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10755466 | |||||
| chr19:10755563
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0002g0152 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.162-4175C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755563 | ||||||
| chr19:10755621
|
C | T | 3 | a0001c0002t0002g0048a0001c0002t0002g0096a0001c0005t0002g0141 | 3 | HG00140.hp2 HG03139.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.162-4117C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755621 | ||||||
| chr19:10755629
|
G | GT | 9 | a0001c0001t0001g0032a0001c0001t0002g0222a0001c0002t0001g0003others(6): Show | 9 | HG00597.hp2 HG01261.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.162-4100dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10755629 | |||||
| chr19:10755641
|
C | CT | 5 | a0001c0001t0001g0145a0001c0002t0002g0273a0001c0002t0006g0161others(2): Show | 5 | HG00140.hp2 HG01981.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-4086dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10755641 | |||||
| chr19:10755641
|
CT | C | 5 | a0001c0002t0001g0162a0001c0002t0002g0084a0001c0002t0002g0163others(2): Show | 5 | HG02738.hp1 HG03942.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-4086delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10755641 | |||||
| chr19:10755656
|
T | G | 2 | a0001c0002t0002g0140a0001c0002t0010g0092 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.162-4082T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755656 | ||||||
| chr19:10755756
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.162-3982C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755756 | ||||||
| chr19:10755788
|
C | T | 5 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0002t0002g0272others(2): Show | 5 | HG01934.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-3950C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755788 | ||||||
| chr19:10755915
|
T | C | 221 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(218): Show | 221 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.162-3823T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755915 | ||||||
| chr19:10755939
|
T | C | 221 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(218): Show | 221 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.162-3799T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10755939 | ||||||
| chr19:10756013
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.162-3725A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756013 | ||||||
| chr19:10756088
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.162-3650G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756088 | ||||||
| chr19:10756212
|
T | C | 70 | a0001c0001t0001g0016a0001c0001t0001g0153a0001c0001t0001g0154others(67): Show | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.162-3526T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756212 | ||||||
| chr19:10756267
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.162-3471A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756267 | ||||||
| chr19:10756367
|
A | T | 1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-3371A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756367 | ||||||
| chr19:10756451
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0008g0087 | 3 | HG01081.hp2 HG01928.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.162-3287C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756451 | ||||||
| chr19:10756543
|
G | A | 222 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(219): Show | 222 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.162-3195G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756543 | ||||||
| chr19:10756772
|
G | A | 153 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.162-2966G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756772 | ||||||
| chr19:10756795
|
T | A | 4 | a0001c0002t0001g0099a0001c0002t0001g0115a0001c0002t0001g0119others(1): Show | 4 | HG02040.hp2 NA18952.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-2943T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756795 | ||||||
| chr19:10756841
|
G | C | 203 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(200): Show | 203 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.162-2897G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756841 | ||||||
| chr19:10756875
|
C | T | 1 | a0001c0002t0001g0007 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.162-2863C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756875 | ||||||
| chr19:10756926
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.162-2812T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756926 | ||||||
| chr19:10756940
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.162-2798C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756940 | ||||||
| chr19:10756985
|
G | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.162-2753G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10756985 | ||||||
| chr19:10757165
|
C | T | 2 | a0001c0002t0002g0048a0001c0002t0002g0090 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.162-2573C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757165 | ||||||
| chr19:10757176
|
G | T | 142 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(139): Show | 142 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.162-2562G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757176 | ||||||
| chr19:10757179
|
C | T | 1 | a0001c0002t0004g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.162-2559C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757179 | ||||||
| chr19:10757258
|
CTTG | C | 10 | a0001c0001t0001g0110a0001c0001t0001g0136a0001c0001t0001g0139others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.162-2475_162-2473d others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10757258 | |||||
| chr19:10757324
|
C | T | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.162-2414C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757324 | ||||||
| chr19:10757347
|
G | T | 3 | a0001c0001t0001g0212a0001c0002t0002g0211a0001c0002t0002g0213 | 3 | HG02698.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.162-2391G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757347 | ||||||
| chr19:10757372
|
C | A | 1 | a0001c0002t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.162-2366C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757372 | ||||||
| chr19:10757557
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.162-2181G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757557 | ||||||
| chr19:10757583
|
T | A | 95 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0102others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.162-2155T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757583 | ||||||
| chr19:10757617
|
C | T | 1 | a0001c0002t0002g0044 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.162-2121C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757617 | ||||||
| chr19:10757741
|
G | C | 51 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0043others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.162-1997G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757741 | ||||||
| chr19:10757827
|
C | A | 1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-1911C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757827 | ||||||
| chr19:10757860
|
G | A | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.162-1878G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757860 | ||||||
| chr19:10757869
|
C | T | 14 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(11): Show | 14 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.162-1869C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757869 | ||||||
| chr19:10757881
|
T | G | 13 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(10): Show | 13 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1857T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757881 | ||||||
| chr19:10757943
|
C | CA | 71 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0040others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.162-1773dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10757943 | |||||
| chr19:10757943
|
C | CAA | 13 | a0001c0001t0001g0150a0001c0001t0002g0152a0001c0002t0002g0043others(10): Show | 13 | HG02145.hp2 HG02451.hp1 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.162-1774_162-1773d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10757943 | |||||
| chr19:10757943
|
C | CAAA | 6 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0002g0277others(3): Show | 6 | HG00323.hp1 HG02738.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-1775_162-1773d others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10757943 | |||||
| chr19:10757960
|
A | G | 7 | a0001c0001t0001g0174a0001c0001t0001g0192a0001c0001t0001g0275others(4): Show | 7 | HG00140.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-1778A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757960 | ||||||
| chr19:10757962
|
A | G | 1 | a0001c0002t0002g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-1776A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10757962 | ||||||
| chr19:10758190
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.162-1548T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758190 | ||||||
| chr19:10758267
|
CTCCTTCC others(61): Show |
C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.162-1467_162-1400d others(70): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758267 | |||||
| chr19:10758283
|
C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1455C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758283 | ||||||
| chr19:10758291
|
T | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1447T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758291 | ||||||
| chr19:10758299
|
C | T | 19 | a0001c0002t0002g0004a0001c0002t0002g0043a0001c0002t0002g0052others(16): Show | 19 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.162-1439C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758299 | ||||||
| chr19:10758307
|
C | T | 14 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(11): Show | 14 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.162-1431C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758307 | ||||||
| chr19:10758327
|
C | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(12): Show | 15 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.162-1411C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758327 | ||||||
| chr19:10758331
|
T | TTCCCTCC others(457): Show |
1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162-1404_162-1403i others(466): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758331 | |||||
| chr19:10758331
|
T | TTCCTTCC others(361): Show |
3 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273 | 3 | HG02615.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162-1396_162-1395i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758331 | |||||
| chr19:10758335
|
T | C | 30 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(27): Show | 30 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.162-1403T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758335 | ||||||
| chr19:10758343
|
T | C | 3 | a0001c0001t0002g0277a0001c0002t0002g0004a0001c0002t0002g0140 | 3 | HG02257.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1395T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758343 | ||||||
| chr19:10758343
|
T | TTCCCTCC others(289): Show |
1 | a0001c0001t0001g0230 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-1392_162-1391i others(298): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758343 | |||||
| chr19:10758343
|
T | TTCCTTCC others(361): Show |
1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758343 | |||||
| chr19:10758343
|
T | TTCCTTCC others(17): Show |
17 | a0001c0002t0002g0043a0001c0002t0002g0052a0001c0002t0002g0054others(14): Show | 17 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.162-1384_162-1383i others(26): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758343 | |||||
| chr19:10758351
|
C | T | 3 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273 | 3 | HG02615.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162-1387C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758351 | ||||||
| chr19:10758359
|
T | C | 3 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273 | 3 | HG02615.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162-1379T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758359 | ||||||
| chr19:10758359
|
TTCCTTCC others(57): Show |
T | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1363_162-1300d others(66): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758359 | |||||
| chr19:10758363
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-1375T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758363 | ||||||
| chr19:10758363
|
T | TTCCCTCC others(361): Show |
1 | a0001c0001t0001g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(389): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0173 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(398): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(361): Show |
1 | a0001c0001t0001g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(361): Show |
1 | a0001c0001t0001g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(361): Show |
2 | a0001c0002t0001g0147a0001c0002t0001g0148 | 2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(361): Show |
104 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(101): Show | 104 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(377): Show |
1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(365): Show |
2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(374): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(377): Show |
1 | a0001c0001t0001g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(376): Show |
1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(385): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758363
|
T | TTCCCTCC others(357): Show |
1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(366): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758363 | |||||
| chr19:10758371
|
C | CTCCT | 5 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp1 HG01109.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-1363_162-1360d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758371 | |||||
| chr19:10758371
|
C | CTCCTTCC others(353): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191 | 3 | HG02559.hp2 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(362): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758371 | |||||
| chr19:10758379
|
C | T | 12 | a0001c0001t0001g0150a0001c0001t0002g0152a0001c0002t0001g0162others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.162-1359C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758379 | ||||||
| chr19:10758387
|
T | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.162-1351T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758387 | ||||||
| chr19:10758391
|
T | C | 1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162-1347T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758391 | ||||||
| chr19:10758395
|
C | CTCCT | 6 | a0001c0001t0001g0150a0001c0001t0002g0152a0001c0002t0002g0063others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-1335_162-1332d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758395 | |||||
| chr19:10758395
|
C | T | 1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162-1343C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758395 | ||||||
| chr19:10758403
|
T | TTCCC | 4 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(1): Show | 4 | HG02615.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-1331_162-1328d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(377): Show |
3 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0002g0011 | 3 | HG00423.hp2 HG00558.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(361): Show |
1 | a0001c0001t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(370): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(309): Show |
1 | a0001c0002t0002g0261 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(318): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(377): Show |
1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(849): Show |
1 | a0001c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(858): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(381): Show |
2 | a0001c0002t0006g0161a0001c0002t0006g0165 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(390): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(377): Show |
1 | a0001c0001t0002g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(365): Show |
2 | a0001c0002t0002g0008a0001c0002t0002g0009 | 2 | HG01516.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.162-1332_162-1331i others(374): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(377): Show |
1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(377): Show |
11 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0002g0012others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.162-1332_162-1331i others(386): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(393): Show |
1 | a0001c0002t0002g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(402): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758403
|
T | TTCCTTCC others(393): Show |
1 | a0001c0002t0002g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162-1332_162-1331i others(402): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758403 | |||||
| chr19:10758407
|
C | T | 94 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.162-1331C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758407 | ||||||
| chr19:10758411
|
T | C | 94 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.162-1327T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758411 | ||||||
| chr19:10758419
|
C | CTCCCTCC others(345): Show |
1 | a0001c0001t0001g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.162-1308_162-1307i others(354): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758419 | |||||
| chr19:10758419
|
C | CTCCCTCC others(349): Show |
1 | a0001c0002t0001g0109 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.162-1308_162-1307i others(358): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758419 | |||||
| chr19:10758419
|
C | CTCCCTCC others(321): Show |
51 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.162-1308_162-1307i others(330): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758419 | |||||
| chr19:10758419
|
C | CTCCCTCC others(325): Show |
1 | a0001c0002t0002g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.162-1308_162-1307i others(334): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758419 | |||||
| chr19:10758419
|
C | CTCCCTCC others(320): Show |
1 | a0001c0002t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.162-1308_162-1307i others(329): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758419 | |||||
| chr19:10758419
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(3): Show | 6 | HG00323.hp1 HG01109.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-1319C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758419 | ||||||
| chr19:10758423
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0002g0152 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.162-1315C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758423 | ||||||
| chr19:10758431
|
C | T | 227 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(224): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.162-1307C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758431 | ||||||
| chr19:10758435
|
C | CTCCCTCC others(317): Show |
2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.162-1292_162-1291i others(326): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(330): Show |
1 | a0001c0002t0002g0074 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.162-1292_162-1291i others(339): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(329): Show |
3 | a0001c0002t0002g0051a0001c0002t0002g0082a0001c0002t0011g0079 | 3 | NA18947.hp1 NA18962.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.162-1292_162-1291i others(338): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(329): Show |
27 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0044others(24): Show | 27 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.162-1292_162-1291i others(338): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(329): Show |
1 | a0001c0001t0001g0251 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162-1292_162-1291i others(338): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(317): Show |
1 | a0001c0002t0002g0005 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.162-1292_162-1291i others(326): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(305): Show |
2 | a0001c0002t0001g0002a0001c0002t0001g0247 | 2 | HG02074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.162-1292_162-1291i others(314): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(310): Show |
1 | a0001c0002t0002g0078 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.162-1276_162-1275i others(319): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(261): Show |
13 | a0001c0002t0002g0043a0001c0002t0002g0054a0001c0002t0002g0055others(10): Show | 13 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1260_162-1259i others(270): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCCTCC others(309): Show |
1 | a0001c0002t0002g0052 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-1260_162-1259i others(318): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCTTCC others(456): Show |
1 | a0001c0001t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162-1300_162-1299i others(465): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCTTCC others(468): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0139 | 3 | HG00323.hp1 HG01109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.162-1300_162-1299i others(477): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCTTCC others(464): Show |
1 | a0001c0001t0002g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-1300_162-1299i others(473): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758435
|
C | CTCCTTCC others(452): Show |
1 | a0001c0001t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.162-1300_162-1299i others(461): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758435 | |||||
| chr19:10758439
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.162-1299C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758439 | ||||||
| chr19:10758443
|
T | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(3): Show | 6 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-1295T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758443 | ||||||
| chr19:10758443
|
T | TTCCTTCC others(452): Show |
1 | a0001c0002t0002g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.162-1284_162-1283i others(461): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758443 | |||||
| chr19:10758443
|
T | TTCCTTCC others(452): Show |
1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162-1284_162-1283i others(461): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758443 | |||||
| chr19:10758443
|
T | TTCCTTCC others(460): Show |
1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-1284_162-1283i others(469): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758443 | |||||
| chr19:10758443
|
T | TTCCTTCC others(464): Show |
1 | a0001c0002t0002g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162-1284_162-1283i others(473): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758443 | |||||
| chr19:10758443
|
T | TTCCTTCC others(464): Show |
1 | a0001c0002t0012g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.162-1284_162-1283i others(473): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758443 | |||||
| chr19:10758447
|
T | CTCCCTCC others(365): Show |
1 | a0001c0001t0001g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.162-1292_162-1291i others(374): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758447 | ||||||
| chr19:10758451
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.162-1287C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758451 | ||||||
| chr19:10758459
|
T | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1279T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758459 | ||||||
| chr19:10758463
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162-1275T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758463 | ||||||
| chr19:10758467
|
C | CTCCTTCC others(480): Show |
2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.162-1268_162-1267i others(489): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758467 | |||||
| chr19:10758467
|
C | T | 11 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(8): Show | 11 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.162-1271C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758467 | ||||||
| chr19:10758469
|
C | CCCTCCTT others(260): Show |
1 | a0001c0002t0002g0059 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.162-1260_162-1259i others(269): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758469 | |||||
| chr19:10758487
|
C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1251C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758487 | ||||||
| chr19:10758494
|
C | A | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1244C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758494 | ||||||
| chr19:10758496
|
T | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.162-1242T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758496 | ||||||
| chr19:10758496
|
T | TCCTC | 13 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(10): Show | 13 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1239_162-1238i others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758496 | |||||
| chr19:10758498
|
CTTCCTCC others(2): Show |
C | 16 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(13): Show | 16 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.162-1220_162-1212d others(11): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10758498 | |||||
| chr19:10758538
|
C | T | 1 | a0001c0002t0001g0099 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.162-1200C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758538 | ||||||
| chr19:10758586
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.162-1152G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758586 | ||||||
| chr19:10758664
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.162-1074A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758664 | ||||||
| chr19:10758790
|
G | A | 1 | a0001c0002t0002g0096 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.162-948G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758790 | ||||||
| chr19:10758899
|
C | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162-839C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758899 | ||||||
| chr19:10758973
|
G | A | 2 | a0001c0002t0001g0006a0001c0002t0001g0007 | 2 | HG00423.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.162-765G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10758973 | ||||||
| chr19:10759077
|
G | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0192a0001c0001t0001g0275others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-661G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10759077 | ||||||
| chr19:10759368
|
G | A | 1 | a0001c0002t0002g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.162-370G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10759368 | ||||||
| chr19:10759577
|
A | T | 3 | a0001c0001t0001g0212a0001c0002t0002g0211a0001c0002t0002g0213 | 3 | HG02698.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.162-161A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10759577 | ||||||
| chr19:10759724
|
T | TC | 10 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0181others(7): Show | 10 | HG00597.hp2 HG01243.hp1 HG03098.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.162-7dupC | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 10759724 | |||||
| chr19:10759731
|
C | A | 1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.162-7C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 1/20 | chr19 | 10759731 | ||||||
| chr19:10759817
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.235+6A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10759817 | ||||||
| chr19:10759823
|
C | A | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.235+12C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10759823 | ||||||
| chr19:10760043
|
C | CT | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+240dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760043 | |||||
| chr19:10760190
|
T | C | 161 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0101others(158): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.235+379T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760190 | ||||||
| chr19:10760197
|
C | CT | 14 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(11): Show | 14 | HG01175.hp2 HG01192.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.235+401dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760197 | |||||
| chr19:10760197
|
CT | C | 19 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+401delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760197 | |||||
| chr19:10760335
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.235+524C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760335 | ||||||
| chr19:10760386
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.235+575G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760386 | ||||||
| chr19:10760499
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.235+688C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760499 | ||||||
| chr19:10760565
|
T | C | 1 | a0001c0002t0002g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+754T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760565 | ||||||
| chr19:10760571
|
G | T | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.235+760G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760571 | ||||||
| chr19:10760601
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.235+790A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760601 | ||||||
| chr19:10760703
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.235+892C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760703 | ||||||
| chr19:10760709
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(10): Show | 13 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+898C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760709 | ||||||
| chr19:10760766
|
C | G | 6 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(3): Show | 6 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+955C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760766 | ||||||
| chr19:10760786
|
G | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+975G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760786 | ||||||
| chr19:10760794
|
G | C | 133 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0108others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.235+983G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760794 | ||||||
| chr19:10760815
|
C | T | 2 | a0001c0002t0002g0012a0001c0002t0002g0017 | 2 | HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.235+1004C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10760815 | ||||||
| chr19:10760827
|
A | ATTTTTTT others(6): Show |
1 | a0001c0002t0002g0012 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.235+1021_235+1033d others(15): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(7): Show |
25 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0036others(22): Show | 25 | HG00558.hp2 HG01069.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.235+1020_235+1033d others(16): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(8): Show |
117 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0027others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.235+1019_235+1033d others(17): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(9): Show |
56 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(53): Show | 56 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.235+1018_235+1033d others(18): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(10): Show |
29 | a0001c0001t0001g0041a0001c0001t0001g0110a0001c0001t0001g0131others(26): Show | 29 | HG00423.hp1 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.235+1017_235+1033d others(19): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(11): Show |
17 | a0001c0001t0001g0108a0001c0001t0003g0088a0001c0002t0001g0119others(14): Show | 17 | HG00438.hp1 HG02155.hp1 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+1033_235+1034i others(20): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(12): Show |
8 | a0001c0002t0002g0043a0001c0002t0002g0055a0001c0002t0002g0057others(5): Show | 8 | NA18941.hp1 NA18971.hp1 NA19009.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+1033_235+1034i others(21): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(13): Show |
4 | a0001c0002t0002g0070a0001c0002t0002g0075a0001c0002t0002g0084others(1): Show | 4 | HG00408.hp2 HG00597.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+1033_235+1034i others(22): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.235+1033_235+1034i others(27): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10760827
|
A | ATTTTTTT others(19): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.235+1033_235+1034i others(28): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10760827 | |||||
| chr19:10761114
|
G | C | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+1303G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761114 | ||||||
| chr19:10761230
|
G | T | 1 | a0001c0001t0003g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.235+1419G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761230 | ||||||
| chr19:10761321
|
G | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+1510G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761321 | ||||||
| chr19:10761352
|
A | G | 1 | a0001c0002t0002g0266 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.235+1541A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761352 | ||||||
| chr19:10761422
|
A | G | 2 | a0001c0002t0002g0144a0001c0002t0002g0276 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.235+1611A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761422 | ||||||
| chr19:10761525
|
C | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0262 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.235+1714C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761525 | ||||||
| chr19:10761723
|
C | T | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+1912C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761723 | ||||||
| chr19:10761755
|
G | T | 121 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.235+1944G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761755 | ||||||
| chr19:10761790
|
C | T | 1 | a0001c0002t0002g0055 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.235+1979C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761790 | ||||||
| chr19:10761791
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.235+1980G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761791 | ||||||
| chr19:10761803
|
A | G | 264 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.235+1992A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10761803 | ||||||
| chr19:10762227
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.235+2416A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762227 | ||||||
| chr19:10762246
|
C | A | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.235+2435C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762246 | ||||||
| chr19:10762253
|
G | T | 7 | a0001c0002t0001g0109a0001c0002t0001g0114a0001c0002t0001g0122others(4): Show | 7 | HG02071.hp2 NA18939.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2442G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762253 | ||||||
| chr19:10762272
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.235+2461A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762272 | ||||||
| chr19:10762331
|
C | A | 1 | a0001c0002t0002g0266 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.235+2520C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762331 | ||||||
| chr19:10762553
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+2742A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762553 | ||||||
| chr19:10762634
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.235+2823A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762634 | ||||||
| chr19:10762673
|
C | T | 20 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(17): Show | 20 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+2862C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762673 | ||||||
| chr19:10762687
|
A | G | 271 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.235+2876A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762687 | ||||||
| chr19:10762738
|
C | T | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+2927C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762738 | ||||||
| chr19:10762818
|
A | C | 1 | a0001c0001t0001g0180 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.235+3007A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762818 | ||||||
| chr19:10762820
|
AGG | A | 3 | a0001c0002t0002g0265a0001c0002t0002g0266a0001c0002t0002g0269 | 3 | HG01069.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.235+3011_235+3012d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10762820 | |||||
| chr19:10762912
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.235+3101C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10762912 | ||||||
| chr19:10763065
|
TTTTTGTT others(3): Show |
T | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0181 | 3 | NA19005.hp1 NA19060.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.235+3273_235+3282d others(12): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10763065 | |||||
| chr19:10763144
|
C | T | 3 | a0001c0002t0002g0044a0001c0002t0002g0080a0001c0002t0007g0045 | 3 | NA18973.hp2 NA18979.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.235+3333C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763144 | ||||||
| chr19:10763355
|
T | C | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+3544T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763355 | ||||||
| chr19:10763404
|
A | G | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.235+3593A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763404 | ||||||
| chr19:10763496
|
G | A | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+3685G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763496 | ||||||
| chr19:10763606
|
G | A | 1 | a0001c0002t0002g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.235+3795G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763606 | ||||||
| chr19:10763859
|
C | T | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+4048C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763859 | ||||||
| chr19:10763940
|
G | T | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.235+4129G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10763940 | ||||||
| chr19:10764014
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.235+4203T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10764014 | ||||||
| chr19:10764191
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.235+4380C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10764191 | ||||||
| chr19:10764339
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235+4528G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10764339 | ||||||
| chr19:10764771
|
T | C | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+4960T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10764771 | ||||||
| chr19:10764815
|
T | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+5004T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10764815 | ||||||
| chr19:10764828
|
C | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+5017C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10764828 | ||||||
| chr19:10764961
|
CT | C | 7 | a0001c0001t0001g0027a0001c0002t0001g0115a0001c0002t0002g0004others(4): Show | 7 | HG02040.hp2 HG02257.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+5166delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10764961 | |||||
| chr19:10765036
|
C | A | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+5225C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765036 | ||||||
| chr19:10765039
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.235+5228G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765039 | ||||||
| chr19:10765115
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235+5304G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765115 | ||||||
| chr19:10765248
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.235+5437A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765248 | ||||||
| chr19:10765418
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.235+5607G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765418 | ||||||
| chr19:10765501
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.235+5690A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765501 | ||||||
| chr19:10765541
|
G | C | 1 | a0001c0002t0002g0096 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.235+5730G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765541 | ||||||
| chr19:10765561
|
A | G | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.235+5750A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765561 | ||||||
| chr19:10765719
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.235+5908G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765719 | ||||||
| chr19:10765735
|
C | T | 5 | a0001c0001t0001g0167a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | NA18941.hp2 NA18962.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+5924C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765735 | ||||||
| chr19:10765756
|
AT | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0244a0001c0001t0001g0246 | 3 | HG01884.hp1 HG01952.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.235+5946delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765756 | ||||||
| chr19:10765884
|
G | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0173 | 3 | HG02257.hp2 HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.235+6073G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10765884 | ||||||
| chr19:10766096
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.235+6285A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766096 | ||||||
| chr19:10766153
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.236-6326C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766153 | ||||||
| chr19:10766165
|
T | G | 121 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-6314T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766165 | ||||||
| chr19:10766243
|
G | A | 1 | a0001c0002t0001g0099 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.236-6236G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766243 | ||||||
| chr19:10766438
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0254 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.236-6041G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766438 | ||||||
| chr19:10766451
|
T | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0108others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.236-6028T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766451 | ||||||
| chr19:10766455
|
G | T | 1 | a0001c0002t0001g0247 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.236-6024G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766455 | ||||||
| chr19:10766711
|
G | A | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.236-5768G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766711 | ||||||
| chr19:10766722
|
C | A | 1 | a0001c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.236-5757C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766722 | ||||||
| chr19:10766732
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.236-5747C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766732 | ||||||
| chr19:10766880
|
C | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0192a0001c0001t0001g0275others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-5599C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10766880 | ||||||
| chr19:10767131
|
C | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.236-5348C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10767131 | ||||||
| chr19:10767176
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.236-5303A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10767176 | ||||||
| chr19:10767218
|
T | TA | 61 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0108others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.236-5245dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10767218 | |||||
| chr19:10767380
|
C | T | 1 | a0001c0002t0001g0099 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.236-5099C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10767380 | ||||||
| chr19:10767468
|
C | T | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.236-5011C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10767468 | ||||||
| chr19:10767594
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-4885G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10767594 | ||||||
| chr19:10767742
|
C | T | 3 | a0001c0002t0002g0053a0001c0002t0002g0083a0001c0002t0002g0086 | 3 | NA18963.hp2 NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.236-4737C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10767742 | ||||||
| chr19:10768167
|
C | T | 259 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.236-4312C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10768167 | ||||||
| chr19:10768173
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.236-4306G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10768173 | ||||||
| chr19:10768178
|
G | A | 1 | a0001c0002t0002g0019 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.236-4301G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10768178 | ||||||
| chr19:10768315
|
G | A | 1 | a0001c0002t0002g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.236-4164G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10768315 | ||||||
| chr19:10768459
|
AAAC | A | 6 | a0001c0002t0002g0276a0001c0003t0001g0168a0001c0003t0001g0177others(3): Show | 6 | HG03471.hp1 NA18747.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-4008_236-4006d others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10768459 | |||||
| chr19:10768471
|
C | A | 2 | a0001c0002t0006g0161a0001c0002t0006g0165 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.236-4008C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10768471 | ||||||
| chr19:10768817
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.236-3662A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10768817 | ||||||
| chr19:10769136
|
C | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.236-3343C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769136 | ||||||
| chr19:10769278
|
A | G | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.236-3201A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769278 | ||||||
| chr19:10769319
|
C | T | 2 | a0001c0001t0002g0091a0001c0005t0001g0143 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.236-3160C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769319 | ||||||
| chr19:10769443
|
G | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.236-3036G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769443 | ||||||
| chr19:10769674
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.236-2805G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769674 | ||||||
| chr19:10769784
|
G | T | 1 | a0001c0002t0002g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.236-2695G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769784 | ||||||
| chr19:10769993
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.236-2486A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10769993 | ||||||
| chr19:10770093
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236-2386C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770093 | ||||||
| chr19:10770104
|
G | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.236-2375G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770104 | ||||||
| chr19:10770187
|
A | G | 1 | a0001c0002t0001g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.236-2292A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770187 | ||||||
| chr19:10770339
|
G | A | 254 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.236-2140G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770339 | ||||||
| chr19:10770567
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0193 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.236-1912C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770567 | ||||||
| chr19:10770574
|
G | C | 54 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.236-1905G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770574 | ||||||
| chr19:10770581
|
G | C | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.236-1898G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770581 | ||||||
| chr19:10770782
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0240 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.236-1697C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770782 | ||||||
| chr19:10770919
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.236-1560A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10770919 | ||||||
| chr19:10771247
|
T | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.236-1232T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10771247 | ||||||
| chr19:10771252
|
A | G | 4 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140others(1): Show | 4 | HG02257.hp1 HG03139.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1227A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10771252 | ||||||
| chr19:10771270
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.236-1209G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10771270 | ||||||
| chr19:10771539
|
CT | C | 121 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-938delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10771539 | |||||
| chr19:10771656
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.236-823T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10771656 | ||||||
| chr19:10771734
|
T | C | 51 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0043others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.236-745T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10771734 | ||||||
| chr19:10772054
|
T | TTTTTA | 122 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(119): Show | 122 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.236-401_236-397dup others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10772054 | |||||
| chr19:10772082
|
T | TTTTTGAT others(9): Show |
1 | a0001c0003t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.236-397_236-396ins others(16): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772082 | ||||||
| chr19:10772083
|
A | T | 1 | a0001c0003t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.236-396A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772083 | ||||||
| chr19:10772091
|
A | T | 1 | a0001c0003t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.236-388A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772091 | ||||||
| chr19:10772138
|
G | A | 1 | a0001c0002t0002g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.236-341G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772138 | ||||||
| chr19:10772161
|
C | A | 1 | a0001c0003t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.236-318C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772161 | ||||||
| chr19:10772174
|
G | GGTTTCAA others(5): Show |
1 | a0001c0003t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.236-302_236-301ins others(12): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr19 | 10772174 | |||||
| chr19:10772268
|
A | G | 1 | a0001c0002t0002g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.236-211A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772268 | ||||||
| chr19:10772269
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.236-210C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772269 | ||||||
| chr19:10772270
|
A | G | 1 | a0001c0002t0002g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.236-209A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772270 | ||||||
| chr19:10772450
|
C | G | 122 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(119): Show | 122 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.236-29C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 2/20 | chr19 | 10772450 | ||||||
| chr19:10772870
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.385+242T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10772870 | ||||||
| chr19:10772905
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.385+277C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10772905 | ||||||
| chr19:10772979
|
G | GT | 173 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(170): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.385+369dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10772979 | |||||
| chr19:10772979
|
G | GTT | 7 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0201others(4): Show | 7 | HG01192.hp2 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+368_385+369dup others(2): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10772979 | |||||
| chr19:10773065
|
C | T | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.385+437C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773065 | ||||||
| chr19:10773066
|
A | G | 264 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.385+438A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773066 | ||||||
| chr19:10773146
|
AT | A | 255 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.385+537delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10773146 | |||||
| chr19:10773300
|
G | A | 263 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.385+672G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773300 | ||||||
| chr19:10773305
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0254 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.385+677G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773305 | ||||||
| chr19:10773427
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+799G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773427 | ||||||
| chr19:10773449
|
AT | A | 238 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.385+838delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10773449 | |||||
| chr19:10773449
|
ATT | A | 20 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0207others(17): Show | 20 | HG00558.hp1 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+837_385+838del others(2): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10773449 | |||||
| chr19:10773574
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0002t0001g0089 | 3 | HG02015.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.385+946G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773574 | ||||||
| chr19:10773623
|
T | A | 1 | a0001c0002t0002g0272 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.385+995T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773623 | ||||||
| chr19:10773630
|
T | A | 1 | a0001c0002t0002g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.385+1002T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773630 | ||||||
| chr19:10773633
|
A | T | 23 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.385+1005A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773633 | ||||||
| chr19:10773637
|
T | A | 1 | a0001c0002t0002g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.385+1009T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773637 | ||||||
| chr19:10773779
|
T | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0244a0001c0001t0001g0246 | 3 | HG01884.hp1 HG01952.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385+1151T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773779 | ||||||
| chr19:10773891
|
T | C | 4 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140others(1): Show | 4 | HG02257.hp1 HG03139.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+1263T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10773891 | ||||||
| chr19:10774040
|
A | C | 1 | a0001c0002t0002g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.385+1412A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774040 | ||||||
| chr19:10774147
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.385+1519A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774147 | ||||||
| chr19:10774247
|
G | A | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.386-1456G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774247 | ||||||
| chr19:10774346
|
A | G | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.386-1357A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774346 | ||||||
| chr19:10774528
|
G | A | 51 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0043others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.386-1175G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774528 | ||||||
| chr19:10774728
|
C | CT | 102 | a0001c0001t0001g0039a0001c0001t0001g0101a0001c0001t0001g0108others(99): Show | 102 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.386-960dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10774728 | |||||
| chr19:10774728
|
C | CTT | 7 | a0001c0002t0001g0094a0001c0002t0001g0100a0001c0002t0001g0105others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-961_386-960dup others(2): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10774728 | |||||
| chr19:10774779
|
A | AT | 25 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(22): Show | 25 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.386-909dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10774779 | |||||
| chr19:10774779
|
A | T | 4 | a0001c0002t0002g0063a0001c0002t0002g0144a0001c0002t0002g0276others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-924A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774779 | ||||||
| chr19:10774779
|
AT | A | 8 | a0001c0001t0003g0195a0001c0002t0001g0115a0001c0002t0002g0004others(5): Show | 8 | HG02040.hp2 HG02257.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-909delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 10774779 | |||||
| chr19:10774783
|
T | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0243a0001c0001t0002g0091others(1): Show | 4 | HG02602.hp2 HG02717.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-920T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774783 | ||||||
| chr19:10774919
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.386-784A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10774919 | ||||||
| chr19:10775051
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.386-652A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775051 | ||||||
| chr19:10775063
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.386-640G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775063 | ||||||
| chr19:10775422
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.386-281T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775422 | ||||||
| chr19:10775428
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.386-275G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775428 | ||||||
| chr19:10775530
|
G | T | 81 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0108others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.386-173G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775530 | ||||||
| chr19:10775619
|
T | C | 1 | a0001c0001t0001g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.386-84T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775619 | ||||||
| chr19:10775697
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.386-6T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 3/20 | chr19 | 10775697 | ||||||
| chr19:10776030
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.589+124C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776030 | ||||||
| chr19:10776105
|
A | G | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.589+199A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776105 | ||||||
| chr19:10776106
|
C | T | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.589+200C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776106 | ||||||
| chr19:10776180
|
C | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.589+274C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776180 | ||||||
| chr19:10776180
|
C | T | 3 | a0001c0001t0002g0091a0001c0005t0001g0143a0001c0005t0002g0141 | 3 | HG00140.hp2 HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.589+274C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776180 | ||||||
| chr19:10776188
|
C | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0081 | 2 | NA19077.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.589+282C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776188 | ||||||
| chr19:10776242
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.589+336G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776242 | ||||||
| chr19:10776261
|
C | A | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.589+355C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776261 | ||||||
| chr19:10776643
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.590-475G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776643 | ||||||
| chr19:10776714
|
T | C | 4 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140others(1): Show | 4 | HG02257.hp1 HG03139.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-404T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776714 | ||||||
| chr19:10776908
|
T | A | 2 | a0001c0002t0001g0107a0001c0002t0001g0218 | 2 | HG02135.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.590-210T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776908 | ||||||
| chr19:10776950
|
T | C | 7 | a0001c0001t0003g0164a0001c0001t0003g0189a0001c0001t0003g0190others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.590-168T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10776950 | ||||||
| chr19:10777012
|
T | A | 2 | a0001c0001t0001g0036a0001c0001t0009g0033 | 2 | HG03710.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.590-106T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 4/20 | chr19 | 10777012 | ||||||
| chr19:10777262
|
C | T | 1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.688+46C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10777262 | ||||||
| chr19:10777280
|
C | T | 1 | a0001c0001t0009g0033 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.688+64C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10777280 | ||||||
| chr19:10777388
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.688+172A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10777388 | ||||||
| chr19:10777877
|
G | A | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.688+661G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10777877 | ||||||
| chr19:10777890
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.688+674C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10777890 | ||||||
| chr19:10777948
|
C | T | 19 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.688+732C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10777948 | ||||||
| chr19:10778019
|
T | TTTTA | 207 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.688+837_688+840dup others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10778019 | |||||
| chr19:10778019
|
T | TTTTATTT others(1): Show |
46 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0027others(43): Show | 46 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.688+833_688+840dup others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10778019 | |||||
| chr19:10778019
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0176a0001c0005t0001g0143 | 3 | HG00323.hp2 HG02965.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.688+829_688+840dup others(12): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10778019 | |||||
| chr19:10778091
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.688+875A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778091 | ||||||
| chr19:10778157
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.688+941C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778157 | ||||||
| chr19:10778390
|
G | A | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.688+1174G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778390 | ||||||
| chr19:10778400
|
T | C | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.688+1184T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778400 | ||||||
| chr19:10778530
|
T | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.688+1314T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778530 | ||||||
| chr19:10778591
|
G | T | 1 | a0001c0001t0001g0278 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.688+1375G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778591 | ||||||
| chr19:10778616
|
C | T | 1 | a0001c0002t0002g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.688+1400C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778616 | ||||||
| chr19:10778791
|
T | C | 2 | a0001c0001t0001g0016a0001c0002t0002g0011 | 2 | HG02735.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.688+1575T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778791 | ||||||
| chr19:10778793
|
C | A | 121 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.688+1577C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10778793 | ||||||
| chr19:10779163
|
T | C | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.688+1947T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10779163 | ||||||
| chr19:10779214
|
C | CA | 9 | a0001c0001t0001g0039a0001c0001t0003g0164a0001c0001t0003g0189others(6): Show | 9 | HG00140.hp2 HG01109.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.688+2013dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779214 | |||||
| chr19:10779359
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.688+2143G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10779359 | ||||||
| chr19:10779474
|
T | TTTTC | 11 | a0001c0001t0001g0202a0001c0001t0001g0207a0001c0001t0001g0215others(8): Show | 11 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.688+2286_688+2289d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779474 | |||||
| chr19:10779474
|
TTTTCTTT others(1): Show |
T | 4 | a0001c0001t0001g0220a0001c0002t0002g0163a0001c0002t0006g0161others(1): Show | 4 | HG02738.hp1 HG02965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+2282_688+2289d others(10): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779474 | |||||
| chr19:10779502
|
C | CTT | 16 | a0001c0002t0002g0004a0001c0002t0002g0042a0001c0002t0002g0043others(13): Show | 16 | HG00408.hp2 HG00438.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.688+2310_688+2311d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTT | 32 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0191others(29): Show | 32 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.688+2309_688+2311d others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTTCTTT | 12 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0002g0008others(9): Show | 12 | HG01516.hp2 HG01934.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.688+2289_688+2290i others(9): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTTCTTT others(1): Show |
9 | a0001c0001t0001g0039a0001c0002t0002g0005a0001c0002t0002g0012others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.688+2289_688+2290i others(10): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTTCTTT others(4): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0007 | 2 | HG00423.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.688+2289_688+2290i others(13): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTTT | 116 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0024others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.688+2308_688+2311d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTTTT | 39 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0038others(36): Show | 39 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.688+2307_688+2311d others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | CTTTTTT | 5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0243others(2): Show | 5 | HG02602.hp1 HG02886.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+2306_688+2311d others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779502
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0231a0001c0001t0002g0277others(3): Show | 6 | HG01358.hp1 HG02965.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+2286C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10779502 | ||||||
| chr19:10779502
|
CT | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(2): Show | 5 | HG00323.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.688+2311delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10779502 | |||||
| chr19:10779999
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.688+2783T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10779999 | ||||||
| chr19:10780025
|
T | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.688+2809T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10780025 | ||||||
| chr19:10780563
|
C | A | 54 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.689-2397C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10780563 | ||||||
| chr19:10780660
|
G | T | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.689-2300G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10780660 | ||||||
| chr19:10781018
|
T | TA | 67 | a0001c0001t0001g0016a0001c0001t0001g0268a0001c0001t0003g0155others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.689-1919dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10781018 | |||||
| chr19:10781018
|
T | TAA | 61 | a0001c0001t0001g0039a0001c0001t0001g0101a0001c0001t0001g0108others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.689-1920_689-1919d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10781018 | |||||
| chr19:10781018
|
TA | T | 107 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(104): Show | 107 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.689-1919delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10781018 | |||||
| chr19:10781096
|
C | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.689-1864C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781096 | ||||||
| chr19:10781170
|
G | A | 271 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.689-1790G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781170 | ||||||
| chr19:10781200
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-1760A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781200 | ||||||
| chr19:10781242
|
G | C | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.689-1718G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781242 | ||||||
| chr19:10781474
|
AC | A | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.689-1482delC | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10781474 | |||||
| chr19:10781546
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.689-1414G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781546 | ||||||
| chr19:10781650
|
G | A | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.689-1310G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781650 | ||||||
| chr19:10781654
|
G | A | 1 | a0001c0002t0002g0096 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.689-1306G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781654 | ||||||
| chr19:10781897
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.689-1063G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781897 | ||||||
| chr19:10781976
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.689-984A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10781976 | ||||||
| chr19:10782172
|
A | G | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.689-788A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782172 | ||||||
| chr19:10782205
|
G | A | 57 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.689-755G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782205 | ||||||
| chr19:10782268
|
A | G | 1 | a0001c0002t0002g0084 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.689-692A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782268 | ||||||
| chr19:10782297
|
G | C | 1 | a0001c0002t0002g0078 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.689-663G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782297 | ||||||
| chr19:10782324
|
G | A | 2 | a0001c0002t0002g0048a0001c0002t0002g0140 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.689-636G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782324 | ||||||
| chr19:10782325
|
C | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.689-635C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782325 | ||||||
| chr19:10782342
|
T | TTTTTTCT others(5): Show |
257 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.689-604_689-593dup others(12): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10782342 | |||||
| chr19:10782342
|
T | TTTTTTCT others(11): Show |
4 | a0001c0001t0001g0199a0001c0002t0002g0090a0001c0002t0002g0140others(1): Show | 4 | HG02717.hp1 HG03239.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-610_689-593dup others(18): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10782342 | |||||
| chr19:10782368
|
C | T | 1 | a0001c0002t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.689-592C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782368 | ||||||
| chr19:10782372
|
C | CTTTTTCT others(6): Show |
1 | a0001c0002t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.689-583_689-582ins others(13): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr19 | 10782372 | |||||
| chr19:10782372
|
C | T | 259 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.689-588C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782372 | ||||||
| chr19:10782398
|
G | A | 56 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.689-562G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782398 | ||||||
| chr19:10782452
|
G | A | 1 | a0001c0002t0002g0005 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.689-508G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782452 | ||||||
| chr19:10782461
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.689-499C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782461 | ||||||
| chr19:10782647
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.689-313C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 5/20 | chr19 | 10782647 | ||||||
| chr19:10783354
|
G | A | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.849+234G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783354 | ||||||
| chr19:10783450
|
G | T | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.849+330G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783450 | ||||||
| chr19:10783482
|
TAAATA | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0027others(14): Show | 17 | HG00597.hp2 HG00621.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.849+366_849+370del others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10783482 | |||||
| chr19:10783564
|
A | G | 261 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.849+444A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783564 | ||||||
| chr19:10783675
|
TTTA | T | 14 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0150others(11): Show | 14 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.849+585_849+587del others(3): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10783675 | |||||
| chr19:10783675
|
TTTATTA | T | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+582_849+587del others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10783675 | |||||
| chr19:10783696
|
A | ATT | 7 | a0001c0002t0001g0094a0001c0002t0001g0100a0001c0002t0001g0105others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.849+577_849+578dup others(2): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10783696 | |||||
| chr19:10783696
|
A | T | 3 | a0001c0002t0001g0111a0001c0002t0002g0074a0001c0005t0001g0143 | 3 | HG02965.hp2 HG03704.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.849+576A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783696 | ||||||
| chr19:10783699
|
A | ATT | 43 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(40): Show | 43 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+580_849+581dup others(2): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10783699 | |||||
| chr19:10783699
|
A | T | 59 | a0001c0001t0001g0174a0001c0002t0001g0094a0001c0002t0001g0100others(56): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.849+579A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783699 | ||||||
| chr19:10783702
|
A | ATT | 4 | a0001c0002t0001g0104a0001c0002t0001g0109a0001c0002t0001g0122others(1): Show | 4 | NA18986.hp1 NA19010.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+583_849+584dup others(2): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10783702 | |||||
| chr19:10783702
|
A | T | 148 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0101others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.849+582A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783702 | ||||||
| chr19:10783705
|
A | T | 251 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.849+585A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783705 | ||||||
| chr19:10783845
|
C | A | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.849+725C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783845 | ||||||
| chr19:10783993
|
C | T | 50 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0043others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.849+873C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10783993 | ||||||
| chr19:10784052
|
G | A | 118 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(115): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.849+932G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784052 | ||||||
| chr19:10784163
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849+1043A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784163 | ||||||
| chr19:10784246
|
T | C | 50 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0043others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.849+1126T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784246 | ||||||
| chr19:10784305
|
G | A | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.849+1185G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784305 | ||||||
| chr19:10784371
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.849+1251G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784371 | ||||||
| chr19:10784540
|
G | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+1420G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784540 | ||||||
| chr19:10784703
|
T | C | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.849+1583T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784703 | ||||||
| chr19:10784794
|
G | A | 1 | a0001c0002t0002g0064 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.849+1674G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784794 | ||||||
| chr19:10784817
|
T | A | 133 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0108others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.849+1697T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784817 | ||||||
| chr19:10784819
|
A | AT | 130 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0108others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.849+1721dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10784819 | |||||
| chr19:10784819
|
A | ATT | 111 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0024others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.849+1720_849+1721d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10784819 | |||||
| chr19:10784819
|
A | ATTT | 24 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 24 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.849+1719_849+1721d others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10784819 | |||||
| chr19:10784819
|
ATTTTTT | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+1716_849+1721d others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10784819 | |||||
| chr19:10784866
|
C | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.850-1698C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784866 | ||||||
| chr19:10784958
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.850-1606G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784958 | ||||||
| chr19:10784969
|
G | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-1595G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784969 | ||||||
| chr19:10784994
|
T | C | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.850-1570T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10784994 | ||||||
| chr19:10785065
|
G | A | 1 | a0001c0010t0002g0077 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.850-1499G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10785065 | ||||||
| chr19:10785084
|
C | T | 1 | a0001c0002t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.850-1480C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10785084 | ||||||
| chr19:10785258
|
T | C | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850-1306T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10785258 | ||||||
| chr19:10785284
|
A | AT | 12 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(9): Show | 12 | HG00642.hp1 HG00738.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-1264dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 10785284 | |||||
| chr19:10785306
|
T | C | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-1258T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10785306 | ||||||
| chr19:10785690
|
A | G | 1 | a0001c0003t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.850-874A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10785690 | ||||||
| chr19:10785728
|
C | G | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.850-836C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10785728 | ||||||
| chr19:10786015
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.850-549G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10786015 | ||||||
| chr19:10786090
|
A | G | 264 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.850-474A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10786090 | ||||||
| chr19:10786228
|
C | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.850-336C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10786228 | ||||||
| chr19:10786511
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850-53C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 6/20 | chr19 | 10786511 | ||||||
| chr19:10786937
|
G | A | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.992+231G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10786937 | ||||||
| chr19:10787084
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.992+378A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787084 | ||||||
| chr19:10787176
|
T | C | 1 | a0001c0002t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.992+470T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787176 | ||||||
| chr19:10787303
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.992+597A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787303 | ||||||
| chr19:10787328
|
A | G | 1 | a0001c0002t0002g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.992+622A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787328 | ||||||
| chr19:10787705
|
A | C | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.992+999A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787705 | ||||||
| chr19:10787737
|
C | T | 122 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(119): Show | 122 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.992+1031C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787737 | ||||||
| chr19:10787752
|
C | CA | 119 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(116): Show | 119 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.992+1065dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr19 | 10787752 | |||||
| chr19:10787752
|
C | CAA | 7 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0166others(4): Show | 7 | HG00597.hp2 HG02572.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+1064_992+1065d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr19 | 10787752 | |||||
| chr19:10787861
|
T | G | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.992+1155T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787861 | ||||||
| chr19:10787869
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.992+1163C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787869 | ||||||
| chr19:10787870
|
A | G | 260 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.992+1164A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787870 | ||||||
| chr19:10787970
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0240 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.992+1264G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10787970 | ||||||
| chr19:10788044
|
C | T | 1 | a0001c0002t0002g0080 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.992+1338C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10788044 | ||||||
| chr19:10788232
|
CA | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0241others(4): Show | 7 | HG01358.hp2 HG01978.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+1545delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr19 | 10788232 | |||||
| chr19:10788246
|
A | AG | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.992+1540_992+1541i others(3): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10788246 | ||||||
| chr19:10788436
|
C | G | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.992+1730C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10788436 | ||||||
| chr19:10788645
|
C | G | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.992+1939C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10788645 | ||||||
| chr19:10788768
|
G | A | 2 | a0001c0001t0003g0194a0001c0001t0003g0197 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.992+2062G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10788768 | ||||||
| chr19:10788910
|
C | A | 3 | a0001c0001t0001g0219a0001c0001t0002g0206a0001c0001t0002g0222 | 3 | HG00558.hp1 NA18942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.992+2204C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10788910 | ||||||
| chr19:10789193
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.992+2487G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789193 | ||||||
| chr19:10789266
|
G | A | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.992+2560G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789266 | ||||||
| chr19:10789343
|
G | C | 1 | a0001c0001t0001g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.992+2637G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789343 | ||||||
| chr19:10789572
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.992+2866C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789572 | ||||||
| chr19:10789818
|
G | A | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.992+3112G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789818 | ||||||
| chr19:10789821
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.992+3115C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789821 | ||||||
| chr19:10789855
|
A | G | 1 | a0001c0002t0002g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.992+3149A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789855 | ||||||
| chr19:10789922
|
C | G | 1 | a0001c0002t0002g0013 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.992+3216C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789922 | ||||||
| chr19:10789957
|
C | T | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.992+3251C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10789957 | ||||||
| chr19:10790293
|
T | TTTTG | 256 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.993-3407_993-3404d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr19 | 10790293 | |||||
| chr19:10790293
|
T | TTTTGTTT others(1): Show |
5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0275others(2): Show | 5 | HG02698.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.993-3411_993-3404d others(10): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr19 | 10790293 | |||||
| chr19:10790757
|
C | T | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.993-2963C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10790757 | ||||||
| chr19:10790759
|
T | C | 3 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273 | 3 | HG02615.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.993-2961T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10790759 | ||||||
| chr19:10790764
|
G | A | 38 | a0001c0001t0002g0160a0001c0002t0001g0001a0001c0002t0001g0002others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.993-2956G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10790764 | ||||||
| chr19:10790882
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.993-2838C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10790882 | ||||||
| chr19:10791075
|
T | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.993-2645T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791075 | ||||||
| chr19:10791157
|
C | T | 259 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.993-2563C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791157 | ||||||
| chr19:10791247
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.993-2473C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791247 | ||||||
| chr19:10791547
|
CCAGCCGG others(6): Show |
C | 18 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(15): Show | 18 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.993-2172_993-2160d others(15): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791547 | ||||||
| chr19:10791706
|
T | TC | 7 | a0001c0002t0001g0100a0001c0002t0001g0119a0001c0002t0001g0162others(4): Show | 7 | HG01261.hp1 HG01934.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.993-2008dupC | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr19 | 10791706 | |||||
| chr19:10791711
|
C | A | 1 | a0001c0002t0002g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.993-2009C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791711 | ||||||
| chr19:10791713
|
G | C | 137 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0102others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.993-2007G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791713 | ||||||
| chr19:10791725
|
G | C | 1 | a0001c0002t0002g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.993-1995G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791725 | ||||||
| chr19:10791944
|
T | C | 68 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(65): Show | 68 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.993-1776T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10791944 | ||||||
| chr19:10792049
|
T | C | 68 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(65): Show | 68 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.993-1671T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792049 | ||||||
| chr19:10792057
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.993-1663C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792057 | ||||||
| chr19:10792118
|
C | A | 24 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.993-1602C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792118 | ||||||
| chr19:10792176
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.993-1544G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792176 | ||||||
| chr19:10792207
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.993-1513G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792207 | ||||||
| chr19:10792459
|
A | G | 1 | a0001c0002t0002g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.993-1261A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792459 | ||||||
| chr19:10792544
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.993-1176A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792544 | ||||||
| chr19:10792647
|
G | A | 68 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(65): Show | 68 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.993-1073G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792647 | ||||||
| chr19:10792694
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.993-1026G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10792694 | ||||||
| chr19:10793039
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.993-681G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10793039 | ||||||
| chr19:10793132
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.993-588A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10793132 | ||||||
| chr19:10793165
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.993-555G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10793165 | ||||||
| chr19:10793296
|
G | A | 40 | a0001c0001t0002g0160a0001c0002t0001g0001a0001c0002t0001g0002others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.993-424G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10793296 | ||||||
| chr19:10793605
|
A | G | 1 | a0001c0002t0001g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.993-115A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 7/20 | chr19 | 10793605 | ||||||
| chr19:10794013
|
G | C | 211 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(208): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1128+158G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794013 | ||||||
| chr19:10794024
|
T | C | 142 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0102others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1128+169T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794024 | ||||||
| chr19:10794226
|
A | G | 23 | a0001c0001t0001g0016a0001c0001t0003g0155a0001c0002t0001g0006others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1128+371A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794226 | ||||||
| chr19:10794344
|
C | CGT | 12 | a0001c0001t0001g0028a0001c0001t0001g0116a0001c0001t0001g0138others(9): Show | 12 | HG00099.hp2 HG01358.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1128+523_1128+524d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGT | 3 | a0001c0001t0001g0255a0001c0001t0001g0262a0001c0002t0002g0270 | 3 | HG01884.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1128+521_1128+524d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGT | 8 | a0001c0001t0002g0160a0001c0002t0001g0094a0001c0002t0001g0100others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+519_1128+524d others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGTG others(1): Show |
6 | a0001c0001t0005g0021a0001c0002t0002g0009a0001c0002t0002g0048others(3): Show | 6 | HG00673.hp2 HG01981.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1128+517_1128+524d others(10): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGTG others(3): Show |
32 | a0001c0001t0001g0153a0001c0001t0005g0020a0001c0002t0001g0026others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1128+515_1128+524d others(12): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGTG others(5): Show |
60 | a0001c0001t0001g0016a0001c0001t0001g0191a0001c0001t0003g0155others(57): Show | 60 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1128+513_1128+524d others(14): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGTG others(7): Show |
13 | a0001c0001t0001g0154a0001c0002t0001g0006a0001c0002t0001g0089others(10): Show | 13 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.1128+511_1128+524d others(16): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGTG others(9): Show |
1 | a0001c0002t0002g0074 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1128+509_1128+524d others(18): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
C | CGTGTGTG others(11): Show |
1 | a0001c0002t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1128+507_1128+524d others(20): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794344
|
CGTGTGT | C | 14 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(11): Show | 14 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128+519_1128+524d others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794344 | |||||
| chr19:10794417
|
T | C | 1 | a0001c0002t0002g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1128+562T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794417 | ||||||
| chr19:10794434
|
A | AAAAC | 18 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(15): Show | 18 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1128+585_1128+588d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794434 | |||||
| chr19:10794537
|
T | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0113others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1128+682T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794537 | ||||||
| chr19:10794717
|
C | A | 48 | a0001c0002t0002g0037a0001c0002t0002g0042a0001c0002t0002g0043others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1129-655C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794717 | ||||||
| chr19:10794740
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1129-632A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794740 | ||||||
| chr19:10794744
|
C | CA | 20 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(17): Show | 20 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1129-619dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 10794744 | |||||
| chr19:10794806
|
C | G | 4 | a0001c0001t0003g0164a0001c0001t0003g0189a0001c0001t0003g0190others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-566C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794806 | ||||||
| chr19:10794876
|
T | A | 3 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0140 | 3 | HG02257.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1129-496T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10794876 | ||||||
| chr19:10795047
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1129-325A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 8/20 | chr19 | 10795047 | ||||||
| chr19:10795480
|
C | T | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1196+41C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10795480 | ||||||
| chr19:10795632
|
G | A | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1196+193G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10795632 | ||||||
| chr19:10795758
|
G | A | 1 | a0001c0002t0002g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1196+319G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10795758 | ||||||
| chr19:10795806
|
A | G | 17 | a0001c0002t0002g0043a0001c0002t0002g0052a0001c0002t0002g0054others(14): Show | 17 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1196+367A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10795806 | ||||||
| chr19:10796082
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1196+643C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796082 | ||||||
| chr19:10796212
|
C | T | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1196+773C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796212 | ||||||
| chr19:10796291
|
C | T | 1 | a0001c0002t0002g0082 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1196+852C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796291 | ||||||
| chr19:10796440
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1197-940A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796440 | ||||||
| chr19:10796527
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1197-853C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796527 | ||||||
| chr19:10796528
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1197-852C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796528 | ||||||
| chr19:10796610
|
A | G | 17 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(14): Show | 17 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1197-770A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796610 | ||||||
| chr19:10796672
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0003 | 2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1197-708C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796672 | ||||||
| chr19:10796742
|
C | T | 1 | a0001c0002t0002g0082 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1197-638C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796742 | ||||||
| chr19:10796749
|
T | A | 23 | a0001c0001t0003g0155a0001c0002t0001g0006a0001c0002t0001g0007others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1197-631T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796749 | ||||||
| chr19:10796789
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1197-591G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10796789 | ||||||
| chr19:10797070
|
G | A | 1 | a0001c0002t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1197-310G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797070 | ||||||
| chr19:10797138
|
G | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0264 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1197-242G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797138 | ||||||
| chr19:10797153
|
C | A | 1 | a0001c0007t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1197-227C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797153 | ||||||
| chr19:10797274
|
C | A | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1197-106C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797274 | ||||||
| chr19:10797285
|
C | T | 1 | a0001c0002t0002g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1197-95C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797285 | ||||||
| chr19:10797318
|
G | C | 21 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1197-62G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797318 | ||||||
| chr19:10797362
|
G | A | 1 | a0001c0001t0009g0033 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1197-18G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 9/20 | chr19 | 10797362 | ||||||
| chr19:10797578
|
C | A | 1 | a0001c0002t0001g0100 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1335+60C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10797578 | ||||||
| chr19:10797842
|
C | G | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1335+324C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10797842 | ||||||
| chr19:10797947
|
G | T | 39 | a0001c0001t0002g0160a0001c0002t0001g0001a0001c0002t0001g0002others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1335+429G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10797947 | ||||||
| chr19:10798014
|
T | G | 21 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1336-472T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798014 | ||||||
| chr19:10798025
|
T | C | 38 | a0001c0001t0002g0160a0001c0002t0001g0001a0001c0002t0001g0002others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1336-461T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798025 | ||||||
| chr19:10798291
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1336-195C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798291 | ||||||
| chr19:10798381
|
A | G | 1 | a0001c0002t0002g0005 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1336-105A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798381 | ||||||
| chr19:10798399
|
C | G | 1 | a0001c0002t0002g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1336-87C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798399 | ||||||
| chr19:10798404
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0002g0152 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1336-82C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798404 | ||||||
| chr19:10798439
|
G | A | 1 | a0003c0008t0001g0267 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1336-47G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 10/20 | chr19 | 10798439 | ||||||
| chr19:10798641
|
GCATGCTG others(81): Show |
G | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1422+145_1422+232d others(90): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10798641 | |||||
| chr19:10799023
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1422+451C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799023 | ||||||
| chr19:10799063
|
G | A | 2 | a0001c0002t0001g0107a0001c0002t0001g0218 | 2 | HG02135.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1422+491G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799063 | ||||||
| chr19:10799238
|
G | A | 67 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(64): Show | 67 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1422+666G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799238 | ||||||
| chr19:10799277
|
C | T | 47 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1422+705C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799277 | ||||||
| chr19:10799285
|
A | G | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1422+713A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799285 | ||||||
| chr19:10799333
|
CTT | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191 | 3 | HG02559.hp2 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1422+762_1422+763d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799333 | ||||||
| chr19:10799531
|
TTTG | T | 32 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0136others(29): Show | 32 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+962_1422+964d others(5): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10799531 | |||||
| chr19:10799532
|
TTG | T | 24 | a0001c0001t0001g0139a0001c0002t0002g0042a0001c0002t0002g0043others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1422+962_1422+963d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10799532 | |||||
| chr19:10799533
|
TG | T | 8 | a0001c0002t0002g0051a0001c0002t0002g0064a0001c0002t0002g0073others(5): Show | 8 | NA19009.hp1 NA19066.hp2 NA19067.hp1 others(5): Show |
intron_variant | MODIFIER | c.1422+962delG | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799533 | ||||||
| chr19:10799534
|
G | GT | 9 | a0001c0001t0001g0151a0001c0001t0001g0207a0001c0001t0001g0215others(6): Show | 9 | HG00642.hp1 HG00642.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1422+979dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10799534 | |||||
| chr19:10799541
|
T | G | 1 | a0001c0002t0001g0112 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1422+969T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799541 | ||||||
| chr19:10799542
|
T | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1422+970T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799542 | ||||||
| chr19:10799560
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1422+988G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799560 | ||||||
| chr19:10799643
|
C | T | 1 | a0001c0002t0001g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1422+1071C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799643 | ||||||
| chr19:10799814
|
G | T | 1 | a0001c0002t0002g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1422+1242G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799814 | ||||||
| chr19:10799886
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1422+1314A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10799886 | ||||||
| chr19:10800002
|
G | A | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1422+1430G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10800002 | ||||||
| chr19:10800104
|
A | G | 145 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0102others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1422+1532A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10800104 | ||||||
| chr19:10800148
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0181 | 3 | NA19005.hp1 NA19060.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1422+1576C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10800148 | ||||||
| chr19:10800325
|
G | GCC | 68 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0110others(65): Show | 68 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1422+1755_1422+175 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10800325 | |||||
| chr19:10800381
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1422+1809T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10800381 | ||||||
| chr19:10800652
|
A | T | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1423-1636A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10800652 | ||||||
| chr19:10800916
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1423-1372C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10800916 | ||||||
| chr19:10801173
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1423-1115G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801173 | ||||||
| chr19:10801175
|
G | A | 5 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0002t0002g0272others(2): Show | 5 | HG01934.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423-1113G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801175 | ||||||
| chr19:10801179
|
G | A | 2 | a0001c0002t0002g0144a0001c0002t0002g0276 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1423-1109G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801179 | ||||||
| chr19:10801254
|
C | T | 3 | a0001c0002t0010g0092a0001c0005t0001g0143a0001c0005t0002g0141 | 3 | HG00140.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1423-1034C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801254 | ||||||
| chr19:10801273
|
G | A | 57 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(54): Show | 57 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1423-1015G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801273 | ||||||
| chr19:10801328
|
A | C | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1423-960A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801328 | ||||||
| chr19:10801605
|
C | CA | 67 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0131others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1423-663dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10801605 | |||||
| chr19:10801605
|
CA | C | 13 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0172others(10): Show | 13 | HG00323.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1423-663delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10801605 | |||||
| chr19:10801908
|
G | GA | 22 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0166others(19): Show | 22 | HG00423.hp1 HG01257.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1423-364dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10801908 | |||||
| chr19:10801908
|
GA | G | 38 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.1423-364delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr19 | 10801908 | |||||
| chr19:10801919
|
A | C | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1423-369A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801919 | ||||||
| chr19:10801925
|
C | A | 2 | a0001c0002t0002g0144a0001c0003t0001g0184 | 2 | HG02976.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1423-363C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10801925 | ||||||
| chr19:10802177
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1423-111G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10802177 | ||||||
| chr19:10802238
|
C | G | 1 | a0001c0002t0002g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1423-50C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 11/20 | chr19 | 10802238 | ||||||
| chr19:10802541
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1493+183T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802541 | ||||||
| chr19:10802638
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1493+280C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802638 | ||||||
| chr19:10802678
|
C | G | 63 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1493+320C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802678 | ||||||
| chr19:10802692
|
G | A | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1493+334G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802692 | ||||||
| chr19:10802751
|
G | A | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1493+393G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802751 | ||||||
| chr19:10802831
|
G | A | 1 | a0001c0002t0002g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1493+473G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802831 | ||||||
| chr19:10802843
|
T | C | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1493+485T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10802843 | ||||||
| chr19:10803073
|
C | T | 57 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(54): Show | 57 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1493+715C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803073 | ||||||
| chr19:10803184
|
G | A | 5 | a0001c0001t0002g0091a0001c0001t0002g0277a0001c0002t0010g0092others(2): Show | 5 | HG00140.hp2 HG02717.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493+826G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803184 | ||||||
| chr19:10803198
|
G | C | 1 | a0001c0001t0002g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1493+840G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803198 | ||||||
| chr19:10803282
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1493+924C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803282 | ||||||
| chr19:10803425
|
C | A | 2 | a0001c0002t0001g0114a0001c0002t0001g0142 | 2 | NA18939.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1493+1067C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803425 | ||||||
| chr19:10803461
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191 | 3 | HG02559.hp2 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1493+1103C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803461 | ||||||
| chr19:10803465
|
C | T | 3 | a0001c0002t0002g0265a0001c0002t0002g0266a0001c0002t0002g0269 | 3 | HG01069.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1493+1107C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803465 | ||||||
| chr19:10803698
|
C | T | 1 | a0001c0002t0001g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1493+1340C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803698 | ||||||
| chr19:10803701
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1493+1343G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803701 | ||||||
| chr19:10803716
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0173 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1493+1358A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803716 | ||||||
| chr19:10803765
|
G | A | 2 | a0001c0002t0006g0161a0001c0002t0006g0165 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1493+1407G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803765 | ||||||
| chr19:10803860
|
A | C | 1 | a0001c0002t0002g0052 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1493+1502A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803860 | ||||||
| chr19:10803991
|
G | C | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1493+1633G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10803991 | ||||||
| chr19:10804043
|
C | G | 42 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1493+1685C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804043 | ||||||
| chr19:10804153
|
G | A | 63 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1494-1763G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804153 | ||||||
| chr19:10804225
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0244a0001c0001t0001g0246 | 3 | HG01884.hp1 HG01952.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1494-1691T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804225 | ||||||
| chr19:10804249
|
A | G | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1494-1667A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804249 | ||||||
| chr19:10804355
|
A | G | 131 | a0001c0001t0002g0091a0001c0001t0002g0277a0001c0002t0001g0001others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1494-1561A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804355 | ||||||
| chr19:10804363
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1494-1553G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804363 | ||||||
| chr19:10804363
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1494-1553G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804363 | ||||||
| chr19:10804564
|
C | T | 18 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0027others(15): Show | 18 | HG00597.hp2 HG00621.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1494-1352C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804564 | ||||||
| chr19:10804628
|
T | C | 59 | a0001c0001t0002g0091a0001c0001t0002g0277a0001c0002t0002g0013others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1494-1288T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804628 | ||||||
| chr19:10804648
|
A | T | 42 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1494-1268A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10804648 | ||||||
| chr19:10805242
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1494-674T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10805242 | ||||||
| chr19:10805249
|
A | G | 131 | a0001c0001t0002g0091a0001c0001t0002g0277a0001c0002t0001g0001others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1494-667A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10805249 | ||||||
| chr19:10805774
|
C | T | 1 | a0001c0002t0002g0064 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1494-142C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10805774 | ||||||
| chr19:10805873
|
C | G | 54 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1494-43C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 12/20 | chr19 | 10805873 | ||||||
| chr19:10805981
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1545+14C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10805981 | ||||||
| chr19:10806008
|
C | T | 40 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1545+41C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806008 | ||||||
| chr19:10806092
|
A | C | 7 | a0001c0002t0001g0099a0001c0002t0001g0104a0001c0002t0001g0115others(4): Show | 7 | HG00438.hp2 HG02040.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+125A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806092 | ||||||
| chr19:10806281
|
A | G | 54 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1545+314A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806281 | ||||||
| chr19:10806307
|
G | A | 1 | a0001c0002t0002g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1545+340G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806307 | ||||||
| chr19:10806430
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1545+463G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806430 | ||||||
| chr19:10806442
|
C | A | 3 | a0001c0002t0002g0074a0001c0002t0002g0259a0001c0002t0002g0260 | 3 | NA18975.hp1 NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1545+475C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806442 | ||||||
| chr19:10806468
|
C | T | 2 | a0001c0002t0006g0161a0001c0002t0006g0165 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1545+501C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806468 | ||||||
| chr19:10806761
|
C | G | 54 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1545+794C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806761 | ||||||
| chr19:10806766
|
G | C | 126 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1545+799G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10806766 | ||||||
| chr19:10807123
|
A | G | 21 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0009others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1545+1156A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807123 | ||||||
| chr19:10807180
|
C | G | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1545+1213C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807180 | ||||||
| chr19:10807182
|
C | T | 8 | a0001c0001t0003g0155a0001c0001t0003g0164a0001c0001t0003g0189others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+1215C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807182 | ||||||
| chr19:10807257
|
C | T | 54 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1545+1290C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807257 | ||||||
| chr19:10807348
|
C | A | 8 | a0001c0001t0003g0155a0001c0001t0003g0164a0001c0001t0003g0189others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-1221C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807348 | ||||||
| chr19:10807539
|
C | CT | 97 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(94): Show | 97 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1546-1003dupT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr19 | 10807539 | |||||
| chr19:10807539
|
C | CTT | 19 | a0001c0002t0001g0218a0001c0002t0002g0043a0001c0002t0002g0051others(16): Show | 19 | HG00438.hp1 HG00673.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1546-1004_1546-100 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr19 | 10807539 | |||||
| chr19:10807539
|
CT | C | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0202others(2): Show | 5 | HG01070.hp2 HG02698.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1003delT | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr19 | 10807539 | |||||
| chr19:10807621
|
T | C | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1546-948T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807621 | ||||||
| chr19:10807659
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-910C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807659 | ||||||
| chr19:10807930
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1546-639G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10807930 | ||||||
| chr19:10808008
|
TGGTG | T | 49 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546-556_1546-553d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr19 | 10808008 | |||||
| chr19:10808145
|
G | GA | 61 | a0001c0001t0002g0091a0001c0001t0002g0277a0001c0002t0002g0013others(58): Show | 61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1546-413dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr19 | 10808145 | |||||
| chr19:10808165
|
G | A | 1 | a0001c0002t0002g0096 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1546-404G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10808165 | ||||||
| chr19:10808496
|
C | T | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1546-73C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 13/20 | chr19 | 10808496 | ||||||
| chr19:10808634
|
G | A | 1 | a0001c0002t0002g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1557+54G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10808634 | ||||||
| chr19:10808723
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1557+143G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10808723 | ||||||
| chr19:10808773
|
G | A | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1557+193G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10808773 | ||||||
| chr19:10808895
|
T | A | 1 | a0001c0010t0002g0077 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1557+315T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10808895 | ||||||
| chr19:10808920
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1557+340A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10808920 | ||||||
| chr19:10809239
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1557+659C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809239 | ||||||
| chr19:10809439
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0240a0001c0001t0001g0248others(1): Show | 4 | HG01074.hp1 HG01168.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+859A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809439 | ||||||
| chr19:10809462
|
T | C | 1 | a0001c0002t0002g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1557+882T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809462 | ||||||
| chr19:10809547
|
G | A | 1 | a0001c0001t0009g0033 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1557+967G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809547 | ||||||
| chr19:10809588
|
T | C | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1557+1008T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809588 | ||||||
| chr19:10809635
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1557+1055C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809635 | ||||||
| chr19:10809639
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0110others(6): Show | 9 | HG00323.hp1 HG01109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+1059C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10809639 | ||||||
| chr19:10810142
|
T | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0193 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1557+1562T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810142 | ||||||
| chr19:10810452
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1558-1812C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810452 | ||||||
| chr19:10810524
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1558-1740G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810524 | ||||||
| chr19:10810530
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1558-1734G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810530 | ||||||
| chr19:10810769
|
T | C | 1 | a0001c0002t0002g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1558-1495T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810769 | ||||||
| chr19:10810849
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1558-1415G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810849 | ||||||
| chr19:10810902
|
G | A | 49 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1558-1362G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810902 | ||||||
| chr19:10810949
|
T | C | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1558-1315T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10810949 | ||||||
| chr19:10811059
|
C | T | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1558-1205C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811059 | ||||||
| chr19:10811068
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1558-1196T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811068 | ||||||
| chr19:10811213
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1558-1051C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811213 | ||||||
| chr19:10811251
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0277 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1558-1013G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811251 | ||||||
| chr19:10811295
|
G | A | 4 | a0001c0001t0001g0199a0001c0002t0002g0004a0001c0002t0002g0140others(1): Show | 4 | HG02257.hp1 HG03239.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-969G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811295 | ||||||
| chr19:10811312
|
T | G | 10 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0181others(7): Show | 10 | NA18747.hp2 NA18948.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-952T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811312 | ||||||
| chr19:10811465
|
A | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0140a0001c0009t0002g0018 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1558-799A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811465 | ||||||
| chr19:10811527
|
C | T | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1558-737C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811527 | ||||||
| chr19:10811617
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1558-647G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811617 | ||||||
| chr19:10811821
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1558-443C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10811821 | ||||||
| chr19:10812051
|
G | C | 2 | a0001c0001t0002g0091a0001c0001t0002g0277 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1558-213G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10812051 | ||||||
| chr19:10812192
|
C | G | 5 | a0001c0002t0002g0063a0001c0002t0002g0090a0001c0002t0002g0144others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-72C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10812192 | ||||||
| chr19:10812252
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1558-12G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 14/20 | chr19 | 10812252 | ||||||
| chr19:10812441
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1671+64C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812441 | ||||||
| chr19:10812615
|
C | T | 1 | a0001c0002t0002g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1671+238C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812615 | ||||||
| chr19:10812621
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1671+244T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812621 | ||||||
| chr19:10812644
|
A | C | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1671+267A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812644 | ||||||
| chr19:10812660
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0192 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1671+283G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812660 | ||||||
| chr19:10812702
|
G | T | 2 | a0001c0002t0010g0092a0001c0005t0002g0141 | 2 | HG00140.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1671+325G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812702 | ||||||
| chr19:10812711
|
C | T | 1 | a0001c0002t0002g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1671+334C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10812711 | ||||||
| chr19:10813366
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1671+989G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10813366 | ||||||
| chr19:10813437
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1671+1060A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10813437 | ||||||
| chr19:10813482
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1671+1105T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10813482 | ||||||
| chr19:10813552
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1671+1175G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10813552 | ||||||
| chr19:10813680
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0191 | 3 | HG02559.hp2 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1671+1303G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10813680 | ||||||
| chr19:10813825
|
C | CA | 66 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0110others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1671+1463dupA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10813825 | |||||
| chr19:10813827
|
A | AAAG | 61 | a0001c0001t0002g0091a0001c0001t0002g0277a0001c0002t0002g0013others(58): Show | 61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1671+1452_1671+145 others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10813827 | |||||
| chr19:10814036
|
C | A | 56 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(53): Show | 56 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1671+1659C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814036 | ||||||
| chr19:10814333
|
G | A | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1671+1956G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814333 | ||||||
| chr19:10814343
|
A | G | 1 | a0001c0002t0002g0011 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1671+1966A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814343 | ||||||
| chr19:10814468
|
GA | G | 56 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(53): Show | 56 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1671+2100delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10814468 | |||||
| chr19:10814501
|
T | C | 1 | a0001c0002t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1671+2124T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814501 | ||||||
| chr19:10814577
|
C | G | 1 | a0001c0001t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1671+2200C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814577 | ||||||
| chr19:10814603
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0240 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1671+2226C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814603 | ||||||
| chr19:10814650
|
C | G | 1 | a0001c0001t0001g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1671+2273C>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814650 | ||||||
| chr19:10814683
|
TA | T | 3 | a0001c0002t0001g0125a0001c0002t0001g0147a0001c0002t0002g0055 | 3 | HG01257.hp1 NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1671+2307delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814683 | ||||||
| chr19:10814684
|
A | T | 123 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.1671+2307A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814684 | ||||||
| chr19:10814820
|
C | T | 57 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(54): Show | 57 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1671+2443C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10814820 | ||||||
| chr19:10815017
|
CCATGG | C | 4 | a0001c0003t0001g0168a0001c0003t0001g0177a0001c0003t0001g0182others(1): Show | 4 | NA18948.hp2 NA18964.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671+2642_1671+264 others(9): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10815017 | |||||
| chr19:10815047
|
G | A | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1671+2670G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815047 | ||||||
| chr19:10815164
|
G | A | 1 | a0001c0005t0002g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1671+2787G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815164 | ||||||
| chr19:10815211
|
G | A | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1671+2834G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815211 | ||||||
| chr19:10815236
|
A | G | 54 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1671+2859A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815236 | ||||||
| chr19:10815412
|
G | A | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1671+3035G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815412 | ||||||
| chr19:10815525
|
T | G | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1671+3148T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815525 | ||||||
| chr19:10815608
|
C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1671+3231C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815608 | ||||||
| chr19:10815817
|
C | A | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1671+3440C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815817 | ||||||
| chr19:10815845
|
T | C | 220 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0024others(217): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1671+3468T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815845 | ||||||
| chr19:10815933
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0226 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1671+3556G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815933 | ||||||
| chr19:10815935
|
G | A | 59 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1671+3558G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10815935 | ||||||
| chr19:10816144
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1671+3767C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816144 | ||||||
| chr19:10816188
|
C | T | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1672-3792C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816188 | ||||||
| chr19:10816212
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0002g0152 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1672-3768C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816212 | ||||||
| chr19:10816273
|
G | C | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1672-3707G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816273 | ||||||
| chr19:10816276
|
C | T | 7 | a0001c0002t0001g0112a0001c0002t0001g0120a0001c0002t0001g0124others(4): Show | 7 | HG00099.hp1 HG01074.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1672-3704C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816276 | ||||||
| chr19:10816338
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1672-3642T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816338 | ||||||
| chr19:10816353
|
C | T | 2 | a0001c0002t0010g0092a0001c0005t0002g0141 | 2 | HG00140.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1672-3627C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816353 | ||||||
| chr19:10816375
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1672-3605G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816375 | ||||||
| chr19:10816402
|
C | A | 2 | a0001c0002t0001g0147a0001c0002t0001g0148 | 2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1672-3578C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816402 | ||||||
| chr19:10816424
|
G | C | 143 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0110others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1672-3556G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816424 | ||||||
| chr19:10816600
|
C | A | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1672-3380C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816600 | ||||||
| chr19:10816643
|
T | G | 1 | a0001c0001t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1672-3337T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816643 | ||||||
| chr19:10816648
|
G | A | 5 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0002t0002g0272others(2): Show | 5 | HG01934.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1672-3332G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816648 | ||||||
| chr19:10816721
|
G | A | 4 | a0001c0002t0002g0044a0001c0002t0002g0080a0001c0002t0007g0045others(1): Show | 4 | NA18947.hp1 NA18973.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1672-3259G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816721 | ||||||
| chr19:10816864
|
T | C | 120 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1672-3116T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816864 | ||||||
| chr19:10816976
|
G | A | 18 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0052others(15): Show | 18 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1672-3004G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10816976 | ||||||
| chr19:10817199
|
A | G | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1672-2781A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817199 | ||||||
| chr19:10817232
|
T | C | 1 | a0001c0002t0002g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1672-2748T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817232 | ||||||
| chr19:10817269
|
G | T | 1 | a0001c0002t0002g0044 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1672-2711G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817269 | ||||||
| chr19:10817350
|
C | CG | 6 | a0001c0001t0001g0039a0001c0001t0001g0201a0001c0001t0001g0215others(3): Show | 6 | HG00673.hp1 HG01175.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1672-2626dupG | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10817350 | |||||
| chr19:10817405
|
C | T | 1 | a0001c0009t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1672-2575C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817405 | ||||||
| chr19:10817443
|
A | G | 4 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0002t0002g0272others(1): Show | 4 | HG02615.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-2537A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817443 | ||||||
| chr19:10817799
|
A | G | 1 | a0001c0002t0002g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1672-2181A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817799 | ||||||
| chr19:10817800
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1672-2180C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817800 | ||||||
| chr19:10817816
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1672-2164T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817816 | ||||||
| chr19:10817816
|
T | TGC | 18 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0036others(15): Show | 18 | HG00642.hp1 HG01099.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1672-2153_1672-215 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10817816 | |||||
| chr19:10817816
|
TGC | T | 8 | a0001c0002t0001g0104a0001c0002t0001g0132a0001c0002t0001g0133others(5): Show | 8 | HG00140.hp2 HG00438.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1672-2153_1672-215 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10817816 | |||||
| chr19:10817816
|
TGCGC | T | 57 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1672-2155_1672-215 others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10817816 | |||||
| chr19:10817818
|
C | T | 56 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0002t0002g0013others(53): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1672-2162C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817818 | ||||||
| chr19:10817820
|
C | T | 3 | a0001c0002t0001g0104a0001c0002t0001g0132a0001c0002t0001g0133 | 3 | HG00438.hp2 NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1672-2160C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817820 | ||||||
| chr19:10817825
|
G | A | 1 | a0001c0002t0006g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1672-2155G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817825 | ||||||
| chr19:10817830
|
C | A | 1 | a0001c0002t0006g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1672-2150C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817830 | ||||||
| chr19:10817837
|
G | A | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1672-2143G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10817837 | ||||||
| chr19:10818177
|
G | C | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1672-1803G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818177 | ||||||
| chr19:10818188
|
C | CCTCCCTC others(31): Show |
13 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0038others(10): Show | 13 | HG02015.hp2 HG02071.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1672-1726_1672-168 others(42): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10818188 | |||||
| chr19:10818188
|
C | CCTCCCTC others(145): Show |
1 | a0001c0001t0001g0258 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1672-1689_1672-168 others(156): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10818188 | |||||
| chr19:10818188
|
CCTCCCTC others(31): Show |
C | 76 | a0001c0001t0001g0034a0001c0001t0001g0095a0001c0001t0001g0102others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1672-1726_1672-168 others(42): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr19 | 10818188 | |||||
| chr19:10818402
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1672-1578T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818402 | ||||||
| chr19:10818474
|
G | C | 19 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0009others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1672-1506G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818474 | ||||||
| chr19:10818492
|
C | T | 2 | a0001c0002t0010g0092a0001c0005t0002g0141 | 2 | HG00140.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1672-1488C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818492 | ||||||
| chr19:10818611
|
G | C | 59 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1672-1369G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818611 | ||||||
| chr19:10818644
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0253 | 2 | HG00741.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1672-1336C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818644 | ||||||
| chr19:10818716
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1672-1264G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818716 | ||||||
| chr19:10818846
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1672-1134C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818846 | ||||||
| chr19:10818904
|
G | A | 3 | a0001c0002t0002g0144a0001c0002t0002g0276a0001c0002t0012g0149 | 3 | HG02622.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1672-1076G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818904 | ||||||
| chr19:10818958
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1672-1022C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10818958 | ||||||
| chr19:10819041
|
G | A | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1672-939G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819041 | ||||||
| chr19:10819098
|
A | G | 10 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0009others(7): Show | 10 | HG01255.hp2 HG01516.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-882A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819098 | ||||||
| chr19:10819629
|
G | A | 59 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1672-351G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819629 | ||||||
| chr19:10819638
|
G | A | 2 | a0001c0002t0002g0004a0001c0002t0002g0140 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1672-342G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819638 | ||||||
| chr19:10819743
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1672-237C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819743 | ||||||
| chr19:10819821
|
G | T | 6 | a0001c0002t0002g0044a0001c0002t0002g0051a0001c0002t0002g0080others(3): Show | 6 | NA18947.hp1 NA18962.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.1672-159G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819821 | ||||||
| chr19:10819846
|
G | A | 1 | a0002c0006t0002g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1672-134G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 15/20 | chr19 | 10819846 | ||||||
| chr19:10820106
|
C | A | 2 | a0001c0002t0002g0048a0001c0002t0013g0263 | 2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1781+17C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10820106 | ||||||
| chr19:10820159
|
T | TCACTGAG | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0262 | 3 | HG01884.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1781+81_1781+87dup others(7): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr19 | 10820159 | |||||
| chr19:10820730
|
G | A | 2 | a0001c0002t0010g0092a0001c0005t0002g0141 | 2 | HG00140.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1781+641G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10820730 | ||||||
| chr19:10820837
|
G | C | 3 | a0001c0002t0002g0073a0001c0002t0002g0081a0001c0002t0002g0198 | 3 | HG00673.hp2 NA19077.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1781+748G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10820837 | ||||||
| chr19:10820976
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1781+887C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10820976 | ||||||
| chr19:10820985
|
A | G | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1781+896A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10820985 | ||||||
| chr19:10821033
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1781+944G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821033 | ||||||
| chr19:10821034
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1781+945G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821034 | ||||||
| chr19:10821066
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1781+977C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821066 | ||||||
| chr19:10821206
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1781+1117A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821206 | ||||||
| chr19:10821540
|
C | CTT | 60 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(57): Show | 60 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1781+1459_1781+146 others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr19 | 10821540 | |||||
| chr19:10821731
|
A | G | 5 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0002t0002g0272others(2): Show | 5 | HG01934.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1781+1642A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821731 | ||||||
| chr19:10821783
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1781+1694G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821783 | ||||||
| chr19:10821910
|
G | A | 1 | a0001c0002t0002g0071 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1781+1821G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821910 | ||||||
| chr19:10821914
|
G | A | 21 | a0001c0002t0002g0042a0001c0002t0002g0043a0001c0002t0002g0052others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.1781+1825G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821914 | ||||||
| chr19:10821947
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1782-1841C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821947 | ||||||
| chr19:10821953
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1782-1835A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821953 | ||||||
| chr19:10821979
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1782-1809G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10821979 | ||||||
| chr19:10822042
|
ACCACACC others(23): Show |
A | 1 | a0003c0008t0001g0267 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1782-1744_1782-171 others(34): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr19 | 10822042 | |||||
| chr19:10822114
|
G | A | 5 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0002t0002g0272others(2): Show | 5 | HG01934.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1782-1674G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822114 | ||||||
| chr19:10822333
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1782-1455G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822333 | ||||||
| chr19:10822346
|
T | C | 129 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1782-1442T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822346 | ||||||
| chr19:10822407
|
T | C | 3 | a0001c0002t0001g0162a0001c0002t0002g0163a0001c0002t0002g0213 | 3 | HG02698.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1782-1381T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822407 | ||||||
| chr19:10822533
|
T | A | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1782-1255T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822533 | ||||||
| chr19:10822539
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1782-1249G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822539 | ||||||
| chr19:10822691
|
G | A | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1782-1097G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822691 | ||||||
| chr19:10822733
|
A | G | 1 | a0001c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1782-1055A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822733 | ||||||
| chr19:10822751
|
A | G | 63 | a0001c0002t0001g0030a0001c0002t0002g0004a0001c0002t0002g0013others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1782-1037A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822751 | ||||||
| chr19:10822837
|
G | T | 277 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0022others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1782-951G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10822837 | ||||||
| chr19:10823060
|
G | A | 1 | a0001c0002t0001g0146 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1782-728G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823060 | ||||||
| chr19:10823062
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1782-726G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823062 | ||||||
| chr19:10823153
|
T | C | 63 | a0001c0002t0001g0030a0001c0002t0002g0004a0001c0002t0002g0013others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1782-635T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823153 | ||||||
| chr19:10823335
|
G | A | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1782-453G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823335 | ||||||
| chr19:10823414
|
A | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0091a0001c0001t0002g0277 | 3 | HG02717.hp2 HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1782-374A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823414 | ||||||
| chr19:10823418
|
T | A | 60 | a0001c0001t0001g0199a0001c0002t0001g0030a0001c0002t0002g0013others(57): Show | 60 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1782-370T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823418 | ||||||
| chr19:10823419
|
A | T | 52 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1782-369A>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823419 | ||||||
| chr19:10823422
|
T | A | 1 | a0001c0002t0002g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1782-366T>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823422 | ||||||
| chr19:10823459
|
G | C | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1782-329G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823459 | ||||||
| chr19:10823615
|
G | A | 1 | a0001c0002t0002g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1782-173G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823615 | ||||||
| chr19:10823639
|
C | T | 1 | a0001c0002t0002g0013 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1782-149C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823639 | ||||||
| chr19:10823645
|
C | A | 1 | a0001c0002t0002g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1782-143C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823645 | ||||||
| chr19:10823726
|
G | C | 3 | a0001c0002t0001g0104a0001c0002t0001g0132a0001c0002t0001g0133 | 3 | HG00438.hp2 NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1782-62G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 16/20 | chr19 | 10823726 | ||||||
| chr19:10823930
|
G | GC | 60 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(57): Show | 60 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1893+31_1893+32ins others(1): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10823930 | ||||||
| chr19:10824147
|
T | C | 129 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1893+248T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824147 | ||||||
| chr19:10824219
|
C | T | 1 | a0001c0002t0002g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1893+320C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824219 | ||||||
| chr19:10824225
|
C | T | 1 | a0001c0002t0002g0266 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1893+326C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824225 | ||||||
| chr19:10824470
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1893+571C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824470 | ||||||
| chr19:10824602
|
C | T | 2 | a0001c0002t0002g0259a0001c0002t0002g0260 | 2 | NA18975.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1894-455C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824602 | ||||||
| chr19:10824674
|
A | C | 1 | a0001c0002t0002g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1894-383A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824674 | ||||||
| chr19:10824675
|
C | A | 1 | a0001c0002t0002g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1894-382C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824675 | ||||||
| chr19:10824702
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1894-355G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824702 | ||||||
| chr19:10824811
|
A | C | 2 | a0001c0002t0001g0001a0001c0002t0002g0043 | 2 | HG03239.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1894-246A>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824811 | ||||||
| chr19:10824830
|
A | G | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1894-227A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824830 | ||||||
| chr19:10824876
|
G | A | 2 | a0001c0002t0002g0004a0001c0009t0002g0018 | 2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1894-181G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 17/20 | chr19 | 10824876 | ||||||
| chr19:10825310
|
G | A | 61 | a0001c0001t0001g0041a0001c0002t0001g0030a0001c0002t0002g0013others(58): Show | 61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2058+89G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825310 | ||||||
| chr19:10825396
|
C | T | 1 | a0001c0002t0010g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2058+175C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825396 | ||||||
| chr19:10825442
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2058+221G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825442 | ||||||
| chr19:10825483
|
A | G | 18 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0113others(15): Show | 18 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.2058+262A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825483 | ||||||
| chr19:10825525
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0002g0163 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2058+304C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825525 | ||||||
| chr19:10825555
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2058+334G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825555 | ||||||
| chr19:10825674
|
A | AAG | 5 | a0001c0002t0002g0063a0001c0002t0002g0090a0001c0002t0002g0144others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2058+471_2058+472d others(4): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr19 | 10825674 | |||||
| chr19:10825674
|
A | AAGAG | 50 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.2058+469_2058+472d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr19 | 10825674 | |||||
| chr19:10825674
|
A | AAGAGAG | 7 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0010g0092others(4): Show | 7 | HG00140.hp2 HG02257.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2058+467_2058+472d others(8): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr19 | 10825674 | |||||
| chr19:10825694
|
A | G | 55 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2058+473A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825694 | ||||||
| chr19:10825853
|
CA | C | 150 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0024others(147): Show | 150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2058+653delA | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr19 | 10825853 | |||||
| chr19:10825898
|
G | T | 1 | a0001c0002t0002g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2058+677G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10825898 | ||||||
| chr19:10826061
|
G | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0241 | 2 | HG01192.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2058+840G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10826061 | ||||||
| chr19:10826137
|
G | C | 1 | a0001c0005t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2058+916G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10826137 | ||||||
| chr19:10826138
|
G | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0241 | 2 | HG01192.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2058+917G>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10826138 | ||||||
| chr19:10826176
|
C | T | 57 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(54): Show | 57 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.2058+955C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10826176 | ||||||
| chr19:10826215
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2058+994A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10826215 | ||||||
| chr19:10827003
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2058+1782C>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10827003 | ||||||
| chr19:10827044
|
G | A | 1 | a0001c0003t0001g0182 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2058+1823G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10827044 | ||||||
| chr19:10827187
|
T | C | 1 | a0001c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2059-1849T>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10827187 | ||||||
| chr19:10827221
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2059-1815C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10827221 | ||||||
| chr19:10827506
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2059-1530C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10827506 | ||||||
| chr19:10827607
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2059-1429C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10827607 | ||||||
| chr19:10828284
|
A | AAAAT | 130 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2059-748_2059-745d others(6): Show |
DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr19 | 10828284 | |||||
| chr19:10828342
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0210 | 3 | HG03710.hp2 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2059-694C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10828342 | ||||||
| chr19:10828383
|
C | T | 54 | a0001c0002t0002g0013a0001c0002t0002g0037a0001c0002t0002g0042others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2059-653C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10828383 | ||||||
| chr19:10828526
|
G | A | 3 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003 | 3 | HG03239.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2059-510G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10828526 | ||||||
| chr19:10828850
|
G | A | 1 | a0001c0002t0002g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2059-186G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10828850 | ||||||
| chr19:10828900
|
G | C | 6 | a0001c0001t0003g0155a0001c0001t0003g0164a0001c0001t0003g0189others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2059-136G>C | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 18/20 | chr19 | 10828900 | ||||||
| chr19:10829493
|
C | T | 1 | a0001c0002t0013g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2291+225C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 19/20 | chr19 | 10829493 | ||||||
| chr19:10829984
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2292-143G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 19/20 | chr19 | 10829984 | ||||||
| chr19:10830042
|
A | G | 59 | a0001c0002t0001g0030a0001c0002t0002g0013a0001c0002t0002g0037others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2292-85A>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 19/20 | chr19 | 10830042 | ||||||
| chr19:10830074
|
G | A | 2 | a0001c0002t0002g0046a0001c0002t0002g0047 | 2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2292-53G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 19/20 | chr19 | 10830074 | ||||||
| chr19:10830468
|
G | A | 1 | a0001c0002t0002g0019 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2543+90G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830468 | ||||||
| chr19:10830605
|
T | G | 1 | a0001c0002t0001g0003 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2543+227T>G | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830605 | ||||||
| chr19:10830712
|
C | T | 2 | a0001c0002t0001g0147a0001c0002t0001g0148 | 2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2544-266C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830712 | ||||||
| chr19:10830777
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2544-201G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830777 | ||||||
| chr19:10830829
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2544-149G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830829 | ||||||
| chr19:10830850
|
C | T | 2 | a0001c0001t0001g0136a0001c0002t0001g0134 | 2 | HG02071.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2544-128C>T | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830850 | ||||||
| chr19:10830851
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2544-127G>A | DNM2 | ENSG00000079805.19 | transcript | ENST00000389253.9 | protein_coding | 20/20 | chr19 | 10830851 |