Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55112 |
|---|---|
| ensemblid | ENSG00000126870.16 |
| hgncid | 21862 |
| symbol | DYNC2I1 |
| name | dynein 2 intermediate chain 1 |
| refseq_nuc | NM_018051.5 |
| refseq_prot | NP_060521.4 |
| ensembl_nuc | ENST00000407559.8 |
| ensembl_prot | ENSP00000384290.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 158856558 |
| end | 158946189 |
| strand | + |
| ver | v1.2 |
| region | chr7:158856558-158946189 |
| region5000 | chr7:158851558-158951189 |
| regionname0 | DYNC2I1_chr7_158856558_158946189 |
| regionname5000 | DYNC2I1_chr7_158851558_158951189 |
| 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 | 0/0 | 1066 | 121 | 17 | 20 | 72 | 1 | 11 | 52 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002 | 0/1 | 1066 | 99 | 16 | 24 | 44 | 3 | 11 | 31 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003 | 0/0 | 1065 | 27 | 4 | 7 | 8 | 2 | 6 | 5 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0004 | 0/0 | 1066 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0005 | 0/0 | 1065 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0006 | 0/0 | 1066 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0007 | 0/0 | 1066 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0008 | 0/0 | 1066 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0009 | 0/0 | 1066 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0010 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0011 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0012 | 0/0 | 203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0013 | 0/0 | 1066 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0014 | 0/0 | 1066 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0015 | 0/0 | 1066 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0016 | 0/0 | 1066 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0017 | 0/0 | 1066 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0018 | 0/0 | 1066 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0019 | 1/0 | 1066 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0020 | 0/0 | 1066 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| 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 | 0/0 | 3201 | 117 | 15 | 20 | 70 | 1 | 11 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0002 | 0/1 | 3201 | 96 | 15 | 23 | 43 | 3 | 11 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0003 | 0/0 | 3198 | 24 | 1 | 7 | 8 | 2 | 6 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0004 | 0/0 | 3201 | 6 | 6 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0005 | 0/0 | 3201 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0006 | 0/0 | 3201 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0007 | 0/0 | 3201 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0008 | 0/0 | 3201 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0009 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0010 | 0/0 | 3198 | 2 | 0 | 0 | 0 | 2 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0011 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0012 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0013 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0014 | 1/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0015 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0016 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0017 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0018 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0019 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0020 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0021 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0022 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0023 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0024 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0025 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0026 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0027 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0028 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| c0029 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| 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 | 0/1 | 589 | 107 | 18 | 27 | 47 | 4 | 10 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0002 | 0/0 | 589 | 82 | 10 | 17 | 46 | 1 | 8 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0003 | 0/0 | 589 | 25 | 2 | 1 | 21 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0004 | 0/0 | 589 | 22 | 1 | 8 | 3 | 4 | 6 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0005 | 0/0 | 589 | 5 | 0 | 0 | 3 | 1 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0006 | 0/0 | 589 | 5 | 5 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0007 | 0/0 | 589 | 5 | 0 | 0 | 5 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0008 | 0/0 | 589 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0009 | 0/0 | 589 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0010 | 1/0 | 589 | 2 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0011 | 0/0 | 589 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0012 | 0/0 | 589 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0013 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0014 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0015 | 0/0 | 589 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0016 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0017 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0018 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0019 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0020 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0021 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0022 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| t0023 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| 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 | 0/0 | 3201 | 117 | 15 | 20 | 70 | 1 | 11 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0012 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0021 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0022 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0023 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0002 | 0/1 | 3201 | 96 | 15 | 23 | 43 | 3 | 11 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0016 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0017 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0019 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0003 | 0/0 | 3198 | 24 | 1 | 7 | 8 | 2 | 6 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0009 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0027 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0004c0004 | 0/0 | 3201 | 6 | 6 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0005c0010 | 0/0 | 3198 | 2 | 0 | 0 | 0 | 2 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0006c0006 | 0/0 | 3201 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0007c0005 | 0/0 | 3201 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0008c0008 | 0/0 | 3201 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0009c0007 | 0/0 | 3201 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0010c0028 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0011c0029 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0012c0013 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0013c0015 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0014c0018 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0015c0026 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0016c0020 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0017c0024 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0018c0025 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0019c0014 | 1/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0020c0011 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3789 | 6 | 1 | 4 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0002 | 0/0 | 3789 | 76 | 7 | 16 | 45 | 0 | 8 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0003 | 0/0 | 3789 | 21 | 0 | 0 | 20 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0005 | 0/0 | 3789 | 5 | 0 | 0 | 3 | 1 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0006 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0009 | 0/0 | 3789 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0012 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0013 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0001t0019 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0012t0002 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0021t0003 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0022t0008 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0001c0023t0018 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0002t0001 | 0/1 | 3789 | 92 | 14 | 23 | 42 | 3 | 9 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0002t0014 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0002t0016 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0002t0017 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0002t0021 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0016t0010 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0017t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0002c0019t0015 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0003t0004 | 0/0 | 3786 | 19 | 1 | 7 | 3 | 2 | 6 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0003t0007 | 0/0 | 3786 | 5 | 0 | 0 | 5 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0009t0011 | 0/0 | 3786 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0003c0027t0022 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0004c0004t0001 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0004c0004t0002 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0004c0004t0006 | 0/0 | 3789 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0005c0010t0004 | 0/0 | 3786 | 2 | 0 | 0 | 0 | 2 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0006c0006t0008 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0007c0005t0002 | 0/0 | 3789 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0008c0008t0003 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0008c0008t0020 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0009c0007t0003 | 0/0 | 3789 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0010c0028t0023 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0011c0029t0004 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0012c0013t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0013c0015t0001 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0014c0018t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0015c0026t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0016c0020t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0017c0024t0001 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0018c0025t0002 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0019c0014t0010 | 1/0 | 3789 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| a0020c0011t0001 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | copy fasta | chr7 | 158851558 | 158951189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0013g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0001t0019g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0012t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0021t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0022t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0001c0023t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0014g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0016g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0017g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0002t0021g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0016t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0017t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0002c0019t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0003t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0009t0011g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0009t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0003c0027t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0004c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0004c0004t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0004c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0004c0004t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0004c0004t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0004c0004t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0005c0010t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0005c0010t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0006c0006t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0006c0006t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0007c0005t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0007c0005t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0008c0008t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0008c0008t0020g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0009c0007t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0009c0007t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0010c0028t0023g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0011c0029t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0012c0013t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0013c0015t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0014c0018t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0015c0026t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0016c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0017c0024t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0018c0025t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0019c0014t0010g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| a0020c0011t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0018 | c0025 | t0002 | g0149 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00140 | hp1 | a0017 | c0024 | t0001 | g0271 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00140 | hp2 | a0003 | c0003 | t0004 | g0249 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00408 | hp1 | a0003 | c0003 | t0007 | g0241 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00621 | hp1 | a0001 | c0001 | t0019 | g0235 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00733 | hp1 | a0011 | c0029 | t0004 | g0250 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01071 | hp2 | a0003 | c0003 | t0004 | g0239 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01081 | hp2 | a0002 | c0019 | t0015 | g0043 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01175 | hp2 | a0003 | c0003 | t0004 | g0252 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01255 | hp1 | a0003 | c0003 | t0004 | g0244 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01257 | hp2 | a0009 | c0007 | t0003 | g0229 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01346 | hp1 | a0003 | c0003 | t0004 | g0258 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01358 | hp1 | a0003 | c0003 | t0004 | g0256 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01361 | hp2 | a0003 | c0003 | t0004 | g0245 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01496 | hp2 | a0003 | c0003 | t0004 | g0254 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0067 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01516 | hp2 | a0005 | c0010 | t0004 | g0247 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0139 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01517 | hp2 | a0005 | c0010 | t0004 | g0251 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01934 | hp2 | a0007 | c0005 | t0002 | g0189 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02015 | hp1 | a0003 | c0003 | t0004 | g0264 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0196 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0224 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02055 | hp2 | a0003 | c0027 | t0022 | g0263 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02080 | hp1 | a0001 | c0001 | t0013 | g0118 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02155 | hp1 | a0003 | c0003 | t0004 | g0266 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02257 | hp2 | a0007 | c0005 | t0002 | g0225 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02258 | hp1 | a0009 | c0007 | t0003 | g0227 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02258 | hp2 | a0004 | c0004 | t0002 | g0192 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0188 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02451 | hp2 | a0002 | c0016 | t0010 | g0090 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02615 | hp2 | a0008 | c0008 | t0003 | g0226 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0234 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0136 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02698 | hp2 | a0003 | c0003 | t0004 | g0238 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02717 | hp1 | a0001 | c0022 | t0008 | g0185 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0233 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0223 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02809 | hp1 | a0006 | c0006 | t0008 | g0187 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02809 | hp2 | a0002 | c0002 | t0021 | g0083 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02818 | hp1 | a0004 | c0004 | t0006 | g0200 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02818 | hp2 | a0006 | c0006 | t0008 | g0186 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02922 | hp1 | a0010 | c0028 | t0023 | g0237 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02922 | hp2 | a0013 | c0015 | t0001 | g0051 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02976 | hp2 | a0003 | c0009 | t0011 | g0261 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03017 | hp2 | a0002 | c0002 | t0014 | g0078 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03209 | hp2 | a0003 | c0003 | t0004 | g0262 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03486 | hp2 | a0004 | c0004 | t0006 | g0199 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03491 | hp1 | a0003 | c0003 | t0004 | g0255 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03491 | hp2 | a0003 | c0003 | t0004 | g0257 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03710 | hp2 | a0002 | c0002 | t0016 | g0029 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03834 | hp2 | a0003 | c0003 | t0004 | g0246 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04184 | hp2 | a0003 | c0003 | t0004 | g0259 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG04228 | hp2 | a0003 | c0003 | t0004 | g0265 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | CHB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CHB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18951 | hp1 | a0003 | c0003 | t0004 | g0267 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18953 | hp1 | a0012 | c0013 | t0001 | g0104 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18957 | hp2 | a0003 | c0003 | t0007 | g0240 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18962 | hp1 | a0016 | c0020 | t0001 | g0001 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18964 | hp2 | a0003 | c0003 | t0007 | g0248 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18965 | hp2 | a0001 | c0012 | t0002 | g0167 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18974 | hp2 | a0014 | c0018 | t0001 | g0074 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18981 | hp2 | a0002 | c0017 | t0001 | g0013 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19030 | hp1 | a0004 | c0004 | t0002 | g0193 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19030 | hp2 | a0004 | c0004 | t0001 | g0170 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19043 | hp2 | a0003 | c0009 | t0011 | g0253 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19060 | hp2 | a0003 | c0003 | t0007 | g0243 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19064 | hp1 | a0003 | c0003 | t0007 | g0260 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19065 | hp2 | a0002 | c0002 | t0017 | g0024 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19066 | hp1 | a0015 | c0026 | t0001 | g0058 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19240 | hp1 | a0008 | c0008 | t0020 | g0228 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ASW | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA20129 | hp2 | a0001 | c0023 | t0018 | g0112 | AFR | ASW | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA20805 | hp1 | a0003 | c0003 | t0004 | g0242 | EUR | TSI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0077 | EUR | TSI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02109 | hp1 | a0020 | c0011 | t0001 | g0038 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18955 | hp1 | a0001 | c0021 | t0003 | g0216 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | USA | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | USA | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| NA21309 | hp2 | a0004 | c0004 | t0006 | g0201 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0056 | REF | REF | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| homoSapiens_grch38 | hp1 | a0019 | c0014 | t0010 | g0011 | REF | REF | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:158871383
|
TGAA | T | 4 | a0003a0005a0010others(1): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
conservative_inframe_deletion | MODERATE | c.313_315delAAG | p.Lys105del | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/25 | 491/3789 | 313/3201 | 105/1066 | INFO_REALIGN_3_PRIME | chr7 | 158871383 | |
| chr7:158871517
|
C | A | 1 | a0020 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.445C>A | p.Arg149Ser | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/25 | 623/3789 | 445/3201 | 149/1066 | chr7 | 158871517 | ||
| chr7:158879714
|
C | G | 2 | a0008a0009 | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
missense_variant | MODERATE | c.604C>G | p.Leu202Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 782/3789 | 604/3201 | 202/1066 | chr7 | 158879714 | ||
| chr7:158879722
|
C | A | 1 | a0012 | 1 | NA18953.hp1 | stop_gained | HIGH | c.612C>A | p.Tyr204* | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 790/3789 | 612/3201 | 204/1066 | chr7 | 158879722 | ||
| chr7:158879785
|
C | G | 19 | a0001a0002a0003others(16): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
missense_variant | MODERATE | c.675C>G | p.Asn225Lys | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 853/3789 | 675/3201 | 225/1066 | chr7 | 158879785 | ||
| chr7:158879824
|
G | T | 1 | a0005 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.714G>T | p.Glu238Asp | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 892/3789 | 714/3201 | 238/1066 | chr7 | 158879824 | ||
| chr7:158879928
|
A | G | 12 | a0001a0003a0004others(9): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
missense_variant | MODERATE | c.818A>G | p.Gln273Arg | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 996/3789 | 818/3201 | 273/1066 | chr7 | 158879928 | ||
| chr7:158887026
|
C | T | 1 | a0018 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.941C>T | p.Ala314Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/25 | 1119/3789 | 941/3201 | 314/1066 | chr7 | 158887026 | ||
| chr7:158891314
|
C | T | 1 | a0008 | 2 | HG02615.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.1040C>T | p.Pro347Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/25 | 1218/3789 | 1040/3201 | 347/1066 | chr7 | 158891314 | ||
| chr7:158905989
|
A | G | 1 | a0017 | 1 | HG00140.hp1 | missense_variant&splice_region_variant | MODERATE | c.1358A>G | p.Asp453Gly | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/25 | 1536/3789 | 1358/3201 | 453/1066 | chr7 | 158905989 | ||
| chr7:158911554
|
C | G | 1 | a0006 | 2 | HG02809.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.1465C>G | p.Arg489Gly | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/25 | 1643/3789 | 1465/3201 | 489/1066 | chr7 | 158911554 | ||
| chr7:158913079
|
G | A | 1 | a0013 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1685G>A | p.Ser562Asn | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/25 | 1863/3789 | 1685/3201 | 562/1066 | chr7 | 158913079 | ||
| chr7:158918774
|
C | T | 1 | a0011 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1826C>T | p.Ala609Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/25 | 2004/3789 | 1826/3201 | 609/1066 | chr7 | 158918774 | ||
| chr7:158923686
|
C | T | 1 | a0010 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2210C>T | p.Thr737Met | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/25 | 2388/3789 | 2210/3201 | 737/1066 | chr7 | 158923686 | ||
| chr7:158926283
|
C | T | 1 | a0007 | 2 | HG01934.hp2 HG02257.hp2 |
missense_variant | MODERATE | c.2354C>T | p.Pro785Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/25 | 2532/3789 | 2354/3201 | 785/1066 | chr7 | 158926283 | ||
| chr7:158926425
|
A | G | 2 | a0004a0007 | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.2395A>G | p.Ile799Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/25 | 2573/3789 | 2395/3201 | 799/1066 | chr7 | 158926425 | ||
| chr7:158927025
|
G | A | 1 | a0016 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.2467G>A | p.Gly823Ser | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/25 | 2645/3789 | 2467/3201 | 823/1066 | chr7 | 158927025 | ||
| chr7:158941970
|
G | A | 1 | a0015 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.2824G>A | p.Ala942Thr | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/25 | 3002/3789 | 2824/3201 | 942/1066 | chr7 | 158941970 | ||
| chr7:158945703
|
C | T | 1 | a0014 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.3125C>T | p.Pro1042Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 3303/3789 | 3125/3201 | 1042/1066 | chr7 | 158945703 | ||
| chr7:158946187
|
A | C | 12 | a0001a0002a0003others(9): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
splice_region_variant | LOW | c.*408A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | chr7 | 158946187 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:158876637
|
T | C | 1 | a0001c0012 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.519T>C | p.Asp173Asp | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/25 | 697/3789 | 519/3201 | 173/1066 | chr7 | 158876637 | ||
| chr7:158879782
|
C | T | 1 | a0015c0026 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.672C>T | p.Asp224Asp | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 850/3789 | 672/3201 | 224/1066 | chr7 | 158879782 | ||
| chr7:158922510
|
G | A | 1 | a0001c0021 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.2055G>A | p.Gln685Gln | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/25 | 2233/3789 | 2055/3201 | 685/1066 | chr7 | 158922510 | ||
| chr7:158922528
|
A | G | 21 | a0001c0001a0001c0012a0001c0021others(18): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
synonymous_variant | LOW | c.2073A>G | p.Lys691Lys | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/25 | 2251/3789 | 2073/3201 | 691/1066 | chr7 | 158922528 | ||
| chr7:158926415
|
G | A | 3 | a0003c0009a0004c0004a0007c0005 | 10 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
synonymous_variant | LOW | c.2385G>A | p.Leu795Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/25 | 2563/3789 | 2385/3201 | 795/1066 | chr7 | 158926415 | ||
| chr7:158927024
|
A | G | 1 | a0016c0020 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.2466A>G | p.Ala822Ala | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/25 | 2644/3789 | 2466/3201 | 822/1066 | chr7 | 158927024 | ||
| chr7:158934192
|
T | G | 1 | a0002c0017 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.2610T>G | p.Pro870Pro | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/25 | 2788/3789 | 2610/3201 | 870/1066 | chr7 | 158934192 | ||
| chr7:158941972
|
G | C | 1 | a0001c0023 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.2826G>C | p.Ala942Ala | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/25 | 3004/3789 | 2826/3201 | 942/1066 | chr7 | 158941972 | ||
| chr7:158942122
|
C | T | 3 | a0002c0019a0003c0027a0005c0010 | 4 | HG01081.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
synonymous_variant | LOW | c.2976C>T | p.Val992Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/25 | 3154/3789 | 2976/3201 | 992/1066 | chr7 | 158942122 | ||
| chr7:158945659
|
T | C | 1 | a0001c0023 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3081T>C | p.Ser1027Ser | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 3259/3789 | 3081/3201 | 1027/1066 | chr7 | 158945659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:158856569
|
C | T | 8 | a0001c0001t0012a0003c0003t0004a0003c0003t0007others(5): Show | 33 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-167C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 167 | chr7 | 158856569 | |||||
| chr7:158856589
|
T | C | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(11): Show | 119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
5_prime_UTR_variant | MODIFIER | c.-147T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 147 | chr7 | 158856589 | |||||
| chr7:158856606
|
C | T | 1 | a0003c0003t0007 | 5 | HG00408.hp1 NA18957.hp2 NA18964.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-130C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 130 | chr7 | 158856606 | |||||
| chr7:158856613
|
T | C | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(11): Show | 119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | chr7 | 158856613 | ||||||
| chr7:158856643
|
C | T | 2 | a0001c0001t0009a0001c0001t0012 | 5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 93 | chr7 | 158856643 | |||||
| chr7:158856654
|
C | T | 1 | a0002c0002t0021 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 82 | chr7 | 158856654 | |||||
| chr7:158856682
|
A | G | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(22): Show | 155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 54 | chr7 | 158856682 | |||||
| chr7:158856721
|
G | A | 1 | a0001c0001t0013 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 15 | chr7 | 158856721 | |||||
| chr7:158945780
|
C | T | 1 | a0002c0002t0017 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 1 | chr7 | 158945780 | |||||
| chr7:158945815
|
C | T | 1 | a0008c0008t0020 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 36 | chr7 | 158945815 | |||||
| chr7:158945832
|
T | G | 1 | a0001c0023t0018 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 53 | chr7 | 158945832 | |||||
| chr7:158945884
|
T | C | 1 | a0002c0002t0014 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 105 | chr7 | 158945884 | |||||
| chr7:158945920
|
G | T | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(20): Show | 125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 141 | chr7 | 158945920 | |||||
| chr7:158945934
|
C | T | 1 | a0002c0002t0016 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 155 | chr7 | 158945934 | |||||
| chr7:158945943
|
G | C | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(20): Show | 125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*164G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 164 | chr7 | 158945943 | |||||
| chr7:158946140
|
A | G | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*361A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 361 | chr7 | 158946140 | |||||
| chr7:158946158
|
T | C | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*379T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 379 | chr7 | 158946158 | |||||
| chr7:158946184
|
C | G | 1 | a0010c0028t0023 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 405 | chr7 | 158946184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:158856911
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+161A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158856911 | ||||||
| chr7:158857062
|
G | A | 1 | a0002c0002t0001g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.15+312G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857062 | ||||||
| chr7:158857095
|
G | T | 156 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(153): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.15+345G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857095 | ||||||
| chr7:158857110
|
G | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+360G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857110 | ||||||
| chr7:158857213
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+463C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857213 | ||||||
| chr7:158857359
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.15+609A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857359 | ||||||
| chr7:158857432
|
A | G | 1 | a0001c0001t0003g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.15+682A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857432 | ||||||
| chr7:158857505
|
A | G | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15+755A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857505 | ||||||
| chr7:158857523
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+773A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857523 | ||||||
| chr7:158857534
|
G | GT | 16 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232others(13): Show | 16 | HG00597.hp2 HG01257.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+789dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857534 | |||||
| chr7:158857534
|
G | GTT | 3 | a0001c0001t0009g0233a0001c0001t0009g0234a0003c0003t0004g0267 | 3 | HG02647.hp2 HG02723.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.15+788_15+789dupTT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857534 | |||||
| chr7:158857538
|
TTG | T | 6 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+790_15+791delGT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857538 | |||||
| chr7:158857539
|
TG | T | 71 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.15+790delG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857539 | ||||||
| chr7:158857540
|
G | GT | 9 | a0001c0001t0001g0273a0002c0002t0001g0097a0002c0002t0001g0098others(6): Show | 9 | HG01981.hp1 HG02004.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+806dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857540 | |||||
| chr7:158857540
|
G | T | 84 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0194others(81): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+790G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857540 | ||||||
| chr7:158857609
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+859C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857609 | ||||||
| chr7:158857712
|
A | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+962A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857712 | ||||||
| chr7:158857768
|
CTTCG | C | 9 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1020_15+1023del others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857768 | |||||
| chr7:158857773
|
T | C | 9 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1023T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857773 | ||||||
| chr7:158857774
|
G | A | 9 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1024G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857774 | ||||||
| chr7:158857787
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.15+1037C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857787 | ||||||
| chr7:158857791
|
C | CT | 5 | a0002c0002t0001g0093a0002c0002t0001g0094a0002c0002t0001g0095others(2): Show | 5 | HG02280.hp2 NA18939.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1060dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | |||||
| chr7:158857791
|
CT | C | 5 | a0002c0002t0001g0006a0002c0002t0001g0007a0002c0002t0001g0008others(2): Show | 5 | HG01070.hp1 HG01167.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1060delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | |||||
| chr7:158857791
|
CTT | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(6): Show | 9 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+1059_15+1060del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | |||||
| chr7:158857791
|
CTTT | C | 41 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0003g0230others(38): Show | 41 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.15+1058_15+1060del others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | |||||
| chr7:158857791
|
CTTTT | C | 113 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(110): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.15+1057_15+1060del others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | |||||
| chr7:158857796
|
T | C | 1 | a0001c0001t0003g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.15+1046T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857796 | ||||||
| chr7:158857853
|
C | A | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1103C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857853 | ||||||
| chr7:158857875
|
C | T | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1125C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857875 | ||||||
| chr7:158858010
|
C | T | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.15+1260C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858010 | ||||||
| chr7:158858033
|
C | T | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1283C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858033 | ||||||
| chr7:158858133
|
A | G | 273 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.15+1383A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858133 | ||||||
| chr7:158858155
|
C | G | 9 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1405C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858155 | ||||||
| chr7:158858250
|
G | A | 123 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.15+1500G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858250 | ||||||
| chr7:158858297
|
A | G | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1547A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858297 | ||||||
| chr7:158858396
|
G | A | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+1646G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858396 | ||||||
| chr7:158858465
|
A | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.15+1715A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858465 | ||||||
| chr7:158858641
|
C | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+1891C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858641 | ||||||
| chr7:158858739
|
C | G | 3 | a0001c0001t0002g0179a0001c0001t0005g0180a0001c0001t0005g0202 | 3 | HG00544.hp2 HG02004.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.15+1989C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858739 | ||||||
| chr7:158858772
|
G | C | 1 | a0003c0003t0004g0239 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.15+2022G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858772 | ||||||
| chr7:158858784
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.15+2034C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858784 | ||||||
| chr7:158858827
|
T | TC | 41 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.15+2083dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858827 | |||||
| chr7:158858828
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+2078C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858828 | ||||||
| chr7:158858850
|
TTCCTCTC others(3): Show |
T | 1 | a0001c0001t0002g0130 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.15+2104_15+2113del others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858850 | |||||
| chr7:158858855
|
C | CTCCCCTC others(5): Show |
1 | a0002c0002t0001g0018 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.15+2112_15+2123dup others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858855 | |||||
| chr7:158858857
|
CCCCTCCC others(10): Show |
C | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+2124_15+2140del others(17): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858857 | |||||
| chr7:158858910
|
T | C | 1 | a0001c0001t0003g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.15+2160T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858910 | ||||||
| chr7:158858922
|
T | TC | 11 | a0001c0001t0002g0114a0001c0001t0002g0119a0001c0001t0002g0131others(8): Show | 11 | HG00597.hp2 HG01243.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+2178dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858922 | |||||
| chr7:158858946
|
C | CCCTCCCC others(8): Show |
26 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.15+2224_15+2238dup others(15): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858946 | |||||
| chr7:158858946
|
C | CCCTCCCC others(23): Show |
1 | a0003c0003t0007g0260 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.15+2209_15+2238dup others(30): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858946 | |||||
| chr7:158858946
|
CCCTCCCC others(8): Show |
C | 6 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+2224_15+2238del others(15): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858946 | |||||
| chr7:158858979
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+2229T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858979 | ||||||
| chr7:158858984
|
T | C | 3 | a0001c0001t0003g0208a0001c0001t0003g0231a0002c0002t0001g0022 | 3 | HG00597.hp2 HG01255.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.15+2234T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858984 | ||||||
| chr7:158858984
|
T | TC | 30 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0273others(27): Show | 30 | HG00597.hp1 HG01169.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.15+2241dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858984 | |||||
| chr7:158858984
|
T | TCCCCTTT others(9): Show |
2 | a0003c0003t0004g0267a0003c0003t0007g0243 | 2 | NA18951.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.15+2238_15+2239ins others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858984 | |||||
| chr7:158858984
|
T | TCCCCTTT others(10): Show |
1 | a0003c0003t0007g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.15+2238_15+2239ins others(17): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858984 | |||||
| chr7:158859040
|
A | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+2290A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859040 | ||||||
| chr7:158859150
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.15+2400C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859150 | ||||||
| chr7:158859564
|
G | C | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+2814G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859564 | ||||||
| chr7:158859660
|
G | A | 5 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+2910G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859660 | ||||||
| chr7:158859714
|
G | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+2964G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859714 | ||||||
| chr7:158859901
|
G | A | 1 | a0002c0002t0001g0028 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+3151G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859901 | ||||||
| chr7:158860056
|
GT | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.15+3321delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158860056 | |||||
| chr7:158860078
|
G | A | 1 | a0001c0001t0002g0135 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.15+3328G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860078 | ||||||
| chr7:158860238
|
T | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+3488T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860238 | ||||||
| chr7:158860338
|
C | T | 96 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(93): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.15+3588C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860338 | ||||||
| chr7:158860382
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+3632C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860382 | ||||||
| chr7:158860626
|
T | C | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15+3876T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860626 | ||||||
| chr7:158860726
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.15+3976A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860726 | ||||||
| chr7:158861034
|
G | A | 272 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.15+4284G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861034 | ||||||
| chr7:158861035
|
G | T | 1 | a0002c0002t0001g0028 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+4285G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861035 | ||||||
| chr7:158861235
|
T | C | 1 | a0002c0002t0001g0095 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.15+4485T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861235 | ||||||
| chr7:158861289
|
G | A | 1 | a0002c0002t0001g0028 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+4539G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861289 | ||||||
| chr7:158861388
|
C | T | 8 | a0001c0001t0002g0135a0001c0001t0002g0174a0001c0001t0002g0175others(5): Show | 8 | HG00544.hp2 HG02155.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+4638C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861388 | ||||||
| chr7:158861515
|
C | A | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.15+4765C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861515 | ||||||
| chr7:158861706
|
G | A | 2 | a0001c0001t0003g0205a0001c0001t0003g0231 | 2 | HG00597.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.15+4956G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861706 | ||||||
| chr7:158861780
|
G | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+5030G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861780 | ||||||
| chr7:158862286
|
A | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0171a0001c0001t0002g0172others(1): Show | 4 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5536A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862286 | ||||||
| chr7:158862303
|
CAG | C | 5 | a0001c0001t0019g0235a0004c0004t0001g0170a0004c0004t0006g0199others(2): Show | 5 | HG00621.hp1 HG02818.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+5554_15+5555del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862303 | ||||||
| chr7:158862352
|
CATTGATT | C | 9 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+5610_15+5616del others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862352 | |||||
| chr7:158862514
|
C | T | 2 | a0008c0008t0003g0226a0008c0008t0020g0228 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15+5764C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862514 | ||||||
| chr7:158862521
|
A | C | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15+5771A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862521 | ||||||
| chr7:158862526
|
G | C | 8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5776G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862526 | ||||||
| chr7:158862552
|
T | TA | 64 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.15+5822dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | |||||
| chr7:158862552
|
T | TAA | 95 | a0001c0001t0001g0270a0001c0001t0002g0105a0001c0001t0002g0106others(92): Show | 95 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.15+5821_15+5822dup others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | |||||
| chr7:158862552
|
T | TAAA | 7 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0137others(4): Show | 7 | HG02056.hp2 HG02683.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+5820_15+5822dup others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | |||||
| chr7:158862552
|
TA | T | 6 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0023t0018g0112others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5822delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | |||||
| chr7:158862635
|
T | G | 1 | a0020c0011t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.15+5885T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862635 | ||||||
| chr7:158862659
|
G | A | 1 | a0003c0003t0004g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.15+5909G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862659 | ||||||
| chr7:158862667
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5917C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862667 | ||||||
| chr7:158862678
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15+5928C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862678 | ||||||
| chr7:158862764
|
A | C | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15+6014A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862764 | ||||||
| chr7:158862843
|
T | C | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+6093T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862843 | ||||||
| chr7:158862955
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.15+6205G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862955 | ||||||
| chr7:158863013
|
A | G | 1 | a0004c0004t0006g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15+6263A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863013 | ||||||
| chr7:158863044
|
A | G | 1 | a0002c0002t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.15+6294A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863044 | ||||||
| chr7:158863083
|
G | A | 1 | a0002c0002t0001g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.15+6333G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863083 | ||||||
| chr7:158863131
|
G | T | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273 | 3 | HG01433.hp1 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.15+6381G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863131 | ||||||
| chr7:158863168
|
C | T | 96 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(93): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.15+6418C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863168 | ||||||
| chr7:158863179
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.15+6429G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863179 | ||||||
| chr7:158863274
|
G | A | 3 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041 | 3 | HG00733.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.15+6524G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863274 | ||||||
| chr7:158863285
|
C | T | 2 | a0007c0005t0002g0189a0007c0005t0002g0225 | 2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.15+6535C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863285 | ||||||
| chr7:158863293
|
C | G | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+6543C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863293 | ||||||
| chr7:158863294
|
A | G | 1 | a0001c0001t0005g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.15+6544A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863294 | ||||||
| chr7:158863310
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.16-6545C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863310 | ||||||
| chr7:158863321
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.16-6534C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863321 | ||||||
| chr7:158863510
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.16-6345G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863510 | ||||||
| chr7:158863527
|
T | C | 1 | a0002c0002t0001g0012 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.16-6328T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863527 | ||||||
| chr7:158863580
|
G | C | 3 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0093 | 3 | HG01358.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.16-6275G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863580 | ||||||
| chr7:158863585
|
A | AG | 8 | a0001c0001t0002g0117a0001c0001t0002g0128a0001c0001t0003g0230others(5): Show | 8 | HG01255.hp2 HG02486.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-6264dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863585 | |||||
| chr7:158863626
|
T | TG | 25 | a0001c0001t0001g0269a0001c0001t0002g0138a0001c0001t0002g0165others(22): Show | 25 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-6221dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863626 | |||||
| chr7:158863629
|
G | C | 2 | a0002c0002t0001g0089a0002c0019t0015g0043 | 2 | HG01081.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.16-6226G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863629 | ||||||
| chr7:158863643
|
G | A | 95 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.16-6212G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863643 | ||||||
| chr7:158863657
|
T | TG | 29 | a0001c0001t0001g0003a0001c0001t0001g0273a0001c0001t0009g0233others(26): Show | 29 | HG00423.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.16-6189dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863657 | |||||
| chr7:158863664
|
G | GC | 110 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(107): Show | 110 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.16-6191_16-6190ins others(1): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863664 | ||||||
| chr7:158863667
|
T | G | 3 | a0001c0022t0008g0185a0006c0006t0008g0186a0006c0006t0008g0187 | 3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.16-6188T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863667 | ||||||
| chr7:158863669
|
T | TG | 5 | a0001c0001t0003g0209a0001c0001t0003g0231a0001c0001t0012g0224others(2): Show | 5 | HG00597.hp2 HG02055.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-6182dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863669 | |||||
| chr7:158863705
|
T | TG | 67 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0002g0117others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.16-6142dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863705 | |||||
| chr7:158863713
|
G | C | 28 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(25): Show | 28 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-6142G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863713 | ||||||
| chr7:158863785
|
C | CG | 88 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(85): Show | 88 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.16-6063dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863785 | |||||
| chr7:158863785
|
C | G | 1 | a0001c0001t0002g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.16-6070C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863785 | ||||||
| chr7:158863788
|
GGGGGAGC others(110): Show |
G | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.16-6043_16-5927del | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863788 | |||||
| chr7:158863847
|
CGGGTGTT others(3): Show |
C | 22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-5994_16-5985del others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863847 | |||||
| chr7:158863869
|
G | T | 9 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-5986G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863869 | ||||||
| chr7:158863899
|
T | TG | 6 | a0001c0001t0002g0134a0001c0001t0003g0207a0001c0001t0003g0211others(3): Show | 6 | HG00544.hp1 HG02698.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-5951dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863899 | |||||
| chr7:158863935
|
T | TG | 7 | a0001c0001t0002g0158a0001c0001t0002g0166a0001c0001t0002g0190others(4): Show | 7 | HG00438.hp2 HG01192.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-5915dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863935 | |||||
| chr7:158864040
|
C | CG | 5 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0002g0183others(2): Show | 5 | HG01192.hp2 NA19001.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-5811dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158864040 | |||||
| chr7:158864045
|
T | G | 1 | a0001c0001t0003g0205 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.16-5810T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864045 | ||||||
| chr7:158864088
|
T | TG | 7 | a0001c0001t0001g0269a0001c0001t0003g0208a0001c0001t0003g0209others(4): Show | 7 | HG00733.hp1 HG01433.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-5761dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158864088 | |||||
| chr7:158864097
|
A | C | 128 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(125): Show | 128 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.16-5758A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864097 | ||||||
| chr7:158864118
|
T | A | 34 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005others(31): Show | 34 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.16-5737T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864118 | ||||||
| chr7:158864120
|
T | TG | 38 | a0001c0001t0001g0269a0001c0001t0002g0128a0001c0001t0002g0130others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.16-5726dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158864120 | |||||
| chr7:158864123
|
G | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.16-5732G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864123 | ||||||
| chr7:158864134
|
G | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.16-5721G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864134 | ||||||
| chr7:158864351
|
CAT | C | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-5503_16-5502del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864351 | ||||||
| chr7:158864537
|
T | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.16-5318T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864537 | ||||||
| chr7:158864568
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.16-5287G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864568 | ||||||
| chr7:158864590
|
G | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-5265G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864590 | ||||||
| chr7:158864628
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.16-5227G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864628 | ||||||
| chr7:158864736
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-5119G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864736 | ||||||
| chr7:158864921
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.16-4934G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864921 | ||||||
| chr7:158865173
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-4682C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865173 | ||||||
| chr7:158865482
|
G | T | 1 | a0001c0001t0002g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-4373G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865482 | ||||||
| chr7:158865676
|
C | G | 1 | a0001c0001t0009g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-4179C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865676 | ||||||
| chr7:158865865
|
A | C | 2 | a0002c0002t0017g0024a0002c0017t0001g0013 | 2 | NA18981.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.16-3990A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865865 | ||||||
| chr7:158866102
|
T | TAAC | 159 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(156): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.16-3752_16-3750dup others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158866102 | |||||
| chr7:158866125
|
A | G | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16-3730A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866125 | ||||||
| chr7:158866225
|
C | T | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3630C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866225 | ||||||
| chr7:158866329
|
T | C | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00408.hp1 HG00733.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.16-3526T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866329 | ||||||
| chr7:158866331
|
G | C | 1 | a0003c0003t0004g0249 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.16-3524G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866331 | ||||||
| chr7:158866884
|
C | CA | 19 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(16): Show | 19 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.16-2957dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158866884 | |||||
| chr7:158866914
|
A | C | 6 | a0002c0002t0001g0033a0002c0002t0001g0066a0002c0002t0001g0067others(3): Show | 6 | HG01346.hp2 HG01516.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-2941A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866914 | ||||||
| chr7:158866963
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-2892A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866963 | ||||||
| chr7:158866983
|
A | G | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-2872A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866983 | ||||||
| chr7:158867018
|
G | GT | 26 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.16-2819dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158867018 | |||||
| chr7:158867018
|
G | GTT | 9 | a0001c0001t0003g0209a0001c0001t0003g0220a0001c0001t0009g0188others(6): Show | 9 | HG02055.hp2 HG02056.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-2820_16-2819dup others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158867018 | |||||
| chr7:158867018
|
GT | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.16-2819delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158867018 | |||||
| chr7:158867128
|
G | C | 1 | a0004c0004t0006g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16-2727G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867128 | ||||||
| chr7:158867193
|
G | C | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-2662G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867193 | ||||||
| chr7:158867298
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.16-2557G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867298 | ||||||
| chr7:158867398
|
C | T | 1 | a0002c0002t0001g0036 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.16-2457C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867398 | ||||||
| chr7:158867436
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-2419G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867436 | ||||||
| chr7:158867650
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.16-2205C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867650 | ||||||
| chr7:158867682
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.16-2173T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867682 | ||||||
| chr7:158867729
|
G | A | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-2126G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867729 | ||||||
| chr7:158867733
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-2122C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867733 | ||||||
| chr7:158867747
|
G | C | 1 | a0001c0001t0002g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2108G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867747 | ||||||
| chr7:158867749
|
C | T | 1 | a0001c0001t0002g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2106C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867749 | ||||||
| chr7:158867750
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2105T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867750 | ||||||
| chr7:158867800
|
C | T | 23 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-2055C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867800 | ||||||
| chr7:158867891
|
C | T | 7 | a0002c0002t0001g0015a0002c0002t0001g0053a0002c0002t0001g0069others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-1964C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867891 | ||||||
| chr7:158868059
|
G | A | 1 | a0001c0001t0006g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.16-1796G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868059 | ||||||
| chr7:158868155
|
C | G | 23 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-1700C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868155 | ||||||
| chr7:158868232
|
C | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.16-1623C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868232 | ||||||
| chr7:158868277
|
C | G | 1 | a0001c0001t0002g0177 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-1578C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868277 | ||||||
| chr7:158868286
|
G | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.16-1569G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868286 | ||||||
| chr7:158868407
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-1448G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868407 | ||||||
| chr7:158868572
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16-1283C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868572 | ||||||
| chr7:158868613
|
G | A | 1 | a0002c0002t0001g0014 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.16-1242G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868613 | ||||||
| chr7:158868663
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.16-1192G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868663 | ||||||
| chr7:158868682
|
G | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-1173G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868682 | ||||||
| chr7:158868964
|
G | C | 1 | a0001c0012t0002g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.16-891G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868964 | ||||||
| chr7:158869005
|
A | G | 1 | a0002c0002t0001g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.16-850A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869005 | ||||||
| chr7:158869067
|
G | A | 158 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.16-788G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869067 | ||||||
| chr7:158869146
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.16-709C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869146 | ||||||
| chr7:158869215
|
CCCCTCTG others(31): Show |
C | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-591_16-554delCC others(36): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158869215 | |||||
| chr7:158869237
|
G | A | 3 | a0003c0003t0004g0238a0003c0003t0004g0254a0003c0003t0004g0258 | 3 | HG01346.hp1 HG01496.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.16-618G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869237 | ||||||
| chr7:158869314
|
A | T | 4 | a0004c0004t0002g0192a0004c0004t0002g0193a0007c0005t0002g0189others(1): Show | 4 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-541A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869314 | ||||||
| chr7:158869340
|
C | T | 2 | a0001c0001t0003g0217a0001c0012t0002g0167 | 2 | HG02129.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.16-515C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869340 | ||||||
| chr7:158869446
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-409C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869446 | ||||||
| chr7:158869491
|
G | A | 24 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(21): Show | 24 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.16-364G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869491 | ||||||
| chr7:158869559
|
T | C | 23 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-296T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869559 | ||||||
| chr7:158869719
|
C | A | 9 | a0002c0002t0001g0037a0002c0002t0001g0054a0002c0002t0001g0070others(6): Show | 9 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-136C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869719 | ||||||
| chr7:158869740
|
C | T | 4 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0089others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-115C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869740 | ||||||
| chr7:158869820
|
T | TTTTAAAC | 161 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(158): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.16-34_16-28dupTTTA others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158869820 | |||||
| chr7:158869986
|
A | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.69+78A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158869986 | ||||||
| chr7:158869998
|
CTT | C | 24 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(21): Show | 24 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.69+92_69+93delTT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158869998 | |||||
| chr7:158870007
|
T | C | 158 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+99T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870007 | ||||||
| chr7:158870149
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005others(40): Show | 43 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.69+241A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870149 | ||||||
| chr7:158870156
|
G | A | 1 | a0002c0002t0001g0095 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.69+248G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870156 | ||||||
| chr7:158870199
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(6): Show | 9 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+291G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870199 | ||||||
| chr7:158870218
|
G | C | 1 | a0004c0004t0006g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.69+310G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870218 | ||||||
| chr7:158870266
|
G | A | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+358G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870266 | ||||||
| chr7:158870362
|
C | CT | 8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+462dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158870362 | |||||
| chr7:158870362
|
CTT | C | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.69+461_69+462delTT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158870362 | |||||
| chr7:158870402
|
G | A | 1 | a0003c0003t0004g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.69+494G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870402 | ||||||
| chr7:158870516
|
C | CTAATTTT others(1): Show |
91 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(88): Show | 91 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.70-600_70-593dupAA others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158870516 | |||||
| chr7:158870540
|
T | C | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.70-602T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870540 | ||||||
| chr7:158870551
|
C | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.70-591C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870551 | ||||||
| chr7:158870713
|
T | A | 158 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.70-429T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870713 | ||||||
| chr7:158870741
|
G | A | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.70-401G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870741 | ||||||
| chr7:158870772
|
G | A | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70-370G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870772 | ||||||
| chr7:158871101
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.70-41G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158871101 | ||||||
| chr7:158871600
|
G | C | 1 | a0020c0011t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.490+38G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871600 | ||||||
| chr7:158871772
|
G | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.490+210G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871772 | ||||||
| chr7:158871786
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+224G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871786 | ||||||
| chr7:158871791
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+229C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871791 | ||||||
| chr7:158871865
|
T | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273others(1): Show | 4 | HG00140.hp1 HG01433.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+303T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871865 | ||||||
| chr7:158871917
|
T | C | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+355T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871917 | ||||||
| chr7:158871971
|
C | T | 3 | a0003c0003t0004g0264a0003c0003t0004g0266a0003c0003t0004g0267 | 3 | HG02015.hp1 HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.490+409C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871971 | ||||||
| chr7:158872015
|
T | C | 2 | a0001c0001t0002g0190a0001c0001t0005g0196 | 2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.490+453T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872015 | ||||||
| chr7:158872231
|
C | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.490+669C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872231 | ||||||
| chr7:158872315
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.490+753C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872315 | ||||||
| chr7:158872425
|
G | A | 1 | a0003c0003t0004g0242 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.490+863G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872425 | ||||||
| chr7:158872507
|
T | C | 161 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(158): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.490+945T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872507 | ||||||
| chr7:158872530
|
T | G | 37 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.490+968T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872530 | ||||||
| chr7:158872549
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.490+987T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872549 | ||||||
| chr7:158872632
|
G | GA | 10 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0163others(7): Show | 10 | HG01257.hp1 HG01516.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.490+1080dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158872632 | |||||
| chr7:158872635
|
A | G | 5 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0272others(2): Show | 5 | HG00140.hp1 HG01433.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+1073A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872635 | ||||||
| chr7:158872755
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490+1193G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872755 | ||||||
| chr7:158872804
|
C | G | 3 | a0001c0001t0002g0126a0001c0001t0002g0132a0001c0001t0002g0153 | 3 | NA18952.hp2 NA19065.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.490+1242C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872804 | ||||||
| chr7:158872915
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+1353C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872915 | ||||||
| chr7:158872947
|
C | T | 1 | a0003c0003t0004g0238 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490+1385C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872947 | ||||||
| chr7:158873027
|
C | T | 1 | a0003c0003t0004g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.490+1465C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873027 | ||||||
| chr7:158873044
|
G | T | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.490+1482G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873044 | ||||||
| chr7:158873057
|
G | A | 24 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(21): Show | 24 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+1495G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873057 | ||||||
| chr7:158873175
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490+1613A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873175 | ||||||
| chr7:158873215
|
T | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.490+1653T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873215 | ||||||
| chr7:158873229
|
G | A | 7 | a0002c0002t0001g0015a0002c0002t0001g0053a0002c0002t0001g0069others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+1667G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873229 | ||||||
| chr7:158873272
|
T | C | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+1710T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873272 | ||||||
| chr7:158873296
|
C | T | 37 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0022t0008g0185others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.490+1734C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873296 | ||||||
| chr7:158873379
|
C | T | 2 | a0001c0001t0009g0188a0001c0001t0009g0233 | 2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.490+1817C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873379 | ||||||
| chr7:158873389
|
T | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+1827T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873389 | ||||||
| chr7:158873405
|
G | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.490+1843G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873405 | ||||||
| chr7:158873818
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+2256G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873818 | ||||||
| chr7:158873943
|
C | T | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0014g0078 | 3 | HG03017.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.490+2381C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873943 | ||||||
| chr7:158873990
|
C | G | 1 | a0001c0001t0002g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.490+2428C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873990 | ||||||
| chr7:158874073
|
T | TA | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.490+2519dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158874073 | |||||
| chr7:158874078
|
A | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.490+2516A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874078 | ||||||
| chr7:158874209
|
A | AT | 32 | a0001c0001t0002g0162a0001c0001t0002g0164a0001c0001t0003g0205others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.491-2384dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158874209 | |||||
| chr7:158874209
|
AT | A | 6 | a0001c0001t0002g0183a0001c0001t0003g0212a0002c0002t0001g0007others(3): Show | 6 | HG02615.hp1 HG02922.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-2384delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158874209 | |||||
| chr7:158874488
|
C | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-2121C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874488 | ||||||
| chr7:158874522
|
G | A | 3 | a0001c0022t0008g0185a0006c0006t0008g0186a0006c0006t0008g0187 | 3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.491-2087G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874522 | ||||||
| chr7:158874732
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.491-1877C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874732 | ||||||
| chr7:158874746
|
C | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-1863C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874746 | ||||||
| chr7:158874784
|
C | G | 1 | a0001c0001t0002g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.491-1825C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874784 | ||||||
| chr7:158874983
|
CCAGTCTC others(3): Show |
C | 1 | a0001c0001t0001g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.491-1625_491-1616d others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874983 | ||||||
| chr7:158875067
|
G | C | 1 | a0001c0001t0002g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.491-1542G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875067 | ||||||
| chr7:158875091
|
C | CT | 64 | a0001c0001t0002g0181a0001c0001t0003g0206a0001c0001t0003g0207others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.491-1498dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | |||||
| chr7:158875091
|
C | CTT | 91 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(88): Show | 91 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.491-1499_491-1498d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | |||||
| chr7:158875091
|
C | CTTT | 5 | a0001c0001t0002g0141a0001c0001t0002g0168a0001c0001t0002g0203others(2): Show | 5 | HG02055.hp1 HG02071.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-1500_491-1498d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | |||||
| chr7:158875091
|
CT | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0268a0002c0002t0001g0002others(53): Show | 56 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.491-1498delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | |||||
| chr7:158875149
|
G | T | 1 | a0001c0001t0002g0135 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.491-1460G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875149 | ||||||
| chr7:158875244
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-1365G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875244 | ||||||
| chr7:158875249
|
G | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.491-1360G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875249 | ||||||
| chr7:158875394
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.491-1215G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875394 | ||||||
| chr7:158875509
|
T | A | 1 | a0001c0001t0002g0135 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.491-1100T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875509 | ||||||
| chr7:158875531
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.491-1078C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875531 | ||||||
| chr7:158875592
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0204 | 2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.491-1017C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875592 | ||||||
| chr7:158875593
|
G | T | 5 | a0003c0003t0004g0257a0003c0003t0004g0264a0003c0003t0004g0265others(2): Show | 5 | HG02015.hp1 HG02155.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-1016G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875593 | ||||||
| chr7:158875822
|
C | T | 74 | a0001c0001t0002g0115a0001c0001t0002g0119a0001c0001t0002g0120others(71): Show | 74 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.491-787C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875822 | ||||||
| chr7:158875833
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.491-776G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875833 | ||||||
| chr7:158875835
|
C | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.491-774C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875835 | ||||||
| chr7:158875854
|
G | A | 8 | a0002c0002t0001g0033a0002c0002t0001g0055a0002c0002t0001g0066others(5): Show | 8 | HG01123.hp2 HG01243.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-755G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875854 | ||||||
| chr7:158875884
|
T | C | 158 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.491-725T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875884 | ||||||
| chr7:158876096
|
T | C | 3 | a0001c0022t0008g0185a0006c0006t0008g0186a0006c0006t0008g0187 | 3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.491-513T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876096 | ||||||
| chr7:158876156
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.491-453A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876156 | ||||||
| chr7:158876346
|
A | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-263A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876346 | ||||||
| chr7:158876359
|
G | A | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-250G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876359 | ||||||
| chr7:158876398
|
T | C | 1 | a0002c0002t0014g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.491-211T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876398 | ||||||
| chr7:158876509
|
C | T | 1 | a0002c0002t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.491-100C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876509 | ||||||
| chr7:158876756
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.573+65T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158876756 | ||||||
| chr7:158876921
|
A | C | 1 | a0002c0002t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.573+230A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158876921 | ||||||
| chr7:158876960
|
A | C | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.573+269A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158876960 | ||||||
| chr7:158877155
|
G | C | 2 | a0001c0001t0003g0212a0001c0001t0003g0222 | 2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.573+464G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877155 | ||||||
| chr7:158877167
|
CAGGCACC others(48): Show |
C | 2 | a0001c0001t0002g0194a0001c0001t0002g0197 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.573+510_573+564del others(55): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158877167 | |||||
| chr7:158877196
|
C | CGCGGTGC others(103): Show |
1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+558_573+559ins others(110): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158877196 | |||||
| chr7:158877278
|
A | C | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+587A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877278 | ||||||
| chr7:158877401
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.573+710C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877401 | ||||||
| chr7:158877406
|
A | G | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.573+715A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877406 | ||||||
| chr7:158877427
|
G | A | 1 | a0002c0002t0001g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.573+736G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877427 | ||||||
| chr7:158877552
|
T | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.573+861T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877552 | ||||||
| chr7:158877577
|
C | T | 1 | a0002c0002t0001g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.573+886C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877577 | ||||||
| chr7:158877631
|
G | T | 1 | a0002c0002t0001g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.573+940G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877631 | ||||||
| chr7:158877778
|
C | G | 1 | a0001c0001t0002g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.573+1087C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877778 | ||||||
| chr7:158877799
|
T | C | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+1108T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877799 | ||||||
| chr7:158877945
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.573+1254C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877945 | ||||||
| chr7:158878006
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.573+1315C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878006 | ||||||
| chr7:158878112
|
GGGGAGGC others(47): Show |
G | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+1425_573+1478d others(56): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878112 | |||||
| chr7:158878138
|
G | C | 2 | a0001c0001t0005g0180a0001c0001t0005g0202 | 2 | HG00544.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.573+1447G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878138 | ||||||
| chr7:158878175
|
G | A | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.573+1484G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878175 | ||||||
| chr7:158878185
|
A | G | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+1494A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878185 | ||||||
| chr7:158878197
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574-1487C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878197 | ||||||
| chr7:158878210
|
CGGGTGCT others(35): Show |
C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.574-1467_574-1426d others(44): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878210 | |||||
| chr7:158878293
|
C | T | 3 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0093 | 3 | HG01358.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.574-1391C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878293 | ||||||
| chr7:158878420
|
C | T | 6 | a0002c0002t0001g0021a0002c0002t0001g0049a0002c0002t0001g0050others(3): Show | 6 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1264C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878420 | ||||||
| chr7:158878425
|
G | A | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.574-1259G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878425 | ||||||
| chr7:158878434
|
G | A | 1 | a0002c0002t0001g0014 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.574-1250G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878434 | ||||||
| chr7:158878436
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.574-1248G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878436 | ||||||
| chr7:158878437
|
C | T | 72 | a0001c0001t0002g0176a0002c0002t0001g0002a0002c0002t0001g0010others(69): Show | 72 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.574-1247C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878437 | ||||||
| chr7:158878471
|
GTGCCGGG others(132): Show |
G | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1195_574-1057d others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878471 | |||||
| chr7:158878514
|
T | A | 217 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(214): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.574-1170T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878514 | ||||||
| chr7:158878516
|
CCGGGCGC others(35): Show |
C | 8 | a0002c0002t0001g0001a0002c0002t0001g0030a0002c0002t0001g0034others(5): Show | 8 | HG00408.hp2 HG02027.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-1150_574-1109d others(44): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878516 | |||||
| chr7:158878518
|
G | A | 136 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.574-1166G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878518 | ||||||
| chr7:158878556
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.574-1128T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878556 | ||||||
| chr7:158878563
|
C | T | 3 | a0001c0001t0002g0137a0001c0001t0002g0151a0001c0023t0018g0112 | 3 | NA18948.hp1 NA18974.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.574-1121C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878563 | ||||||
| chr7:158878602
|
G | A | 2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.574-1082G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878602 | ||||||
| chr7:158878618
|
T | C | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1066T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878618 | ||||||
| chr7:158878630
|
A | T | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1054A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878630 | ||||||
| chr7:158878647
|
T | A | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1037T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878647 | ||||||
| chr7:158878648
|
C | G | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1036C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878648 | ||||||
| chr7:158878730
|
CTG | C | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-951_574-950del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878730 | |||||
| chr7:158878732
|
G | C | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-952G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878732 | ||||||
| chr7:158878740
|
C | T | 1 | a0004c0004t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-944C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878740 | ||||||
| chr7:158878783
|
G | A | 1 | a0004c0004t0006g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-901G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878783 | ||||||
| chr7:158878785
|
C | T | 2 | a0002c0002t0001g0007a0002c0002t0001g0052 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.574-899C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878785 | ||||||
| chr7:158878826
|
A | G | 23 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-858A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878826 | ||||||
| chr7:158878853
|
T | TGGCCAGG others(119): Show |
22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.574-764_574-763ins others(126): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878853 | |||||
| chr7:158878884
|
ACCATGTG others(90): Show |
A | 1 | a0006c0006t0008g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.574-749_574-653del others(97): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878884 | |||||
| chr7:158878941
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0160 | 2 | NA18969.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.574-743G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878941 | ||||||
| chr7:158878976
|
C | T | 5 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0022t0008g0185others(2): Show | 5 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-708C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878976 | ||||||
| chr7:158878977
|
G | C | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.574-707G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878977 | ||||||
| chr7:158878988
|
G | C | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-696G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878988 | ||||||
| chr7:158879050
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.574-634C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879050 | ||||||
| chr7:158879099
|
C | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.574-585C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879099 | ||||||
| chr7:158879442
|
A | G | 1 | a0006c0006t0008g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.574-242A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879442 | ||||||
| chr7:158879531
|
A | G | 2 | a0002c0002t0001g0085a0002c0002t0001g0100 | 2 | NA18985.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.574-153A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879531 | ||||||
| chr7:158879581
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.574-103C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879581 | ||||||
| chr7:158879582
|
G | A | 1 | a0004c0004t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-102G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879582 | ||||||
| chr7:158879601
|
G | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574-83G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879601 | ||||||
| chr7:158879610
|
C | A | 1 | a0002c0002t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-74C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879610 | ||||||
| chr7:158880037
|
C | T | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.879+48C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880037 | ||||||
| chr7:158880057
|
C | T | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.879+68C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880057 | ||||||
| chr7:158880255
|
G | A | 1 | a0001c0012t0002g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.879+266G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880255 | ||||||
| chr7:158880353
|
A | G | 1 | a0004c0004t0002g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.879+364A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880353 | ||||||
| chr7:158880570
|
A | T | 2 | a0001c0001t0002g0155a0014c0018t0001g0074 | 2 | HG01433.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.879+581A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880570 | ||||||
| chr7:158880913
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.879+924A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880913 | ||||||
| chr7:158881160
|
G | A | 2 | a0001c0001t0003g0212a0001c0001t0003g0222 | 2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.879+1171G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881160 | ||||||
| chr7:158881169
|
G | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0022t0008g0185others(3): Show | 6 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+1180G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881169 | ||||||
| chr7:158881675
|
A | C | 1 | a0001c0001t0002g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.879+1686A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881675 | ||||||
| chr7:158881733
|
A | G | 1 | a0011c0029t0004g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.879+1744A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881733 | ||||||
| chr7:158881830
|
C | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.879+1841C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881830 | ||||||
| chr7:158881873
|
T | C | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.879+1884T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881873 | ||||||
| chr7:158882066
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.879+2077G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882066 | ||||||
| chr7:158882288
|
A | C | 1 | a0001c0001t0002g0183 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.880-2276A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882288 | ||||||
| chr7:158882400
|
A | G | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-2164A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882400 | ||||||
| chr7:158882559
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.880-2005C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882559 | ||||||
| chr7:158882575
|
C | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-1989C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882575 | ||||||
| chr7:158882625
|
C | G | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-1939C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882625 | ||||||
| chr7:158882708
|
A | G | 1 | a0002c0002t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.880-1856A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882708 | ||||||
| chr7:158882734
|
A | G | 40 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.880-1830A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882734 | ||||||
| chr7:158882873
|
C | CT | 13 | a0003c0003t0004g0242a0003c0003t0004g0244a0003c0003t0004g0245others(10): Show | 13 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-1690dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158882873 | |||||
| chr7:158882875
|
C | A | 13 | a0003c0003t0004g0242a0003c0003t0004g0244a0003c0003t0004g0245others(10): Show | 13 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-1689C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882875 | ||||||
| chr7:158882875
|
C | CA | 21 | a0002c0002t0001g0023a0002c0002t0001g0110a0003c0003t0004g0238others(18): Show | 21 | HG00140.hp2 HG01071.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-1673dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158882875 | |||||
| chr7:158882875
|
CA | C | 120 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(117): Show | 120 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.880-1673delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158882875 | |||||
| chr7:158882971
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-1593C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882971 | ||||||
| chr7:158883209
|
TTTC | T | 3 | a0001c0001t0013g0118a0003c0003t0007g0240a0003c0003t0007g0241 | 3 | HG00408.hp1 HG02080.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.880-1346_880-1344d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883209 | |||||
| chr7:158883218
|
CT | C | 43 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273others(40): Show | 43 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-1329delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883218 | |||||
| chr7:158883221
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.880-1343T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883221 | ||||||
| chr7:158883257
|
G | A | 2 | a0001c0001t0005g0180a0001c0001t0005g0202 | 2 | HG00544.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.880-1307G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883257 | ||||||
| chr7:158883382
|
A | AT | 30 | a0001c0001t0002g0125a0001c0001t0002g0179a0001c0001t0003g0221others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.880-1168dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883382 | |||||
| chr7:158883384
|
T | TA | 5 | a0003c0003t0004g0257a0003c0003t0004g0264a0003c0003t0004g0265others(2): Show | 5 | HG02015.hp1 HG02155.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1180_880-1179i others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883384 | ||||||
| chr7:158883385
|
T | A | 8 | a0001c0001t0001g0003a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-1179T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883385 | ||||||
| chr7:158883415
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-1149C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883415 | ||||||
| chr7:158883484
|
C | T | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-1080C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883484 | ||||||
| chr7:158883513
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.880-1051T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883513 | ||||||
| chr7:158883586
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.880-978A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883586 | ||||||
| chr7:158883598
|
T | TAGAA | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-963_880-962ins others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883598 | |||||
| chr7:158883631
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.880-933T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883631 | ||||||
| chr7:158883658
|
C | CT | 14 | a0001c0001t0001g0270a0002c0002t0001g0015a0002c0002t0001g0020others(11): Show | 14 | HG01175.hp1 HG02080.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.880-883dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883658 | |||||
| chr7:158883658
|
CT | C | 146 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.880-883delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883658 | |||||
| chr7:158883658
|
CTT | C | 5 | a0001c0001t0002g0197a0001c0001t0009g0188a0001c0001t0009g0233others(2): Show | 5 | HG01169.hp1 HG01496.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-884_880-883del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883658 | |||||
| chr7:158883686
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.880-878C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883686 | ||||||
| chr7:158883818
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.880-746C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883818 | ||||||
| chr7:158883821
|
A | G | 159 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(156): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.880-743A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883821 | ||||||
| chr7:158883857
|
A | G | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-707A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883857 | ||||||
| chr7:158883944
|
G | A | 1 | a0003c0009t0011g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.880-620G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883944 | ||||||
| chr7:158884004
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.880-560G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884004 | ||||||
| chr7:158884046
|
A | AT | 27 | a0001c0001t0001g0003a0001c0001t0013g0118a0003c0003t0004g0238others(24): Show | 27 | HG00408.hp1 HG01071.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-502dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158884046 | |||||
| chr7:158884046
|
AT | A | 10 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(7): Show | 10 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-502delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158884046 | |||||
| chr7:158884075
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.880-489C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884075 | ||||||
| chr7:158884083
|
C | T | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.880-481C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884083 | ||||||
| chr7:158884205
|
C | T | 3 | a0001c0022t0008g0185a0006c0006t0008g0186a0006c0006t0008g0187 | 3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.880-359C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884205 | ||||||
| chr7:158884256
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.880-308G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884256 | ||||||
| chr7:158884410
|
TAACTGGT others(3): Show |
T | 3 | a0002c0002t0001g0053a0002c0002t0001g0091a0002c0016t0010g0090 | 3 | HG02451.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.880-151_880-142del others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158884410 | |||||
| chr7:158884453
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-111A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884453 | ||||||
| chr7:158884510
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.880-54A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884510 | ||||||
| chr7:158884799
|
C | T | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.935+180C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158884799 | ||||||
| chr7:158885112
|
C | T | 8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.935+493C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885112 | ||||||
| chr7:158885137
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.935+518A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885137 | ||||||
| chr7:158885303
|
G | A | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.935+684G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885303 | ||||||
| chr7:158885345
|
C | CT | 16 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.935+740dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr7 | 158885345 | |||||
| chr7:158885430
|
C | G | 1 | a0001c0001t0002g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.935+811C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885430 | ||||||
| chr7:158885494
|
A | G | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+875A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885494 | ||||||
| chr7:158885613
|
A | AT | 75 | a0001c0001t0002g0115a0001c0001t0002g0119a0001c0001t0002g0120others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.935+996dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr7 | 158885613 | |||||
| chr7:158885794
|
A | G | 5 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.935+1175A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885794 | ||||||
| chr7:158885915
|
C | G | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-1106C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885915 | ||||||
| chr7:158886048
|
T | C | 2 | a0003c0003t0004g0244a0003c0003t0004g0246 | 2 | HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.936-973T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886048 | ||||||
| chr7:158886398
|
T | C | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-623T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886398 | ||||||
| chr7:158886430
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.936-591G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886430 | ||||||
| chr7:158886434
|
G | A | 1 | a0003c0009t0011g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.936-587G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886434 | ||||||
| chr7:158886505
|
T | C | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.936-516T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886505 | ||||||
| chr7:158886639
|
T | A | 1 | a0002c0002t0001g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.936-382T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886639 | ||||||
| chr7:158886862
|
A | G | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-159A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886862 | ||||||
| chr7:158886928
|
T | C | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.936-93T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886928 | ||||||
| chr7:158886949
|
AT | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.936-71delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886949 | ||||||
| chr7:158887130
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0160 | 2 | NA18969.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.990+55A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887130 | ||||||
| chr7:158887167
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.990+92C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887167 | ||||||
| chr7:158887224
|
G | A | 1 | a0002c0002t0001g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.990+149G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887224 | ||||||
| chr7:158887252
|
AATTG | A | 96 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(93): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.990+183_990+186del others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158887252 | |||||
| chr7:158887487
|
T | C | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.990+412T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887487 | ||||||
| chr7:158887506
|
A | G | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.990+431A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887506 | ||||||
| chr7:158887958
|
G | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.990+883G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887958 | ||||||
| chr7:158887987
|
T | C | 1 | a0002c0002t0001g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.990+912T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887987 | ||||||
| chr7:158888019
|
C | CT | 42 | a0001c0001t0001g0003a0001c0001t0001g0270a0001c0001t0002g0105others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.990+968dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | |||||
| chr7:158888019
|
C | CTTTT | 19 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.990+965_990+968dup others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | |||||
| chr7:158888019
|
C | CTTTTT | 11 | a0003c0003t0004g0245a0003c0003t0004g0252a0003c0003t0004g0259others(8): Show | 11 | HG00408.hp1 HG01175.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+964_990+968dup others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | |||||
| chr7:158888019
|
CT | C | 7 | a0001c0001t0002g0168a0001c0001t0002g0175a0001c0001t0003g0212others(4): Show | 7 | HG01255.hp2 HG02683.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.990+968delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | |||||
| chr7:158888114
|
T | C | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1039T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888114 | ||||||
| chr7:158888185
|
C | T | 4 | a0004c0004t0001g0170a0004c0004t0006g0199a0004c0004t0006g0200others(1): Show | 4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1110C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888185 | ||||||
| chr7:158888297
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+1222A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888297 | ||||||
| chr7:158888410
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.990+1335G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888410 | ||||||
| chr7:158888468
|
C | CAT | 11 | a0001c0001t0002g0116a0001c0001t0005g0139a0001c0001t0009g0188others(8): Show | 11 | HG01175.hp2 HG01255.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+1409_990+1410d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888468 | |||||
| chr7:158888618
|
C | T | 6 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0022t0008g0185others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+1543C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888618 | ||||||
| chr7:158888630
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.990+1555C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888630 | ||||||
| chr7:158888808
|
C | T | 6 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0022t0008g0185others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+1733C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888808 | ||||||
| chr7:158888850
|
CTGT | C | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1780_990+1782d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888850 | |||||
| chr7:158888918
|
G | A | 4 | a0001c0001t0002g0115a0001c0001t0002g0122a0001c0001t0002g0156others(1): Show | 4 | NA18939.hp2 NA18954.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1843G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888918 | ||||||
| chr7:158888966
|
T | C | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.990+1891T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888966 | ||||||
| chr7:158889036
|
T | TAC | 5 | a0002c0002t0001g0006a0002c0002t0001g0063a0002c0002t0001g0073others(2): Show | 5 | HG01123.hp2 HG01891.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+1990_990+1991d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
T | TACAC | 3 | a0001c0001t0006g0004a0001c0001t0006g0005a0002c0002t0001g0064 | 3 | HG02451.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+1988_990+1991d others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0273others(1): Show | 4 | HG00140.hp1 HG01934.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1982_990+1991d others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.990+1980_990+1991d others(14): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
TAC | T | 13 | a0001c0001t0002g0132a0001c0001t0003g0220a0001c0022t0008g0185others(10): Show | 13 | HG01255.hp2 HG01257.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.990+1990_990+1991d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
TACAC | T | 115 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(112): Show | 115 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.990+1988_990+1991d others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
TACACAC | T | 3 | a0003c0003t0004g0264a0003c0003t0004g0266a0003c0003t0004g0267 | 3 | HG02015.hp1 HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.990+1986_990+1991d others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889036
|
TACACACA others(1): Show |
T | 28 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(25): Show | 28 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.990+1984_990+1991d others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | |||||
| chr7:158889065
|
A | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0097 | 2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.990+1990A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889065 | ||||||
| chr7:158889080
|
C | CT | 11 | a0001c0001t0002g0159a0001c0001t0002g0161a0001c0001t0002g0173others(8): Show | 11 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+2023dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889080 | |||||
| chr7:158889080
|
CT | C | 34 | a0001c0001t0005g0136a0001c0001t0009g0188a0001c0001t0009g0233others(31): Show | 34 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.990+2023delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889080 | |||||
| chr7:158889083
|
T | C | 6 | a0001c0001t0002g0124a0001c0001t0002g0133a0001c0001t0002g0142others(3): Show | 6 | HG02165.hp2 NA18942.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+2008T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889083 | ||||||
| chr7:158889085
|
T | C | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+2010T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889085 | ||||||
| chr7:158889086
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.990+2011T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889086 | ||||||
| chr7:158889151
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+2076G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889151 | ||||||
| chr7:158889157
|
TGCAAGCT others(5): Show |
T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.990+2083_990+2094d others(14): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889157 | ||||||
| chr7:158889174
|
G | A | 2 | a0003c0003t0004g0244a0003c0003t0004g0246 | 2 | HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.991-2091G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889174 | ||||||
| chr7:158889421
|
G | A | 1 | a0003c0003t0007g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.991-1844G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889421 | ||||||
| chr7:158889428
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.991-1837C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889428 | ||||||
| chr7:158889436
|
A | T | 31 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.991-1829A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889436 | ||||||
| chr7:158889442
|
C | T | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.991-1823C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889442 | ||||||
| chr7:158889692
|
AAAC | A | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1558_991-1556d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889692 | |||||
| chr7:158889794
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.991-1471A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889794 | ||||||
| chr7:158889835
|
TCTCTA | T | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1426_991-1422d others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889835 | |||||
| chr7:158890005
|
C | CA | 112 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.991-1236dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158890005 | |||||
| chr7:158890005
|
C | CAA | 7 | a0001c0001t0002g0122a0001c0001t0002g0135a0003c0003t0004g0262others(4): Show | 7 | HG00733.hp1 HG02055.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-1237_991-1236d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158890005 | |||||
| chr7:158890005
|
CA | C | 23 | a0001c0001t0003g0230a0001c0023t0018g0112a0002c0002t0001g0010others(20): Show | 23 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.991-1236delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158890005 | |||||
| chr7:158890111
|
G | C | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-1154G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890111 | ||||||
| chr7:158890226
|
A | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.991-1039A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890226 | ||||||
| chr7:158890331
|
G | A | 7 | a0003c0003t0004g0257a0003c0003t0004g0262a0003c0003t0004g0264others(4): Show | 7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-934G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890331 | ||||||
| chr7:158890488
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.991-777G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890488 | ||||||
| chr7:158890628
|
G | A | 1 | a0002c0002t0001g0093 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.991-637G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890628 | ||||||
| chr7:158890717
|
G | A | 1 | a0004c0004t0002g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.991-548G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890717 | ||||||
| chr7:158890849
|
G | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.991-416G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890849 | ||||||
| chr7:158890893
|
G | A | 58 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0009others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.991-372G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890893 | ||||||
| chr7:158890991
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.991-274C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890991 | ||||||
| chr7:158891000
|
C | G | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.991-265C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891000 | ||||||
| chr7:158891112
|
G | T | 4 | a0001c0022t0008g0185a0001c0023t0018g0112a0006c0006t0008g0186others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-153G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891112 | ||||||
| chr7:158891134
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.991-131T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891134 | ||||||
| chr7:158891190
|
G | C | 2 | a0001c0001t0002g0148a0001c0001t0013g0118 | 2 | HG02080.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.991-75G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891190 | ||||||
| chr7:158891392
|
A | T | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1059+59A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891392 | ||||||
| chr7:158891461
|
A | G | 98 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(95): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1059+128A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891461 | ||||||
| chr7:158891494
|
C | T | 3 | a0002c0002t0001g0007a0002c0002t0001g0052a0013c0015t0001g0051 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+161C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891494 | ||||||
| chr7:158891582
|
C | T | 15 | a0003c0003t0004g0242a0003c0003t0004g0244a0003c0003t0004g0245others(12): Show | 15 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059+249C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891582 | ||||||
| chr7:158891583
|
G | A | 1 | a0003c0003t0004g0238 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1059+250G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891583 | ||||||
| chr7:158891613
|
A | G | 6 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0022t0008g0185others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+280A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891613 | ||||||
| chr7:158891678
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1059+345C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891678 | ||||||
| chr7:158891855
|
AAGGGAAG others(63): Show |
A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+556_1059+625d others(72): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158891855 | |||||
| chr7:158891920
|
C | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1059+587C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891920 | ||||||
| chr7:158891998
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1059+665C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891998 | ||||||
| chr7:158892025
|
G | C | 1 | a0002c0002t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+692G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892025 | ||||||
| chr7:158892302
|
G | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+969G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892302 | ||||||
| chr7:158892321
|
A | G | 1 | a0008c0008t0020g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1059+988A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892321 | ||||||
| chr7:158892404
|
A | G | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+1071A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892404 | ||||||
| chr7:158892485
|
A | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+1152A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892485 | ||||||
| chr7:158892509
|
A | G | 1 | a0002c0002t0001g0044 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1059+1176A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892509 | ||||||
| chr7:158892566
|
T | C | 157 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1059+1233T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892566 | ||||||
| chr7:158892615
|
A | AT | 97 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(94): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1059+1292dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158892615 | |||||
| chr7:158892717
|
G | T | 1 | a0001c0001t0005g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1059+1384G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892717 | ||||||
| chr7:158892805
|
G | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+1472G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892805 | ||||||
| chr7:158892812
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1059+1479G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892812 | ||||||
| chr7:158892907
|
T | C | 157 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1059+1574T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892907 | ||||||
| chr7:158892938
|
C | CA | 15 | a0002c0002t0001g0022a0002c0002t0001g0023a0003c0003t0004g0242others(12): Show | 15 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059+1623dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158892938 | |||||
| chr7:158892938
|
CA | C | 120 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(117): Show | 120 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1059+1623delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158892938 | |||||
| chr7:158892962
|
A | G | 2 | a0006c0006t0008g0186a0006c0006t0008g0187 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1059+1629A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892962 | ||||||
| chr7:158893167
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1059+1834C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893167 | ||||||
| chr7:158893215
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1059+1882A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893215 | ||||||
| chr7:158893291
|
G | T | 1 | a0001c0001t0002g0175 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1059+1958G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893291 | ||||||
| chr7:158893379
|
T | A | 1 | a0003c0003t0004g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1059+2046T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893379 | ||||||
| chr7:158893646
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+2313C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893646 | ||||||
| chr7:158893663
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+2330C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893663 | ||||||
| chr7:158893699
|
T | TGCATATC others(5): Show |
4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+2367_1059+237 others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158893699 | |||||
| chr7:158893718
|
C | T | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1059+2385C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893718 | ||||||
| chr7:158893863
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1059+2530G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893863 | ||||||
| chr7:158893928
|
A | G | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+2595A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893928 | ||||||
| chr7:158893935
|
T | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+2602T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893935 | ||||||
| chr7:158894004
|
C | T | 85 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(82): Show | 85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1059+2671C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894004 | ||||||
| chr7:158894089
|
G | A | 1 | a0001c0001t0003g0205 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1059+2756G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894089 | ||||||
| chr7:158894112
|
T | C | 1 | a0002c0002t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059+2779T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894112 | ||||||
| chr7:158894112
|
T | TGCATATC others(5): Show |
1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1059+2787_1059+279 others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894112 | |||||
| chr7:158894112
|
T | TGCATATC others(17): Show |
4 | a0001c0001t0006g0004a0001c0001t0006g0005a0002c0002t0001g0041others(1): Show | 4 | HG00642.hp2 HG01496.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+2798_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894112 | |||||
| chr7:158894120
|
C | CTACCGCA others(17): Show |
125 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1059+2798_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894120 | |||||
| chr7:158894120
|
C | CTACTGCA others(17): Show |
2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | NA18943.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1059+2790_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894120 | |||||
| chr7:158894120
|
C | CTACTGCA others(17): Show |
3 | a0003c0003t0004g0264a0003c0003t0004g0266a0003c0003t0004g0267 | 3 | HG02015.hp1 HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1059+2790_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894120 | |||||
| chr7:158894132
|
A | ATACCGCA others(5): Show |
12 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 12 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1059+2804_1059+281 others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894132 | |||||
| chr7:158894132
|
A | ATACCGCA others(17): Show |
103 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1059+2815_1059+281 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894132 | |||||
| chr7:158894132
|
A | C | 158 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1059+2799A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894132 | ||||||
| chr7:158894172
|
G | C | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0014g0078 | 3 | HG03017.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1059+2839G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894172 | ||||||
| chr7:158894182
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1059+2849G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894182 | ||||||
| chr7:158894216
|
GCATATCC others(53): Show |
G | 1 | a0011c0029t0004g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1059+2887_1059+294 others(64): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894216 | |||||
| chr7:158894463
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1059+3130T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894463 | ||||||
| chr7:158894824
|
C | T | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1059+3491C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894824 | ||||||
| chr7:158894865
|
GT | G | 121 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(118): Show | 121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1059+3534delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894865 | |||||
| chr7:158895102
|
T | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1059+3769T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895102 | ||||||
| chr7:158895118
|
T | C | 1 | a0001c0001t0012g0224 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+3785T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895118 | ||||||
| chr7:158895136
|
A | G | 1 | a0002c0002t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1059+3803A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895136 | ||||||
| chr7:158895184
|
G | T | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1059+3851G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895184 | ||||||
| chr7:158895236
|
C | G | 1 | a0001c0001t0002g0204 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1059+3903C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895236 | ||||||
| chr7:158895307
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+3974C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895307 | ||||||
| chr7:158895712
|
C | T | 2 | a0008c0008t0003g0226a0008c0008t0020g0228 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+4379C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895712 | ||||||
| chr7:158895809
|
G | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+4476G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895809 | ||||||
| chr7:158895934
|
G | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+4601G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895934 | ||||||
| chr7:158896134
|
T | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+4801T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896134 | ||||||
| chr7:158896575
|
A | G | 1 | a0001c0022t0008g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1060-5164A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896575 | ||||||
| chr7:158896654
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-5085G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896654 | ||||||
| chr7:158896738
|
G | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-5001G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896738 | ||||||
| chr7:158896776
|
T | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-4963T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896776 | ||||||
| chr7:158896856
|
T | C | 1 | a0001c0001t0002g0157 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1060-4883T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896856 | ||||||
| chr7:158896866
|
GT | G | 161 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273others(158): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1060-4859delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158896866 | |||||
| chr7:158896884
|
G | A | 1 | a0011c0029t0004g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1060-4855G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896884 | ||||||
| chr7:158896985
|
C | CT | 28 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(25): Show | 28 | HG00140.hp1 HG00642.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1060-4738dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158896985 | |||||
| chr7:158896985
|
CT | C | 24 | a0001c0001t0002g0151a0001c0001t0002g0171a0001c0001t0003g0205others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1060-4738delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158896985 | |||||
| chr7:158896994
|
T | A | 1 | a0001c0001t0002g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1060-4745T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896994 | ||||||
| chr7:158897058
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1060-4681G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897058 | ||||||
| chr7:158897288
|
C | T | 4 | a0004c0004t0001g0170a0004c0004t0006g0199a0004c0004t0006g0200others(1): Show | 4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-4451C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897288 | ||||||
| chr7:158897433
|
C | T | 2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1060-4306C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897433 | ||||||
| chr7:158897508
|
A | G | 273 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1060-4231A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897508 | ||||||
| chr7:158897511
|
T | C | 1 | a0004c0004t0002g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060-4228T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897511 | ||||||
| chr7:158897596
|
A | G | 3 | a0001c0001t0002g0107a0007c0005t0002g0189a0007c0005t0002g0225 | 3 | HG01891.hp2 HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1060-4143A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897596 | ||||||
| chr7:158897624
|
A | G | 106 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(103): Show | 106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1060-4115A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897624 | ||||||
| chr7:158897659
|
A | G | 1 | a0004c0004t0002g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060-4080A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897659 | ||||||
| chr7:158897768
|
T | G | 1 | a0001c0001t0002g0175 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1060-3971T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897768 | ||||||
| chr7:158897776
|
C | T | 35 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1060-3963C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897776 | ||||||
| chr7:158897885
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1060-3854G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897885 | ||||||
| chr7:158898087
|
A | C | 6 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0022t0008g0185others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-3652A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898087 | ||||||
| chr7:158898175
|
A | G | 115 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1060-3564A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898175 | ||||||
| chr7:158898530
|
G | A | 12 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0037others(9): Show | 12 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1060-3209G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898530 | ||||||
| chr7:158898726
|
G | A | 164 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(161): Show | 164 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1060-3013G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898726 | ||||||
| chr7:158898870
|
GT | G | 5 | a0002c0002t0001g0009a0002c0002t0001g0056a0002c0002t0001g0061others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-2857delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158898870 | |||||
| chr7:158898936
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1060-2803A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898936 | ||||||
| chr7:158899312
|
A | G | 2 | a0003c0003t0004g0256a0003c0003t0004g0259 | 2 | HG01358.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1060-2427A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899312 | ||||||
| chr7:158899351
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1060-2388C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899351 | ||||||
| chr7:158899359
|
T | C | 121 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(118): Show | 121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1060-2380T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899359 | ||||||
| chr7:158899455
|
T | C | 3 | a0004c0004t0006g0199a0004c0004t0006g0200a0004c0004t0006g0201 | 3 | HG02818.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1060-2284T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899455 | ||||||
| chr7:158899777
|
T | G | 1 | a0002c0002t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1060-1962T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899777 | ||||||
| chr7:158899807
|
T | C | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060-1932T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899807 | ||||||
| chr7:158899823
|
A | G | 1 | a0007c0005t0002g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1060-1916A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899823 | ||||||
| chr7:158899952
|
C | T | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-1787C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899952 | ||||||
| chr7:158900068
|
C | G | 93 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(90): Show | 93 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1060-1671C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900068 | ||||||
| chr7:158900116
|
C | CT | 5 | a0001c0001t0002g0105a0001c0001t0002g0165a0002c0002t0001g0039others(2): Show | 5 | HG01175.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-1607dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900116 | |||||
| chr7:158900116
|
CT | C | 22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1060-1607delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900116 | |||||
| chr7:158900433
|
T | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-1306T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900433 | ||||||
| chr7:158900731
|
G | GT | 67 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273others(64): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1060-990dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | |||||
| chr7:158900731
|
G | GTT | 85 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(82): Show | 85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1060-991_1060-990d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | |||||
| chr7:158900731
|
G | GTTT | 11 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0002g0121others(8): Show | 11 | HG01243.hp2 HG02071.hp1 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.1060-992_1060-990d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | |||||
| chr7:158900731
|
GT | G | 10 | a0001c0001t0006g0005a0002c0002t0001g0015a0002c0002t0001g0034others(7): Show | 10 | HG01943.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060-990delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | |||||
| chr7:158900788
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-951G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900788 | ||||||
| chr7:158900974
|
A | G | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-765A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900974 | ||||||
| chr7:158901073
|
C | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1060-666C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158901073 | ||||||
| chr7:158901282
|
C | T | 5 | a0002c0002t0001g0007a0002c0002t0001g0052a0002c0002t0001g0096others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-457C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158901282 | ||||||
| chr7:158901839
|
T | C | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1137+23T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158901839 | ||||||
| chr7:158902050
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1137+234A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158902050 | ||||||
| chr7:158902110
|
G | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1138-266G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158902110 | ||||||
| chr7:158902216
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1138-160C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158902216 | ||||||
| chr7:158902873
|
C | G | 1 | a0001c0001t0002g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1357+278C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158902873 | ||||||
| chr7:158902893
|
G | C | 2 | a0002c0002t0001g0031a0002c0002t0001g0032 | 2 | NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1357+298G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158902893 | ||||||
| chr7:158903341
|
C | CTG | 171 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1357+747_1357+748d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158903341 | |||||
| chr7:158903728
|
C | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1357+1133C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158903728 | ||||||
| chr7:158904123
|
C | T | 31 | a0001c0001t0002g0183a0003c0003t0004g0238a0003c0003t0004g0239others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1357+1528C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904123 | ||||||
| chr7:158904364
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1358-1625C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904364 | ||||||
| chr7:158904412
|
A | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1358-1577A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904412 | ||||||
| chr7:158904526
|
T | A | 1 | a0001c0001t0002g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1358-1463T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904526 | ||||||
| chr7:158904674
|
T | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1358-1315T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904674 | ||||||
| chr7:158904874
|
G | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1358-1115G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904874 | ||||||
| chr7:158905140
|
C | CT | 16 | a0001c0001t0002g0123a0001c0001t0012g0223a0001c0001t0012g0224others(13): Show | 16 | HG01257.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1358-831dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | |||||
| chr7:158905140
|
C | CTTTTTTT others(3): Show |
3 | a0003c0003t0004g0255a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG02976.hp2 HG03491.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1358-840_1358-831d others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | |||||
| chr7:158905140
|
C | CTTTTTTT others(4): Show |
26 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1358-841_1358-831d others(13): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | |||||
| chr7:158905140
|
C | CTTTTTTT others(5): Show |
1 | a0003c0003t0004g0252 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1358-842_1358-831d others(14): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | |||||
| chr7:158905140
|
CT | C | 10 | a0001c0001t0002g0171a0001c0001t0002g0177a0001c0001t0002g0194others(7): Show | 10 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-831delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | |||||
| chr7:158905184
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1358-805G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905184 | ||||||
| chr7:158905200
|
G | A | 1 | a0002c0002t0001g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1358-789G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905200 | ||||||
| chr7:158905372
|
C | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1358-617C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905372 | ||||||
| chr7:158905431
|
G | A | 2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1358-558G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905431 | ||||||
| chr7:158905618
|
T | G | 1 | a0001c0001t0001g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1358-371T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905618 | ||||||
| chr7:158905784
|
G | T | 4 | a0001c0022t0008g0185a0002c0016t0010g0090a0006c0006t0008g0186others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1358-205G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905784 | ||||||
| chr7:158906121
|
G | A | 4 | a0004c0004t0001g0170a0004c0004t0006g0199a0004c0004t0006g0200others(1): Show | 4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+30G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906121 | ||||||
| chr7:158906271
|
C | T | 1 | a0002c0002t0001g0032 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1460+180C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906271 | ||||||
| chr7:158906276
|
C | T | 1 | a0001c0001t0002g0165 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1460+185C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906276 | ||||||
| chr7:158906410
|
T | C | 1 | a0002c0002t0001g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1460+319T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906410 | ||||||
| chr7:158906521
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1460+430C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906521 | ||||||
| chr7:158906686
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1460+595G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906686 | ||||||
| chr7:158906865
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+774A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906865 | ||||||
| chr7:158907106
|
T | C | 158 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1460+1015T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907106 | ||||||
| chr7:158907164
|
GA | G | 132 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(129): Show | 132 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1460+1086delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907164 | |||||
| chr7:158907273
|
C | CT | 106 | a0001c0001t0001g0268a0001c0001t0002g0105a0001c0001t0002g0106others(103): Show | 106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1460+1207dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | |||||
| chr7:158907273
|
C | CTT | 7 | a0001c0001t0002g0165a0001c0001t0002g0177a0001c0001t0002g0181others(4): Show | 7 | HG02080.hp1 HG02683.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1460+1206_1460+120 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | |||||
| chr7:158907273
|
CT | C | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273others(3): Show | 6 | HG01169.hp2 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+1207delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | |||||
| chr7:158907273
|
CTT | C | 29 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1460+1206_1460+120 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | |||||
| chr7:158907418
|
T | C | 8 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0249others(5): Show | 8 | HG00140.hp2 HG01071.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+1327T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907418 | ||||||
| chr7:158907586
|
C | T | 6 | a0002c0002t0001g0021a0002c0002t0001g0049a0002c0002t0001g0050others(3): Show | 6 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+1495C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907586 | ||||||
| chr7:158907648
|
C | T | 1 | a0002c0002t0001g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1460+1557C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907648 | ||||||
| chr7:158907669
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1460+1578G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907669 | ||||||
| chr7:158907852
|
A | G | 98 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(95): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1460+1761A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907852 | ||||||
| chr7:158907891
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1460+1800G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907891 | ||||||
| chr7:158907908
|
C | T | 98 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(95): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1460+1817C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907908 | ||||||
| chr7:158908398
|
G | A | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1460+2307G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908398 | ||||||
| chr7:158908490
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1460+2399G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908490 | ||||||
| chr7:158908691
|
G | A | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+2600G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908691 | ||||||
| chr7:158908733
|
C | G | 98 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(95): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1460+2642C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908733 | ||||||
| chr7:158908860
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1461-2690C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908860 | ||||||
| chr7:158909017
|
A | T | 30 | a0003c0003t0004g0238a0003c0003t0004g0239a0003c0003t0004g0242others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1461-2533A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909017 | ||||||
| chr7:158909277
|
G | A | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1461-2273G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909277 | ||||||
| chr7:158909305
|
T | C | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1461-2245T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909305 | ||||||
| chr7:158909330
|
C | CA | 33 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0208others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1461-2195dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | |||||
| chr7:158909330
|
C | CAA | 6 | a0001c0001t0001g0003a0001c0001t0003g0207a0001c0001t0003g0232others(3): Show | 6 | HG00423.hp2 HG00544.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461-2196_1461-219 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | |||||
| chr7:158909330
|
CA | C | 94 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0272others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1461-2195delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | |||||
| chr7:158909330
|
CAA | C | 9 | a0001c0001t0002g0183a0001c0001t0002g0194a0001c0001t0005g0196others(6): Show | 9 | HG01167.hp2 HG02015.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1461-2196_1461-219 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | |||||
| chr7:158909416
|
A | G | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1461-2134A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909416 | ||||||
| chr7:158909588
|
C | T | 5 | a0001c0022t0008g0185a0001c0023t0018g0112a0002c0016t0010g0090others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461-1962C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909588 | ||||||
| chr7:158909653
|
A | G | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1461-1897A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909653 | ||||||
| chr7:158909891
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1461-1659G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909891 | ||||||
| chr7:158909931
|
C | G | 1 | a0003c0003t0004g0239 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1461-1619C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909931 | ||||||
| chr7:158909955
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1461-1595C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909955 | ||||||
| chr7:158909985
|
C | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461-1565C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909985 | ||||||
| chr7:158910250
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1461-1300G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910250 | ||||||
| chr7:158910328
|
T | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1461-1222T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910328 | ||||||
| chr7:158910402
|
ACCTGTGG others(22): Show |
A | 98 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(95): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1461-1139_1461-111 others(33): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158910402 | |||||
| chr7:158910413
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1461-1137C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910413 | ||||||
| chr7:158910435
|
G | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1461-1115G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910435 | ||||||
| chr7:158910437
|
G | T | 4 | a0001c0022t0008g0185a0002c0016t0010g0090a0006c0006t0008g0186others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461-1113G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910437 | ||||||
| chr7:158910574
|
G | T | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1461-976G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910574 | ||||||
| chr7:158910613
|
G | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1461-937G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910613 | ||||||
| chr7:158910644
|
C | CGAGGGCA others(4): Show |
1 | a0002c0002t0016g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1461-893_1461-883d others(13): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158910644 | |||||
| chr7:158910757
|
T | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1461-793T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910757 | ||||||
| chr7:158910863
|
C | A | 10 | a0002c0002t0001g0019a0002c0002t0001g0037a0002c0002t0001g0054others(7): Show | 10 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1461-687C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910863 | ||||||
| chr7:158910983
|
A | G | 1 | a0012c0013t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1461-567A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910983 | ||||||
| chr7:158910984
|
G | A | 1 | a0012c0013t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1461-566G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910984 | ||||||
| chr7:158911023
|
G | T | 8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461-527G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158911023 | ||||||
| chr7:158911127
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1461-423G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158911127 | ||||||
| chr7:158911363
|
G | A | 98 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(95): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1461-187G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158911363 | ||||||
| chr7:158911914
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1590+235C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158911914 | ||||||
| chr7:158911984
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1590+305T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158911984 | ||||||
| chr7:158912308
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0273 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1590+629C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912308 | ||||||
| chr7:158912424
|
G | C | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1591-561G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912424 | ||||||
| chr7:158912576
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1591-409G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912576 | ||||||
| chr7:158912720
|
C | CCTAAGAA others(31): Show |
1 | a0003c0003t0007g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1591-264_1591-227d others(40): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr7 | 158912720 | |||||
| chr7:158912752
|
G | A | 1 | a0002c0016t0010g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1591-233G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912752 | ||||||
| chr7:158913353
|
A | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1702+257A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913353 | ||||||
| chr7:158913475
|
C | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1702+379C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913475 | ||||||
| chr7:158913556
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1702+460G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913556 | ||||||
| chr7:158913559
|
T | G | 8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1702+463T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913559 | ||||||
| chr7:158913563
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1702+467A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913563 | ||||||
| chr7:158913702
|
G | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1703-531G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913702 | ||||||
| chr7:158913715
|
A | AT | 5 | a0001c0022t0008g0185a0001c0023t0018g0112a0002c0016t0010g0090others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1703-518_1703-517i others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913715 | ||||||
| chr7:158913716
|
A | T | 136 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1703-517A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913716 | ||||||
| chr7:158913794
|
C | T | 1 | a0009c0007t0003g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1703-439C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913794 | ||||||
| chr7:158913801
|
T | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1703-432T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913801 | ||||||
| chr7:158913959
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1703-274C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913959 | ||||||
| chr7:158913989
|
C | T | 7 | a0001c0001t0005g0196a0002c0002t0001g0002a0002c0002t0001g0016others(4): Show | 7 | HG01358.hp2 HG02015.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1703-244C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913989 | ||||||
| chr7:158914340
|
T | C | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1791+19T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914340 | ||||||
| chr7:158914380
|
A | G | 11 | a0001c0001t0002g0123a0001c0001t0005g0196a0001c0001t0012g0223others(8): Show | 11 | HG01358.hp2 HG02015.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1791+59A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914380 | ||||||
| chr7:158914381
|
T | C | 1 | a0001c0001t0002g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1791+60T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914381 | ||||||
| chr7:158914546
|
G | A | 11 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0006g0199others(8): Show | 11 | HG01257.hp2 HG01934.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1791+225G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914546 | ||||||
| chr7:158914608
|
G | GC | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+288dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158914608 | |||||
| chr7:158914616
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(6): Show | 9 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1791+295G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914616 | ||||||
| chr7:158914703
|
A | T | 4 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0197others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+382A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914703 | ||||||
| chr7:158914734
|
C | T | 1 | a0001c0001t0006g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1791+413C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914734 | ||||||
| chr7:158914784
|
C | G | 1 | a0001c0001t0003g0211 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1791+463C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914784 | ||||||
| chr7:158914798
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1791+477G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914798 | ||||||
| chr7:158914874
|
A | G | 1 | a0003c0003t0007g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1791+553A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914874 | ||||||
| chr7:158914968
|
G | C | 1 | a0001c0001t0002g0130 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1791+647G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914968 | ||||||
| chr7:158915048
|
A | G | 33 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0014others(30): Show | 33 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1791+727A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915048 | ||||||
| chr7:158915052
|
CGCTAGTT others(31): Show |
C | 17 | a0003c0003t0004g0242a0003c0003t0004g0244a0003c0003t0004g0245others(14): Show | 17 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1791+735_1791+772d others(40): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915052 | |||||
| chr7:158915090
|
T | TGCTGGTT others(69): Show |
2 | a0002c0002t0001g0006a0002c0002t0001g0059 | 2 | HG01943.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1791+810_1791+811i others(78): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915090 | |||||
| chr7:158915128
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+807C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915128 | ||||||
| chr7:158915196
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0097 | 2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1791+875G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915196 | ||||||
| chr7:158915216
|
G | A | 1 | a0001c0001t0012g0223 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1791+895G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915216 | ||||||
| chr7:158915222
|
C | T | 3 | a0001c0023t0018g0112a0002c0002t0001g0062a0002c0002t0001g0065 | 3 | NA18945.hp1 NA19002.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1791+901C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915222 | ||||||
| chr7:158915231
|
A | C | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+910A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915231 | ||||||
| chr7:158915234
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1791+913G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915234 | ||||||
| chr7:158915238
|
T | C | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+917T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915238 | ||||||
| chr7:158915240
|
C | G | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+919C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915240 | ||||||
| chr7:158915248
|
C | G | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+927C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915248 | ||||||
| chr7:158915251
|
T | A | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+930T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915251 | ||||||
| chr7:158915255
|
A | G | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+934A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915255 | ||||||
| chr7:158915261
|
T | G | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+940T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915261 | ||||||
| chr7:158915278
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+957G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915278 | ||||||
| chr7:158915278
|
G | GTGGTTGA others(943): Show |
1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+964_1791+965i others(952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915278 | |||||
| chr7:158915286
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005others(1): Show | 4 | HG00140.hp1 HG02257.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+965G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915286 | ||||||
| chr7:158915307
|
C | G | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+986C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915307 | ||||||
| chr7:158915309
|
G | C | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+988G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915309 | ||||||
| chr7:158915309
|
G | GGACACGC others(31): Show |
8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1031_1791+106 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915309 | |||||
| chr7:158915347
|
C | CGACACGC others(183): Show |
96 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(93): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1791+1064_1791+106 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915347 | |||||
| chr7:158915347
|
C | CGACACGC others(183): Show |
2 | a0002c0002t0001g0007a0002c0002t0001g0052 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1791+1064_1791+106 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915347 | |||||
| chr7:158915347
|
C | CGACACGC others(183): Show |
2 | a0002c0002t0001g0067a0002c0002t0001g0103 | 2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1791+1068_1791+106 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915347 | |||||
| chr7:158915348
|
G | GACACGCT others(449): Show |
2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1061_1791+106 others(460): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915348 | |||||
| chr7:158915352
|
CGCTGGTT others(31): Show |
C | 2 | a0002c0002t0001g0062a0002c0002t0001g0065 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+1069_1791+110 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915352 | |||||
| chr7:158915362
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1041C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915362 | ||||||
| chr7:158915383
|
G | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1062G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915383 | ||||||
| chr7:158915386
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1791+1065G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915386 | ||||||
| chr7:158915390
|
T | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1791+1069T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915390 | ||||||
| chr7:158915392
|
C | CTGGTTGA others(369): Show |
1 | a0002c0002t0001g0079 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1098_1791+109 others(380): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915392 | |||||
| chr7:158915400
|
C | CATTAAGG others(863): Show |
1 | a0001c0001t0002g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1099_1791+110 others(874): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915400 | |||||
| chr7:158915400
|
C | CATTAAGG others(4799): Show |
1 | a0001c0001t0002g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1791+1251_1791+125 others(4810): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915400 | |||||
| chr7:158915400
|
C | G | 4 | a0001c0001t0005g0196a0002c0002t0001g0025a0002c0019t0015g0043others(1): Show | 4 | HG00140.hp1 HG01081.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1079C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915400 | ||||||
| chr7:158915421
|
G | C | 2 | a0001c0001t0003g0205a0001c0001t0003g0231 | 2 | HG00597.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1791+1100G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915421 | ||||||
| chr7:158915423
|
C | T | 1 | a0002c0002t0001g0079 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1102C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915423 | ||||||
| chr7:158915424
|
G | GACACGCT others(297): Show |
1 | a0002c0002t0001g0025 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1791+1116_1791+111 others(308): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915424 | |||||
| chr7:158915424
|
G | T | 1 | a0002c0002t0001g0079 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1103G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915424 | ||||||
| chr7:158915428
|
C | T | 1 | a0002c0002t0001g0098 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1791+1107C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915428 | ||||||
| chr7:158915429
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1791+1108G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915429 | ||||||
| chr7:158915438
|
G | C | 11 | a0001c0001t0002g0174a0001c0001t0005g0196a0002c0002t0001g0025others(8): Show | 11 | HG00140.hp1 HG01081.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1791+1117G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915438 | ||||||
| chr7:158915458
|
C | T | 3 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107 | 3 | HG01891.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1791+1137C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915458 | ||||||
| chr7:158915459
|
G | A | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1138G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915459 | ||||||
| chr7:158915459
|
G | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1138G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915459 | ||||||
| chr7:158915466
|
C | T | 4 | a0002c0002t0001g0025a0002c0002t0001g0079a0003c0009t0011g0253others(1): Show | 4 | HG02976.hp2 HG03654.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1145C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915466 | ||||||
| chr7:158915467
|
G | A | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1146G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915467 | ||||||
| chr7:158915483
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1162G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915483 | ||||||
| chr7:158915499
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1178C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915499 | ||||||
| chr7:158915500
|
G | A | 22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1791+1179G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915500 | ||||||
| chr7:158915506
|
G | C | 3 | a0003c0003t0004g0256a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG01358.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1185G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915506 | ||||||
| chr7:158915514
|
G | C | 4 | a0002c0002t0001g0025a0002c0002t0001g0079a0003c0009t0011g0253others(1): Show | 4 | HG02976.hp2 HG03654.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1193G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915514 | ||||||
| chr7:158915517
|
A | T | 10 | a0001c0001t0002g0174a0001c0001t0003g0222a0001c0001t0005g0196others(7): Show | 10 | HG00140.hp1 HG01081.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1196A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915517 | ||||||
| chr7:158915527
|
G | T | 8 | a0001c0001t0002g0174a0001c0001t0003g0222a0002c0002t0001g0025others(5): Show | 8 | HG00140.hp1 HG01358.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1206G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915527 | ||||||
| chr7:158915534
|
C | T | 1 | a0003c0003t0004g0256 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1213C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915534 | ||||||
| chr7:158915535
|
C | A | 1 | a0001c0001t0003g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1214C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915535 | ||||||
| chr7:158915535
|
C | G | 1 | a0003c0003t0004g0256 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1214C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915535 | ||||||
| chr7:158915537
|
C | T | 1 | a0003c0003t0004g0256 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1216C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915537 | ||||||
| chr7:158915538
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1217G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915538 | ||||||
| chr7:158915543
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1222G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915543 | ||||||
| chr7:158915544
|
G | C | 5 | a0001c0001t0003g0222a0002c0002t0001g0025a0002c0002t0001g0079others(2): Show | 5 | HG02976.hp2 HG03654.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1223G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915544 | ||||||
| chr7:158915552
|
G | C | 4 | a0001c0001t0003g0222a0003c0003t0004g0256a0003c0009t0011g0253others(1): Show | 4 | HG01358.hp1 HG02976.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1231G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915552 | ||||||
| chr7:158915573
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1252C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915573 | ||||||
| chr7:158915573
|
C | G | 6 | a0001c0001t0003g0222a0002c0002t0001g0025a0002c0002t0001g0079others(3): Show | 6 | HG01358.hp1 HG02976.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1791+1252C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915573 | ||||||
| chr7:158915582
|
C | G | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1261C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915582 | ||||||
| chr7:158915590
|
G | C | 4 | a0001c0001t0002g0174a0001c0001t0003g0222a0003c0009t0011g0253others(1): Show | 4 | HG02976.hp2 HG04204.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1269G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915590 | ||||||
| chr7:158915611
|
A | C | 3 | a0003c0003t0004g0239a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG01071.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1290A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915611 | ||||||
| chr7:158915611
|
A | G | 4 | a0001c0001t0002g0174a0001c0001t0003g0222a0001c0001t0005g0196others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1290A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915611 | ||||||
| chr7:158915613
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1292C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915613 | ||||||
| chr7:158915619
|
G | A | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1298G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915619 | ||||||
| chr7:158915620
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1299C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915620 | ||||||
| chr7:158915628
|
C | A | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1307C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915628 | ||||||
| chr7:158915628
|
C | CATTA | 5 | a0002c0002t0001g0025a0002c0002t0001g0079a0003c0009t0011g0253others(2): Show | 5 | HG00140.hp1 HG02976.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1308_1791+130 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915628 | |||||
| chr7:158915628
|
C | CATTAAGG others(1619): Show |
1 | a0001c0001t0002g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1308_1791+130 others(1630): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915628 | |||||
| chr7:158915628
|
C | CATTAAGG others(2033): Show |
1 | a0001c0001t0003g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1308_1791+130 others(2044): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915628 | |||||
| chr7:158915645
|
C | G | 3 | a0001c0001t0005g0196a0002c0019t0015g0043a0017c0024t0001g0271 | 3 | HG00140.hp1 HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1324C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915645 | ||||||
| chr7:158915647
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1326C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915647 | ||||||
| chr7:158915647
|
C | T | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1326C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915647 | ||||||
| chr7:158915648
|
G | T | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1327G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915648 | ||||||
| chr7:158915654
|
G | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1333G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915654 | ||||||
| chr7:158915655
|
T | TGGTTGAC others(210): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1362_1791+136 others(221): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915655 | |||||
| chr7:158915662
|
C | G | 4 | a0002c0002t0001g0025a0002c0002t0001g0079a0003c0009t0011g0253others(1): Show | 4 | HG02976.hp2 HG03654.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1341C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915662 | ||||||
| chr7:158915683
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1362G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915683 | ||||||
| chr7:158915685
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1364C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915685 | ||||||
| chr7:158915686
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1365G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915686 | ||||||
| chr7:158915690
|
C | T | 186 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1791+1369C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915690 | ||||||
| chr7:158915691
|
G | A | 3 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112 | 3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1791+1370G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915691 | ||||||
| chr7:158915699
|
A | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1378A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915699 | ||||||
| chr7:158915721
|
G | A | 3 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112 | 3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1791+1400G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915721 | ||||||
| chr7:158915723
|
C | T | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1402C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915723 | ||||||
| chr7:158915724
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1403G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915724 | ||||||
| chr7:158915724
|
G | T | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1403G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915724 | ||||||
| chr7:158915728
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1407C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915728 | ||||||
| chr7:158915730
|
C | G | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1409C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915730 | ||||||
| chr7:158915732
|
G | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1411G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915732 | ||||||
| chr7:158915738
|
C | G | 1 | a0002c0002t0001g0079 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1417C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915738 | ||||||
| chr7:158915759
|
G | C | 3 | a0001c0001t0003g0212a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG02976.hp2 NA18990.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1438G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915759 | ||||||
| chr7:158915761
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1440C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915761 | ||||||
| chr7:158915762
|
T | A | 1 | a0001c0001t0003g0212 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1791+1441T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915762 | ||||||
| chr7:158915762
|
T | G | 7 | a0001c0001t0005g0196a0002c0002t0001g0025a0002c0002t0001g0079others(4): Show | 7 | HG00140.hp1 HG02015.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1791+1441T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915762 | ||||||
| chr7:158915766
|
C | CGCTGGCT others(145): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1450_1791+145 others(156): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915766 | |||||
| chr7:158915768
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1447C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915768 | ||||||
| chr7:158915776
|
G | C | 3 | a0001c0001t0003g0212a0002c0019t0015g0043a0017c0024t0001g0271 | 3 | HG00140.hp1 HG01081.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1791+1455G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915776 | ||||||
| chr7:158915797
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1476G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915797 | ||||||
| chr7:158915797
|
G | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1476G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915797 | ||||||
| chr7:158915799
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1478C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915799 | ||||||
| chr7:158915800
|
G | A | 3 | a0002c0019t0015g0043a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1479G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915800 | ||||||
| chr7:158915814
|
C | G | 2 | a0001c0001t0002g0174a0001c0001t0003g0222 | 2 | HG04204.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1791+1493C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915814 | ||||||
| chr7:158915835
|
G | C | 2 | a0001c0001t0002g0174a0001c0001t0003g0222 | 2 | HG04204.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1791+1514G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915835 | ||||||
| chr7:158915836
|
T | TCGACACG others(104): Show |
1 | a0001c0001t0003g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1516_1791+151 others(115): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915836 | |||||
| chr7:158915838
|
A | ACGGTGGT others(1339): Show |
1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1517_1791+151 others(1350): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915838 | ||||||
| chr7:158915838
|
A | G | 13 | a0001c0001t0002g0174a0001c0001t0002g0183a0001c0001t0005g0196others(10): Show | 13 | HG01081.hp1 HG02015.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1791+1517A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915838 | ||||||
| chr7:158915842
|
C | CGGTGGTT others(26): Show |
1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1522_1791+152 others(37): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915842 | |||||
| chr7:158915845
|
T | C | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1524T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915845 | ||||||
| chr7:158915851
|
A | G | 91 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(88): Show | 91 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1791+1530A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915851 | ||||||
| chr7:158915852
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1531C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915852 | ||||||
| chr7:158915873
|
G | C | 4 | a0001c0001t0002g0174a0001c0001t0005g0196a0002c0002t0001g0025others(1): Show | 4 | HG02015.hp2 HG03654.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1552G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915873 | ||||||
| chr7:158915875
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1554C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915875 | ||||||
| chr7:158915880
|
C | T | 2 | a0002c0002t0001g0014a0002c0002t0001g0046 | 2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1791+1559C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915880 | ||||||
| chr7:158915881
|
G | A | 1 | a0001c0001t0003g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1560G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915881 | ||||||
| chr7:158915882
|
C | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1561C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915882 | ||||||
| chr7:158915886
|
T | C | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1791+1565T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915886 | ||||||
| chr7:158915890
|
G | C | 6 | a0001c0001t0002g0174a0001c0001t0005g0196a0002c0019t0015g0043others(3): Show | 6 | HG00140.hp1 HG01081.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+1569G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915890 | ||||||
| chr7:158915890
|
G | GATTAAGG others(366): Show |
1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+1588_1791+158 others(377): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915890 | |||||
| chr7:158915911
|
G | C | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1590G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915911 | ||||||
| chr7:158915914
|
G | A | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1593G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915914 | ||||||
| chr7:158915914
|
G | T | 1 | a0001c0001t0002g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1593G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915914 | ||||||
| chr7:158915918
|
C | T | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1597C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915918 | ||||||
| chr7:158915919
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1598G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915919 | ||||||
| chr7:158915920
|
C | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1599C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915920 | ||||||
| chr7:158915928
|
C | G | 4 | a0001c0001t0003g0222a0002c0002t0001g0025a0002c0002t0001g0079others(1): Show | 4 | HG03654.hp1 HG03688.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1607C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915928 | ||||||
| chr7:158915949
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1628G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915949 | ||||||
| chr7:158915949
|
G | C | 5 | a0001c0001t0003g0222a0001c0001t0005g0196a0003c0009t0011g0253others(2): Show | 5 | HG00140.hp1 HG02015.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1628G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915949 | ||||||
| chr7:158915949
|
G | GTCAACAC others(107): Show |
1 | a0001c0001t0002g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1629_1791+163 others(118): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915949 | |||||
| chr7:158915951
|
T | C | 9 | a0001c0001t0002g0174a0001c0001t0003g0222a0001c0001t0005g0196others(6): Show | 9 | HG00140.hp1 HG02015.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1791+1630T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915951 | ||||||
| chr7:158915957
|
A | AGTGGTTG others(3282): Show |
1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3293): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915957 | |||||
| chr7:158915957
|
A | G | 9 | a0001c0001t0002g0174a0001c0001t0003g0222a0001c0001t0005g0196others(6): Show | 9 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1791+1636A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915957 | ||||||
| chr7:158915958
|
G | C | 4 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0084others(1): Show | 4 | HG01081.hp2 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1637G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915958 | ||||||
| chr7:158915958
|
G | GTGGTTGA others(598): Show |
1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(609): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | |||||
| chr7:158915958
|
G | GTGGTTGA others(2634): Show |
2 | a0001c0001t0001g0268a0001c0001t0001g0272 | 2 | HG01934.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2645): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | |||||
| chr7:158915958
|
G | GTGGTTGA others(2634): Show |
2 | a0001c0001t0001g0269a0001c0001t0001g0273 | 2 | HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2645): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | |||||
| chr7:158915958
|
G | GTGGTTGA others(2634): Show |
1 | a0001c0001t0001g0270 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2645): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | |||||
| chr7:158915958
|
G | GTGGTTGA others(2748): Show |
2 | a0001c0001t0003g0214a0001c0001t0003g0217 | 2 | HG02129.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2759): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | |||||
| chr7:158915958
|
G | GTGGTTGA others(3200): Show |
1 | a0001c0001t0003g0220 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3211): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | |||||
| chr7:158915962
|
T | C | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1641T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915962 | ||||||
| chr7:158915965
|
A | ACATGAAG others(294): Show |
1 | a0002c0002t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1791+1647_1791+164 others(305): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915965 | |||||
| chr7:158915966
|
C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0213 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3348): Show |
1 | a0001c0001t0003g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3359): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3125): Show |
3 | a0001c0001t0003g0208a0001c0001t0003g0210a0001c0001t0003g0232 | 3 | NA18944.hp2 NA19079.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0212 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7257): Show |
1 | a0001c0001t0002g0177 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7268): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
5 | a0004c0004t0002g0192a0004c0004t0006g0199a0004c0004t0006g0201others(2): Show | 5 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
1 | a0004c0004t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
1 | a0004c0004t0002g0193 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
1 | a0004c0004t0006g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0005g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2682): Show |
1 | a0001c0001t0002g0130 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2693): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(6394): Show |
1 | a0001c0001t0002g0165 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(6405): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0198 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
1 | a0001c0001t0002g0145 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
1 | a0001c0001t0002g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2679): Show |
23 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0124others(20): Show | 23 | HG00741.hp2 HG01192.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(6766): Show |
1 | a0001c0001t0002g0176 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(6777): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7596): Show |
2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(7607): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2679): Show |
9 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7520): Show |
1 | a0018c0025t0002g0149 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7520): Show |
1 | a0001c0001t0002g0156 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7520): Show |
1 | a0001c0001t0002g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
3 | a0001c0001t0002g0126a0001c0001t0002g0181a0001c0001t0002g0184 | 3 | HG02273.hp2 HG03654.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7520): Show |
1 | a0001c0001t0002g0129 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7485): Show |
1 | a0001c0001t0002g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7496): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7941): Show |
2 | a0001c0001t0002g0147a0001c0001t0002g0179 | 2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7941): Show |
1 | a0001c0001t0002g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7941): Show |
1 | a0001c0001t0002g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2641): Show |
1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2680): Show |
1 | a0001c0001t0002g0135 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2691): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2983): Show |
1 | a0001c0001t0002g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2994): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2679): Show |
1 | a0001c0001t0002g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7941): Show |
1 | a0001c0001t0002g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7748): Show |
1 | a0001c0001t0002g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7759): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(1999): Show |
1 | a0001c0001t0002g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2010): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0012t0002g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2679): Show |
1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2679): Show |
2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(8242): Show |
2 | a0001c0001t0002g0123a0002c0002t0001g0095 | 2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(8253): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0183 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(4612): Show |
1 | a0001c0001t0002g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(4623): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2676): Show |
3 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0197 | 3 | HG01167.hp2 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2687): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2679): Show |
1 | a0001c0001t0002g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2718): Show |
1 | a0001c0001t0012g0223 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2729): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(2718): Show |
1 | a0001c0001t0012g0224 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2729): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3166): Show |
2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(3177): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3166): Show |
1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3177): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3125): Show |
10 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0209others(7): Show | 10 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0207 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3505): Show |
1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3516): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7979): Show |
1 | a0001c0001t0002g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7990): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3432): Show |
1 | a0001c0001t0009g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3443): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3356): Show |
1 | a0001c0001t0009g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3367): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(3356): Show |
1 | a0001c0001t0009g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3367): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | CATTAAGG others(7561): Show |
1 | a0001c0001t0002g0204 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1791+1663_1791+166 others(7572): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | |||||
| chr7:158915966
|
C | G | 5 | a0001c0001t0002g0174a0001c0001t0003g0222a0002c0002t0001g0084others(2): Show | 5 | HG02976.hp2 HG03688.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1645C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915966 | ||||||
| chr7:158915979
|
T | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1658T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915979 | ||||||
| chr7:158915987
|
G | A | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1666G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915987 | ||||||
| chr7:158915987
|
G | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1666G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915987 | ||||||
| chr7:158915987
|
G | GTTTACAC others(69): Show |
9 | a0001c0001t0002g0203a0002c0002t0001g0039a0002c0002t0001g0040others(6): Show | 9 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(80): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915987 | |||||
| chr7:158915987
|
G | GTTTACAC others(4000): Show |
1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(4011): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915987 | |||||
| chr7:158915989
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1791+1668C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915989 | ||||||
| chr7:158915989
|
C | T | 93 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(90): Show | 93 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1791+1668C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915989 | ||||||
| chr7:158915990
|
G | A | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1669G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915990 | ||||||
| chr7:158915990
|
G | T | 93 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(90): Show | 93 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1791+1669G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915990 | ||||||
| chr7:158915996
|
C | G | 12 | a0001c0001t0002g0203a0001c0023t0018g0112a0002c0002t0001g0039others(9): Show | 12 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1791+1675C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915996 | ||||||
| chr7:158916004
|
C | G | 93 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(90): Show | 93 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.1791+1683C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916004 | ||||||
| chr7:158916021
|
A | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1700A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916021 | ||||||
| chr7:158916025
|
G | C | 12 | a0001c0001t0002g0203a0001c0001t0005g0196a0002c0002t0001g0039others(9): Show | 12 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1791+1704G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916025 | ||||||
| chr7:158916025
|
G | GTCGACAT others(446): Show |
4 | a0002c0002t0001g0066a0002c0002t0001g0068a0002c0002t0001g0073others(1): Show | 4 | HG01123.hp2 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1706_1791+170 others(457): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916025 | |||||
| chr7:158916025
|
G | GTCGACAT others(484): Show |
1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(495): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916025 | |||||
| chr7:158916026
|
T | TCGACATG others(142): Show |
1 | a0002c0002t0001g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(153): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | |||||
| chr7:158916026
|
T | TCGACATG others(142): Show |
1 | a0002c0002t0017g0024 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(153): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | |||||
| chr7:158916026
|
T | TCGACATG others(142): Show |
83 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1791+1706_1791+170 others(153): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | |||||
| chr7:158916026
|
T | TCGACATG others(329): Show |
1 | a0002c0002t0001g0076 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(340): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | |||||
| chr7:158916027
|
C | CGACATGC others(3087): Show |
1 | a0009c0007t0003g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(3098): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916027 | ||||||
| chr7:158916027
|
C | CGACATGC others(3090): Show |
3 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227 | 3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1791+1706_1791+170 others(3101): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916027 | ||||||
| chr7:158916027
|
C | T | 118 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1791+1706C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916027 | ||||||
| chr7:158916028
|
T | A | 9 | a0001c0001t0002g0203a0002c0002t0001g0039a0002c0002t0001g0040others(6): Show | 9 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1791+1707T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916028 | ||||||
| chr7:158916028
|
T | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1791+1707T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916028 | ||||||
| chr7:158916028
|
T | TACACGCT others(4238): Show |
1 | a0003c0027t0022g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4238): Show |
1 | a0003c0003t0004g0242 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4577): Show |
1 | a0003c0003t0004g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4588): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4574): Show |
1 | a0003c0003t0004g0267 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4585): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4238): Show |
1 | a0003c0003t0004g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4613): Show |
2 | a0003c0003t0004g0257a0003c0003t0004g0265 | 2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(4624): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4276): Show |
1 | a0003c0003t0007g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4287): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4238): Show |
8 | a0003c0003t0004g0244a0003c0003t0004g0245a0003c0003t0004g0252others(5): Show | 8 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(3747): Show |
1 | a0003c0003t0007g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(3758): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4537): Show |
2 | a0006c0006t0008g0186a0006c0006t0008g0187 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(4548): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4233): Show |
1 | a0003c0003t0004g0256 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4244): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(5176): Show |
1 | a0003c0003t0004g0238 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5187): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(5100): Show |
1 | a0003c0003t0004g0249 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5111): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(5214): Show |
2 | a0003c0003t0004g0254a0003c0003t0004g0258 | 2 | HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(5225): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(5176): Show |
1 | a0003c0003t0004g0255 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5187): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4577): Show |
1 | a0003c0003t0004g0264 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4588): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4238): Show |
1 | a0003c0003t0007g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(4238): Show |
1 | a0003c0003t0004g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(5176): Show |
1 | a0003c0003t0004g0239 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5187): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916028
|
T | TACACGCT others(5179): Show |
1 | a0003c0003t0004g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5190): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | |||||
| chr7:158916034
|
C | G | 5 | a0001c0001t0005g0196a0002c0002t0001g0066a0002c0002t0001g0068others(2): Show | 5 | HG01123.hp2 HG01346.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1713C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916034 | ||||||
| chr7:158916042
|
G | C | 97 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1791+1721G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916042 | ||||||
| chr7:158916062
|
C | T | 3 | a0001c0001t0002g0126a0001c0001t0002g0132a0002c0019t0015g0043 | 3 | HG01081.hp2 NA19065.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1791+1741C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916062 | ||||||
| chr7:158916063
|
G | A | 4 | a0002c0002t0001g0066a0002c0002t0001g0068a0002c0002t0001g0073others(1): Show | 4 | HG01123.hp2 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1742G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916063 | ||||||
| chr7:158916063
|
G | C | 88 | a0001c0001t0005g0180a0001c0001t0005g0196a0001c0001t0005g0202others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1791+1742G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916063 | ||||||
| chr7:158916063
|
G | GTCGACAC others(6316): Show |
2 | a0001c0022t0008g0185a0002c0016t0010g0090 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(6327): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916063 | |||||
| chr7:158916064
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+1743T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916064 | ||||||
| chr7:158916065
|
T | C | 119 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1791+1744T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916065 | ||||||
| chr7:158916066
|
G | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1791+1745G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916066 | ||||||
| chr7:158916070
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1749C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916070 | ||||||
| chr7:158916071
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1750G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916071 | ||||||
| chr7:158916072
|
C | G | 88 | a0001c0001t0005g0180a0001c0001t0005g0196a0001c0001t0005g0202others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1791+1751C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916072 | ||||||
| chr7:158916080
|
G | C | 7 | a0002c0002t0001g0033a0002c0002t0001g0055a0002c0002t0001g0066others(4): Show | 7 | HG01081.hp2 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1759G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916080 | ||||||
| chr7:158916086
|
G | GGAT | 108 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1791+1766_1791+176 others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | |||||
| chr7:158916086
|
G | GGATGATT others(34): Show |
1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1768_1791+176 others(45): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | |||||
| chr7:158916086
|
G | GGATGATT others(107): Show |
8 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041others(5): Show | 8 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1791+1768_1791+176 others(118): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | |||||
| chr7:158916086
|
G | GGATGATT others(110): Show |
1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1791+1768_1791+176 others(121): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | |||||
| chr7:158916086
|
G | GGATGATT others(148): Show |
1 | a0002c0002t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1791+1768_1791+176 others(159): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | |||||
| chr7:158916097
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1791+1776C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916097 | ||||||
| chr7:158916098
|
G | A | 179 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1791+1777G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916098 | ||||||
| chr7:158916098
|
G | C | 11 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(8): Show | 11 | HG01081.hp2 HG01433.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1791+1777G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916098 | ||||||
| chr7:158916100
|
C | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1779C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916100 | ||||||
| chr7:158916100
|
C | T | 3 | a0001c0001t0005g0196a0003c0003t0004g0256a0003c0003t0004g0259 | 3 | HG01358.hp1 HG02015.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1791+1779C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916100 | ||||||
| chr7:158916101
|
G | A | 86 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1791+1780G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916101 | ||||||
| chr7:158916107
|
C | CTGGTTGA others(145): Show |
1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+1814_1791+181 others(156): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916107 | |||||
| chr7:158916107
|
C | G | 1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+1786C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916107 | ||||||
| chr7:158916114
|
A | G | 86 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1791+1793A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916114 | ||||||
| chr7:158916115
|
C | G | 15 | a0001c0001t0002g0203a0002c0002t0001g0025a0002c0002t0001g0039others(12): Show | 15 | HG00140.hp1 HG00733.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1791+1794C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916115 | ||||||
| chr7:158916124
|
T | TGATTGTG others(329): Show |
3 | a0001c0001t0003g0214a0001c0001t0003g0217a0001c0001t0003g0220 | 3 | HG02083.hp1 HG02129.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1791+1814_1791+181 others(340): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916124 | |||||
| chr7:158916136
|
G | A | 1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+1815G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916136 | ||||||
| chr7:158916136
|
G | C | 4 | a0003c0009t0011g0253a0003c0009t0011g0261a0010c0028t0023g0237others(1): Show | 4 | HG00140.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1815G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916136 | ||||||
| chr7:158916143
|
T | C | 130 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1791+1822T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916143 | ||||||
| chr7:158916144
|
G | T | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1791+1823G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916144 | ||||||
| chr7:158916145
|
G | C | 117 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1791+1824G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916145 | ||||||
| chr7:158916145
|
G | GTGGTTGA others(31): Show |
1 | a0011c0029t0004g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1791+1856_1791+189 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916145 | |||||
| chr7:158916146
|
T | TCGTTGAC others(590): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1825_1791+182 others(601): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916146 | ||||||
| chr7:158916153
|
C | G | 85 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0202others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1791+1832C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916153 | ||||||
| chr7:158916157
|
A | T | 2 | a0003c0003t0004g0262a0003c0027t0022g0263 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1791+1836A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916157 | ||||||
| chr7:158916174
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1853G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916174 | ||||||
| chr7:158916174
|
G | C | 4 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0019t0015g0043others(1): Show | 4 | HG01081.hp2 HG02922.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1853G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916174 | ||||||
| chr7:158916176
|
C | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1855C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916176 | ||||||
| chr7:158916177
|
G | A | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1856G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916177 | ||||||
| chr7:158916183
|
C | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1862C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916183 | ||||||
| chr7:158916191
|
C | G | 89 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(86): Show | 89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1791+1870C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916191 | ||||||
| chr7:158916212
|
G | C | 7 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(4): Show | 7 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1891G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916212 | ||||||
| chr7:158916214
|
C | CGACACGC others(780): Show |
1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1893_1791+189 others(791): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916214 | ||||||
| chr7:158916215
|
T | A | 3 | a0001c0001t0005g0196a0002c0002t0001g0060a0017c0024t0001g0271 | 3 | HG00140.hp1 HG01975.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1894T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916215 | ||||||
| chr7:158916215
|
T | G | 113 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(110): Show | 113 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1791+1894T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916215 | ||||||
| chr7:158916221
|
C | G | 7 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(4): Show | 7 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1900C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916221 | ||||||
| chr7:158916229
|
C | G | 14 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(11): Show | 14 | HG01123.hp2 HG01243.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1791+1908C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916229 | ||||||
| chr7:158916242
|
T | G | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1921T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916242 | ||||||
| chr7:158916242
|
T | TGTGAAAC others(31): Show |
1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1928_1791+192 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916242 | |||||
| chr7:158916250
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1929G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916250 | ||||||
| chr7:158916250
|
G | C | 10 | a0001c0001t0002g0203a0002c0002t0001g0033a0002c0002t0001g0039others(7): Show | 10 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1929G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916250 | ||||||
| chr7:158916252
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1931C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916252 | ||||||
| chr7:158916253
|
T | G | 132 | a0001c0001t0002g0203a0001c0001t0003g0205a0001c0001t0003g0206others(129): Show | 132 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1791+1932T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916253 | ||||||
| chr7:158916257
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1936C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916257 | ||||||
| chr7:158916259
|
C | G | 10 | a0001c0001t0002g0203a0002c0002t0001g0033a0002c0002t0001g0039others(7): Show | 10 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1938C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916259 | ||||||
| chr7:158916263
|
T | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1942T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916263 | ||||||
| chr7:158916267
|
C | G | 11 | a0001c0001t0002g0203a0002c0002t0001g0033a0002c0002t0001g0039others(8): Show | 11 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1791+1946C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916267 | ||||||
| chr7:158916271
|
T | A | 109 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1791+1950T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916271 | ||||||
| chr7:158916288
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1967C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916288 | ||||||
| chr7:158916288
|
C | G | 6 | a0002c0002t0001g0025a0002c0002t0001g0072a0002c0002t0001g0079others(3): Show | 6 | HG01257.hp1 HG02976.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1791+1967C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916288 | ||||||
| chr7:158916290
|
C | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0072a0002c0002t0001g0079 | 3 | HG01257.hp1 HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1969C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916290 | ||||||
| chr7:158916291
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1970G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916291 | ||||||
| chr7:158916291
|
G | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1970G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916291 | ||||||
| chr7:158916297
|
G | C | 27 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(24): Show | 27 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1791+1976G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916297 | ||||||
| chr7:158916305
|
G | C | 6 | a0002c0002t0001g0025a0002c0002t0001g0072a0002c0002t0001g0079others(3): Show | 6 | HG01081.hp2 HG01257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+1984G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916305 | ||||||
| chr7:158916305
|
G | GATTAAGG others(107): Show |
1 | a0002c0002t0001g0073 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1791+2004_1791+200 others(118): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916305 | |||||
| chr7:158916326
|
G | A | 10 | a0001c0001t0002g0203a0002c0002t0001g0033a0002c0002t0001g0039others(7): Show | 10 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+2005G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916326 | ||||||
| chr7:158916326
|
G | C | 92 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1791+2005G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916326 | ||||||
| chr7:158916328
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+2007C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916328 | ||||||
| chr7:158916329
|
T | G | 108 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1791+2008T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916329 | ||||||
| chr7:158916333
|
C | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0073a0002c0002t0001g0079 | 3 | HG01123.hp2 HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+2012C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916333 | ||||||
| chr7:158916335
|
C | G | 92 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1791+2014C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916335 | ||||||
| chr7:158916343
|
C | G | 92 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1791+2022C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916343 | ||||||
| chr7:158916363
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2042C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916363 | ||||||
| chr7:158916364
|
G | A | 90 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(87): Show | 90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1791+2043G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916364 | ||||||
| chr7:158916364
|
G | C | 3 | a0002c0002t0001g0084a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG02976.hp2 HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2043G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916364 | ||||||
| chr7:158916366
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1791+2045C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916366 | ||||||
| chr7:158916367
|
G | A | 2 | a0002c0002t0001g0044a0002c0002t0001g0057 | 2 | NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1791+2046G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916367 | ||||||
| chr7:158916367
|
G | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1791+2046G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916367 | ||||||
| chr7:158916371
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2050C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916371 | ||||||
| chr7:158916373
|
C | G | 4 | a0002c0002t0001g0033a0002c0002t0001g0084a0003c0009t0011g0253others(1): Show | 4 | HG02976.hp2 HG03017.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2052C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916373 | ||||||
| chr7:158916381
|
C | G | 4 | a0001c0001t0005g0139a0002c0002t0001g0084a0003c0009t0011g0253others(1): Show | 4 | HG01517.hp1 HG02976.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2060C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916381 | ||||||
| chr7:158916402
|
G | A | 1 | a0002c0002t0001g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1791+2081G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916402 | ||||||
| chr7:158916402
|
G | C | 4 | a0001c0001t0005g0196a0002c0002t0001g0084a0003c0009t0011g0253others(1): Show | 4 | HG02015.hp2 HG02976.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2081G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916402 | ||||||
| chr7:158916402
|
G | GTCGCTGG others(1125): Show |
1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+2084_1791+208 others(1136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916402 | |||||
| chr7:158916404
|
C | CGGCATGC others(31): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2084_1791+208 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916404 | |||||
| chr7:158916404
|
C | T | 6 | a0002c0002t0001g0055a0002c0002t0001g0066a0002c0002t0001g0068others(3): Show | 6 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+2083C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916404 | ||||||
| chr7:158916405
|
G | T | 4 | a0002c0002t0001g0055a0002c0002t0001g0066a0002c0002t0001g0068others(1): Show | 4 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+2084G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916405 | ||||||
| chr7:158916409
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1791+2088C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916409 | ||||||
| chr7:158916411
|
C | G | 5 | a0002c0002t0001g0055a0002c0002t0001g0066a0002c0002t0001g0068others(2): Show | 5 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+2090C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916411 | ||||||
| chr7:158916419
|
C | G | 3 | a0002c0002t0001g0084a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG02976.hp2 HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2098C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916419 | ||||||
| chr7:158916440
|
G | A | 1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+2119G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916440 | ||||||
| chr7:158916440
|
G | GTCGACAC others(183): Show |
1 | a0002c0002t0001g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1791+2135_1791+213 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916440 | |||||
| chr7:158916443
|
G | T | 25 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1791+2122G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916443 | ||||||
| chr7:158916447
|
C | T | 4 | a0002c0002t0001g0055a0002c0002t0001g0066a0002c0002t0001g0068others(1): Show | 4 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+2126C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916447 | ||||||
| chr7:158916449
|
C | CTGGTTGA others(221): Show |
3 | a0002c0002t0001g0040a0002c0002t0001g0048a0002c0002t0001g0067 | 3 | HG00733.hp2 HG01516.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1791+2135_1791+213 others(232): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916449 | |||||
| chr7:158916457
|
C | G | 8 | a0001c0001t0002g0203a0002c0002t0001g0007a0002c0002t0001g0039others(5): Show | 8 | HG01175.hp1 HG01496.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1791+2136C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916457 | ||||||
| chr7:158916459
|
T | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2138T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916459 | ||||||
| chr7:158916461
|
T | A | 109 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1791+2140T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916461 | ||||||
| chr7:158916469
|
T | C | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2148T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916469 | ||||||
| chr7:158916478
|
G | A | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2157G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916478 | ||||||
| chr7:158916478
|
G | C | 3 | a0001c0001t0005g0196a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG02015.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2157G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916478 | ||||||
| chr7:158916480
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2159C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916480 | ||||||
| chr7:158916480
|
C | T | 5 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0084others(2): Show | 5 | HG02976.hp2 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+2159C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916480 | ||||||
| chr7:158916481
|
T | G | 108 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1791+2160T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916481 | ||||||
| chr7:158916485
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1791+2164T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916485 | ||||||
| chr7:158916485
|
T | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2164T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916485 | ||||||
| chr7:158916487
|
C | G | 5 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0084others(2): Show | 5 | HG02976.hp2 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+2166C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916487 | ||||||
| chr7:158916490
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2169G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916490 | ||||||
| chr7:158916495
|
C | G | 90 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(87): Show | 90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1791+2174C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916495 | ||||||
| chr7:158916499
|
A | T | 1 | a0001c0001t0002g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1791+2178A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916499 | ||||||
| chr7:158916516
|
G | C | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2195G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916516 | ||||||
| chr7:158916518
|
C | T | 6 | a0002c0002t0001g0020a0002c0002t0001g0025a0002c0002t0001g0045others(3): Show | 6 | HG02486.hp1 HG03654.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1791+2197C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916518 | ||||||
| chr7:158916519
|
T | G | 108 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1791+2198T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916519 | ||||||
| chr7:158916523
|
C | T | 6 | a0002c0002t0001g0084a0003c0003t0004g0257a0003c0003t0004g0264others(3): Show | 6 | HG02015.hp1 HG02155.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+2202C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916523 | ||||||
| chr7:158916525
|
C | G | 1 | a0002c0002t0001g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1791+2204C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916525 | ||||||
| chr7:158916533
|
C | CATTAAGG others(183): Show |
1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1792-2185_1792-218 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916533 | |||||
| chr7:158916533
|
C | G | 88 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-2207C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916533 | ||||||
| chr7:158916540
|
G | A | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-2200G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916540 | ||||||
| chr7:158916554
|
G | C | 6 | a0001c0001t0005g0196a0002c0002t0001g0039a0002c0002t0001g0041others(3): Show | 6 | HG01081.hp2 HG01175.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-2186G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916554 | ||||||
| chr7:158916561
|
C | T | 1 | a0002c0002t0001g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1792-2179C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916561 | ||||||
| chr7:158916562
|
G | A | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-2178G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916562 | ||||||
| chr7:158916563
|
C | G | 6 | a0001c0001t0005g0196a0002c0002t0001g0039a0002c0002t0001g0041others(3): Show | 6 | HG01081.hp2 HG01175.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-2177C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916563 | ||||||
| chr7:158916571
|
C | CATTAAGG others(69): Show |
1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-2149_1792-214 others(80): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916571 | |||||
| chr7:158916571
|
C | G | 5 | a0002c0002t0001g0039a0002c0002t0001g0041a0002c0002t0001g0072others(2): Show | 5 | HG01175.hp1 HG01257.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-2169C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916571 | ||||||
| chr7:158916571
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-2169C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916571 | ||||||
| chr7:158916592
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-2148G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916592 | ||||||
| chr7:158916592
|
G | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1792-2148G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916592 | ||||||
| chr7:158916592
|
G | GTCGCTGG others(26): Show |
2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2145_1792-214 others(37): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916592 | |||||
| chr7:158916595
|
G | A | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1792-2145G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916595 | ||||||
| chr7:158916599
|
C | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2141C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916599 | ||||||
| chr7:158916601
|
C | G | 89 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(86): Show | 89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1792-2139C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916601 | ||||||
| chr7:158916609
|
C | G | 89 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(86): Show | 89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1792-2131C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916609 | ||||||
| chr7:158916630
|
G | A | 4 | a0002c0002t0001g0039a0002c0002t0001g0041a0002c0002t0001g0103others(1): Show | 4 | HG01175.hp1 HG01496.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-2110G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916630 | ||||||
| chr7:158916630
|
G | C | 90 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(87): Show | 90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1792-2110G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916630 | ||||||
| chr7:158916632
|
C | G | 1 | a0001c0001t0005g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1792-2108C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916632 | ||||||
| chr7:158916632
|
C | T | 2 | a0002c0002t0001g0048a0002c0002t0001g0059 | 2 | HG01943.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1792-2108C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916632 | ||||||
| chr7:158916633
|
T | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-2107T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916633 | ||||||
| chr7:158916633
|
T | G | 107 | a0001c0001t0001g0269a0001c0001t0002g0203a0001c0001t0005g0180others(104): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1792-2107T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916633 | ||||||
| chr7:158916637
|
C | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2103C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916637 | ||||||
| chr7:158916639
|
C | G | 90 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(87): Show | 90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1792-2101C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916639 | ||||||
| chr7:158916647
|
C | G | 91 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(88): Show | 91 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1792-2093C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916647 | ||||||
| chr7:158916651
|
T | A | 109 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1792-2089T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916651 | ||||||
| chr7:158916655
|
G | A | 109 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1792-2085G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916655 | ||||||
| chr7:158916668
|
C | A | 85 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1792-2072C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916668 | ||||||
| chr7:158916668
|
C | G | 16 | a0002c0002t0001g0033a0002c0002t0001g0039a0002c0002t0001g0040others(13): Show | 16 | HG00733.hp2 HG01123.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1792-2072C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916668 | ||||||
| chr7:158916670
|
C | T | 7 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041others(4): Show | 7 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-2070C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916670 | ||||||
| chr7:158916671
|
G | A | 4 | a0001c0001t0012g0223a0001c0001t0012g0224a0003c0009t0011g0253others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-2069G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916671 | ||||||
| chr7:158916671
|
G | T | 4 | a0002c0002t0001g0039a0002c0002t0001g0041a0002c0002t0001g0103others(1): Show | 4 | HG01175.hp1 HG01496.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-2069G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916671 | ||||||
| chr7:158916676
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2064G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916676 | ||||||
| chr7:158916677
|
G | C | 87 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(84): Show | 87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792-2063G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916677 | ||||||
| chr7:158916685
|
G | C | 102 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(99): Show | 102 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1792-2055G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916685 | ||||||
| chr7:158916685
|
G | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2055G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916685 | ||||||
| chr7:158916693
|
A | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1792-2047A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916693 | ||||||
| chr7:158916706
|
G | A | 2 | a0001c0001t0002g0203a0002c0002t0001g0072 | 2 | HG01257.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1792-2034G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916706 | ||||||
| chr7:158916706
|
G | C | 4 | a0001c0001t0005g0196a0002c0002t0001g0025a0002c0002t0001g0079others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-2034G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916706 | ||||||
| chr7:158916708
|
C | T | 88 | a0001c0001t0005g0180a0001c0001t0005g0196a0001c0001t0005g0202others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-2032C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916708 | ||||||
| chr7:158916709
|
T | G | 11 | a0001c0001t0002g0203a0001c0001t0005g0196a0002c0002t0001g0039others(8): Show | 11 | HG01081.hp2 HG01175.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1792-2031T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916709 | ||||||
| chr7:158916710
|
G | A | 107 | a0001c0001t0002g0203a0001c0001t0005g0180a0001c0001t0005g0196others(104): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1792-2030G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916710 | ||||||
| chr7:158916713
|
C | T | 6 | a0002c0002t0001g0039a0002c0002t0001g0041a0002c0002t0001g0103others(3): Show | 6 | HG01175.hp1 HG01496.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-2027C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916713 | ||||||
| chr7:158916715
|
C | G | 87 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(84): Show | 87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792-2025C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916715 | ||||||
| chr7:158916723
|
C | G | 3 | a0001c0001t0005g0196a0002c0002t0001g0025a0002c0002t0001g0079 | 3 | HG02015.hp2 HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2017C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916723 | ||||||
| chr7:158916744
|
G | GTCGCTGG others(140): Show |
1 | a0002c0002t0001g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1792-1994_1792-199 others(151): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916744 | |||||
| chr7:158916746
|
C | T | 3 | a0002c0002t0001g0072a0002c0002t0001g0091a0002c0019t0015g0043 | 3 | HG01081.hp2 HG01257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1792-1994C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916746 | ||||||
| chr7:158916747
|
T | G | 200 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1792-1993T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916747 | ||||||
| chr7:158916747
|
T | TACACGCT others(31): Show |
1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1792-1917_1792-188 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916747 | |||||
| chr7:158916748
|
A | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1792-1992A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916748 | ||||||
| chr7:158916751
|
C | T | 83 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1792-1989C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916751 | ||||||
| chr7:158916753
|
C | G | 1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1987C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916753 | ||||||
| chr7:158916761
|
C | CAGTAAGG others(400): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1978_1792-197 others(411): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916761 | |||||
| chr7:158916761
|
C | G | 3 | a0002c0002t0001g0025a0002c0002t0001g0048a0002c0002t0001g0079 | 3 | HG03654.hp1 HG03942.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1979C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916761 | ||||||
| chr7:158916764
|
T | C | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1976T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916764 | ||||||
| chr7:158916764
|
T | TAAGGATG others(178): Show |
7 | a0002c0002t0001g0040a0002c0002t0001g0055a0002c0002t0001g0066others(4): Show | 7 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1955_1792-195 others(189): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916764 | |||||
| chr7:158916764
|
T | TAAGGATG others(178): Show |
1 | a0002c0002t0001g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1792-1955_1792-195 others(189): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916764 | |||||
| chr7:158916782
|
G | C | 2 | a0002c0002t0001g0025a0002c0002t0001g0079 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1958G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916782 | ||||||
| chr7:158916782
|
G | GTCGCTGG others(216): Show |
1 | a0002c0002t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1792-1955_1792-195 others(227): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916782 | |||||
| chr7:158916785
|
G | A | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1955G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916785 | ||||||
| chr7:158916789
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1951C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916789 | ||||||
| chr7:158916799
|
C | G | 12 | a0002c0002t0001g0033a0002c0002t0001g0040a0002c0002t0001g0048others(9): Show | 12 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1792-1941C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916799 | ||||||
| chr7:158916800
|
A | G | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-1940A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916800 | ||||||
| chr7:158916802
|
T | C | 9 | a0002c0002t0001g0033a0002c0002t0001g0040a0002c0002t0001g0048others(6): Show | 9 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1792-1938T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916802 | ||||||
| chr7:158916819
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1921C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916819 | ||||||
| chr7:158916820
|
G | C | 10 | a0002c0002t0001g0033a0002c0002t0001g0040a0002c0002t0001g0048others(7): Show | 10 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1920G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916820 | ||||||
| chr7:158916820
|
G | GTCGCTGG others(216): Show |
1 | a0002c0002t0001g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1792-1917_1792-191 others(227): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916820 | |||||
| chr7:158916820
|
G | T | 1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1792-1920G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916820 | ||||||
| chr7:158916822
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1918C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916822 | ||||||
| chr7:158916823
|
G | GACACGCT others(3472): Show |
1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1792-1904_1792-190 others(3483): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916823 | |||||
| chr7:158916827
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1913C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916827 | ||||||
| chr7:158916829
|
C | G | 1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1911C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916829 | ||||||
| chr7:158916837
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1903C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916837 | ||||||
| chr7:158916858
|
G | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1882G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916858 | ||||||
| chr7:158916858
|
G | GTCGCTGG others(216): Show |
1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1880_1792-187 others(227): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916858 | |||||
| chr7:158916860
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1880C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916860 | ||||||
| chr7:158916861
|
T | G | 107 | a0001c0001t0005g0180a0001c0001t0005g0196a0001c0001t0005g0202others(104): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1792-1879T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916861 | ||||||
| chr7:158916862
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1878A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916862 | ||||||
| chr7:158916865
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1875C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916865 | ||||||
| chr7:158916867
|
C | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1873C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916867 | ||||||
| chr7:158916875
|
C | G | 9 | a0001c0001t0005g0196a0002c0002t0001g0015a0002c0002t0001g0025others(6): Show | 9 | HG02015.hp2 HG02109.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1792-1865C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916875 | ||||||
| chr7:158916879
|
T | A | 108 | a0001c0001t0005g0180a0001c0001t0005g0196a0001c0001t0005g0202others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1792-1861T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916879 | ||||||
| chr7:158916896
|
C | G | 104 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1792-1844C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916896 | ||||||
| chr7:158916898
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1842C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916898 | ||||||
| chr7:158916898
|
C | T | 88 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-1842C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916898 | ||||||
| chr7:158916899
|
G | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0084 | 3 | HG03654.hp1 HG03688.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1841G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916899 | ||||||
| chr7:158916905
|
G | C | 17 | a0001c0001t0005g0196a0002c0002t0001g0025a0002c0002t0001g0033others(14): Show | 17 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1792-1835G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916905 | ||||||
| chr7:158916913
|
G | C | 97 | a0001c0001t0005g0180a0001c0001t0005g0196a0001c0001t0005g0202others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1792-1827G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916913 | ||||||
| chr7:158916914
|
A | G | 3 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0084 | 3 | HG03654.hp1 HG03688.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1826A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916914 | ||||||
| chr7:158916926
|
T | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1814T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916926 | ||||||
| chr7:158916934
|
G | C | 4 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0084others(1): Show | 4 | HG01081.hp2 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-1806G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916934 | ||||||
| chr7:158916934
|
G | GTCGCTGG others(368): Show |
1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1804_1792-180 others(379): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916934 | |||||
| chr7:158916936
|
C | T | 88 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-1804C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916936 | ||||||
| chr7:158916937
|
T | G | 10 | a0001c0001t0005g0196a0002c0002t0001g0025a0002c0002t0001g0059others(7): Show | 10 | HG01081.hp2 HG01257.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1803T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916937 | ||||||
| chr7:158916941
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1799C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916941 | ||||||
| chr7:158916943
|
C | CTGGTTGA others(442): Show |
1 | a0002c0002t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1792-1775_1792-177 others(453): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916943 | |||||
| chr7:158916943
|
C | CTGGTTGA others(31): Show |
2 | a0002c0002t0001g0048a0002c0002t0001g0091 | 2 | HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1792-1789_1792-178 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916943 | |||||
| chr7:158916943
|
C | G | 5 | a0002c0002t0001g0025a0002c0002t0001g0059a0002c0002t0001g0072others(2): Show | 5 | HG01257.hp1 HG01943.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1797C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916943 | ||||||
| chr7:158916951
|
C | G | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1789C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916951 | ||||||
| chr7:158916952
|
A | G | 8 | a0002c0002t0001g0033a0002c0002t0001g0040a0002c0002t0001g0055others(5): Show | 8 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1788A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916952 | ||||||
| chr7:158916963
|
T | G | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1777T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916963 | ||||||
| chr7:158916963
|
TTG | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1774_1792-177 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916963 | |||||
| chr7:158916971
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1792-1769C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916971 | ||||||
| chr7:158916972
|
G | C | 10 | a0001c0001t0005g0196a0002c0002t0001g0033a0002c0002t0001g0040others(7): Show | 10 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1768G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916972 | ||||||
| chr7:158916974
|
C | A | 88 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(85): Show | 88 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-1766C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916974 | ||||||
| chr7:158916974
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1766C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916974 | ||||||
| chr7:158916975
|
T | G | 204 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1792-1765T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916975 | ||||||
| chr7:158916981
|
C | G | 10 | a0001c0001t0005g0196a0002c0002t0001g0033a0002c0002t0001g0040others(7): Show | 10 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1759C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916981 | ||||||
| chr7:158916989
|
C | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1751C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916989 | ||||||
| chr7:158916990
|
A | G | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1750A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916990 | ||||||
| chr7:158917001
|
TTG | T | 7 | a0002c0002t0001g0016a0002c0002t0001g0025a0002c0002t0001g0048others(4): Show | 7 | HG01943.hp2 HG02486.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1736_1792-173 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917001 | |||||
| chr7:158917002
|
T | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1738T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917002 | ||||||
| chr7:158917003
|
G | GTGAAACG others(442): Show |
3 | a0002c0002t0001g0039a0002c0002t0001g0041a0002c0002t0001g0103 | 3 | HG01175.hp1 HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1792-1727_1792-172 others(453): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917003 | |||||
| chr7:158917003
|
G | GTGAAACG others(442): Show |
83 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1792-1727_1792-172 others(453): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917003 | |||||
| chr7:158917010
|
G | C | 4 | a0002c0019t0015g0043a0003c0009t0011g0253a0003c0009t0011g0261others(1): Show | 4 | HG01081.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1730G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917010 | ||||||
| chr7:158917017
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1723C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917017 | ||||||
| chr7:158917019
|
C | G | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1721C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917019 | ||||||
| chr7:158917039
|
TTG | T | 8 | a0002c0002t0001g0033a0002c0002t0001g0040a0002c0002t0001g0055others(5): Show | 8 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1698_1792-169 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917039 | |||||
| chr7:158917048
|
G | A | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1692G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917048 | ||||||
| chr7:158917048
|
G | C | 96 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(93): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1792-1692G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917048 | ||||||
| chr7:158917048
|
G | GTCGCTGG others(480): Show |
1 | a0002c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1689_1792-168 others(491): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917048 | |||||
| chr7:158917048
|
G | GTCTACAC others(221): Show |
1 | a0001c0001t0002g0198 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1792-1690_1792-168 others(232): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917048 | |||||
| chr7:158917050
|
C | T | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1690C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917050 | ||||||
| chr7:158917051
|
G | GACACGCT others(31): Show |
2 | a0001c0001t0009g0188a0001c0001t0009g0233 | 2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1792-1654_1792-161 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917051 | |||||
| chr7:158917055
|
C | G | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1685C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917055 | ||||||
| chr7:158917055
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1792-1685C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917055 | ||||||
| chr7:158917057
|
C | G | 98 | a0001c0001t0002g0198a0001c0001t0005g0180a0001c0001t0005g0202others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1792-1683C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917057 | ||||||
| chr7:158917065
|
C | CATTAAGG others(485): Show |
1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1664_1792-166 others(496): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | |||||
| chr7:158917065
|
C | CATTAAGG others(67): Show |
1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1661_1792-166 others(78): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | |||||
| chr7:158917065
|
C | CATTAAGG others(31): Show |
8 | a0002c0002t0001g0033a0002c0002t0001g0040a0002c0002t0001g0055others(5): Show | 8 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1655_1792-165 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | |||||
| chr7:158917065
|
C | CATTTAGG others(449): Show |
1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1792-1672_1792-167 others(460): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | |||||
| chr7:158917065
|
C | G | 96 | a0001c0001t0002g0198a0001c0001t0005g0180a0001c0001t0005g0202others(93): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1792-1675C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917065 | ||||||
| chr7:158917086
|
G | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1654G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917086 | ||||||
| chr7:158917088
|
C | T | 2 | a0002c0002t0001g0067a0002c0002t0001g0103 | 2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1792-1652C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917088 | ||||||
| chr7:158917089
|
T | G | 111 | a0001c0001t0002g0198a0001c0001t0002g0203a0001c0001t0005g0180others(108): Show | 111 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1792-1651T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917089 | ||||||
| chr7:158917089
|
T | TACACGCT others(259): Show |
2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(270): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(943): Show |
2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(954): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(943): Show |
1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(954): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(942): Show |
1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(953): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(942): Show |
5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(953): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(259): Show |
66 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(63): Show | 66 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(270): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(3890): Show |
1 | a0001c0001t0002g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(3901): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(3890): Show |
1 | a0001c0001t0002g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(3901): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5027): Show |
1 | a0001c0001t0002g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5038): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0197 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0130 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0135 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5065): Show |
1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5076): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(4002): Show |
1 | a0001c0001t0002g0105 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(4013): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
2 | a0001c0001t0002g0145a0001c0001t0002g0178 | 2 | HG00741.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0175 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(6467): Show |
1 | a0001c0001t0002g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(6478): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(676): Show |
1 | a0004c0004t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(687): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917089
|
T | TACACGCT others(5103): Show |
3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0117 | 3 | HG01243.hp2 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | |||||
| chr7:158917093
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1647C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917093 | ||||||
| chr7:158917094
|
G | GCTGGTTG others(183): Show |
3 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227 | 3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917094 | |||||
| chr7:158917094
|
G | GCTGGTTG others(259): Show |
1 | a0009c0007t0003g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(270): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917094 | |||||
| chr7:158917095
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1645C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917095 | ||||||
| chr7:158917096
|
T | TGGTTGAG others(256): Show |
1 | a0001c0001t0002g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(267): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917096 | |||||
| chr7:158917103
|
C | CATTAAGG others(102): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1617_1792-161 others(113): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917103 | |||||
| chr7:158917103
|
C | G | 26 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1792-1637C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917103 | ||||||
| chr7:158917107
|
A | T | 3 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227 | 3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1792-1633A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917107 | ||||||
| chr7:158917116
|
T | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1624T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917116 | ||||||
| chr7:158917124
|
C | G | 26 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1792-1616C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917124 | ||||||
| chr7:158917127
|
G | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1792-1613G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917127 | ||||||
| chr7:158917131
|
C | T | 3 | a0002c0019t0015g0043a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1609C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917131 | ||||||
| chr7:158917132
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1608G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917132 | ||||||
| chr7:158917133
|
C | G | 4 | a0001c0001t0005g0196a0008c0008t0003g0226a0008c0008t0020g0228others(1): Show | 4 | HG02015.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1607C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917133 | ||||||
| chr7:158917141
|
G | C | 26 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1792-1599G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917141 | ||||||
| chr7:158917141
|
G | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1599G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917141 | ||||||
| chr7:158917154
|
T | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1586T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917154 | ||||||
| chr7:158917161
|
T | C | 31 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(28): Show | 31 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1792-1579T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917161 | ||||||
| chr7:158917162
|
G | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1578G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917162 | ||||||
| chr7:158917164
|
T | C | 31 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(28): Show | 31 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1792-1576T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917164 | ||||||
| chr7:158917169
|
C | CGCTGGTT others(143): Show |
1 | a0001c0001t0003g0209 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1792-1570_1792-156 others(154): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917169 | |||||
| chr7:158917169
|
C | CGCTGGTT others(146): Show |
22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1792-1570_1792-156 others(157): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917169 | |||||
| chr7:158917169
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1571C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917169 | ||||||
| chr7:158917170
|
G | GC | 7 | a0001c0001t0005g0196a0001c0023t0018g0112a0003c0009t0011g0253others(4): Show | 7 | HG02015.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-1570_1792-156 others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917170 | ||||||
| chr7:158917178
|
C | G | 25 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1792-1562C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917178 | ||||||
| chr7:158917182
|
A | G | 8 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(5): Show | 8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792-1558A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917182 | ||||||
| chr7:158917199
|
G | C | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1541G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917199 | ||||||
| chr7:158917202
|
G | T | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-1538G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917202 | ||||||
| chr7:158917208
|
C | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1532C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917208 | ||||||
| chr7:158917215
|
A | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1525A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917215 | ||||||
| chr7:158917216
|
G | C | 24 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1792-1524G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917216 | ||||||
| chr7:158917216
|
G | GATTAAGG others(220): Show |
1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-1505_1792-150 others(231): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917216 | |||||
| chr7:158917229
|
T | C | 95 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1792-1511T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917229 | ||||||
| chr7:158917236
|
T | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1504T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917236 | ||||||
| chr7:158917237
|
G | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1503G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917237 | ||||||
| chr7:158917239
|
T | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1501T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917239 | ||||||
| chr7:158917244
|
C | T | 2 | a0001c0001t0001g0003a0002c0002t0001g0048 | 2 | HG02257.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1792-1496C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917244 | ||||||
| chr7:158917248
|
C | G | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1492C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917248 | ||||||
| chr7:158917249
|
G | A | 2 | a0001c0001t0002g0195a0001c0001t0002g0197 | 2 | HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1792-1491G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917249 | ||||||
| chr7:158917249
|
G | GTTGACAT others(4837): Show |
1 | a0001c0001t0002g0194 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1792-1431_1792-143 others(4848): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917249 | |||||
| chr7:158917253
|
A | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1487A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917253 | ||||||
| chr7:158917275
|
G | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1465G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917275 | ||||||
| chr7:158917282
|
T | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1458T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917282 | ||||||
| chr7:158917284
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1456C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917284 | ||||||
| chr7:158917292
|
A | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1448A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917292 | ||||||
| chr7:158917292
|
A | G | 3 | a0002c0019t0015g0043a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1448A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917292 | ||||||
| chr7:158917307
|
T | G | 3 | a0002c0002t0001g0007a0002c0002t0001g0052a0013c0015t0001g0051 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1792-1433T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917307 | ||||||
| chr7:158917310
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1430G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917310 | ||||||
| chr7:158917316
|
A | ACTAAACA others(161): Show |
5 | a0002c0002t0001g0015a0002c0002t0001g0053a0002c0002t0001g0069others(2): Show | 5 | HG02486.hp1 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792-1370_1792-136 others(172): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917316 | |||||
| chr7:158917316
|
ACTAAACA others(245): Show |
A | 3 | a0002c0019t0015g0043a0003c0009t0011g0253a0003c0009t0011g0261 | 3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1348_1792-109 others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917316 | |||||
| chr7:158917317
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1423C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917317 | ||||||
| chr7:158917318
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1422T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917318 | ||||||
| chr7:158917320
|
A | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1420A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917320 | ||||||
| chr7:158917323
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1417A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917323 | ||||||
| chr7:158917325
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1415C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917325 | ||||||
| chr7:158917326
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1414C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917326 | ||||||
| chr7:158917327
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1413C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917327 | ||||||
| chr7:158917328
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1412C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917328 | ||||||
| chr7:158917331
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1409C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917331 | ||||||
| chr7:158917331
|
CCCTCCAC others(119): Show |
C | 8 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(5): Show | 8 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1288_1792-116 others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917331 | |||||
| chr7:158917333
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1407C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917333 | ||||||
| chr7:158917335
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1405C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917335 | ||||||
| chr7:158917336
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1404C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917336 | ||||||
| chr7:158917338
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1402C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917338 | ||||||
| chr7:158917340
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1400C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917340 | ||||||
| chr7:158917342
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1398C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917342 | ||||||
| chr7:158917343
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1397C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917343 | ||||||
| chr7:158917345
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1395C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917345 | ||||||
| chr7:158917347
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1393C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917347 | ||||||
| chr7:158917350
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1390C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917350 | ||||||
| chr7:158917354
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1386T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917354 | ||||||
| chr7:158917359
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1381C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917359 | ||||||
| chr7:158917363
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1377A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917363 | ||||||
| chr7:158917364
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1376C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917364 | ||||||
| chr7:158917374
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1366C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917374 | ||||||
| chr7:158917375
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1365C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917375 | ||||||
| chr7:158917377
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1363C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917377 | ||||||
| chr7:158917378
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1362C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917378 | ||||||
| chr7:158917380
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1360C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917380 | ||||||
| chr7:158917381
|
A | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1359A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917381 | ||||||
| chr7:158917385
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1355C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917385 | ||||||
| chr7:158917388
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1352C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917388 | ||||||
| chr7:158917390
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1350T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917390 | ||||||
| chr7:158917392
|
T | C | 6 | a0002c0002t0001g0015a0002c0002t0001g0027a0002c0002t0001g0053others(3): Show | 6 | HG02486.hp1 HG02976.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1348T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917392 | ||||||
| chr7:158917392
|
T | TGCCTCTC others(119): Show |
86 | a0001c0001t0005g0180a0001c0001t0005g0202a0002c0002t0001g0001others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1792-1289_1792-128 others(130): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917392 | |||||
| chr7:158917392
|
T | TGCCTCTC others(161): Show |
1 | a0002c0002t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1792-1307_1792-130 others(172): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917392 | |||||
| chr7:158917393
|
G | GCCTCTCA others(77): Show |
2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | NA18943.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1792-1289_1792-128 others(88): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917393 | |||||
| chr7:158917394
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1346C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917394 | ||||||
| chr7:158917395
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1345C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917395 | ||||||
| chr7:158917397
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1343C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917397 | ||||||
| chr7:158917398
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1342T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917398 | ||||||
| chr7:158917401
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1339C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917401 | ||||||
| chr7:158917404
|
A | AACACCTC others(287): Show |
22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1792-1289_1792-128 others(298): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917404 | |||||
| chr7:158917405
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1335A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917405 | ||||||
| chr7:158917406
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1334C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917406 | ||||||
| chr7:158917416
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1324C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917416 | ||||||
| chr7:158917417
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1323C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917417 | ||||||
| chr7:158917419
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1321C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917419 | ||||||
| chr7:158917420
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1320C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917420 | ||||||
| chr7:158917422
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1318C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917422 | ||||||
| chr7:158917423
|
A | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1317A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917423 | ||||||
| chr7:158917427
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1313C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917427 | ||||||
| chr7:158917430
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1310C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917430 | ||||||
| chr7:158917432
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1308T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917432 | ||||||
| chr7:158917433
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1307C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917433 | ||||||
| chr7:158917434
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1306C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917434 | ||||||
| chr7:158917435
|
G | A | 2 | a0002c0002t0001g0060a0002c0002t0001g0109 | 2 | HG00741.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1792-1305G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917435 | ||||||
| chr7:158917436
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1304C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917436 | ||||||
| chr7:158917437
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1303C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917437 | ||||||
| chr7:158917439
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1301C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917439 | ||||||
| chr7:158917440
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1300T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917440 | ||||||
| chr7:158917442
|
G | A | 4 | a0001c0001t0005g0196a0002c0002t0001g0060a0002c0002t0001g0109others(1): Show | 4 | HG00741.hp1 HG01975.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1298G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917442 | ||||||
| chr7:158917442
|
G | GCTAAACA others(161): Show |
1 | a0002c0002t0001g0076 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1792-1289_1792-128 others(172): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917442 | |||||
| chr7:158917442
|
GCTAAACA others(77): Show |
G | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792-1263_1792-118 others(88): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917442 | |||||
| chr7:158917443
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1297C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917443 | ||||||
| chr7:158917447
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1293A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917447 | ||||||
| chr7:158917448
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1292C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917448 | ||||||
| chr7:158917450
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1290C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917450 | ||||||
| chr7:158917451
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1289C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917451 | ||||||
| chr7:158917452
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1792-1288T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917452 | ||||||
| chr7:158917453
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1287C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917453 | ||||||
| chr7:158917454
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1286C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917454 | ||||||
| chr7:158917457
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1283T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917457 | ||||||
| chr7:158917457
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1792-1283T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917457 | ||||||
| chr7:158917457
|
T | TCCTCCAC others(35): Show |
1 | a0020c0011t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1792-1264_1792-126 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917457 | |||||
| chr7:158917462
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1278C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917462 | ||||||
| chr7:158917466
|
C | CGGTGGTT others(93): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1274_1792-127 others(104): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917466 | ||||||
| chr7:158917468
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1272C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917468 | ||||||
| chr7:158917469
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1271C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917469 | ||||||
| chr7:158917471
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1269C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917471 | ||||||
| chr7:158917476
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1264C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917476 | ||||||
| chr7:158917476
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1792-1264C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917476 | ||||||
| chr7:158917477
|
A | G | 4 | a0002c0002t0001g0060a0002c0002t0001g0076a0002c0002t0001g0098others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-1263A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917477 | ||||||
| chr7:158917477
|
ACCTCTCA others(35): Show |
A | 2 | a0003c0003t0007g0248a0003c0003t0007g0260 | 2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1792-1222_1792-118 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917477 | |||||
| chr7:158917479
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1261C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917479 | ||||||
| chr7:158917485
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1255C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917485 | ||||||
| chr7:158917489
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1251A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917489 | ||||||
| chr7:158917490
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1250C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917490 | ||||||
| chr7:158917492
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1248C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917492 | ||||||
| chr7:158917493
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1247C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917493 | ||||||
| chr7:158917495
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1245C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917495 | ||||||
| chr7:158917496
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1244C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917496 | ||||||
| chr7:158917499
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1241T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917499 | ||||||
| chr7:158917499
|
T | TCCTCCAC others(119): Show |
1 | a0002c0002t0001g0098 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1792-1223_1792-122 others(130): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917499 | |||||
| chr7:158917504
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1236C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917504 | ||||||
| chr7:158917508
|
C | CGGTGGTT others(138): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1232_1792-123 others(149): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917508 | ||||||
| chr7:158917511
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1229C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917511 | ||||||
| chr7:158917514
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1226C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917514 | ||||||
| chr7:158917516
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1224T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917516 | ||||||
| chr7:158917518
|
T | C | 8 | a0001c0001t0003g0221a0002c0002t0001g0006a0002c0002t0001g0007others(5): Show | 8 | HG01943.hp2 HG02074.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1222T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917518 | ||||||
| chr7:158917519
|
G | A | 1 | a0002c0002t0001g0098 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1792-1221G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917519 | ||||||
| chr7:158917519
|
G | GCCTCTCA others(749): Show |
1 | a0001c0001t0003g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1792-1089_1792-108 others(760): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917519 | |||||
| chr7:158917519
|
GCCTCTCA others(77): Show |
G | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1792-1120_1792-103 others(88): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917519 | |||||
| chr7:158917520
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1220C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917520 | ||||||
| chr7:158917521
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1219C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917521 | ||||||
| chr7:158917523
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1217C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917523 | ||||||
| chr7:158917524
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1216T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917524 | ||||||
| chr7:158917526
|
A | G | 1 | a0004c0004t0006g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1792-1214A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917526 | ||||||
| chr7:158917527
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1213C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917527 | ||||||
| chr7:158917531
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1209A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917531 | ||||||
| chr7:158917532
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1208C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917532 | ||||||
| chr7:158917534
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1206C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917534 | ||||||
| chr7:158917535
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1205C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917535 | ||||||
| chr7:158917536
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792-1204T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917536 | ||||||
| chr7:158917537
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1203C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917537 | ||||||
| chr7:158917538
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1202C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917538 | ||||||
| chr7:158917541
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1199T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917541 | ||||||
| chr7:158917541
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792-1199T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917541 | ||||||
| chr7:158917541
|
T | TCCTCCAC others(35): Show |
91 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(88): Show | 91 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1792-1179_1792-113 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917541 | |||||
| chr7:158917541
|
T | TCCTCCAC others(455): Show |
1 | a0004c0004t0006g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1792-1181_1792-118 others(466): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917541 | |||||
| chr7:158917543
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1197C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917543 | ||||||
| chr7:158917546
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1194C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917546 | ||||||
| chr7:158917551
|
T | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1189T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917551 | ||||||
| chr7:158917552
|
C | CTGGTTGA others(10): Show |
1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1188_1792-118 others(21): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917552 | ||||||
| chr7:158917553
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1187C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917553 | ||||||
| chr7:158917555
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1185C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917555 | ||||||
| chr7:158917556
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1184C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917556 | ||||||
| chr7:158917557
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1183C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917557 | ||||||
| chr7:158917559
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1181C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917559 | ||||||
| chr7:158917560
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1180C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917560 | ||||||
| chr7:158917562
|
C | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1178C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917562 | ||||||
| chr7:158917565
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1175C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917565 | ||||||
| chr7:158917568
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1172G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917568 | ||||||
| chr7:158917568
|
G | GCTAAACA others(119): Show |
1 | a0002c0002t0014g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1792-1138_1792-101 others(130): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917568 | |||||
| chr7:158917603
|
A | G | 2 | a0007c0005t0002g0189a0007c0005t0002g0225 | 2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1137A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917603 | ||||||
| chr7:158917610
|
A | G | 2 | a0007c0005t0002g0189a0007c0005t0002g0225 | 2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1130A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917610 | ||||||
| chr7:158917620
|
T | C | 2 | a0007c0005t0002g0189a0007c0005t0002g0225 | 2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1120T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917620 | ||||||
| chr7:158917625
|
T | C | 2 | a0007c0005t0002g0189a0007c0005t0002g0225 | 2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1115T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917625 | ||||||
| chr7:158917625
|
TCCTCCAC others(35): Show |
T | 3 | a0002c0002t0001g0007a0002c0002t0001g0052a0013c0015t0001g0051 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1792-1095_1792-105 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917625 | |||||
| chr7:158917644
|
C | T | 6 | a0004c0004t0001g0170a0004c0004t0002g0192a0004c0004t0002g0193others(3): Show | 6 | HG02258.hp2 HG02818.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1096C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917644 | ||||||
| chr7:158917645
|
G | A | 2 | a0007c0005t0002g0189a0007c0005t0002g0225 | 2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1095G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917645 | ||||||
| chr7:158917652
|
G | A | 6 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(3): Show | 6 | HG01081.hp2 HG01934.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1088G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917652 | ||||||
| chr7:158917686
|
C | T | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1054C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917686 | ||||||
| chr7:158917687
|
A | G | 8 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(5): Show | 8 | HG01081.hp2 HG01257.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792-1053A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917687 | ||||||
| chr7:158917698
|
A | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1042A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917698 | ||||||
| chr7:158917704
|
C | T | 6 | a0002c0002t0001g0015a0002c0002t0001g0053a0002c0002t0001g0069others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1036C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917704 | ||||||
| chr7:158917732
|
T | C | 118 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1792-1008T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917732 | ||||||
| chr7:158917744
|
C | T | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-996C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917744 | ||||||
| chr7:158917783
|
T | G | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-957T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917783 | ||||||
| chr7:158917805
|
T | A | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-935T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917805 | ||||||
| chr7:158917951
|
A | G | 8 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(5): Show | 8 | HG01081.hp2 HG01257.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792-789A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917951 | ||||||
| chr7:158918075
|
T | C | 2 | a0002c0002t0001g0067a0002c0002t0001g0103 | 2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1792-665T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918075 | ||||||
| chr7:158918121
|
C | T | 23 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1792-619C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918121 | ||||||
| chr7:158918188
|
G | A | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-552G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918188 | ||||||
| chr7:158918250
|
C | T | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1792-490C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918250 | ||||||
| chr7:158918363
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1792-377C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918363 | ||||||
| chr7:158918604
|
T | C | 95 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1792-136T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918604 | ||||||
| chr7:158918735
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG01433.hp1 | splice_region_variant&intron_variant | LOW | c.1792-5G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918735 | ||||||
| chr7:158918893
|
A | G | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+24A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158918893 | ||||||
| chr7:158918952
|
AT | A | 91 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(88): Show | 91 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1921+87delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158918952 | |||||
| chr7:158918963
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1921+94A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158918963 | ||||||
| chr7:158919112
|
T | A | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+243T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919112 | ||||||
| chr7:158919251
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1921+382A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919251 | ||||||
| chr7:158919259
|
T | G | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1921+390T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919259 | ||||||
| chr7:158919379
|
C | CAA | 3 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0093 | 3 | HG01358.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1921+512_1921+513d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158919379 | |||||
| chr7:158919496
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1921+627G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919496 | ||||||
| chr7:158919548
|
G | C | 3 | a0002c0002t0001g0066a0002c0002t0001g0068a0002c0002t0001g0080 | 3 | HG01346.hp2 HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1921+679G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919548 | ||||||
| chr7:158919561
|
G | A | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+692G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919561 | ||||||
| chr7:158919881
|
GC | G | 95 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1921+1017delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158919881 | |||||
| chr7:158919895
|
G | A | 3 | a0001c0001t0002g0157a0001c0001t0012g0223a0001c0001t0012g0224 | 3 | HG02055.hp1 HG02723.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1921+1026G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919895 | ||||||
| chr7:158919945
|
C | T | 1 | a0001c0001t0005g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1921+1076C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919945 | ||||||
| chr7:158919952
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1921+1083G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919952 | ||||||
| chr7:158919954
|
AGAACACG others(90): Show |
A | 1 | a0003c0003t0007g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1921+1110_1921+120 others(101): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158919954 | |||||
| chr7:158920047
|
A | G | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1921+1178A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920047 | ||||||
| chr7:158920073
|
G | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1921+1204G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920073 | ||||||
| chr7:158920076
|
T | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+1207T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920076 | ||||||
| chr7:158920083
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1921+1214G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920083 | ||||||
| chr7:158920141
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1921+1272C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920141 | ||||||
| chr7:158920160
|
T | A | 2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1921+1291T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920160 | ||||||
| chr7:158920190
|
G | A | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1921+1321G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920190 | ||||||
| chr7:158920227
|
G | A | 1 | a0002c0002t0001g0063 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1921+1358G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920227 | ||||||
| chr7:158920229
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1921+1360C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920229 | ||||||
| chr7:158920385
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1921+1516G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920385 | ||||||
| chr7:158920439
|
C | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1921+1570C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920439 | ||||||
| chr7:158920574
|
G | A | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1921+1705G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920574 | ||||||
| chr7:158920621
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1921+1752C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920621 | ||||||
| chr7:158920633
|
CGTG | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1743_1922-174 others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920633 | ||||||
| chr7:158920901
|
A | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1922-1476A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920901 | ||||||
| chr7:158920967
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1922-1410G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920967 | ||||||
| chr7:158920995
|
C | T | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1382C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920995 | ||||||
| chr7:158921082
|
C | T | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1295C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921082 | ||||||
| chr7:158921123
|
AC | A | 4 | a0004c0004t0002g0192a0004c0004t0002g0193a0007c0005t0002g0189others(1): Show | 4 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1253delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921123 | ||||||
| chr7:158921238
|
T | C | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1139T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921238 | ||||||
| chr7:158921311
|
G | A | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1922-1066G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921311 | ||||||
| chr7:158921321
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1922-1056C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921321 | ||||||
| chr7:158921407
|
G | A | 4 | a0008c0008t0003g0226a0008c0008t0020g0228a0009c0007t0003g0227others(1): Show | 4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-970G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921407 | ||||||
| chr7:158921428
|
G | A | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-949G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921428 | ||||||
| chr7:158921467
|
A | G | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1922-910A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921467 | ||||||
| chr7:158921525
|
C | T | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-852C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921525 | ||||||
| chr7:158921547
|
C | T | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-830C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921547 | ||||||
| chr7:158921552
|
G | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0197 | 3 | HG01167.hp2 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1922-825G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921552 | ||||||
| chr7:158921635
|
G | A | 2 | a0003c0003t0004g0254a0003c0003t0004g0258 | 2 | HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1922-742G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921635 | ||||||
| chr7:158921751
|
C | T | 3 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112 | 3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1922-626C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921751 | ||||||
| chr7:158921800
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1922-577A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921800 | ||||||
| chr7:158922051
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1922-326G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922051 | ||||||
| chr7:158922174
|
A | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1922-203A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922174 | ||||||
| chr7:158922187
|
C | T | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1922-190C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922187 | ||||||
| chr7:158922230
|
A | C | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1922-147A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922230 | ||||||
| chr7:158922361
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1922-16T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922361 | ||||||
| chr7:158922370
|
TC | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
splice_region_variant&intron_variant | LOW | c.1922-4delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158922370 | |||||
| chr7:158922571
|
G | C | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+22G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922571 | ||||||
| chr7:158922573
|
A | G | 125 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(122): Show | 125 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2094+24A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922573 | ||||||
| chr7:158922575
|
G | A | 2 | a0003c0003t0004g0254a0003c0003t0004g0258 | 2 | HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2094+26G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922575 | ||||||
| chr7:158922655
|
G | A | 1 | a0001c0001t0002g0198 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2094+106G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922655 | ||||||
| chr7:158922878
|
G | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2094+329G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922878 | ||||||
| chr7:158922896
|
T | G | 1 | a0004c0004t0006g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2094+347T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922896 | ||||||
| chr7:158922931
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+382C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922931 | ||||||
| chr7:158922952
|
A | C | 3 | a0004c0004t0006g0199a0004c0004t0006g0200a0004c0004t0006g0201 | 3 | HG02818.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2094+403A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922952 | ||||||
| chr7:158923028
|
C | A | 4 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0009t0011g0253others(1): Show | 4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+479C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923028 | ||||||
| chr7:158923073
|
G | C | 1 | a0003c0009t0011g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2095-498G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923073 | ||||||
| chr7:158923294
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2095-277C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923294 | ||||||
| chr7:158923336
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2095-235G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923336 | ||||||
| chr7:158923943
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2257+210C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158923943 | ||||||
| chr7:158924059
|
C | T | 1 | a0002c0002t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2257+326C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924059 | ||||||
| chr7:158924221
|
T | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2257+488T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924221 | ||||||
| chr7:158924452
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2257+719C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924452 | ||||||
| chr7:158924493
|
A | G | 2 | a0001c0001t0005g0196a0002c0019t0015g0043 | 2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.2257+760A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924493 | ||||||
| chr7:158924587
|
C | T | 2 | a0002c0002t0001g0022a0002c0002t0001g0097 | 2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2257+854C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924587 | ||||||
| chr7:158924603
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2257+870C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924603 | ||||||
| chr7:158924614
|
T | TAAAAGAT others(316): Show |
1 | a0001c0001t0012g0224 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2257+895_2257+896i others(325): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr7 | 158924614 | |||||
| chr7:158924614
|
T | TAAAAGAT others(326): Show |
1 | a0001c0001t0012g0223 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2257+895_2257+896i others(335): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr7 | 158924614 | |||||
| chr7:158924623
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0006g0004a0001c0001t0006g0005 | 3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2257+890T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924623 | ||||||
| chr7:158924798
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2257+1065A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924798 | ||||||
| chr7:158925170
|
G | A | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2258-1017G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925170 | ||||||
| chr7:158925223
|
C | G | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2258-964C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925223 | ||||||
| chr7:158925531
|
A | T | 1 | a0004c0004t0002g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2258-656A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925531 | ||||||
| chr7:158925564
|
A | G | 3 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041 | 3 | HG00733.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2258-623A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925564 | ||||||
| chr7:158925707
|
G | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2258-480G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925707 | ||||||
| chr7:158926102
|
A | G | 104 | a0001c0001t0001g0268a0001c0001t0005g0136a0001c0001t0005g0139others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2258-85A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158926102 | ||||||
| chr7:158926114
|
T | C | 32 | a0001c0001t0005g0136a0001c0001t0005g0180a0001c0001t0005g0202others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.2258-73T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158926114 | ||||||
| chr7:158926304
|
C | T | 30 | a0001c0001t0002g0168a0001c0001t0003g0205a0001c0001t0003g0206others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.2371+4C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926304 | ||||||
| chr7:158926358
|
C | G | 1 | a0001c0001t0002g0176 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2372-44C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926358 | ||||||
| chr7:158926370
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2372-32C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926370 | ||||||
| chr7:158926393
|
C | T | 220 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.2372-9C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926393 | ||||||
| chr7:158926562
|
G | A | 124 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2433+99G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/24 | chr7 | 158926562 | ||||||
| chr7:158926734
|
T | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2434-258T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/24 | chr7 | 158926734 | ||||||
| chr7:158926765
|
G | A | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2434-227G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/24 | chr7 | 158926765 | ||||||
| chr7:158927100
|
A | C | 1 | a0001c0001t0002g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2485+57A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927100 | ||||||
| chr7:158927231
|
G | A | 1 | a0001c0001t0003g0219 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2485+188G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927231 | ||||||
| chr7:158927306
|
G | A | 93 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(90): Show | 93 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.2485+263G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927306 | ||||||
| chr7:158927310
|
G | A | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2485+267G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927310 | ||||||
| chr7:158927396
|
TTG | T | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2485+355_2485+356d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927396 | |||||
| chr7:158927408
|
T | TA | 121 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(118): Show | 121 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2485+379dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927408 | |||||
| chr7:158927446
|
A | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2485+403A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927446 | ||||||
| chr7:158927557
|
AT | A | 94 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(91): Show | 94 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.2485+528delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927557 | |||||
| chr7:158927712
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2485+669C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927712 | ||||||
| chr7:158927827
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2485+784C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927827 | ||||||
| chr7:158927834
|
GAGCCACC others(4): Show |
G | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2485+796_2485+806d others(13): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927834 | |||||
| chr7:158927875
|
G | A | 2 | a0001c0001t0006g0004a0001c0001t0006g0005 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2485+832G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927875 | ||||||
| chr7:158928037
|
A | C | 2 | a0001c0001t0005g0196a0001c0001t0006g0005 | 2 | HG02015.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2485+994A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928037 | ||||||
| chr7:158928108
|
G | A | 92 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(89): Show | 92 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.2485+1065G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928108 | ||||||
| chr7:158928110
|
G | T | 1 | a0001c0001t0002g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2485+1067G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928110 | ||||||
| chr7:158928271
|
T | TGATCTCA others(311): Show |
1 | a0001c0001t0003g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2485+1243_2485+124 others(322): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928271 | |||||
| chr7:158928271
|
T | TGATCTCA others(312): Show |
14 | a0001c0001t0003g0206a0001c0001t0003g0209a0001c0001t0003g0210others(11): Show | 14 | HG00423.hp1 HG00597.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.2485+1243_2485+124 others(323): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928271 | |||||
| chr7:158928271
|
T | TGATCTCA others(313): Show |
6 | a0001c0001t0003g0205a0001c0001t0003g0207a0001c0001t0003g0208others(3): Show | 6 | HG00544.hp1 HG03688.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2485+1243_2485+124 others(324): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928271 | |||||
| chr7:158928296
|
T | A | 1 | a0001c0001t0003g0210 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2485+1253T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928296 | ||||||
| chr7:158928310
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2485+1267C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928310 | ||||||
| chr7:158928333
|
C | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2485+1290C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928333 | ||||||
| chr7:158928401
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2485+1358C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928401 | ||||||
| chr7:158928589
|
G | C | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2485+1546G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928589 | ||||||
| chr7:158928682
|
G | A | 1 | a0001c0012t0002g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2485+1639G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928682 | ||||||
| chr7:158928748
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2485+1705A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928748 | ||||||
| chr7:158928776
|
TAGTC | T | 136 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2486-1674_2486-167 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928776 | |||||
| chr7:158928808
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2486-1647C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928808 | ||||||
| chr7:158928813
|
A | G | 239 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2486-1642A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928813 | ||||||
| chr7:158928835
|
C | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2486-1620C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928835 | ||||||
| chr7:158928856
|
G | A | 95 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2486-1599G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928856 | ||||||
| chr7:158929030
|
A | G | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2486-1425A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929030 | ||||||
| chr7:158929255
|
C | A | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2486-1200C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929255 | ||||||
| chr7:158929288
|
C | T | 1 | a0002c0002t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2486-1167C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929288 | ||||||
| chr7:158929385
|
A | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2486-1070A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929385 | ||||||
| chr7:158929385
|
AGGCCTGG others(49): Show |
A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2486-1048_2486-993 others(59): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158929385 | |||||
| chr7:158929391
|
G | A | 7 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(4): Show | 7 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2486-1064G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929391 | ||||||
| chr7:158929408
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2486-1047G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929408 | ||||||
| chr7:158929441
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0273 | 3 | HG01433.hp1 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2486-1014G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929441 | ||||||
| chr7:158929459
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2486-996T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929459 | ||||||
| chr7:158929487
|
A | G | 10 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112others(7): Show | 10 | HG01255.hp2 HG01257.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2486-968A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929487 | ||||||
| chr7:158929499
|
C | G | 2 | a0008c0008t0003g0226a0008c0008t0020g0228 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2486-956C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929499 | ||||||
| chr7:158929501
|
G | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2486-954G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929501 | ||||||
| chr7:158929555
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2486-900G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929555 | ||||||
| chr7:158929624
|
G | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2486-831G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929624 | ||||||
| chr7:158929630
|
C | T | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2486-825C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929630 | ||||||
| chr7:158929837
|
G | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0197 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2486-618G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929837 | ||||||
| chr7:158930062
|
T | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2486-393T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930062 | ||||||
| chr7:158930132
|
T | G | 2 | a0003c0009t0011g0253a0003c0009t0011g0261 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2486-323T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930132 | ||||||
| chr7:158930322
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2486-133G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930322 | ||||||
| chr7:158930323
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2486-132T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930323 | ||||||
| chr7:158930624
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2546+109A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930624 | ||||||
| chr7:158930643
|
T | C | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+128T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930643 | ||||||
| chr7:158930648
|
G | A | 4 | a0004c0004t0001g0170a0004c0004t0006g0199a0004c0004t0006g0200others(1): Show | 4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546+133G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930648 | ||||||
| chr7:158930661
|
A | G | 1 | a0004c0004t0006g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2546+146A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930661 | ||||||
| chr7:158930713
|
G | A | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2546+198G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930713 | ||||||
| chr7:158930763
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2546+248G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930763 | ||||||
| chr7:158930767
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2546+252C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930767 | ||||||
| chr7:158930772
|
G | A | 6 | a0002c0002t0001g0015a0002c0002t0001g0053a0002c0002t0001g0069others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+257G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930772 | ||||||
| chr7:158931015
|
G | A | 1 | a0009c0007t0003g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2546+500G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931015 | ||||||
| chr7:158931093
|
A | C | 3 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0027t0022g0263 | 3 | HG01081.hp2 HG02015.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2546+578A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931093 | ||||||
| chr7:158931228
|
T | C | 1 | a0003c0009t0011g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2546+713T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931228 | ||||||
| chr7:158931244
|
A | G | 22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.2546+729A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931244 | ||||||
| chr7:158931305
|
C | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+790C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931305 | ||||||
| chr7:158931318
|
T | C | 24 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.2546+803T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931318 | ||||||
| chr7:158931472
|
C | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2546+957C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931472 | ||||||
| chr7:158931544
|
C | T | 1 | a0004c0004t0002g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2546+1029C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931544 | ||||||
| chr7:158931636
|
A | G | 22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.2546+1121A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931636 | ||||||
| chr7:158931910
|
G | T | 1 | a0013c0015t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2546+1395G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931910 | ||||||
| chr7:158931914
|
A | T | 1 | a0003c0003t0007g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2546+1399A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931914 | ||||||
| chr7:158932027
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2546+1512A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932027 | ||||||
| chr7:158932098
|
G | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2546+1583G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932098 | ||||||
| chr7:158932123
|
G | A | 1 | a0001c0001t0005g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2546+1608G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932123 | ||||||
| chr7:158932198
|
C | T | 82 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(79): Show | 82 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.2546+1683C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932198 | ||||||
| chr7:158932214
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+1699C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932214 | ||||||
| chr7:158932448
|
A | G | 1 | a0003c0003t0007g0260 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2547-1681A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932448 | ||||||
| chr7:158932449
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2547-1680C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932449 | ||||||
| chr7:158932563
|
C | CCGA | 24 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.2547-1564_2547-156 others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr7 | 158932563 | |||||
| chr7:158932898
|
T | A | 3 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112 | 3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2547-1231T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932898 | ||||||
| chr7:158932932
|
G | A | 3 | a0003c0009t0011g0253a0003c0009t0011g0261a0004c0004t0001g0170 | 3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2547-1197G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932932 | ||||||
| chr7:158933043
|
C | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2547-1086C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933043 | ||||||
| chr7:158933073
|
TC | T | 5 | a0002c0002t0001g0009a0002c0002t0001g0056a0002c0002t0001g0061others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-1055delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933073 | ||||||
| chr7:158933177
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2547-952G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933177 | ||||||
| chr7:158933216
|
C | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2547-913C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933216 | ||||||
| chr7:158933498
|
G | A | 1 | a0003c0003t0007g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2547-631G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933498 | ||||||
| chr7:158933523
|
C | T | 3 | a0004c0004t0006g0199a0004c0004t0006g0200a0004c0004t0006g0201 | 3 | HG02818.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2547-606C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933523 | ||||||
| chr7:158933601
|
A | G | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2547-528A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933601 | ||||||
| chr7:158933763
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2547-366T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933763 | ||||||
| chr7:158933771
|
T | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2547-358T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933771 | ||||||
| chr7:158933785
|
G | A | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2547-344G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933785 | ||||||
| chr7:158933964
|
G | A | 109 | a0001c0001t0005g0136a0001c0001t0005g0139a0001c0001t0005g0180others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2547-165G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933964 | ||||||
| chr7:158933993
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-136G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933993 | ||||||
| chr7:158934107
|
T | TC | 242 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2547-22_2547-21ins others(1): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158934107 | ||||||
| chr7:158934323
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2646+95T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | chr7 | 158934323 | ||||||
| chr7:158934324
|
C | CT | 239 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2647-91dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr7 | 158934324 | |||||
| chr7:158934332
|
A | C | 3 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112 | 3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2647-86A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | chr7 | 158934332 | ||||||
| chr7:158934387
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2647-31G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | chr7 | 158934387 | ||||||
| chr7:158934578
|
A | G | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2778+29A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934578 | ||||||
| chr7:158934585
|
T | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2778+36T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934585 | ||||||
| chr7:158934612
|
G | T | 108 | a0001c0001t0005g0136a0001c0001t0005g0139a0001c0001t0005g0180others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2778+63G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934612 | ||||||
| chr7:158934781
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2778+232G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934781 | ||||||
| chr7:158934813
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2778+264T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934813 | ||||||
| chr7:158934900
|
C | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2778+351C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934900 | ||||||
| chr7:158934922
|
C | T | 95 | a0001c0001t0005g0136a0001c0001t0005g0180a0001c0001t0005g0202others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2778+373C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934922 | ||||||
| chr7:158934981
|
A | G | 1 | a0001c0012t0002g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2778+432A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934981 | ||||||
| chr7:158935209
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+660C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935209 | ||||||
| chr7:158935219
|
A | G | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2778+670A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935219 | ||||||
| chr7:158935246
|
C | T | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+697C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935246 | ||||||
| chr7:158935460
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2778+911T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935460 | ||||||
| chr7:158935485
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2778+936C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935485 | ||||||
| chr7:158935926
|
ACGGTGGC others(16): Show |
A | 1 | a0002c0002t0001g0062 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2778+1381_2778+140 others(27): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158935926 | |||||
| chr7:158936052
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2778+1503G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936052 | ||||||
| chr7:158936185
|
C | T | 1 | a0001c0001t0009g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2778+1636C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936185 | ||||||
| chr7:158936283
|
A | G | 72 | a0001c0001t0002g0115a0001c0001t0002g0119a0001c0001t0002g0120others(69): Show | 72 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2778+1734A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936283 | ||||||
| chr7:158936417
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2778+1868C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936417 | ||||||
| chr7:158936447
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2778+1898G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936447 | ||||||
| chr7:158936550
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2778+2001C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936550 | ||||||
| chr7:158936645
|
C | T | 3 | a0001c0001t0012g0223a0001c0001t0012g0224a0001c0023t0018g0112 | 3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2778+2096C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936645 | ||||||
| chr7:158936831
|
A | G | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2778+2282A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936831 | ||||||
| chr7:158936840
|
C | T | 1 | a0001c0001t0005g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2778+2291C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936840 | ||||||
| chr7:158937237
|
T | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2778+2688T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937237 | ||||||
| chr7:158937242
|
G | T | 1 | a0009c0007t0003g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2778+2693G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937242 | ||||||
| chr7:158937352
|
C | T | 3 | a0003c0009t0011g0253a0003c0009t0011g0261a0004c0004t0001g0170 | 3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2778+2803C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937352 | ||||||
| chr7:158937423
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2778+2874G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937423 | ||||||
| chr7:158937499
|
G | A | 3 | a0003c0009t0011g0253a0003c0009t0011g0261a0004c0004t0001g0170 | 3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2778+2950G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937499 | ||||||
| chr7:158937622
|
G | GA | 7 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234others(4): Show | 7 | HG01257.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2778+3086dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAA | 20 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(17): Show | 20 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.2778+3083_2778+308 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA | 98 | a0001c0001t0005g0136a0001c0001t0005g0139a0001c0001t0005g0180others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2778+3080_2778+308 others(11): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(6): Show |
1 | a0002c0002t0001g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2778+3074_2778+308 others(17): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(7): Show |
5 | a0002c0002t0001g0015a0002c0002t0001g0069a0002c0002t0001g0091others(2): Show | 5 | HG02109.hp1 HG02486.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(18): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(8): Show |
3 | a0003c0009t0011g0253a0003c0009t0011g0261a0004c0004t0001g0170 | 3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(19): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(9): Show |
1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(20): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(10): Show |
1 | a0003c0027t0022g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(21): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(11): Show |
1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(22): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(19): Show |
1 | a0001c0001t0012g0223 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(30): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(20): Show |
2 | a0001c0001t0001g0268a0001c0001t0012g0224 | 2 | HG01934.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(31): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(21): Show |
4 | a0001c0001t0001g0270a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 4 | HG01981.hp1 HG02148.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(32): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937622
|
G | GAAAAAAA others(22): Show |
1 | a0001c0001t0001g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(33): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | |||||
| chr7:158937756
|
A | T | 93 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(90): Show | 93 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.2778+3207A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937756 | ||||||
| chr7:158937888
|
A | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2778+3339A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937888 | ||||||
| chr7:158938101
|
A | G | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2778+3552A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938101 | ||||||
| chr7:158938115
|
A | T | 1 | a0001c0001t0002g0204 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2778+3566A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938115 | ||||||
| chr7:158938157
|
C | T | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2778+3608C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938157 | ||||||
| chr7:158938263
|
C | G | 1 | a0009c0007t0003g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2779-3662C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938263 | ||||||
| chr7:158938476
|
G | A | 3 | a0001c0001t0005g0196a0002c0019t0015g0043a0003c0027t0022g0263 | 3 | HG01081.hp2 HG02015.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2779-3449G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938476 | ||||||
| chr7:158938506
|
G | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2779-3419G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938506 | ||||||
| chr7:158938605
|
A | C | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2779-3320A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938605 | ||||||
| chr7:158938625
|
G | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2779-3300G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938625 | ||||||
| chr7:158938695
|
G | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-3230G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938695 | ||||||
| chr7:158938741
|
G | T | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2779-3184G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938741 | ||||||
| chr7:158938842
|
T | C | 1 | a0002c0002t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2779-3083T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938842 | ||||||
| chr7:158939233
|
C | A | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2779-2692C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939233 | ||||||
| chr7:158939239
|
G | C | 1 | a0002c0002t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2779-2686G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939239 | ||||||
| chr7:158939272
|
C | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0273a0002c0002t0021g0083others(1): Show | 4 | HG01433.hp1 HG01981.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2779-2653C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939272 | ||||||
| chr7:158939273
|
C | CCAAA | 139 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0270others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2779-2647_2779-264 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158939273 | |||||
| chr7:158939273
|
C | CCCAAA | 4 | a0001c0001t0001g0269a0001c0001t0001g0273a0002c0002t0021g0083others(1): Show | 4 | HG01433.hp1 HG01981.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2779-2651_2779-265 others(9): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158939273 | |||||
| chr7:158939422
|
G | T | 1 | a0002c0002t0001g0079 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2779-2503G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939422 | ||||||
| chr7:158939514
|
T | C | 1 | a0009c0007t0003g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2779-2411T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939514 | ||||||
| chr7:158939756
|
C | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2779-2169C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939756 | ||||||
| chr7:158939867
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2779-2058A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939867 | ||||||
| chr7:158939991
|
G | A | 1 | a0003c0009t0011g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2779-1934G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939991 | ||||||
| chr7:158940063
|
A | T | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2779-1862A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940063 | ||||||
| chr7:158940158
|
C | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-1767C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940158 | ||||||
| chr7:158940180
|
A | C | 1 | a0017c0024t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2779-1745A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940180 | ||||||
| chr7:158940216
|
A | G | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2779-1709A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940216 | ||||||
| chr7:158940268
|
G | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2779-1657G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940268 | ||||||
| chr7:158940344
|
C | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2779-1581C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940344 | ||||||
| chr7:158940387
|
C | T | 1 | a0003c0003t0007g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2779-1538C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940387 | ||||||
| chr7:158940492
|
C | T | 1 | a0003c0003t0004g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2779-1433C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940492 | ||||||
| chr7:158940599
|
C | T | 3 | a0001c0001t0002g0124a0001c0001t0002g0133a0001c0001t0002g0144 | 3 | NA18942.hp1 NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2779-1326C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940599 | ||||||
| chr7:158940836
|
C | T | 1 | a0002c0019t0015g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2779-1089C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940836 | ||||||
| chr7:158941363
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2779-562G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941363 | ||||||
| chr7:158941386
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2779-539G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941386 | ||||||
| chr7:158941582
|
C | T | 24 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.2779-343C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941582 | ||||||
| chr7:158941591
|
C | A | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2779-334C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941591 | ||||||
| chr7:158941722
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2779-203C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941722 | ||||||
| chr7:158941778
|
C | T | 1 | a0001c0012t0002g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2779-147C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941778 | ||||||
| chr7:158942432
|
C | G | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3002+284C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942432 | ||||||
| chr7:158942448
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3002+300G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942448 | ||||||
| chr7:158942569
|
G | A | 239 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.3002+421G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942569 | ||||||
| chr7:158942670
|
T | C | 1 | a0010c0028t0023g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3002+522T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942670 | ||||||
| chr7:158942898
|
A | G | 1 | a0001c0001t0009g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3002+750A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942898 | ||||||
| chr7:158943037
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3002+889C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943037 | ||||||
| chr7:158943060
|
C | T | 1 | a0001c0023t0018g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3002+912C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943060 | ||||||
| chr7:158943106
|
G | A | 1 | a0003c0003t0004g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3002+958G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943106 | ||||||
| chr7:158943342
|
C | A | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3002+1194C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943342 | ||||||
| chr7:158943346
|
C | T | 1 | a0001c0001t0002g0165 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3002+1198C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943346 | ||||||
| chr7:158943421
|
C | G | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3002+1273C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943421 | ||||||
| chr7:158943576
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3002+1428G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943576 | ||||||
| chr7:158943633
|
G | C | 21 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.3002+1485G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943633 | ||||||
| chr7:158943684
|
C | T | 1 | a0009c0007t0003g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3002+1536C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943684 | ||||||
| chr7:158943694
|
AGCATGTT others(4): Show |
A | 4 | a0001c0001t0012g0223a0001c0001t0012g0224a0002c0019t0015g0043others(1): Show | 4 | HG01081.hp2 HG02055.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002+1548_3002+155 others(15): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr7 | 158943694 | |||||
| chr7:158943757
|
T | C | 3 | a0003c0003t0004g0244a0003c0003t0004g0246a0011c0029t0004g0250 | 3 | HG00733.hp1 HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3002+1609T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943757 | ||||||
| chr7:158943819
|
C | T | 1 | a0001c0001t0003g0211 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3002+1671C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943819 | ||||||
| chr7:158943870
|
C | T | 2 | a0003c0003t0004g0257a0003c0003t0004g0265 | 2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3003-1711C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943870 | ||||||
| chr7:158943871
|
G | A | 9 | a0001c0001t0006g0004a0001c0001t0006g0005a0004c0004t0002g0192others(6): Show | 9 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3003-1710G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943871 | ||||||
| chr7:158943901
|
G | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0171a0001c0001t0002g0172others(1): Show | 4 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.3003-1680G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943901 | ||||||
| chr7:158944004
|
G | C | 1 | a0001c0001t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3003-1577G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944004 | ||||||
| chr7:158944065
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3003-1516G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944065 | ||||||
| chr7:158944123
|
G | A | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0014g0078 | 3 | HG03017.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3003-1458G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944123 | ||||||
| chr7:158944150
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3003-1431G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944150 | ||||||
| chr7:158944172
|
G | A | 103 | a0001c0001t0005g0136a0001c0001t0005g0139a0001c0001t0005g0180others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.3003-1409G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944172 | ||||||
| chr7:158944187
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3003-1394C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944187 | ||||||
| chr7:158944212
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3003-1369G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944212 | ||||||
| chr7:158944422
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.3003-1159G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944422 | ||||||
| chr7:158944505
|
G | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3003-1076G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944505 | ||||||
| chr7:158944628
|
G | A | 1 | a0004c0004t0006g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3003-953G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944628 | ||||||
| chr7:158944674
|
A | G | 9 | a0001c0001t0006g0004a0001c0001t0006g0005a0004c0004t0002g0192others(6): Show | 9 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3003-907A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944674 | ||||||
| chr7:158944763
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0269others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.3003-818T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944763 | ||||||
| chr7:158944870
|
G | A | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3003-711G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944870 | ||||||
| chr7:158944907
|
C | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3003-674C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944907 | ||||||
| chr7:158945026
|
C | T | 2 | a0002c0019t0015g0043a0003c0027t0022g0263 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3003-555C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945026 | ||||||
| chr7:158945112
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3003-469T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945112 | ||||||
| chr7:158945141
|
G | C | 1 | a0002c0002t0001g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3003-440G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945141 | ||||||
| chr7:158945178
|
C | T | 2 | a0002c0002t0001g0096a0002c0002t0001g0111 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3003-403C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945178 | ||||||
| chr7:158945435
|
T | G | 1 | a0002c0017t0001g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3003-146T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945435 | ||||||
| chr7:158945529
|
C | T | 3 | a0001c0001t0009g0188a0001c0001t0009g0233a0001c0001t0009g0234 | 3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3003-52C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945529 |