Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4137 |
|---|---|
| ensemblid | ENSG00000186868.18 |
| hgncid | 6893 |
| symbol | MAPT |
| name | microtubule associated protein tau |
| refseq_nuc | NM_001377265.1 |
| refseq_prot | NP_001364194.1 |
| ensembl_nuc | ENST00000262410.10 |
| ensembl_prot | ENSP00000262410.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 45894554 |
| end | 46028334 |
| strand | + |
| ver | v1.2 |
| region | chr17:45894554-46028334 |
| region5000 | chr17:45889554-46033334 |
| regionname0 | MAPT_chr17_45894554_46028334 |
| regionname5000 | MAPT_chr17_45889554_46033334 |
| 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 | 833 | 123 | 42 | 28 | 34 | 8 | 11 | 26 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002 | 0/1 | 833 | 69 | 4 | 17 | 38 | 1 | 8 | 24 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0003 | 0/0 | 833 | 21 | 2 | 8 | 1 | 4 | 6 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004 | 0/0 | 833 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0005 | 0/0 | 833 | 6 | 2 | 2 | 0 | 1 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0006 | 0/0 | 833 | 6 | 1 | 4 | 1 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0007 | 0/0 | 833 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0008 | 0/0 | 833 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0009 | 0/0 | 833 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0010 | 0/0 | 833 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0011 | 0/0 | 833 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0012 | 0/0 | 833 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0013 | 0/0 | 833 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0014 | 0/0 | 833 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0015 | 0/0 | 833 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| 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 | 2502 | 119 | 40 | 28 | 32 | 8 | 11 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0002 | 0/0 | 2502 | 43 | 3 | 9 | 24 | 1 | 6 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0003 | 0/1 | 2502 | 25 | 0 | 8 | 14 | 0 | 2 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0004 | 0/0 | 2502 | 21 | 2 | 8 | 1 | 4 | 6 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0005 | 0/0 | 2502 | 13 | 12 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0006 | 0/0 | 2502 | 6 | 1 | 4 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0007 | 0/0 | 2502 | 6 | 2 | 2 | 0 | 1 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0008 | 0/0 | 2502 | 4 | 4 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0009 | 0/0 | 2502 | 3 | 3 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0010 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0011 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0012 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0013 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0014 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0015 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0016 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0017 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0018 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0019 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| c0020 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| 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 | 0/0 | 4316 | 64 | 2 | 18 | 37 | 3 | 4 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0002 | 0/0 | 4314 | 63 | 26 | 18 | 7 | 3 | 9 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0003 | 0/0 | 4312 | 52 | 10 | 14 | 21 | 3 | 4 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0004 | 0/0 | 4311 | 17 | 2 | 6 | 1 | 2 | 6 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0005 | 0/0 | 4312 | 11 | 11 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0006 | 0/0 | 4313 | 6 | 0 | 1 | 4 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0007 | 0/0 | 4312 | 6 | 6 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0008 | 0/0 | 4314 | 4 | 3 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0009 | 0/0 | 4315 | 4 | 4 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0010 | 0/0 | 4315 | 3 | 3 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0011 | 0/0 | 4310 | 2 | 0 | 1 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0012 | 0/0 | 4314 | 2 | 0 | 1 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0013 | 0/0 | 4315 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0014 | 0/0 | 4313 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0015 | 0/0 | 4309 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0016 | 0/0 | 4311 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0017 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0018 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0019 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0020 | 0/1 | 4314 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0021 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0022 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0023 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0024 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0025 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0026 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0027 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0028 | 0/0 | 4316 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| t0029 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| 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 | 2502 | 119 | 40 | 28 | 32 | 8 | 11 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0010 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0015 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0017 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002 | 0/0 | 2502 | 43 | 3 | 9 | 24 | 1 | 6 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003 | 0/1 | 2502 | 25 | 0 | 8 | 14 | 0 | 2 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0018 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0003c0004 | 0/0 | 2502 | 21 | 2 | 8 | 1 | 4 | 6 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004c0005 | 0/0 | 2502 | 13 | 12 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0005c0007 | 0/0 | 2502 | 6 | 2 | 2 | 0 | 1 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0006c0006 | 0/0 | 2502 | 6 | 1 | 4 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0007c0008 | 0/0 | 2502 | 4 | 4 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0008c0009 | 0/0 | 2502 | 3 | 3 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0009c0011 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0010c0020 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0011c0012 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0012c0016 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0013c0014 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0014c0013 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0015c0019 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6817 | 35 | 1 | 11 | 19 | 3 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0002 | 0/0 | 6815 | 42 | 21 | 9 | 0 | 3 | 9 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0003 | 0/0 | 6813 | 26 | 7 | 7 | 10 | 2 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0005 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0006 | 0/0 | 6814 | 3 | 0 | 0 | 3 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0007 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0008 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0009 | 0/0 | 6816 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0010 | 0/0 | 6816 | 3 | 3 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0012 | 0/0 | 6815 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0023 | 0/0 | 6815 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0026 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0001t0027 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0010t0013 | 0/0 | 6816 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0015t0001 | 0/0 | 6817 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0001c0017t0002 | 0/0 | 6815 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0001 | 0/0 | 6817 | 13 | 1 | 2 | 8 | 0 | 2 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0002 | 0/0 | 6815 | 2 | 1 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0003 | 0/0 | 6813 | 19 | 0 | 5 | 11 | 0 | 3 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0006 | 0/0 | 6814 | 3 | 0 | 1 | 1 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0008 | 0/0 | 6815 | 2 | 1 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0012 | 0/0 | 6815 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0017 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0018 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0002t0021 | 0/0 | 6815 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003t0001 | 0/0 | 6817 | 14 | 0 | 4 | 9 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003t0002 | 0/0 | 6815 | 7 | 0 | 3 | 4 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003t0019 | 0/0 | 6815 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003t0020 | 0/1 | 6815 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003t0024 | 0/0 | 6815 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0003t0028 | 0/0 | 6817 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0002c0018t0002 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0003c0004t0004 | 0/0 | 6812 | 17 | 2 | 6 | 1 | 2 | 6 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0003c0004t0011 | 0/0 | 6811 | 2 | 0 | 1 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0003c0004t0015 | 0/0 | 6810 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0003c0004t0016 | 0/0 | 6812 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004c0005t0001 | 0/0 | 6817 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004c0005t0002 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004c0005t0005 | 0/0 | 6813 | 8 | 8 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004c0005t0007 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0004c0005t0025 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0005c0007t0003 | 0/0 | 6813 | 6 | 2 | 2 | 0 | 1 | 1 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0006c0006t0002 | 0/0 | 6815 | 6 | 1 | 4 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0007c0008t0003 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0007c0008t0014 | 0/0 | 6814 | 2 | 2 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0007c0008t0029 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0008c0009t0009 | 0/0 | 6816 | 3 | 3 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0009c0011t0002 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0009c0011t0008 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0010c0020t0007 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0011c0012t0022 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0012c0016t0002 | 0/0 | 6815 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0013c0014t0002 | 0/0 | 6815 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0014c0013t0007 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| a0015c0019t0005 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | copy fasta | chr17 | 45889554 | 46033334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0010g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0012g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0023g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0026g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0001t0027g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0010t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0010t0013g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0015t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0001c0017t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0012g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0017g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0018g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0002t0021g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0019g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0020g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0024g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0003t0028g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0002c0018t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0011g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0011g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0015g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0003c0004t0016g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0004c0005t0025g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0005c0007t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0005c0007t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0005c0007t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0005c0007t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0005c0007t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0005c0007t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0006c0006t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0006c0006t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0006c0006t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0006c0006t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0006c0006t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0006c0006t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0007c0008t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0007c0008t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0007c0008t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0007c0008t0029g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0008c0009t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0008c0009t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0008c0009t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0009c0011t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0009c0011t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0010c0020t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0011c0012t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0012c0016t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0013c0014t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0014c0013t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| a0015c0019t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0006 | g0215 | EUR | GBR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00140 | hp1 | a0003 | c0004 | t0004 | g0006 | EUR | GBR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | GBR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00280 | hp1 | a0003 | c0004 | t0016 | g0007 | EUR | FIN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0054 | EUR | FIN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0229 | EUR | FIN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0102 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00408 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0174 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0151 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00544 | hp1 | a0001 | c0017 | t0002 | g0218 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0092 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0169 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | CHS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00642 | hp1 | a0006 | c0006 | t0002 | g0063 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0177 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01071 | hp2 | a0012 | c0016 | t0002 | g0111 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01074 | hp1 | a0003 | c0004 | t0004 | g0011 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01081 | hp1 | a0006 | c0006 | t0002 | g0209 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01081 | hp2 | a0005 | c0007 | t0003 | g0084 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01099 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0103 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01106 | hp2 | a0006 | c0006 | t0002 | g0120 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0041 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01109 | hp2 | a0004 | c0005 | t0001 | g0104 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01167 | hp2 | a0003 | c0004 | t0011 | g0015 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01175 | hp1 | a0005 | c0007 | t0003 | g0230 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01175 | hp2 | a0002 | c0003 | t0028 | g0090 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0141 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0244 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01243 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01255 | hp1 | a0003 | c0004 | t0004 | g0005 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01258 | hp1 | a0006 | c0006 | t0002 | g0115 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01261 | hp2 | a0002 | c0002 | t0006 | g0214 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0213 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0132 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01358 | hp1 | a0002 | c0002 | t0021 | g0069 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01361 | hp2 | a0003 | c0004 | t0015 | g0014 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01433 | hp2 | a0003 | c0004 | t0004 | g0018 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01515 | hp1 | a0005 | c0007 | t0003 | g0051 | EUR | IBS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01516 | hp1 | a0003 | c0004 | t0004 | g0003 | EUR | IBS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01517 | hp2 | a0003 | c0004 | t0011 | g0002 | EUR | IBS | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01928 | hp1 | a0002 | c0003 | t0002 | g0155 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0061 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01943 | hp1 | a0002 | c0002 | t0003 | g0076 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01952 | hp2 | a0003 | c0004 | t0004 | g0004 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01993 | hp1 | a0001 | c0001 | t0012 | g0143 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02055 | hp1 | a0011 | c0012 | t0022 | g0022 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02055 | hp2 | a0005 | c0007 | t0003 | g0234 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02071 | hp1 | a0002 | c0002 | t0006 | g0070 | EAS | KHV | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02074 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | KHV | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0048 | EAS | KHV | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02257 | hp1 | a0003 | c0004 | t0004 | g0020 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02258 | hp1 | a0010 | c0020 | t0007 | g0117 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0075 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02280 | hp2 | a0004 | c0005 | t0005 | g0204 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02451 | hp1 | a0004 | c0005 | t0005 | g0195 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02451 | hp2 | a0004 | c0005 | t0007 | g0077 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02572 | hp1 | a0005 | c0007 | t0003 | g0056 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02572 | hp2 | a0006 | c0006 | t0002 | g0186 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02602 | hp1 | a0003 | c0004 | t0004 | g0013 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02615 | hp2 | a0001 | c0001 | t0027 | g0093 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02622 | hp2 | a0009 | c0011 | t0008 | g0097 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0171 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02698 | hp2 | a0005 | c0007 | t0003 | g0203 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02717 | hp1 | a0007 | c0008 | t0014 | g0191 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02717 | hp2 | a0009 | c0011 | t0002 | g0030 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02723 | hp2 | a0007 | c0008 | t0003 | g0185 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02735 | hp1 | a0001 | c0001 | t0023 | g0088 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02735 | hp2 | a0003 | c0004 | t0004 | g0019 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02738 | hp1 | a0003 | c0004 | t0004 | g0016 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02809 | hp1 | a0004 | c0005 | t0007 | g0170 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02809 | hp2 | a0004 | c0005 | t0005 | g0167 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0192 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02895 | hp2 | a0004 | c0005 | t0005 | g0038 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02897 | hp2 | a0004 | c0005 | t0005 | g0039 | AFR | GWD | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02922 | hp1 | a0007 | c0008 | t0029 | g0060 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02965 | hp1 | a0001 | c0010 | t0013 | g0208 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02965 | hp2 | a0015 | c0019 | t0005 | g0189 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02976 | hp1 | a0002 | c0002 | t0008 | g0035 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02976 | hp2 | a0004 | c0005 | t0005 | g0025 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03139 | hp1 | a0002 | c0018 | t0002 | g0081 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03139 | hp2 | a0004 | c0005 | t0002 | g0180 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03195 | hp2 | a0007 | c0008 | t0014 | g0026 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03225 | hp1 | a0008 | c0009 | t0009 | g0032 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0052 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03239 | hp1 | a0003 | c0004 | t0004 | g0012 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0106 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0109 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03579 | hp2 | a0001 | c0010 | t0013 | g0129 | AFR | MSL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03669 | hp1 | a0002 | c0002 | t0012 | g0058 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03688 | hp1 | a0002 | c0003 | t0019 | g0044 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0173 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03704 | hp1 | a0003 | c0004 | t0004 | g0021 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0101 | SAS | BEB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0147 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG04199 | hp2 | a0003 | c0004 | t0004 | g0010 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0145 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18522 | hp1 | a0004 | c0005 | t0005 | g0124 | AFR | YRI | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | YRI | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0094 | EAS | CHB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | CHB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18906 | hp1 | a0008 | c0009 | t0009 | g0033 | AFR | YRI | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | YRI | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18940 | hp1 | a0002 | c0003 | t0024 | g0222 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18947 | hp1 | a0006 | c0006 | t0002 | g0095 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18950 | hp2 | a0002 | c0003 | t0002 | g0146 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18959 | hp2 | a0002 | c0002 | t0003 | g0149 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18962 | hp1 | a0002 | c0002 | t0017 | g0112 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0251 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18986 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18991 | hp2 | a0002 | c0003 | t0001 | g0118 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19002 | hp2 | a0002 | c0003 | t0002 | g0219 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | LWK | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19030 | hp2 | a0008 | c0009 | t0009 | g0107 | AFR | LWK | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19043 | hp1 | a0014 | c0013 | t0007 | g0040 | AFR | LWK | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | LWK | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19068 | hp1 | a0002 | c0003 | t0002 | g0200 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19068 | hp2 | a0002 | c0002 | t0018 | g0091 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19070 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19081 | hp1 | a0002 | c0002 | t0008 | g0172 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19085 | hp1 | a0001 | c0015 | t0001 | g0098 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19085 | hp2 | a0003 | c0004 | t0004 | g0008 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19240 | hp1 | a0004 | c0005 | t0005 | g0190 | AFR | YRI | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ASW | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ASW | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01123 | hp1 | a0013 | c0014 | t0002 | g0049 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG01123 | hp2 | a0003 | c0004 | t0004 | g0009 | AMR | CLM | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02109 | hp1 | a0003 | c0004 | t0004 | g0017 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02109 | hp2 | a0004 | c0005 | t0025 | g0121 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ACB | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | USA | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | USA | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0020 | g0114 | REF | REF | MAPT_chr17_45889554_46033334 | MAPT | chr17 | 45889554 | 46033334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45962387
|
C | T | 1 | a0010 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.50C>T | p.Thr17Met | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/13 | 200/6815 | 50/2502 | 17/833 | chr17 | 45962387 | ||
| chr17:45983006
|
G | T | 1 | a0009 | 2 | HG02622.hp2 HG02717.hp2 |
missense_variant | MODERATE | c.427G>T | p.Ala143Ser | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 577/6815 | 427/2502 | 143/833 | chr17 | 45983006 | ||
| chr17:45983043
|
G | A | 1 | a0009 | 2 | HG02622.hp2 HG02717.hp2 |
missense_variant | MODERATE | c.464G>A | p.Arg155His | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 614/6815 | 464/2502 | 155/833 | chr17 | 45983043 | ||
| chr17:45983126
|
G | A | 1 | a0006 | 6 | HG00642.hp1 HG01081.hp1 HG01106.hp2 others(3): Show |
missense_variant | MODERATE | c.547G>A | p.Glu183Lys | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 697/6815 | 547/2502 | 183/833 | chr17 | 45983126 | ||
| chr17:45983370
|
A | G | 1 | a0015 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.791A>G | p.Lys264Arg | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 941/6815 | 791/2502 | 264/833 | chr17 | 45983370 | ||
| chr17:45983409
|
C | T | 1 | a0003 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
missense_variant | MODERATE | c.830C>T | p.Pro277Leu | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 980/6815 | 830/2502 | 277/833 | chr17 | 45983409 | ||
| chr17:45983441
|
G | A | 1 | a0008 | 3 | HG03225.hp1 NA18906.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.862G>A | p.Gly288Arg | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1012/6815 | 862/2502 | 288/833 | chr17 | 45983441 | ||
| chr17:45983493
|
A | G | 1 | a0005 | 6 | HG01081.hp2 HG01175.hp1 HG01515.hp1 others(3): Show |
missense_variant | MODERATE | c.914A>G | p.Gln305Arg | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1064/6815 | 914/2502 | 305/833 | chr17 | 45983493 | ||
| chr17:45983657
|
G | A | 1 | a0003 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
missense_variant | MODERATE | c.1078G>A | p.Asp360Asn | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1228/6815 | 1078/2502 | 360/833 | chr17 | 45983657 | ||
| chr17:45983670
|
T | C | 1 | a0003 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
missense_variant | MODERATE | c.1091T>C | p.Val364Ala | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1241/6815 | 1091/2502 | 364/833 | chr17 | 45983670 | ||
| chr17:45983757
|
C | T | 4 | a0004a0008a0010others(1): Show | 18 | HG01109.hp2 HG02109.hp2 HG02258.hp1 others(15): Show |
missense_variant | MODERATE | c.1178C>T | p.Ser393Leu | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1328/6815 | 1178/2502 | 393/833 | chr17 | 45983757 | ||
| chr17:45983898
|
G | A | 1 | a0011 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1319G>A | p.Gly440Glu | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1469/6815 | 1319/2502 | 440/833 | chr17 | 45983898 | ||
| chr17:45983912
|
C | T | 1 | a0003 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
missense_variant | MODERATE | c.1333C>T | p.Arg445Trp | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1483/6815 | 1333/2502 | 445/833 | chr17 | 45983912 | ||
| chr17:45990016
|
T | C | 4 | a0002a0006a0007others(1): Show | 81 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
missense_variant | MODERATE | c.1546T>C | p.Tyr516His | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/13 | 1696/6815 | 1546/2502 | 516/833 | chr17 | 45990016 | ||
| chr17:45990034
|
T | C | 1 | a0003 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
missense_variant | MODERATE | c.1564T>C | p.Ser522Pro | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/13 | 1714/6815 | 1564/2502 | 522/833 | chr17 | 45990034 | ||
| chr17:45991482
|
T | C | 1 | a0014 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1628T>C | p.Ile543Thr | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/13 | 1778/6815 | 1628/2502 | 543/833 | chr17 | 45991482 | ||
| chr17:45991484
|
G | A | 1 | a0013 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.1630G>A | p.Ala544Thr | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/13 | 1780/6815 | 1630/2502 | 544/833 | chr17 | 45991484 | ||
| chr17:45991562
|
G | A | 1 | a0007 | 4 | HG02717.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1708G>A | p.Ala570Thr | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/13 | 1858/6815 | 1708/2502 | 570/833 | chr17 | 45991562 | ||
| chr17:45996468
|
G | A | 1 | a0012 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1802G>A | p.Arg601His | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/13 | 1952/6815 | 1802/2502 | 601/833 | chr17 | 45996468 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45982882
|
G | A | 1 | a0003c0004 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.303G>A | p.Pro101Pro | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 453/6815 | 303/2502 | 101/833 | chr17 | 45982882 | ||
| chr17:45983491
|
C | G | 1 | a0002c0018 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.912C>G | p.Pro304Pro | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1062/6815 | 912/2502 | 304/833 | chr17 | 45983491 | ||
| chr17:45983659
|
C | T | 3 | a0002c0003a0002c0018a0006c0006 | 32 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(29): Show |
synonymous_variant | LOW | c.1080C>T | p.Asp360Asp | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/13 | 1230/6815 | 1080/2502 | 360/833 | chr17 | 45983659 | ||
| chr17:45991492
|
G | A | 1 | a0001c0015 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1638G>A | p.Pro546Pro | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/13 | 1788/6815 | 1638/2502 | 546/833 | chr17 | 45991492 | ||
| chr17:45991558
|
G | A | 1 | a0003c0004 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1704G>A | p.Pro568Pro | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/13 | 1854/6815 | 1704/2502 | 568/833 | chr17 | 45991558 | ||
| chr17:45996523
|
A | G | 1 | a0003c0004 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1857A>G | p.Ala619Ala | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/13 | 2007/6815 | 1857/2502 | 619/833 | chr17 | 45996523 | ||
| chr17:45996607
|
T | C | 1 | a0003c0004 | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1941T>C | p.Asn647Asn | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/13 | 2091/6815 | 1941/2502 | 647/833 | chr17 | 45996607 | ||
| chr17:45996652
|
G | A | 2 | a0001c0010a0005c0007 | 8 | HG01081.hp2 HG01175.hp1 HG01515.hp1 others(5): Show |
synonymous_variant | LOW | c.1986G>A | p.Pro662Pro | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/13 | 2136/6815 | 1986/2502 | 662/833 | chr17 | 45996652 | ||
| chr17:46024075
|
T | C | 1 | a0001c0017 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.2406T>C | p.Asn802Asn | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2556/6815 | 2406/2502 | 802/833 | chr17 | 46024075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45894571
|
C | A | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-133C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/13 | 67767 | chr17 | 45894571 | |||||
| chr17:45894605
|
C | T | 1 | a0007c0008t0029 | 1 | HG02922.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-99C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/13 | chr17 | 45894605 | ||||||
| chr17:45894606
|
G | A | 1 | a0002c0002t0017 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/13 | 67732 | chr17 | 45894606 | |||||
| chr17:45894658
|
C | T | 1 | a0002c0003t0028 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/13 | 67680 | chr17 | 45894658 | |||||
| chr17:45894659
|
TC | T | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-42delC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/13 | 67676 | INFO_REALIGN_3_PRIME | chr17 | 45894659 | ||||
| chr17:45962325
|
A | G | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-13A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/13 | 13 | chr17 | 45962325 | |||||
| chr17:46024197
|
T | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*26T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 26 | chr17 | 46024197 | |||||
| chr17:46024247
|
G | A | 3 | a0001c0001t0005a0004c0005t0005a0015c0019t0005 | 11 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*76G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 76 | chr17 | 46024247 | |||||
| chr17:46024409
|
A | AT | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*241dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 242 | INFO_REALIGN_3_PRIME | chr17 | 46024409 | ||||
| chr17:46024483
|
T | TC | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*317dupC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 318 | INFO_REALIGN_3_PRIME | chr17 | 46024483 | ||||
| chr17:46024505
|
A | G | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*334A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 334 | chr17 | 46024505 | |||||
| chr17:46024635
|
G | A | 2 | a0001c0001t0012a0002c0002t0012 | 2 | HG01993.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*464G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 464 | chr17 | 46024635 | |||||
| chr17:46025072
|
G | T | 1 | a0001c0001t0027 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 901 | chr17 | 46025072 | |||||
| chr17:46025077
|
C | CCT | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*909_*910dupCT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 911 | INFO_REALIGN_3_PRIME | chr17 | 46025077 | ||||
| chr17:46025218
|
C | T | 3 | a0001c0001t0026a0007c0008t0014a0007c0008t0029 | 4 | HG02717.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1047C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1047 | chr17 | 46025218 | |||||
| chr17:46025238
|
T | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1067T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1067 | chr17 | 46025238 | |||||
| chr17:46025272
|
A | G | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1101 | chr17 | 46025272 | |||||
| chr17:46025316
|
C | CT | 22 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(19): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1145_*1146insT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1146 | chr17 | 46025316 | |||||
| chr17:46025323
|
G | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1152G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1152 | chr17 | 46025323 | |||||
| chr17:46025375
|
TCA | T | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1208_*1209delAC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1208 | INFO_REALIGN_3_PRIME | chr17 | 46025375 | ||||
| chr17:46025499
|
A | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1328A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1328 | chr17 | 46025499 | |||||
| chr17:46025567
|
T | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1396T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1396 | chr17 | 46025567 | |||||
| chr17:46025848
|
G | A | 1 | a0002c0002t0018 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1677G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1677 | chr17 | 46025848 | |||||
| chr17:46025930
|
T | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1759T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1759 | chr17 | 46025930 | |||||
| chr17:46026079
|
TAG | T | 8 | a0001c0001t0003a0001c0001t0006a0002c0002t0003others(5): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1909_*1910delAG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1909 | chr17 | 46026079 | |||||
| chr17:46026088
|
G | GA | 8 | a0001c0001t0006a0002c0002t0006a0003c0004t0004others(5): Show | 29 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1935dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1936 | INFO_REALIGN_3_PRIME | chr17 | 46026088 | ||||
| chr17:46026131
|
G | A | 1 | a0002c0003t0019 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1960G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 1960 | chr17 | 46026131 | |||||
| chr17:46026250
|
C | T | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2079C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2079 | chr17 | 46026250 | |||||
| chr17:46026338
|
G | A | 1 | a0002c0003t0020 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2167G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2167 | chr17 | 46026338 | |||||
| chr17:46026440
|
G | T | 3 | a0001c0001t0005a0004c0005t0005a0015c0019t0005 | 11 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2269G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2269 | chr17 | 46026440 | |||||
| chr17:46026459
|
T | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2288T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2288 | chr17 | 46026459 | |||||
| chr17:46026460
|
G | A | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2289G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2289 | chr17 | 46026460 | |||||
| chr17:46026561
|
C | CT | 3 | a0003c0004t0004a0003c0004t0011a0003c0004t0016 | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2390_*2391insT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2391 | chr17 | 46026561 | |||||
| chr17:46026912
|
TG | T | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2743delG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2743 | INFO_REALIGN_3_PRIME | chr17 | 46026912 | ||||
| chr17:46026977
|
A | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2806A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2806 | chr17 | 46026977 | |||||
| chr17:46026981
|
G | A | 1 | a0003c0004t0016 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2810G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2810 | chr17 | 46026981 | |||||
| chr17:46027044
|
TCTC | T | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2876_*2878delCCT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2876 | INFO_REALIGN_3_PRIME | chr17 | 46027044 | ||||
| chr17:46027143
|
T | C | 4 | a0003c0004t0004a0003c0004t0011a0003c0004t0015others(1): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2972T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2972 | chr17 | 46027143 | |||||
| chr17:46027162
|
C | T | 1 | a0001c0010t0013 | 2 | HG02965.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2991C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 2991 | chr17 | 46027162 | |||||
| chr17:46027210
|
CCTT | C | 15 | a0001c0001t0005a0001c0001t0007a0001c0001t0026others(12): Show | 43 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3043_*3045delCTT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3043 | INFO_REALIGN_3_PRIME | chr17 | 46027210 | ||||
| chr17:46027246
|
T | TG | 8 | a0001c0001t0001a0001c0001t0009a0001c0015t0001others(5): Show | 69 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*3079dupG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3080 | INFO_REALIGN_3_PRIME | chr17 | 46027246 | ||||
| chr17:46027304
|
A | G | 1 | a0002c0003t0024 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3133A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3133 | chr17 | 46027304 | |||||
| chr17:46027741
|
T | C | 1 | a0002c0002t0021 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3570T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3570 | chr17 | 46027741 | |||||
| chr17:46028019
|
A | G | 5 | a0001c0001t0007a0004c0005t0007a0004c0005t0025others(2): Show | 7 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3848A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3848 | chr17 | 46028019 | |||||
| chr17:46028029
|
A | G | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(34): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*3858A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3858 | chr17 | 46028029 | |||||
| chr17:46028122
|
G | A | 1 | a0011c0012t0022 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3951G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 3951 | chr17 | 46028122 | |||||
| chr17:46028325
|
T | C | 1 | a0001c0001t0023 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4154T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 13/13 | 4154 | chr17 | 46028325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45894776
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+90G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45894776 | ||||||
| chr17:45894810
|
C | G | 45 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0216others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-18+124C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45894810 | ||||||
| chr17:45895048
|
C | CGT | 20 | a0001c0001t0001g0181a0001c0001t0001g0250a0001c0001t0002g0166others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+404_-18+405dup others(2): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
C | CGTGT | 22 | a0001c0001t0001g0187a0001c0001t0002g0193a0001c0001t0002g0199others(19): Show | 22 | HG01167.hp1 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18+402_-18+405dup others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0002g0206a0001c0001t0003g0253a0001c0001t0007g0205 | 3 | HG02004.hp2 HG02280.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-18+398_-18+405dup others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-18+396_-18+405dup others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
C | CGTGTGTG others(5): Show |
1 | a0001c0010t0013g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18+394_-18+405dup others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
CGT | C | 79 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.-18+404_-18+405del others(2): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
CGTGT | C | 12 | a0001c0001t0001g0042a0001c0001t0002g0036a0001c0001t0002g0037others(9): Show | 12 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+402_-18+405del others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
CGTGTGT | C | 10 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0031others(7): Show | 10 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+400_-18+405del others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895048
|
CGTGTGTG others(3): Show |
C | 1 | a0011c0012t0022g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18+396_-18+405del others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45895048 | |||||
| chr17:45895092
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-18+406G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895092 | ||||||
| chr17:45895186
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-18+500T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895186 | ||||||
| chr17:45895215
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+529C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895215 | ||||||
| chr17:45895415
|
AG | A | 20 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(17): Show | 20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+730delG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895415 | ||||||
| chr17:45895549
|
C | T | 161 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.-18+863C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895549 | ||||||
| chr17:45895652
|
G | A | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+966G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895652 | ||||||
| chr17:45895714
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1028A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895714 | ||||||
| chr17:45895755
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1069G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895755 | ||||||
| chr17:45895768
|
T | C | 2 | a0002c0002t0003g0108a0002c0003t0001g0169 | 2 | HG00621.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-18+1082T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895768 | ||||||
| chr17:45895867
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1181C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45895867 | ||||||
| chr17:45896042
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1356C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896042 | ||||||
| chr17:45896047
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1361A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896047 | ||||||
| chr17:45896132
|
T | G | 59 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-18+1446T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896132 | ||||||
| chr17:45896281
|
G | A | 3 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0176 | 3 | HG00558.hp2 HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.-18+1595G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896281 | ||||||
| chr17:45896286
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1600C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896286 | ||||||
| chr17:45896533
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+1847T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896533 | ||||||
| chr17:45896626
|
G | T | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-18+1940G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896626 | ||||||
| chr17:45896659
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-18+1973C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896659 | ||||||
| chr17:45896699
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2013C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896699 | ||||||
| chr17:45896781
|
C | T | 57 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(54): Show | 57 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-18+2095C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896781 | ||||||
| chr17:45896806
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+2120A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896806 | ||||||
| chr17:45896864
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2178C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896864 | ||||||
| chr17:45896977
|
TCGC | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2293_-18+2295d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45896977 | |||||
| chr17:45896988
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2302G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45896988 | ||||||
| chr17:45897110
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2424G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897110 | ||||||
| chr17:45897111
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2425A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897111 | ||||||
| chr17:45897183
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2497G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897183 | ||||||
| chr17:45897228
|
G | A | 33 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(30): Show | 33 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-18+2542G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897228 | ||||||
| chr17:45897460
|
G | T | 3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+2774G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897460 | ||||||
| chr17:45897523
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+2837C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897523 | ||||||
| chr17:45897584
|
G | C | 4 | a0001c0001t0002g0024a0002c0003t0002g0023a0004c0005t0005g0025others(1): Show | 4 | HG01243.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+2898G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897584 | ||||||
| chr17:45897897
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+3211T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897897 | ||||||
| chr17:45897919
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+3233T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45897919 | ||||||
| chr17:45897994
|
ATTACTGT others(15): Show |
A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+3322_-18+3343d others(24): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45897994 | |||||
| chr17:45898049
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+3363A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45898049 | ||||||
| chr17:45898051
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+3365G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45898051 | ||||||
| chr17:45898124
|
C | T | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+3438C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45898124 | ||||||
| chr17:45898698
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+4012T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45898698 | ||||||
| chr17:45898869
|
A | G | 166 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0133others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-18+4183A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45898869 | ||||||
| chr17:45898904
|
C | T | 5 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0003g0028others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+4218C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45898904 | ||||||
| chr17:45899253
|
G | A | 2 | a0004c0005t0005g0038a0004c0005t0005g0039 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-18+4567G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899253 | ||||||
| chr17:45899261
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+4575G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899261 | ||||||
| chr17:45899278
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+4592G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899278 | ||||||
| chr17:45899318
|
T | C | 54 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+4632T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899318 | ||||||
| chr17:45899378
|
G | C | 1 | a0002c0002t0001g0055 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-18+4692G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899378 | ||||||
| chr17:45899447
|
C | A | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG00733.hp2 HG00738.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+4761C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899447 | ||||||
| chr17:45899611
|
T | C | 1 | a0005c0007t0003g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18+4925T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899611 | ||||||
| chr17:45899640
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-18+4954C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899640 | ||||||
| chr17:45899652
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+4966A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899652 | ||||||
| chr17:45899683
|
A | G | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+4997A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899683 | ||||||
| chr17:45899814
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-18+5128C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899814 | ||||||
| chr17:45899886
|
G | T | 3 | a0002c0002t0001g0100a0002c0003t0001g0101a0002c0003t0001g0102 | 3 | HG00408.hp1 HG03831.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-18+5200G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899886 | ||||||
| chr17:45899942
|
A | G | 2 | a0001c0001t0001g0226a0002c0002t0003g0225 | 2 | HG00408.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-18+5256A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45899942 | ||||||
| chr17:45900336
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+5650C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900336 | ||||||
| chr17:45900382
|
G | GGCTGGCC others(4): Show |
21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+5696_-18+5697i others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900382 | ||||||
| chr17:45900461
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+5775C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900461 | ||||||
| chr17:45900480
|
T | G | 54 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+5794T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900480 | ||||||
| chr17:45900675
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+5989C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900675 | ||||||
| chr17:45900735
|
T | C | 1 | a0001c0001t0003g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18+6049T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900735 | ||||||
| chr17:45900735
|
T | G | 1 | a0004c0005t0005g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-18+6049T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900735 | ||||||
| chr17:45900754
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6068A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900754 | ||||||
| chr17:45900857
|
G | A | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+6171G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900857 | ||||||
| chr17:45900929
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6243G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900929 | ||||||
| chr17:45900940
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6254G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900940 | ||||||
| chr17:45900942
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6256T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900942 | ||||||
| chr17:45900954
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6268G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45900954 | ||||||
| chr17:45901168
|
G | A | 22 | a0001c0001t0010g0109a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+6482G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901168 | ||||||
| chr17:45901238
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6552A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901238 | ||||||
| chr17:45901259
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6573T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901259 | ||||||
| chr17:45901273
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-18+6587G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901273 | ||||||
| chr17:45901312
|
G | A | 2 | a0001c0001t0002g0057a0002c0002t0012g0058 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-18+6626G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901312 | ||||||
| chr17:45901375
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-18+6689G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901375 | ||||||
| chr17:45901568
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+6882T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901568 | ||||||
| chr17:45901622
|
A | G | 54 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+6936A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901622 | ||||||
| chr17:45901624
|
G | A | 2 | a0004c0005t0005g0190a0007c0008t0014g0191 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18+6938G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901624 | ||||||
| chr17:45901846
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18+7160C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901846 | ||||||
| chr17:45901873
|
A | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7187A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901873 | ||||||
| chr17:45901874
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7188T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901874 | ||||||
| chr17:45901875
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7189T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901875 | ||||||
| chr17:45901881
|
G | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7195G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901881 | ||||||
| chr17:45901906
|
G | T | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7220G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901906 | ||||||
| chr17:45901911
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7225T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901911 | ||||||
| chr17:45901912
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7226T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901912 | ||||||
| chr17:45901914
|
C | CT | 5 | a0001c0001t0001g0249a0001c0001t0002g0125a0001c0001t0002g0207others(2): Show | 5 | HG01934.hp1 HG02280.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+7244dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45901914 | |||||
| chr17:45901914
|
CT | C | 56 | a0001c0001t0001g0210a0001c0001t0002g0027a0001c0001t0002g0031others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-18+7244delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45901914 | |||||
| chr17:45901919
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7233T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901919 | ||||||
| chr17:45901921
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7235T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901921 | ||||||
| chr17:45901922
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7236T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901922 | ||||||
| chr17:45901923
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7237T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901923 | ||||||
| chr17:45901925
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7239T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901925 | ||||||
| chr17:45901927
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7241T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901927 | ||||||
| chr17:45901929
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7243T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901929 | ||||||
| chr17:45901936
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7250T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901936 | ||||||
| chr17:45901938
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7252T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901938 | ||||||
| chr17:45901939
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7253T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901939 | ||||||
| chr17:45901940
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7254T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901940 | ||||||
| chr17:45901942
|
C | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7256C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901942 | ||||||
| chr17:45901945
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7259T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901945 | ||||||
| chr17:45901947
|
C | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7261C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901947 | ||||||
| chr17:45901948
|
C | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7262C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901948 | ||||||
| chr17:45901950
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7264T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901950 | ||||||
| chr17:45901951
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7265T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901951 | ||||||
| chr17:45901952
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7266T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901952 | ||||||
| chr17:45901954
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7268A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901954 | ||||||
| chr17:45901955
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7269T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901955 | ||||||
| chr17:45901956
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7270A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901956 | ||||||
| chr17:45901958
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7272T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901958 | ||||||
| chr17:45901962
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7276T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901962 | ||||||
| chr17:45901963
|
A | AGAGAGAT others(4): Show |
1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7277_-18+7278i others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901963 | ||||||
| chr17:45901964
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7278T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901964 | ||||||
| chr17:45901966
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7280A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901966 | ||||||
| chr17:45901974
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7288T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901974 | ||||||
| chr17:45901976
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7290A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901976 | ||||||
| chr17:45901981
|
G | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7295G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901981 | ||||||
| chr17:45901985
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7299T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901985 | ||||||
| chr17:45901988
|
C | T | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7302C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901988 | ||||||
| chr17:45901996
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7310T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45901996 | ||||||
| chr17:45902001
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7315T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902001 | ||||||
| chr17:45902002
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7316A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902002 | ||||||
| chr17:45902004
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7318A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902004 | ||||||
| chr17:45902005
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7319T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902005 | ||||||
| chr17:45902006
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7320T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902006 | ||||||
| chr17:45902007
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7321T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902007 | ||||||
| chr17:45902008
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7322T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902008 | ||||||
| chr17:45902009
|
C | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7323C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902009 | ||||||
| chr17:45902010
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7324T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902010 | ||||||
| chr17:45902011
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7325T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902011 | ||||||
| chr17:45902012
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7326A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902012 | ||||||
| chr17:45902019
|
T | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7333T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902019 | ||||||
| chr17:45902020
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7334T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902020 | ||||||
| chr17:45902023
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7337A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902023 | ||||||
| chr17:45902024
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7338T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902024 | ||||||
| chr17:45902031
|
A | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7345A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902031 | ||||||
| chr17:45902032
|
A | T | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7346A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902032 | ||||||
| chr17:45902033
|
G | C | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7347G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902033 | ||||||
| chr17:45902035
|
G | T | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+7349G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902035 | ||||||
| chr17:45902102
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+7416T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902102 | ||||||
| chr17:45902105
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-18+7419C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902105 | ||||||
| chr17:45902138
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+7452G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902138 | ||||||
| chr17:45902256
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+7570G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902256 | ||||||
| chr17:45902365
|
C | T | 1 | a0001c0015t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-18+7679C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902365 | ||||||
| chr17:45902456
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+7770A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902456 | ||||||
| chr17:45902605
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+7919C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902605 | ||||||
| chr17:45902606
|
A | G | 179 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0133others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-18+7920A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902606 | ||||||
| chr17:45902735
|
C | G | 5 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0003g0028others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+8049C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902735 | ||||||
| chr17:45902857
|
T | C | 1 | a0002c0002t0003g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-18+8171T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45902857 | ||||||
| chr17:45903164
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+8478A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903164 | ||||||
| chr17:45903199
|
A | T | 1 | a0004c0005t0001g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+8513A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903199 | ||||||
| chr17:45903201
|
C | T | 1 | a0002c0002t0003g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-18+8515C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903201 | ||||||
| chr17:45903274
|
G | C | 3 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0003g0252 | 3 | HG00642.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-18+8588G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903274 | ||||||
| chr17:45903275
|
G | A | 1 | a0002c0003t0019g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-18+8589G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903275 | ||||||
| chr17:45903339
|
G | T | 1 | a0007c0008t0014g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+8653G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903339 | ||||||
| chr17:45903396
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+8710A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903396 | ||||||
| chr17:45903577
|
T | TG | 3 | a0001c0001t0003g0223a0002c0003t0001g0061a0004c0005t0001g0104 | 3 | HG01109.hp2 HG01934.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-18+8893dupG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903577 | |||||
| chr17:45903632
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+8946G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903632 | ||||||
| chr17:45903640
|
G | A | 3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+8954G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903640 | ||||||
| chr17:45903644
|
G | C | 1 | a0002c0003t0002g0146 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-18+8958G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903644 | ||||||
| chr17:45903650
|
G | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8964G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903650 | ||||||
| chr17:45903651
|
G | A | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8965G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903651 | ||||||
| chr17:45903652
|
T | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8966T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903652 | ||||||
| chr17:45903653
|
T | G | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8967T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903653 | ||||||
| chr17:45903654
|
G | A | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8968G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903654 | ||||||
| chr17:45903657
|
G | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8971G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903657 | ||||||
| chr17:45903658
|
T | G | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8972T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903658 | ||||||
| chr17:45903659
|
G | A | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8973G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903659 | ||||||
| chr17:45903660
|
A | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8974A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903660 | ||||||
| chr17:45903662
|
C | A | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8976C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903662 | ||||||
| chr17:45903663
|
C | T | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8977C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903663 | ||||||
| chr17:45903665
|
A | T | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8979A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903665 | ||||||
| chr17:45903666
|
G | T | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+8980G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903666 | ||||||
| chr17:45903714
|
C | CAAAAAA | 18 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+9040_-18+9045d others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903714 | |||||
| chr17:45903714
|
CA | C | 22 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9045delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903714 | |||||
| chr17:45903737
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9051C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903737 | ||||||
| chr17:45903750
|
T | G | 2 | a0001c0001t0001g0211a0001c0001t0006g0212 | 2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-18+9064T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903750 | ||||||
| chr17:45903755
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+9069A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903755 | ||||||
| chr17:45903755
|
A | T | 1 | a0001c0001t0006g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-18+9069A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903755 | ||||||
| chr17:45903755
|
AT | A | 15 | a0001c0001t0001g0065a0001c0001t0002g0066a0001c0001t0002g0067others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+9077delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903755 | |||||
| chr17:45903755
|
ATTTTTTT others(70): Show |
A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9071_-18+9147d others(79): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903755 | |||||
| chr17:45903756
|
T | TA | 35 | a0001c0001t0002g0031a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 35 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-18+9070_-18+9071i others(3): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903756 | ||||||
| chr17:45903757
|
T | A | 4 | a0001c0001t0002g0027a0001c0001t0002g0125a0002c0002t0003g0147others(1): Show | 4 | HG03579.hp1 HG04115.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+9071T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903757 | ||||||
| chr17:45903758
|
T | A | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+9072T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903758 | ||||||
| chr17:45903764
|
A | T | 1 | a0005c0007t0003g0051 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-18+9078A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903764 | ||||||
| chr17:45903767
|
T | TATATAAT others(32): Show |
1 | a0007c0008t0014g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+9094_-18+9132d others(41): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903767 | |||||
| chr17:45903810
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-18+9124T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903810 | ||||||
| chr17:45903811
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-18+9125A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903811 | ||||||
| chr17:45903838
|
A | AT | 173 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-18+9156dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903838 | |||||
| chr17:45903838
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9152A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903838 | ||||||
| chr17:45903839
|
T | TTTTTATA others(16): Show |
1 | a0002c0003t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-18+9156_-18+9157i others(25): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903839 | |||||
| chr17:45903839
|
T | TTTTTATA others(16): Show |
47 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(44): Show | 47 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-18+9156_-18+9157i others(25): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903839 | |||||
| chr17:45903840
|
T | TTTTATAT others(17): Show |
7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0196others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+9156_-18+9157i others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903840 | |||||
| chr17:45903841
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9155T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903841 | ||||||
| chr17:45903841
|
T | TA | 3 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-18+9155_-18+9156i others(3): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903841 | ||||||
| chr17:45903841
|
TTATATAT others(304): Show |
T | 1 | a0002c0002t0006g0070 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-18+9157_-18+9467d others(2): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903841 | |||||
| chr17:45903855
|
T | A | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-18+9169T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903855 | ||||||
| chr17:45903863
|
A | AT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9179dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903863 | |||||
| chr17:45903866
|
ATAT | A | 18 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+9181_-18+9183d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903866 | ||||||
| chr17:45903870
|
ATTATATA others(1): Show |
A | 9 | a0001c0001t0002g0053a0001c0001t0009g0034a0001c0001t0010g0052others(6): Show | 9 | HG00642.hp1 HG01071.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+9202_-18+9209d others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903870 | |||||
| chr17:45903875
|
ATATT | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9193_-18+9196d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903875 | |||||
| chr17:45903884
|
T | A | 1 | a0004c0005t0001g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+9198T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903884 | ||||||
| chr17:45903885
|
A | T | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9199A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903885 | ||||||
| chr17:45903886
|
T | A | 1 | a0004c0005t0001g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+9200T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903886 | ||||||
| chr17:45903887
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9201T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903887 | ||||||
| chr17:45903895
|
T | A | 2 | a0003c0004t0004g0003a0003c0004t0011g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+9209T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903895 | ||||||
| chr17:45903902
|
AT | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9219delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903902 | |||||
| chr17:45903903
|
T | TTTATATA | 3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+9227_-18+9233d others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903903 | |||||
| chr17:45903903
|
T | TTTATATA others(7): Show |
8 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0166others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+9220_-18+9233d others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903903 | |||||
| chr17:45903912
|
T | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+9226T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903912 | ||||||
| chr17:45903913
|
A | T | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+9227A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903913 | ||||||
| chr17:45903918
|
TTTA | T | 22 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(19): Show | 22 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9234_-18+9236d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903918 | |||||
| chr17:45903920
|
T | C | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+9234T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903920 | ||||||
| chr17:45903921
|
A | ATATATAT others(24): Show |
44 | a0001c0001t0001g0042a0001c0001t0001g0135a0001c0001t0001g0136others(41): Show | 44 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-18+9251_-18+9281d others(33): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903921 | |||||
| chr17:45903921
|
A | ATATATTA others(39): Show |
1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-18+9240_-18+9241i others(48): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903921 | |||||
| chr17:45903937
|
T | A | 1 | a0002c0002t0006g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18+9251T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903937 | ||||||
| chr17:45903944
|
A | ATTATATA others(3): Show |
4 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9258_-18+9259i others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903944 | ||||||
| chr17:45903944
|
A | T | 11 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0166others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+9258A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903944 | ||||||
| chr17:45903945
|
A | ATATATAT | 3 | a0001c0001t0001g0216a0001c0001t0002g0043a0001c0001t0026g0192 | 3 | HG00099.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+9296_-18+9302d others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903945 | |||||
| chr17:45903945
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0006g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-18+9282_-18+9302d others(23): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903945 | |||||
| chr17:45903945
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18+9281_-18+9282i others(47): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903945 | |||||
| chr17:45903945
|
A | T | 51 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.-18+9259A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903945 | ||||||
| chr17:45903945
|
ATATATAT | A | 6 | a0001c0001t0001g0165a0001c0001t0001g0247a0001c0001t0003g0122others(3): Show | 6 | HG01071.hp2 HG02074.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+9296_-18+9302d others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903945 | |||||
| chr17:45903945
|
ATATATAT others(14): Show |
A | 1 | a0006c0006t0002g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-18+9282_-18+9302d others(23): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903945 | |||||
| chr17:45903951
|
A | T | 4 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9265A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903951 | ||||||
| chr17:45903952
|
T | TTATATAT others(38): Show |
1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+9310_-18+9311i others(47): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903952 | |||||
| chr17:45903952
|
T | TTATATAT others(31): Show |
5 | a0001c0001t0002g0024a0002c0003t0002g0023a0004c0005t0005g0025others(2): Show | 5 | HG01243.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+9295_-18+9296i others(40): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903952 | |||||
| chr17:45903952
|
T | TTATATAT others(17): Show |
4 | a0001c0001t0001g0164a0001c0001t0003g0144a0001c0001t0005g0194others(1): Show | 4 | HG01928.hp2 HG01993.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9281_-18+9282i others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903952 | |||||
| chr17:45903952
|
T | TTATATAT others(48): Show |
4 | a0001c0001t0003g0196a0004c0005t0002g0180a0004c0005t0005g0195others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+9281_-18+9282i others(57): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903952 | |||||
| chr17:45903953
|
TATA | T | 16 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(13): Show | 16 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+9268_-18+9270d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903953 | ||||||
| chr17:45903958
|
A | T | 2 | a0002c0003t0019g0044a0004c0005t0005g0190 | 2 | HG03688.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18+9272A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903958 | ||||||
| chr17:45903958
|
AT | A | 16 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(13): Show | 16 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+9274delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903958 | |||||
| chr17:45903959
|
T | A | 3 | a0001c0001t0001g0065a0002c0002t0003g0064a0003c0004t0004g0004 | 3 | HG01952.hp2 HG02074.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-18+9273T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903959 | ||||||
| chr17:45903965
|
A | T | 17 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(14): Show | 17 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+9279A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903965 | ||||||
| chr17:45903966
|
T | A | 1 | a0003c0004t0004g0004 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-18+9280T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903966 | ||||||
| chr17:45903966
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+9288_-18+9289i others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903966 | |||||
| chr17:45903966
|
T | TTTATATA others(3): Show |
1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-18+9281_-18+9282i others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903966 | |||||
| chr17:45903972
|
A | ATTATATA others(55): Show |
1 | a0001c0001t0001g0249 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-18+9302_-18+9303i others(64): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903972 | |||||
| chr17:45903973
|
T | TATTA | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0005others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+9287_-18+9288i others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903973 | ||||||
| chr17:45903973
|
T | TTATATAT others(4): Show |
1 | a0001c0010t0013g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18+9291_-18+9301d others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903973 | |||||
| chr17:45903979
|
A | AT | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0005others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+9295dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903979 | |||||
| chr17:45903986
|
A | AC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9300_-18+9301i others(3): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903986 | ||||||
| chr17:45903987
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9301T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903987 | ||||||
| chr17:45903987
|
TTTA | T | 16 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(13): Show | 16 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+9303_-18+9305d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903987 | |||||
| chr17:45903990
|
A | T | 1 | a0001c0001t0002g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+9304A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903990 | ||||||
| chr17:45903993
|
T | C | 3 | a0001c0001t0002g0193a0001c0001t0026g0192a0001c0010t0013g0129 | 3 | HG01167.hp1 HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+9307T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45903993 | ||||||
| chr17:45903997
|
TTATATA | T | 16 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(13): Show | 16 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+9313_-18+9318d others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45903997 | |||||
| chr17:45904005
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9319T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904005 | ||||||
| chr17:45904006
|
A | ATATATAT | 4 | a0001c0001t0002g0024a0002c0003t0002g0023a0004c0005t0005g0025others(1): Show | 4 | HG01243.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9336_-18+9342d others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904006 | |||||
| chr17:45904006
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-18+9365_-18+9410d others(48): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904006 | |||||
| chr17:45904013
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9327T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904013 | ||||||
| chr17:45904019
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9333A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904019 | ||||||
| chr17:45904020
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9334T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904020 | ||||||
| chr17:45904026
|
AT | A | 3 | a0001c0001t0003g0229a0001c0001t0003g0231a0005c0007t0003g0230 | 3 | HG00323.hp1 HG01175.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-18+9343delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904026 | |||||
| chr17:45904027
|
T | TTTATATA others(24): Show |
1 | a0001c0001t0002g0071 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-18+9365_-18+9395d others(33): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904027 | |||||
| chr17:45904028
|
T | A | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9342T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904028 | ||||||
| chr17:45904029
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9343T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904029 | ||||||
| chr17:45904033
|
T | A | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9347T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904033 | ||||||
| chr17:45904034
|
A | T | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9348A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904034 | ||||||
| chr17:45904035
|
TTATATAT others(56): Show |
T | 7 | a0001c0001t0002g0053a0001c0001t0009g0034a0001c0001t0010g0052others(4): Show | 7 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+9388_-18+9450d others(65): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904035 | |||||
| chr17:45904036
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9350T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904036 | ||||||
| chr17:45904041
|
AT | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9358delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904041 | |||||
| chr17:45904042
|
T | A | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9356T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904042 | ||||||
| chr17:45904043
|
T | A | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9357T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904043 | ||||||
| chr17:45904043
|
TTA | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0002g0027others(9): Show | 12 | HG01884.hp2 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+9365_-18+9366d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904043 | |||||
| chr17:45904044
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9358T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904044 | ||||||
| chr17:45904045
|
A | T | 1 | a0002c0003t0019g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-18+9359A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904045 | ||||||
| chr17:45904045
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0003g0248 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+9375_-18+9388d others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904045 | |||||
| chr17:45904051
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9365A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904051 | ||||||
| chr17:45904052
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9366T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904052 | ||||||
| chr17:45904057
|
T | G | 8 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(5): Show | 8 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+9371T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904057 | ||||||
| chr17:45904060
|
T | TC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9374_-18+9375i others(3): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904060 | ||||||
| chr17:45904061
|
A | T | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9375A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904061 | ||||||
| chr17:45904062
|
T | G | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9376T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904062 | ||||||
| chr17:45904067
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9381T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904067 | ||||||
| chr17:45904074
|
T | G | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9388T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904074 | ||||||
| chr17:45904075
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9389T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904075 | ||||||
| chr17:45904076
|
A | T | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9390A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904076 | ||||||
| chr17:45904080
|
A | T | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+9394A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904080 | ||||||
| chr17:45904082
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9396T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904082 | ||||||
| chr17:45904084
|
T | A | 1 | a0001c0010t0013g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18+9398T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904084 | ||||||
| chr17:45904087
|
AT | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9404delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904087 | |||||
| chr17:45904089
|
TTATATAT others(28): Show |
T | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+9409_-18+9443d others(37): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904089 | |||||
| chr17:45904090
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9404T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904090 | ||||||
| chr17:45904106
|
T | A | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9420T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904106 | ||||||
| chr17:45904106
|
TTATATAT others(11): Show |
T | 1 | a0002c0002t0003g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-18+9426_-18+9443d others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904106 | |||||
| chr17:45904107
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9421T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904107 | ||||||
| chr17:45904108
|
A | T | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+9422A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904108 | ||||||
| chr17:45904108
|
ATATATAT | A | 3 | a0001c0001t0001g0211a0001c0001t0002g0072a0002c0002t0003g0145 | 3 | HG04115.hp1 HG04204.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-18+9444_-18+9450d others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904108 | |||||
| chr17:45904115
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9429T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904115 | ||||||
| chr17:45904129
|
TTATATAT others(1): Show |
T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9451_-18+9458d others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904129 | |||||
| chr17:45904152
|
GT | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9468delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904152 | |||||
| chr17:45904161
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9475T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904161 | ||||||
| chr17:45904166
|
ATAT | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9482_-18+9484d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904166 | |||||
| chr17:45904170
|
TTATA | T | 45 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(42): Show | 45 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-18+9491_-18+9494d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904170 | |||||
| chr17:45904178
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9492A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904178 | ||||||
| chr17:45904180
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9494A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904180 | ||||||
| chr17:45904188
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9502G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904188 | ||||||
| chr17:45904203
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9517C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904203 | ||||||
| chr17:45904205
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9519A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904205 | ||||||
| chr17:45904205
|
AATATATT others(2): Show |
A | 4 | a0001c0001t0003g0196a0001c0001t0027g0093a0014c0013t0007g0040others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9542_-18+9550d others(11): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904205 | |||||
| chr17:45904221
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9535T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904221 | ||||||
| chr17:45904221
|
TATATATA others(12): Show |
T | 1 | a0002c0002t0001g0158 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-18+9555_-18+9573d others(21): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904221 | |||||
| chr17:45904222
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-18+9555_-18+9580d others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904222 | |||||
| chr17:45904223
|
T | G | 3 | a0002c0003t0001g0150a0002c0003t0001g0198a0005c0007t0003g0056 | 3 | HG02572.hp1 NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-18+9537T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904223 | ||||||
| chr17:45904225
|
T | C | 2 | a0004c0005t0005g0190a0007c0008t0014g0191 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18+9539T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904225 | ||||||
| chr17:45904230
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9544T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904230 | ||||||
| chr17:45904237
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9551T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904237 | ||||||
| chr17:45904239
|
TA | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9555delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904239 | |||||
| chr17:45904250
|
A | ATT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9565_-18+9566i others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904250 | |||||
| chr17:45904258
|
TATATTAT others(56): Show |
T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9577_-18+9639d others(65): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904258 | |||||
| chr17:45904320
|
TAA | T | 18 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+9635_-18+9636d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904320 | ||||||
| chr17:45904330
|
T | A | 2 | a0001c0001t0002g0057a0002c0002t0012g0058 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-18+9644T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904330 | ||||||
| chr17:45904330
|
T | TTATATTA others(30): Show |
1 | a0002c0002t0001g0220 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-18+9644_-18+9645i others(39): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904330 | ||||||
| chr17:45904336
|
TTA | T | 2 | a0001c0001t0026g0192a0001c0010t0013g0129 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+9660_-18+9661d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904336 | |||||
| chr17:45904338
|
A | ATATATAT others(31): Show |
40 | a0001c0001t0001g0065a0001c0001t0001g0099a0001c0001t0001g0128others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18+9671_-18+9708d others(40): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904338 | |||||
| chr17:45904338
|
A | ATATATAT others(30): Show |
1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+9682_-18+9683i others(39): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904338 | |||||
| chr17:45904338
|
A | ATATATAT others(29): Show |
2 | a0002c0002t0001g0055a0002c0002t0012g0058 | 2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-18+9659_-18+9660i others(38): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904338 | |||||
| chr17:45904338
|
A | T | 22 | a0002c0002t0001g0220a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9652A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904338 | ||||||
| chr17:45904338
|
ATATATAT others(2): Show |
A | 4 | a0001c0001t0002g0193a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG00642.hp2 HG01167.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9673_-18+9681d others(11): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904338 | |||||
| chr17:45904346
|
ATT | A | 11 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0003g0028others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+9661_-18+9662d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904346 | ||||||
| chr17:45904357
|
TATATATA | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9672_-18+9678d others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904357 | ||||||
| chr17:45904367
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9681A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904367 | ||||||
| chr17:45904368
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9682A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904368 | ||||||
| chr17:45904376
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9690T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904376 | ||||||
| chr17:45904429
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9743G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904429 | ||||||
| chr17:45904465
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+9779A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904465 | ||||||
| chr17:45904546
|
G | A | 6 | a0001c0001t0001g0074a0002c0002t0003g0076a0002c0002t0017g0112others(3): Show | 6 | HG01106.hp1 HG01943.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+9860G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904546 | ||||||
| chr17:45904547
|
C | T | 6 | a0001c0001t0001g0074a0002c0002t0003g0076a0002c0002t0017g0112others(3): Show | 6 | HG01106.hp1 HG01943.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+9861C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904547 | ||||||
| chr17:45904553
|
A | G | 3 | a0001c0001t0002g0031a0001c0001t0008g0029a0009c0011t0002g0030 | 3 | HG01884.hp2 HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-18+9867A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904553 | ||||||
| chr17:45904592
|
C | T | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9906C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904592 | ||||||
| chr17:45904607
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-18+9921G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904607 | ||||||
| chr17:45904696
|
C | CT | 24 | a0001c0001t0001g0153a0001c0001t0001g0164a0001c0001t0002g0199others(21): Show | 24 | HG01928.hp1 HG01928.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18+10021dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904696 | |||||
| chr17:45904696
|
CTT | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+10020_-18+1002 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45904696 | |||||
| chr17:45904703
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+10017T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904703 | ||||||
| chr17:45904793
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+10107A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904793 | ||||||
| chr17:45904848
|
T | C | 1 | a0001c0001t0002g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-18+10162T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904848 | ||||||
| chr17:45904920
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+10234C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45904920 | ||||||
| chr17:45905041
|
T | A | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10355T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905041 | ||||||
| chr17:45905042
|
T | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10356T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905042 | ||||||
| chr17:45905044
|
T | A | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10358T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905044 | ||||||
| chr17:45905055
|
T | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10369T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905055 | ||||||
| chr17:45905058
|
G | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10372G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905058 | ||||||
| chr17:45905059
|
C | G | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10373C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905059 | ||||||
| chr17:45905061
|
G | T | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+10375G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905061 | ||||||
| chr17:45905082
|
C | G | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+10396C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905082 | ||||||
| chr17:45905260
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-18+10574G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905260 | ||||||
| chr17:45905537
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+10851A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905537 | ||||||
| chr17:45905595
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+10909T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905595 | ||||||
| chr17:45905597
|
A | T | 1 | a0006c0006t0002g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-18+10911A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905597 | ||||||
| chr17:45905642
|
G | C | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-18+10956G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905642 | ||||||
| chr17:45905793
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+11107T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905793 | ||||||
| chr17:45905997
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+11311G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45905997 | ||||||
| chr17:45906435
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+11749A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45906435 | ||||||
| chr17:45906715
|
G | A | 17 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(14): Show | 17 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+12029G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45906715 | ||||||
| chr17:45906776
|
C | T | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+12090C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45906776 | ||||||
| chr17:45906791
|
G | A | 3 | a0002c0002t0003g0213a0002c0002t0006g0214a0002c0002t0006g0215 | 3 | HG00099.hp1 HG01261.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+12105G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45906791 | ||||||
| chr17:45906848
|
C | T | 2 | a0002c0002t0003g0076a0002c0003t0001g0075 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-18+12162C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45906848 | ||||||
| chr17:45906887
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+12201G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45906887 | ||||||
| chr17:45907033
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+12347C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907033 | ||||||
| chr17:45907280
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+12594T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907280 | ||||||
| chr17:45907303
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+12617A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907303 | ||||||
| chr17:45907306
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+12620T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907306 | ||||||
| chr17:45907320
|
C | A | 1 | a0002c0002t0003g0062 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-18+12634C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907320 | ||||||
| chr17:45907418
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-18+12732C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907418 | ||||||
| chr17:45907498
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+12812C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907498 | ||||||
| chr17:45907548
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-18+12862A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907548 | ||||||
| chr17:45907766
|
A | G | 13 | a0001c0001t0001g0065a0001c0001t0001g0099a0001c0001t0001g0128others(10): Show | 13 | HG00621.hp1 HG02071.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18+13080A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907766 | ||||||
| chr17:45907791
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+13105G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907791 | ||||||
| chr17:45907881
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+13195C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45907881 | ||||||
| chr17:45908231
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+13545C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908231 | ||||||
| chr17:45908260
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0003g0122a0002c0003t0001g0118 | 3 | HG02074.hp1 NA18943.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-18+13574C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908260 | ||||||
| chr17:45908270
|
C | A | 134 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(131): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+13584C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908270 | ||||||
| chr17:45908296
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+13610T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908296 | ||||||
| chr17:45908357
|
G | A | 9 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(6): Show | 9 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+13671G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908357 | ||||||
| chr17:45908407
|
A | G | 3 | a0001c0001t0003g0223a0001c0017t0002g0218a0002c0003t0002g0219 | 3 | HG00544.hp1 NA19002.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-18+13721A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908407 | ||||||
| chr17:45908712
|
T | A | 7 | a0001c0001t0002g0036a0001c0001t0002g0179a0001c0001t0003g0196others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+14026T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908712 | ||||||
| chr17:45908773
|
C | T | 1 | a0002c0003t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-18+14087C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908773 | ||||||
| chr17:45908813
|
G | A | 171 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-18+14127G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908813 | ||||||
| chr17:45908942
|
G | A | 3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+14256G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908942 | ||||||
| chr17:45908963
|
A | C | 6 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039others(3): Show | 6 | HG01109.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+14277A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45908963 | ||||||
| chr17:45908966
|
GT | G | 6 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039others(3): Show | 6 | HG01109.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+14284delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45908966 | |||||
| chr17:45909030
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+14344C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909030 | ||||||
| chr17:45909054
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+14368A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909054 | ||||||
| chr17:45909066
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+14380G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909066 | ||||||
| chr17:45909087
|
C | T | 1 | a0001c0001t0003g0157 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-18+14401C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909087 | ||||||
| chr17:45909096
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+14410A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909096 | ||||||
| chr17:45909149
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-18+14463T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909149 | ||||||
| chr17:45909163
|
G | T | 1 | a0001c0001t0003g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18+14477G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909163 | ||||||
| chr17:45909626
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+14940G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909626 | ||||||
| chr17:45909640
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+14954G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909640 | ||||||
| chr17:45909788
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+15102G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909788 | ||||||
| chr17:45909818
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+15132T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45909818 | ||||||
| chr17:45909869
|
C | CA | 11 | a0001c0001t0001g0165a0001c0001t0002g0078a0001c0001t0007g0205others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+15207dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45909869 | |||||
| chr17:45909869
|
C | CAAAA | 17 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+15204_-18+1520 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45909869 | |||||
| chr17:45909869
|
CA | C | 85 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(82): Show | 85 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-18+15207delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45909869 | |||||
| chr17:45909869
|
CAA | C | 8 | a0001c0001t0001g0245a0001c0001t0002g0031a0002c0002t0003g0251others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+15206_-18+1520 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45909869 | |||||
| chr17:45909869
|
CAAAAAAA others(1): Show |
C | 20 | a0001c0001t0002g0024a0001c0001t0002g0046a0001c0001t0002g0047others(17): Show | 20 | HG00280.hp2 HG01071.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-18+15200_-18+1520 others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45909869 | |||||
| chr17:45910180
|
G | A | 1 | a0001c0001t0010g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-18+15494G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910180 | ||||||
| chr17:45910357
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+15671G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910357 | ||||||
| chr17:45910435
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+15749T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910435 | ||||||
| chr17:45910452
|
C | T | 2 | a0004c0005t0025g0121a0012c0016t0002g0111 | 2 | HG01071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-18+15766C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910452 | ||||||
| chr17:45910503
|
G | A | 1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-18+15817G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910503 | ||||||
| chr17:45910576
|
T | A | 42 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(39): Show | 42 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-18+15890T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910576 | ||||||
| chr17:45910666
|
T | TA | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(43): Show | 46 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.-18+16000dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45910666 | |||||
| chr17:45910666
|
TA | T | 9 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0072others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+16000delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45910666 | |||||
| chr17:45910666
|
TAAAA | T | 18 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(15): Show | 18 | HG01074.hp1 HG01099.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+15997_-18+1600 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45910666 | |||||
| chr17:45910839
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+16153A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910839 | ||||||
| chr17:45910900
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-18+16214G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45910900 | ||||||
| chr17:45911125
|
G | A | 2 | a0001c0001t0002g0079a0004c0005t0007g0077 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+16439G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911125 | ||||||
| chr17:45911130
|
T | C | 1 | a0008c0009t0009g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+16444T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911130 | ||||||
| chr17:45911257
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+16571G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911257 | ||||||
| chr17:45911452
|
A | C | 5 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0001t0026g0192others(2): Show | 5 | HG02280.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+16766A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911452 | ||||||
| chr17:45911487
|
G | A | 1 | a0002c0002t0003g0213 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-18+16801G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911487 | ||||||
| chr17:45911518
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+16832T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911518 | ||||||
| chr17:45911559
|
G | A | 2 | a0002c0003t0001g0118a0002c0003t0019g0044 | 2 | HG03688.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-18+16873G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911559 | ||||||
| chr17:45911721
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17035A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911721 | ||||||
| chr17:45911743
|
G | A | 5 | a0001c0001t0001g0074a0002c0002t0017g0112a0002c0003t0002g0073others(2): Show | 5 | HG01106.hp1 HG02300.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+17057G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911743 | ||||||
| chr17:45911763
|
CA | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17084delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45911763 | |||||
| chr17:45911784
|
A | ACAAC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17098_-18+1709 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911784 | ||||||
| chr17:45911790
|
A | G | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+17104A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911790 | ||||||
| chr17:45911791
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17105A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911791 | ||||||
| chr17:45911793
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17107G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911793 | ||||||
| chr17:45911855
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17169T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45911855 | ||||||
| chr17:45912062
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+17376G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912062 | ||||||
| chr17:45912143
|
TA | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17459delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45912143 | |||||
| chr17:45912231
|
A | G | 1 | a0001c0001t0003g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18+17545A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912231 | ||||||
| chr17:45912323
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17637T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912323 | ||||||
| chr17:45912532
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17846T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912532 | ||||||
| chr17:45912543
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17857A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912543 | ||||||
| chr17:45912675
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+17989A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912675 | ||||||
| chr17:45912706
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+18020A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45912706 | ||||||
| chr17:45913112
|
G | A | 1 | a0003c0004t0004g0005 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-18+18426G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913112 | ||||||
| chr17:45913184
|
A | T | 5 | a0001c0001t0003g0082a0001c0001t0027g0093a0004c0005t0025g0121others(2): Show | 5 | HG01071.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+18498A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913184 | ||||||
| chr17:45913251
|
A | C | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+18565A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913251 | ||||||
| chr17:45913296
|
G | A | 22 | a0001c0001t0002g0166a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+18610G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913296 | ||||||
| chr17:45913553
|
A | G | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+18867A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913553 | ||||||
| chr17:45913764
|
T | C | 1 | a0003c0004t0004g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-18+19078T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913764 | ||||||
| chr17:45913886
|
AC | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19202delC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45913886 | |||||
| chr17:45913906
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19220A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45913906 | ||||||
| chr17:45914010
|
C | T | 8 | a0001c0001t0002g0166a0001c0001t0002g0168a0001c0001t0003g0105others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+19324C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914010 | ||||||
| chr17:45914102
|
T | TA | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19421dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914102 | |||||
| chr17:45914143
|
A | C | 21 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(18): Show | 21 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19457A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914143 | ||||||
| chr17:45914148
|
A | T | 242 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-18+19462A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914148 | ||||||
| chr17:45914149
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19463T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914149 | ||||||
| chr17:45914187
|
A | G | 54 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+19501A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914187 | ||||||
| chr17:45914205
|
G | GAGGGTGT others(8): Show |
20 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(17): Show | 20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+19523_-18+1953 others(19): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914205 | |||||
| chr17:45914205
|
G | GAGGGTGT others(53): Show |
1 | a0003c0004t0004g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-18+19537_-18+1953 others(64): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914205 | |||||
| chr17:45914205
|
G | GAGGGTGT others(68): Show |
20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+19537_-18+1953 others(79): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914205 | |||||
| chr17:45914276
|
G | A | 5 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0003g0028others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+19590G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914276 | ||||||
| chr17:45914277
|
G | C | 26 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(23): Show | 26 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18+19591G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914277 | ||||||
| chr17:45914353
|
T | TG | 7 | a0002c0002t0003g0062a0002c0002t0018g0091a0002c0003t0001g0061others(4): Show | 7 | HG00408.hp1 HG00621.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+19673dupG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914353 | |||||
| chr17:45914354
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-18+19668G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914354 | ||||||
| chr17:45914372
|
A | G | 1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-18+19686A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914372 | ||||||
| chr17:45914415
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19729G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914415 | ||||||
| chr17:45914476
|
C | G | 1 | a0003c0004t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18+19790C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914476 | ||||||
| chr17:45914506
|
G | A | 5 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0001t0026g0192others(2): Show | 5 | HG02280.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+19820G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914506 | ||||||
| chr17:45914522
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+19836G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914522 | ||||||
| chr17:45914723
|
C | CT | 12 | a0001c0001t0001g0181a0001c0001t0002g0053a0001c0001t0002g0079others(9): Show | 12 | HG00609.hp1 HG00609.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+20052dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914723 | |||||
| chr17:45914723
|
CT | C | 22 | a0002c0002t0003g0175a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+20052delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45914723 | |||||
| chr17:45914867
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20181C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914867 | ||||||
| chr17:45914878
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20192G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914878 | ||||||
| chr17:45914917
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20231A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914917 | ||||||
| chr17:45914939
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20253G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45914939 | ||||||
| chr17:45915090
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20404G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915090 | ||||||
| chr17:45915097
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20411G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915097 | ||||||
| chr17:45915215
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20529C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915215 | ||||||
| chr17:45915324
|
A | AGT | 5 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0001t0026g0192others(2): Show | 5 | HG02280.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+20648_-18+2064 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45915324 | |||||
| chr17:45915440
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20754A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915440 | ||||||
| chr17:45915480
|
T | TTGTGATA others(30): Show |
21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20799_-18+2083 others(41): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45915480 | |||||
| chr17:45915506
|
A | G | 2 | a0008c0009t0009g0107a0011c0012t0022g0022 | 2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-18+20820A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915506 | ||||||
| chr17:45915523
|
CTG | C | 3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+20844_-18+2084 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45915523 | |||||
| chr17:45915573
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+20887T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915573 | ||||||
| chr17:45915576
|
C | T | 1 | a0006c0006t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-18+20890C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915576 | ||||||
| chr17:45915577
|
G | A | 54 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0046others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+20891G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45915577 | ||||||
| chr17:45916010
|
T | G | 107 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(104): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-18+21324T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916010 | ||||||
| chr17:45916073
|
G | A | 1 | a0002c0003t0020g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-18+21387G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916073 | ||||||
| chr17:45916288
|
C | T | 1 | a0007c0008t0014g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+21602C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916288 | ||||||
| chr17:45916343
|
G | C | 8 | a0001c0001t0002g0027a0001c0001t0003g0028a0001c0001t0008g0029others(5): Show | 8 | HG01109.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+21657G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916343 | ||||||
| chr17:45916352
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+21666G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916352 | ||||||
| chr17:45916387
|
C | T | 8 | a0001c0001t0002g0053a0001c0001t0009g0034a0001c0001t0010g0052others(5): Show | 8 | HG02647.hp2 HG02818.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+21701C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916387 | ||||||
| chr17:45916422
|
G | C | 2 | a0002c0002t0003g0076a0002c0003t0001g0075 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-18+21736G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916422 | ||||||
| chr17:45916655
|
T | C | 57 | a0001c0001t0001g0148a0001c0001t0001g0210a0001c0001t0001g0211others(54): Show | 57 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+21969T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916655 | ||||||
| chr17:45916809
|
A | G | 1 | a0002c0003t0001g0182 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-18+22123A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916809 | ||||||
| chr17:45916886
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22200T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916886 | ||||||
| chr17:45916992
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22306C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45916992 | ||||||
| chr17:45917020
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22334C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917020 | ||||||
| chr17:45917069
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22383A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917069 | ||||||
| chr17:45917120
|
C | T | 1 | a0001c0001t0006g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-18+22434C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917120 | ||||||
| chr17:45917142
|
GAGA | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22461_-18+2246 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45917142 | |||||
| chr17:45917257
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22571G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917257 | ||||||
| chr17:45917282
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22596C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917282 | ||||||
| chr17:45917397
|
A | G | 41 | a0001c0001t0001g0148a0001c0001t0001g0210a0001c0001t0001g0211others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18+22711A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917397 | ||||||
| chr17:45917465
|
G | T | 1 | a0004c0005t0005g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18+22779G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917465 | ||||||
| chr17:45917586
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+22900A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917586 | ||||||
| chr17:45917676
|
A | G | 1 | a0005c0007t0003g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+22990A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917676 | ||||||
| chr17:45917732
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+23046G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917732 | ||||||
| chr17:45917770
|
C | CT | 10 | a0001c0001t0002g0027a0001c0001t0002g0036a0001c0001t0002g0179others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+23097dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45917770 | |||||
| chr17:45917773
|
TTTTTTTT others(4): Show |
T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+23097_-18+2310 others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45917773 | |||||
| chr17:45917778
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-18+23092T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917778 | ||||||
| chr17:45917784
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-18+23098C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917784 | ||||||
| chr17:45917919
|
C | T | 2 | a0004c0005t0005g0190a0007c0008t0014g0191 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18+23233C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917919 | ||||||
| chr17:45917927
|
C | A | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+23241C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917927 | ||||||
| chr17:45917934
|
G | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+23248G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45917934 | ||||||
| chr17:45918266
|
T | C | 1 | a0002c0003t0002g0146 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-18+23580T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918266 | ||||||
| chr17:45918566
|
C | G | 73 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-18+23880C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918566 | ||||||
| chr17:45918624
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+23938A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918624 | ||||||
| chr17:45918774
|
T | C | 113 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-18+24088T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918774 | ||||||
| chr17:45918786
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18+24100G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918786 | ||||||
| chr17:45918796
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-18+24110G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918796 | ||||||
| chr17:45918843
|
A | C | 1 | a0001c0001t0007g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+24157A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45918843 | ||||||
| chr17:45919011
|
A | G | 1 | a0002c0003t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-18+24325A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919011 | ||||||
| chr17:45919064
|
TA | T | 23 | a0002c0002t0008g0172a0003c0004t0004g0001a0003c0004t0004g0003others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+24393delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45919064 | |||||
| chr17:45919195
|
A | G | 121 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-18+24509A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919195 | ||||||
| chr17:45919198
|
G | A | 1 | a0001c0001t0003g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-18+24512G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919198 | ||||||
| chr17:45919208
|
G | C | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+24522G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919208 | ||||||
| chr17:45919350
|
GC | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+24672delC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45919350 | |||||
| chr17:45919355
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+24669C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919355 | ||||||
| chr17:45919542
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+24856T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919542 | ||||||
| chr17:45919567
|
C | T | 52 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0152others(49): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+24881C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919567 | ||||||
| chr17:45919594
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+24908A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919594 | ||||||
| chr17:45919615
|
G | A | 2 | a0014c0013t0007g0040a0015c0019t0005g0189 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+24929G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45919615 | ||||||
| chr17:45920006
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+25320T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920006 | ||||||
| chr17:45920093
|
A | G | 2 | a0004c0005t0005g0190a0007c0008t0014g0191 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18+25407A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920093 | ||||||
| chr17:45920133
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+25447A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920133 | ||||||
| chr17:45920154
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+25468C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920154 | ||||||
| chr17:45920159
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-18+25473G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920159 | ||||||
| chr17:45920231
|
C | T | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+25545C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920231 | ||||||
| chr17:45920535
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+25849G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920535 | ||||||
| chr17:45920543
|
G | A | 1 | a0001c0001t0003g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-18+25857G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920543 | ||||||
| chr17:45920785
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+26099C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920785 | ||||||
| chr17:45920857
|
G | A | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+26171G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920857 | ||||||
| chr17:45920912
|
C | T | 2 | a0003c0004t0004g0001a0003c0004t0004g0018 | 2 | HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-18+26226C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920912 | ||||||
| chr17:45920962
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+26276C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45920962 | ||||||
| chr17:45921170
|
C | T | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+26484C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921170 | ||||||
| chr17:45921208
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+26522T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921208 | ||||||
| chr17:45921332
|
T | C | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+26646T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921332 | ||||||
| chr17:45921401
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+26715T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921401 | ||||||
| chr17:45921456
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+26770A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921456 | ||||||
| chr17:45921544
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+26858C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921544 | ||||||
| chr17:45921733
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-18+27047C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921733 | ||||||
| chr17:45921734
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+27048G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921734 | ||||||
| chr17:45921837
|
G | A | 6 | a0001c0001t0001g0216a0001c0001t0002g0217a0001c0001t0003g0054others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+27151G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921837 | ||||||
| chr17:45921938
|
G | A | 1 | a0002c0002t0003g0225 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-18+27252G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45921938 | ||||||
| chr17:45922040
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+27354A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922040 | ||||||
| chr17:45922163
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+27477G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922163 | ||||||
| chr17:45922278
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-18+27592A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922278 | ||||||
| chr17:45922419
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+27733C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922419 | ||||||
| chr17:45922427
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+27741G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922427 | ||||||
| chr17:45922469
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18+27783C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922469 | ||||||
| chr17:45922486
|
A | AAC | 66 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0148others(63): Show | 66 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-18+27832_-18+2783 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACAC | 6 | a0001c0001t0002g0199a0002c0002t0003g0213a0002c0002t0006g0214others(3): Show | 6 | HG00099.hp1 HG01261.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+27830_-18+2783 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACAC | 2 | a0001c0010t0013g0129a0004c0005t0005g0025 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+27828_-18+2783 others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(3): Show |
13 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0168others(10): Show | 13 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+27824_-18+2783 others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(5): Show |
2 | a0001c0001t0002g0166a0001c0001t0008g0029 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-18+27822_-18+2783 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(7): Show |
4 | a0001c0001t0002g0178a0002c0002t0003g0048a0007c0008t0014g0026others(1): Show | 4 | HG02055.hp1 HG02132.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+27820_-18+2783 others(18): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(9): Show |
1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+27818_-18+2783 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(11): Show |
9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(6): Show | 9 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+27816_-18+2783 others(22): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(13): Show |
3 | a0001c0001t0002g0047a0002c0002t0003g0244a0005c0007t0003g0051 | 3 | HG01192.hp2 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-18+27814_-18+2783 others(24): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
A | AACACACA others(15): Show |
4 | a0001c0001t0001g0216a0001c0001t0002g0046a0002c0002t0001g0045others(1): Show | 4 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+27812_-18+2783 others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
AAC | A | 7 | a0001c0001t0003g0229a0001c0001t0009g0034a0001c0001t0010g0052others(4): Show | 7 | HG00323.hp1 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+27832_-18+2783 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922486
|
AACACACA others(7): Show |
A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+27820_-18+2783 others(18): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45922486 | |||||
| chr17:45922746
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-18+28060T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922746 | ||||||
| chr17:45922836
|
G | A | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+28150G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922836 | ||||||
| chr17:45922863
|
T | C | 1 | a0006c0006t0002g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-18+28177T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922863 | ||||||
| chr17:45922868
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+28182A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922868 | ||||||
| chr17:45922906
|
A | C | 1 | a0002c0003t0002g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-18+28220A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922906 | ||||||
| chr17:45922946
|
G | A | 1 | a0009c0011t0002g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+28260G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45922946 | ||||||
| chr17:45923139
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+28453C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923139 | ||||||
| chr17:45923164
|
C | T | 3 | a0002c0002t0003g0213a0002c0002t0006g0214a0002c0002t0006g0215 | 3 | HG00099.hp1 HG01261.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+28478C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923164 | ||||||
| chr17:45923244
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+28558G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923244 | ||||||
| chr17:45923283
|
T | A | 1 | a0011c0012t0022g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18+28597T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923283 | ||||||
| chr17:45923405
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+28719G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923405 | ||||||
| chr17:45923521
|
G | T | 3 | a0001c0001t0002g0027a0001c0001t0003g0028a0009c0011t0002g0030 | 3 | HG02486.hp1 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+28835G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923521 | ||||||
| chr17:45923522
|
G | T | 3 | a0001c0001t0002g0027a0001c0001t0003g0028a0009c0011t0002g0030 | 3 | HG02486.hp1 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+28836G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923522 | ||||||
| chr17:45923548
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+28862T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923548 | ||||||
| chr17:45923862
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+29176G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45923862 | ||||||
| chr17:45924013
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+29327C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924013 | ||||||
| chr17:45924014
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-18+29328G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924014 | ||||||
| chr17:45924183
|
G | GC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+29503dupC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45924183 | |||||
| chr17:45924255
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+29569A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924255 | ||||||
| chr17:45924295
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+29609A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924295 | ||||||
| chr17:45924312
|
C | CT | 5 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208others(2): Show | 5 | HG02280.hp1 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+29629dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45924312 | |||||
| chr17:45924591
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+29905T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924591 | ||||||
| chr17:45924696
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+30010A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924696 | ||||||
| chr17:45924772
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+30086A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924772 | ||||||
| chr17:45924847
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-18+30161G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924847 | ||||||
| chr17:45924884
|
A | T | 224 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-18+30198A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924884 | ||||||
| chr17:45924905
|
A | G | 118 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.-18+30219A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924905 | ||||||
| chr17:45924914
|
G | A | 18 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0166others(15): Show | 18 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+30228G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924914 | ||||||
| chr17:45924994
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-18+30308A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45924994 | ||||||
| chr17:45925065
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+30379C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925065 | ||||||
| chr17:45925120
|
T | A | 1 | a0002c0003t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-18+30434T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925120 | ||||||
| chr17:45925189
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+30503A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925189 | ||||||
| chr17:45925229
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+30543C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925229 | ||||||
| chr17:45925266
|
A | T | 167 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-18+30580A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925266 | ||||||
| chr17:45925444
|
C | T | 1 | a0002c0003t0020g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-18+30758C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925444 | ||||||
| chr17:45925505
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+30819C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925505 | ||||||
| chr17:45925574
|
GT | G | 116 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-18+30892delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45925574 | |||||
| chr17:45925603
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+30917A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925603 | ||||||
| chr17:45925767
|
A | AAAG | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31083_-18+3108 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45925767 | |||||
| chr17:45925823
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-18+31137G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925823 | ||||||
| chr17:45925936
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-18+31250C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45925936 | ||||||
| chr17:45926031
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31345T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926031 | ||||||
| chr17:45926080
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31394A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926080 | ||||||
| chr17:45926214
|
GA | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31540delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45926214 | |||||
| chr17:45926233
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31547C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926233 | ||||||
| chr17:45926259
|
T | TAA | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31574_-18+3157 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45926259 | |||||
| chr17:45926266
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-18+31580T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926266 | ||||||
| chr17:45926527
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+31841A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926527 | ||||||
| chr17:45926550
|
C | G | 3 | a0001c0001t0001g0074a0002c0003t0001g0177a0002c0003t0002g0103 | 3 | HG00738.hp1 HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-18+31864C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926550 | ||||||
| chr17:45926710
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+32024T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926710 | ||||||
| chr17:45926911
|
G | GTGTGTAT others(35): Show |
2 | a0002c0003t0001g0101a0014c0013t0007g0040 | 2 | HG03831.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+32242_-18+3228 others(46): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45926911 | |||||
| chr17:45926928
|
CATATATA others(23): Show |
C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+32250_-18+3227 others(34): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45926928 | |||||
| chr17:45926953
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+32267A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926953 | ||||||
| chr17:45926966
|
T | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-18+32280T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45926966 | ||||||
| chr17:45927020
|
T | C | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+32334T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927020 | ||||||
| chr17:45927076
|
T | G | 17 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+32390T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927076 | ||||||
| chr17:45927106
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+32420A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927106 | ||||||
| chr17:45927131
|
A | T | 1 | a0013c0014t0002g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-18+32445A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927131 | ||||||
| chr17:45927265
|
G | A | 1 | a0001c0010t0013g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18+32579G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927265 | ||||||
| chr17:45927287
|
G | A | 3 | a0001c0001t0002g0207a0001c0001t0007g0205a0001c0010t0013g0208 | 3 | HG02280.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+32601G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927287 | ||||||
| chr17:45927302
|
C | T | 1 | a0002c0002t0021g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-18+32616C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927302 | ||||||
| chr17:45927303
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-18+32617G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927303 | ||||||
| chr17:45927405
|
G | A | 1 | a0002c0002t0003g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-18+32719G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927405 | ||||||
| chr17:45927558
|
A | G | 51 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0152others(48): Show | 51 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-18+32872A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927558 | ||||||
| chr17:45927589
|
G | C | 2 | a0002c0002t0001g0220a0002c0002t0003g0151 | 2 | HG00438.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-18+32903G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927589 | ||||||
| chr17:45927626
|
C | T | 1 | a0005c0007t0003g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+32940C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927626 | ||||||
| chr17:45927780
|
C | T | 6 | a0001c0001t0026g0192a0001c0010t0013g0129a0004c0005t0001g0104others(3): Show | 6 | HG01109.hp2 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+33094C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927780 | ||||||
| chr17:45927818
|
G | A | 1 | a0002c0002t0003g0213 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-18+33132G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927818 | ||||||
| chr17:45927820
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33134G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927820 | ||||||
| chr17:45927860
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33174A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927860 | ||||||
| chr17:45927888
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33202T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927888 | ||||||
| chr17:45927931
|
C | T | 45 | a0001c0001t0001g0148a0001c0001t0001g0210a0001c0001t0001g0211others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-18+33245C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927931 | ||||||
| chr17:45927957
|
G | A | 2 | a0001c0001t0002g0228a0002c0003t0001g0102 | 2 | HG00408.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18+33271G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927957 | ||||||
| chr17:45927963
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33277G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927963 | ||||||
| chr17:45927995
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33309G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45927995 | ||||||
| chr17:45928002
|
G | GA | 52 | a0001c0001t0001g0074a0001c0001t0001g0148a0001c0001t0001g0210others(49): Show | 52 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.-18+33341dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45928002 | |||||
| chr17:45928002
|
GA | G | 67 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(64): Show | 67 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-18+33341delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45928002 | |||||
| chr17:45928002
|
GAA | G | 22 | a0001c0001t0001g0236a0001c0001t0002g0031a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+33340_-18+3334 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45928002 | |||||
| chr17:45928002
|
GAAAAAAA others(4): Show |
G | 2 | a0001c0001t0001g0165a0002c0003t0001g0118 | 2 | HG02074.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-18+33331_-18+3334 others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45928002 | |||||
| chr17:45928040
|
C | T | 1 | a0002c0003t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-18+33354C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928040 | ||||||
| chr17:45928047
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33361A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928047 | ||||||
| chr17:45928111
|
C | G | 3 | a0001c0001t0002g0199a0001c0001t0002g0206a0002c0002t0003g0145 | 3 | HG04199.hp1 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-18+33425C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928111 | ||||||
| chr17:45928124
|
T | C | 2 | a0001c0001t0026g0192a0001c0010t0013g0129 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+33438T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928124 | ||||||
| chr17:45928249
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+33563A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928249 | ||||||
| chr17:45928368
|
C | A | 1 | a0005c0007t0003g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18+33682C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928368 | ||||||
| chr17:45928455
|
C | G | 119 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.-18+33769C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928455 | ||||||
| chr17:45928591
|
T | C | 1 | a0001c0001t0003g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-17-33730T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928591 | ||||||
| chr17:45928686
|
A | T | 7 | a0001c0001t0026g0192a0001c0010t0013g0129a0001c0010t0013g0208others(4): Show | 7 | HG01109.hp2 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-33635A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928686 | ||||||
| chr17:45928719
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-33602A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928719 | ||||||
| chr17:45928757
|
G | A | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-33564G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928757 | ||||||
| chr17:45928764
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-33557T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928764 | ||||||
| chr17:45928791
|
G | GTTCACAC others(22): Show |
1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-17-33529_-17-3350 others(33): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45928791 | |||||
| chr17:45928857
|
A | G | 169 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.-17-33464A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928857 | ||||||
| chr17:45928886
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-33435T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928886 | ||||||
| chr17:45928887
|
G | A | 1 | a0003c0004t0004g0001 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-17-33434G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45928887 | ||||||
| chr17:45929087
|
C | CT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-33226dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45929087 | |||||
| chr17:45929111
|
C | A | 1 | a0001c0001t0005g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-17-33210C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929111 | ||||||
| chr17:45929235
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-33086T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929235 | ||||||
| chr17:45929481
|
G | A | 1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-32840G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929481 | ||||||
| chr17:45929530
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-32791T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929530 | ||||||
| chr17:45929588
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-32733T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929588 | ||||||
| chr17:45929590
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-32731A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929590 | ||||||
| chr17:45929932
|
A | G | 3 | a0001c0001t0026g0192a0001c0010t0013g0129a0001c0010t0013g0208 | 3 | HG02895.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-17-32389A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929932 | ||||||
| chr17:45929945
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-17-32376T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45929945 | ||||||
| chr17:45930026
|
C | T | 1 | a0002c0003t0020g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-17-32295C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930026 | ||||||
| chr17:45930047
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-17-32274G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930047 | ||||||
| chr17:45930127
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-32194C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930127 | ||||||
| chr17:45930152
|
C | A | 1 | a0001c0001t0010g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-17-32169C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930152 | ||||||
| chr17:45930173
|
A | G | 2 | a0001c0001t0026g0192a0001c0010t0013g0129 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-17-32148A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930173 | ||||||
| chr17:45930184
|
G | A | 51 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0152others(48): Show | 51 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17-32137G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930184 | ||||||
| chr17:45930210
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17-32111G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930210 | ||||||
| chr17:45930264
|
G | A | 6 | a0001c0001t0001g0074a0002c0002t0017g0112a0002c0003t0001g0177others(3): Show | 6 | HG00738.hp1 HG01106.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-32057G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930264 | ||||||
| chr17:45930361
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-31960C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930361 | ||||||
| chr17:45930398
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-31923T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930398 | ||||||
| chr17:45930407
|
CAAAA | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-31900_-17-3189 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45930407 | |||||
| chr17:45930419
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-31902A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930419 | ||||||
| chr17:45930512
|
C | T | 1 | a0001c0001t0003g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-17-31809C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930512 | ||||||
| chr17:45930735
|
T | C | 119 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.-17-31586T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930735 | ||||||
| chr17:45930873
|
G | A | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-31448G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930873 | ||||||
| chr17:45930924
|
G | T | 1 | a0002c0003t0002g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-31397G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45930924 | ||||||
| chr17:45931068
|
G | A | 1 | a0002c0002t0003g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-17-31253G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45931068 | ||||||
| chr17:45931243
|
T | C | 3 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-31078T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45931243 | ||||||
| chr17:45931480
|
G | C | 1 | a0001c0001t0003g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-17-30841G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45931480 | ||||||
| chr17:45931595
|
C | T | 3 | a0001c0001t0026g0192a0001c0010t0013g0129a0015c0019t0005g0189 | 3 | HG02895.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-17-30726C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45931595 | ||||||
| chr17:45932005
|
C | T | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-30316C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932005 | ||||||
| chr17:45932090
|
G | GA | 23 | a0002c0002t0018g0091a0002c0003t0028g0090a0003c0004t0004g0001others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-30219dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45932090 | |||||
| chr17:45932090
|
GA | G | 40 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0152others(37): Show | 40 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-30219delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45932090 | |||||
| chr17:45932505
|
G | A | 1 | a0011c0012t0022g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-17-29816G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932505 | ||||||
| chr17:45932510
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29811C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932510 | ||||||
| chr17:45932555
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29766A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932555 | ||||||
| chr17:45932594
|
C | CA | 29 | a0001c0001t0001g0074a0001c0001t0001g0133a0001c0001t0001g0134others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-29706dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45932594 | |||||
| chr17:45932594
|
CA | C | 6 | a0001c0001t0002g0227a0001c0001t0003g0085a0001c0001t0003g0252others(3): Show | 6 | HG00438.hp1 HG00642.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-29706delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45932594 | |||||
| chr17:45932674
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29647A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932674 | ||||||
| chr17:45932752
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29569G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932752 | ||||||
| chr17:45932898
|
A | G | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-29423A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932898 | ||||||
| chr17:45932998
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29323C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45932998 | ||||||
| chr17:45933005
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0003g0028a0009c0011t0002g0030 | 3 | HG02486.hp1 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-29316C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933005 | ||||||
| chr17:45933039
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29282A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933039 | ||||||
| chr17:45933086
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29235C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933086 | ||||||
| chr17:45933097
|
A | AC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29224_-17-2922 others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933097 | ||||||
| chr17:45933112
|
G | A | 167 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-17-29209G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933112 | ||||||
| chr17:45933157
|
A | ATTGTGTT others(2): Show |
7 | a0001c0001t0002g0036a0001c0001t0002g0179a0001c0001t0003g0196others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-29160_-17-2915 others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933157 | |||||
| chr17:45933176
|
A | G | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-29145A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933176 | ||||||
| chr17:45933245
|
C | CTT | 119 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0148others(116): Show | 119 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-17-29063_-17-2906 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933245 | |||||
| chr17:45933245
|
C | CTTT | 20 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-29064_-17-2906 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933245 | |||||
| chr17:45933245
|
C | CTTTTT | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-29066_-17-2906 others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933245 | |||||
| chr17:45933295
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-29026A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933295 | ||||||
| chr17:45933618
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-28703G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933618 | ||||||
| chr17:45933630
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17-28691G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933630 | ||||||
| chr17:45933652
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-28669A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933652 | ||||||
| chr17:45933707
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-28614G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45933707 | ||||||
| chr17:45933840
|
A | AT | 157 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-17-28463dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933840 | |||||
| chr17:45933840
|
A | ATT | 38 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0226others(35): Show | 38 | HG00642.hp2 HG01243.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-28464_-17-2846 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933840 | |||||
| chr17:45933840
|
ATT | A | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-28464_-17-2846 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45933840 | |||||
| chr17:45934160
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-28161A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934160 | ||||||
| chr17:45934270
|
T | C | 1 | a0002c0002t0006g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-17-28051T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934270 | ||||||
| chr17:45934295
|
C | T | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-28026C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934295 | ||||||
| chr17:45934383
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27938A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934383 | ||||||
| chr17:45934459
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27862A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934459 | ||||||
| chr17:45934598
|
T | TA | 8 | a0001c0001t0002g0168a0001c0001t0026g0192a0001c0010t0013g0129others(5): Show | 8 | HG01109.hp2 HG02622.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-27722dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45934598 | |||||
| chr17:45934646
|
C | T | 1 | a0004c0005t0005g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-27675C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934646 | ||||||
| chr17:45934730
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27591A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934730 | ||||||
| chr17:45934882
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27439T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934882 | ||||||
| chr17:45934891
|
CG | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27429delG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934891 | ||||||
| chr17:45934894
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27427T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934894 | ||||||
| chr17:45934977
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-27344G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934977 | ||||||
| chr17:45934990
|
T | A | 1 | a0002c0002t0001g0100 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-17-27331T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45934990 | ||||||
| chr17:45935097
|
T | C | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-27224T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935097 | ||||||
| chr17:45935342
|
C | G | 2 | a0001c0001t0003g0028a0009c0011t0002g0030 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-17-26979C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935342 | ||||||
| chr17:45935549
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26772T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935549 | ||||||
| chr17:45935623
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26698C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935623 | ||||||
| chr17:45935637
|
A | C | 1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-17-26684A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935637 | ||||||
| chr17:45935658
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26663T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935658 | ||||||
| chr17:45935737
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26584G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935737 | ||||||
| chr17:45935823
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26498C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935823 | ||||||
| chr17:45935869
|
A | G | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-26452A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935869 | ||||||
| chr17:45935915
|
G | T | 14 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0166others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-26406G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935915 | ||||||
| chr17:45935980
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26341T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935980 | ||||||
| chr17:45935998
|
T | C | 1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-17-26323T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935998 | ||||||
| chr17:45935999
|
C | T | 1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-17-26322C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45935999 | ||||||
| chr17:45936081
|
C | G | 3 | a0001c0001t0002g0031a0001c0001t0007g0184a0002c0018t0002g0081 | 3 | HG01884.hp2 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-17-26240C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936081 | ||||||
| chr17:45936109
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26212G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936109 | ||||||
| chr17:45936117
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-26204A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936117 | ||||||
| chr17:45936243
|
C | T | 1 | a0009c0011t0002g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-17-26078C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936243 | ||||||
| chr17:45936572
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-25749A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936572 | ||||||
| chr17:45936598
|
T | TC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-25723_-17-2572 others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936598 | ||||||
| chr17:45936600
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-25721T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936600 | ||||||
| chr17:45936688
|
C | T | 1 | a0005c0007t0003g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-17-25633C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936688 | ||||||
| chr17:45936771
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-25550G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936771 | ||||||
| chr17:45936833
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-17-25488G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936833 | ||||||
| chr17:45936897
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-25424T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45936897 | ||||||
| chr17:45937013
|
T | C | 15 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0166others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-25308T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937013 | ||||||
| chr17:45937018
|
G | A | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-25303G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937018 | ||||||
| chr17:45937067
|
G | A | 3 | a0001c0001t0026g0192a0004c0005t0025g0121a0012c0016t0002g0111 | 3 | HG01071.hp2 HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-17-25254G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937067 | ||||||
| chr17:45937268
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-17-25053C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937268 | ||||||
| chr17:45937402
|
A | T | 1 | a0002c0003t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-17-24919A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937402 | ||||||
| chr17:45937599
|
GAA | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-24712_-17-2471 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45937599 | |||||
| chr17:45937615
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-24706G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937615 | ||||||
| chr17:45937616
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-24705G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937616 | ||||||
| chr17:45937731
|
T | C | 2 | a0002c0002t0001g0220a0002c0002t0003g0151 | 2 | HG00438.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-17-24590T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937731 | ||||||
| chr17:45937786
|
G | C | 19 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0166others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-24535G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937786 | ||||||
| chr17:45937934
|
A | C | 1 | a0002c0002t0021g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-17-24387A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937934 | ||||||
| chr17:45937964
|
G | A | 2 | a0002c0003t0020g0114a0006c0006t0002g0120 | 2 | HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-17-24357G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45937964 | ||||||
| chr17:45938080
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-24241A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938080 | ||||||
| chr17:45938098
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-24223A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938098 | ||||||
| chr17:45938258
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-24063G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938258 | ||||||
| chr17:45938379
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23942A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938379 | ||||||
| chr17:45938450
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23871A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938450 | ||||||
| chr17:45938544
|
C | T | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-23777C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938544 | ||||||
| chr17:45938563
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23758G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938563 | ||||||
| chr17:45938645
|
A | AT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23667dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45938645 | |||||
| chr17:45938791
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23530G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938791 | ||||||
| chr17:45938802
|
C | A | 1 | a0001c0001t0003g0232 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-17-23519C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938802 | ||||||
| chr17:45938810
|
A | AT | 19 | a0001c0001t0001g0164a0001c0001t0001g0221a0001c0001t0002g0036others(16): Show | 19 | HG00642.hp1 HG01175.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-23490dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45938810 | |||||
| chr17:45938810
|
A | ATT | 68 | a0001c0001t0001g0042a0001c0001t0001g0133a0001c0001t0001g0134others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17-23491_-17-2349 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45938810 | |||||
| chr17:45938810
|
A | ATTT | 13 | a0001c0001t0002g0031a0001c0001t0003g0083a0001c0001t0003g0144others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-23492_-17-2349 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45938810 | |||||
| chr17:45938810
|
AT | A | 18 | a0001c0001t0002g0024a0001c0001t0002g0159a0001c0001t0002g0161others(15): Show | 18 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-23490delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45938810 | |||||
| chr17:45938844
|
C | A | 14 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0166others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-23477C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938844 | ||||||
| chr17:45938970
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-17-23351C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938970 | ||||||
| chr17:45938971
|
G | A | 14 | a0001c0001t0002g0024a0001c0001t0002g0096a0001c0001t0002g0166others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-23350G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938971 | ||||||
| chr17:45938975
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23346G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938975 | ||||||
| chr17:45938978
|
T | A | 1 | a0001c0001t0008g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-23343T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45938978 | ||||||
| chr17:45939096
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23225A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939096 | ||||||
| chr17:45939193
|
A | C | 2 | a0002c0002t0002g0154a0002c0003t0002g0146 | 2 | NA18950.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-17-23128A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939193 | ||||||
| chr17:45939235
|
A | AG | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-23085dupG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45939235 | |||||
| chr17:45939738
|
G | A | 1 | a0002c0002t0003g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-17-22583G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939738 | ||||||
| chr17:45939758
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-22563G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939758 | ||||||
| chr17:45939793
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-22528C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939793 | ||||||
| chr17:45939814
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-22507T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939814 | ||||||
| chr17:45939853
|
G | A | 2 | a0001c0001t0003g0028a0009c0011t0002g0030 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-17-22468G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939853 | ||||||
| chr17:45939917
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-22404A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939917 | ||||||
| chr17:45939976
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-22345A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45939976 | ||||||
| chr17:45940087
|
G | A | 2 | a0001c0001t0002g0207a0001c0001t0007g0205 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-17-22234G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45940087 | ||||||
| chr17:45940300
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-22021C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45940300 | ||||||
| chr17:45940359
|
G | T | 17 | a0001c0001t0001g0165a0001c0001t0002g0066a0001c0001t0002g0067others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-21962G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45940359 | ||||||
| chr17:45940503
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-17-21818C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45940503 | ||||||
| chr17:45940504
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-21817G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45940504 | ||||||
| chr17:45940575
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-21746G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45940575 | ||||||
| chr17:45941033
|
A | G | 27 | a0001c0001t0002g0178a0002c0002t0002g0171a0003c0004t0004g0001others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-17-21288A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941033 | ||||||
| chr17:45941061
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-17-21260A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941061 | ||||||
| chr17:45941122
|
T | A | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-21199T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941122 | ||||||
| chr17:45941122
|
T | C | 25 | a0001c0001t0002g0125a0001c0001t0002g0207a0001c0001t0007g0205others(22): Show | 25 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-21199T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941122 | ||||||
| chr17:45941153
|
T | C | 43 | a0001c0001t0002g0053a0001c0001t0002g0078a0001c0001t0002g0159others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.-17-21168T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941153 | ||||||
| chr17:45941282
|
C | A | 7 | a0001c0001t0002g0159a0001c0001t0009g0034a0001c0001t0010g0052others(4): Show | 7 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-21039C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941282 | ||||||
| chr17:45941291
|
T | C | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-21030T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941291 | ||||||
| chr17:45941377
|
A | G | 3 | a0001c0001t0002g0125a0010c0020t0007g0117a0014c0013t0007g0040 | 3 | HG02258.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-17-20944A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941377 | ||||||
| chr17:45941398
|
G | A | 171 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0128others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.-17-20923G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941398 | ||||||
| chr17:45941440
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-20881A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941440 | ||||||
| chr17:45941589
|
C | CCCTTCCT others(145): Show |
1 | a0004c0005t0005g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-17-20705_-17-2070 others(156): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941589 | |||||
| chr17:45941589
|
C | CCCTTCCT others(121): Show |
4 | a0001c0001t0002g0024a0002c0003t0002g0023a0007c0008t0014g0026others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-20705_-17-2070 others(132): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941589 | |||||
| chr17:45941589
|
CCCTT | C | 6 | a0001c0001t0002g0027a0001c0001t0002g0162a0001c0001t0002g0227others(3): Show | 6 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-20717_-17-2071 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941589 | |||||
| chr17:45941600
|
T | TTCCTTCC others(9): Show |
2 | a0001c0001t0003g0122a0002c0003t0001g0182 | 2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-17-20720_-17-2070 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941600 | |||||
| chr17:45941604
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-17-20717T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941604 | ||||||
| chr17:45941612
|
CTCCCCCC others(1): Show |
C | 3 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-20704_-17-2069 others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941612 | |||||
| chr17:45941617
|
C | T | 234 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.-17-20704C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941617 | ||||||
| chr17:45941635
|
T | C | 3 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-20686T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941635 | ||||||
| chr17:45941641
|
T | TCCTTCCC others(9): Show |
1 | a0001c0001t0010g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-20665_-17-2065 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941641 | |||||
| chr17:45941641
|
T | TCCTTCCC others(25): Show |
1 | a0001c0001t0003g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-17-20666_-17-2066 others(36): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941641 | |||||
| chr17:45941648
|
C | CCCCTTCC others(9): Show |
1 | a0001c0001t0003g0202 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-17-20666_-17-2066 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941648 | |||||
| chr17:45941656
|
A | C | 9 | a0001c0001t0002g0036a0001c0001t0002g0168a0001c0001t0003g0105others(6): Show | 9 | HG01071.hp2 HG02293.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-20665A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941656 | ||||||
| chr17:45941664
|
C | A | 1 | a0012c0016t0002g0111 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-17-20657C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941664 | ||||||
| chr17:45941665
|
C | T | 1 | a0006c0006t0002g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-17-20656C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941665 | ||||||
| chr17:45941665
|
CCCTTCCC others(17): Show |
C | 1 | a0001c0001t0007g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-17-20649_-17-2062 others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941665 | |||||
| chr17:45941668
|
TTCCCCCC others(5): Show |
T | 1 | a0001c0001t0002g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-20649_-17-2063 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941668 | |||||
| chr17:45941672
|
C | A | 1 | a0002c0002t0001g0140 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-17-20649C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941672 | ||||||
| chr17:45941672
|
C | CTCCTTCC others(5): Show |
1 | a0009c0011t0002g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-17-20649_-17-2064 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941672 | ||||||
| chr17:45941672
|
C | T | 1 | a0006c0006t0002g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-17-20649C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941672 | ||||||
| chr17:45941672
|
CCCCTTCC others(33): Show |
C | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-20648_-17-2060 others(44): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941672 | ||||||
| chr17:45941673
|
C | CCCTTCCA others(25): Show |
1 | a0004c0005t0005g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-20642_-17-2064 others(36): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941673 | |||||
| chr17:45941673
|
C | CCCTTCCC others(9): Show |
29 | a0001c0001t0001g0128a0001c0001t0001g0210a0001c0001t0001g0216others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-20641_-17-2062 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941673 | |||||
| chr17:45941673
|
C | T | 2 | a0006c0006t0002g0186a0009c0011t0002g0030 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-17-20648C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941673 | ||||||
| chr17:45941680
|
C | CCCCTTCC others(49): Show |
2 | a0001c0001t0002g0168a0001c0001t0003g0105 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-20641_-17-2064 others(60): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941680 | ||||||
| chr17:45941680
|
C | CCCCTTCC others(5): Show |
1 | a0002c0002t0001g0140 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-17-20641_-17-2064 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941680 | ||||||
| chr17:45941680
|
C | CCCCTTCC others(41): Show |
1 | a0001c0001t0002g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-17-20641_-17-2064 others(52): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941680 | ||||||
| chr17:45941680
|
C | CCCCTTCC others(5): Show |
1 | a0001c0001t0005g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-17-20641_-17-2064 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941680 | ||||||
| chr17:45941680
|
C | CTCCT | 5 | a0001c0001t0001g0247a0001c0001t0002g0166a0001c0001t0003g0196others(2): Show | 5 | HG01071.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-20624_-17-2062 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941680
|
C | CTCCTTCC others(5): Show |
1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-17-20632_-17-2062 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941680
|
C | CTCCTTCC others(13): Show |
3 | a0002c0002t0001g0131a0002c0002t0001g0176a0002c0002t0003g0108 | 3 | HG00558.hp2 HG00621.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-17-20626_-17-2062 others(24): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941680
|
C | CTCCTTCC others(33): Show |
1 | a0002c0002t0001g0130 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(44): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941680
|
C | CTCCTTCC others(9): Show |
3 | a0001c0001t0002g0206a0001c0001t0027g0093a0010c0020t0007g0117 | 3 | HG02258.hp1 HG02615.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-17-20636_-17-2062 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941680
|
C | CTCCTTCC others(21): Show |
1 | a0001c0001t0001g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-20621_-17-2062 others(32): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941680
|
C | T | 2 | a0008c0009t0009g0107a0009c0011t0002g0030 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-17-20641C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941680 | ||||||
| chr17:45941680
|
CTCCTTCC others(29): Show |
C | 1 | a0002c0002t0002g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17-20620_-17-2058 others(40): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941680 | |||||
| chr17:45941681
|
T | C | 4 | a0001c0001t0003g0156a0002c0002t0002g0154a0002c0003t0001g0169others(1): Show | 4 | HG00621.hp1 HG01928.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-20640T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941681 | ||||||
| chr17:45941681
|
T | TCCTTCCT others(29): Show |
1 | a0001c0001t0002g0161 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(40): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941681 | |||||
| chr17:45941681
|
TCCTTCCT others(17): Show |
T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA18991.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-17-20620_-17-2059 others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941681 | |||||
| chr17:45941684
|
T | C | 2 | a0001c0001t0003g0197a0002c0002t0001g0140 | 2 | HG02004.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-17-20637T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941684 | ||||||
| chr17:45941684
|
T | TTCCCCCC others(5): Show |
1 | a0005c0007t0003g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-20634_-17-2063 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941684 | |||||
| chr17:45941685
|
T | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0168a0001c0001t0003g0105 | 3 | HG02622.hp1 HG03453.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-17-20636T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941685 | ||||||
| chr17:45941685
|
T | TCCTTCCT others(25): Show |
73 | a0001c0001t0001g0065a0001c0001t0001g0099a0001c0001t0001g0133others(70): Show | 73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-17-20626_-17-2062 others(36): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941685 | |||||
| chr17:45941685
|
T | TCCTTCCT others(41): Show |
3 | a0001c0001t0003g0232a0001c0001t0003g0238a0002c0002t0003g0062 | 3 | NA19011.hp1 NA19054.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-17-20626_-17-2062 others(52): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941685 | |||||
| chr17:45941685
|
T | TCCTTCCT others(57): Show |
10 | a0001c0001t0001g0187a0002c0002t0001g0100a0002c0002t0003g0086others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-20626_-17-2062 others(68): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941685 | |||||
| chr17:45941685
|
T | TCCTTCCT others(69): Show |
1 | a0006c0006t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(80): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941685 | |||||
| chr17:45941685
|
T | TCCTTCCT others(9): Show |
1 | a0002c0002t0003g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-17-20632_-17-2061 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941685 | |||||
| chr17:45941688
|
T | C | 1 | a0002c0003t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-20633T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941688 | ||||||
| chr17:45941688
|
T | TTCCTTCC others(25): Show |
1 | a0001c0001t0001g0074 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(36): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941688 | |||||
| chr17:45941689
|
T | C | 1 | a0002c0003t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-20632T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941689 | ||||||
| chr17:45941689
|
T | TCCTTCCC others(21): Show |
5 | a0001c0001t0001g0237a0001c0001t0001g0249a0002c0003t0002g0103others(2): Show | 5 | HG01106.hp1 HG01934.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-20626_-17-2062 others(32): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941689 | |||||
| chr17:45941689
|
TCCTTCCT others(9): Show |
T | 5 | a0001c0001t0002g0024a0001c0001t0008g0029a0004c0005t0005g0025others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-20620_-17-2060 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941689 | |||||
| chr17:45941692
|
T | C | 2 | a0002c0002t0002g0154a0002c0003t0002g0155 | 2 | HG01928.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-17-20629T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941692 | ||||||
| chr17:45941692
|
T | TTCCC | 2 | a0001c0001t0003g0144a0002c0003t0002g0146 | 2 | HG01928.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-17-20626_-17-2062 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941692 | |||||
| chr17:45941693
|
T | TCCCTCCT others(17): Show |
1 | a0002c0003t0001g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941693 | |||||
| chr17:45941693
|
T | TCCCTCCT others(33): Show |
1 | a0001c0001t0002g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(44): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941693 | |||||
| chr17:45941693
|
T | TCCCTCCT others(21): Show |
1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-17-20626_-17-2062 others(32): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941693 | |||||
| chr17:45941693
|
TCCTTCCT others(5): Show |
T | 2 | a0001c0001t0002g0199a0002c0002t0003g0048 | 2 | HG02132.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-17-20620_-17-2060 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941693 | |||||
| chr17:45941696
|
T | C | 25 | a0001c0001t0002g0043a0001c0001t0003g0122a0001c0001t0003g0156others(22): Show | 25 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-20625T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941696 | ||||||
| chr17:45941697
|
T | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0179 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-17-20624T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941697 | ||||||
| chr17:45941697
|
TCCTG | T | 17 | a0001c0001t0001g0042a0001c0001t0002g0142a0001c0001t0002g0193others(14): Show | 17 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-20616_-17-2061 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941697 | |||||
| chr17:45941697
|
TCCTGCCT others(1): Show |
T | 25 | a0001c0001t0001g0139a0001c0001t0002g0031a0001c0001t0003g0122others(22): Show | 25 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-20620_-17-2061 others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941697 | |||||
| chr17:45941701
|
G | GCCTTCCT others(5): Show |
5 | a0001c0001t0003g0248a0001c0001t0003g0253a0002c0002t0003g0094others(2): Show | 5 | HG01123.hp1 HG01358.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-20617_-17-2061 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941701 | |||||
| chr17:45941701
|
G | GCCTTCCT others(13): Show |
6 | a0001c0001t0009g0034a0001c0001t0010g0052a0002c0002t0008g0035others(3): Show | 6 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-20617_-17-2061 others(24): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941701 | |||||
| chr17:45941701
|
G | T | 38 | a0001c0001t0001g0152a0001c0001t0001g0181a0001c0001t0001g0221others(35): Show | 38 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-20620G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941701 | ||||||
| chr17:45941701
|
GCCTGCCT others(5): Show |
G | 6 | a0001c0001t0002g0027a0001c0001t0002g0207a0001c0001t0002g0227others(3): Show | 6 | HG00642.hp2 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-20616_-17-2060 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941701 | |||||
| chr17:45941701
|
GCCTGCCT others(9): Show |
G | 4 | a0001c0001t0010g0109a0004c0005t0001g0104a0004c0005t0005g0038others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-20616_-17-2060 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941701 | |||||
| chr17:45941705
|
G | T | 167 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-17-20616G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941705 | ||||||
| chr17:45941705
|
GCCTTCCT others(29): Show |
G | 1 | a0003c0004t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-17-20600_-17-2056 others(40): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941705 | |||||
| chr17:45941708
|
T | C | 1 | a0002c0002t0003g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-17-20613T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941708 | ||||||
| chr17:45941709
|
T | G | 4 | a0001c0001t0002g0224a0002c0003t0001g0177a0005c0007t0003g0203others(1): Show | 4 | HG00738.hp1 HG02622.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-20612T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941709 | ||||||
| chr17:45941713
|
T | G | 5 | a0001c0001t0002g0053a0001c0001t0003g0144a0002c0002t0002g0154others(2): Show | 5 | HG01928.hp1 HG01928.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-20608T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941713 | ||||||
| chr17:45941713
|
T | TCCTG | 3 | a0001c0001t0002g0228a0002c0002t0003g0145a0003c0004t0004g0001 | 3 | HG01099.hp2 HG04204.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-17-20605_-17-2060 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45941713 | |||||
| chr17:45941717
|
T | G | 112 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-17-20604T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941717 | ||||||
| chr17:45941721
|
T | G | 2 | a0001c0001t0001g0249a0002c0003t0001g0169 | 2 | HG00621.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-17-20600T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941721 | ||||||
| chr17:45941725
|
T | G | 20 | a0001c0001t0012g0143a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-20596T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941725 | ||||||
| chr17:45941729
|
T | G | 3 | a0001c0001t0003g0144a0002c0002t0003g0048a0002c0002t0003g0145 | 3 | HG01928.hp2 HG02132.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-17-20592T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941729 | ||||||
| chr17:45941737
|
T | G | 19 | a0003c0004t0004g0003a0003c0004t0004g0004a0003c0004t0004g0005others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-20584T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941737 | ||||||
| chr17:45941741
|
T | G | 22 | a0001c0001t0002g0168a0001c0001t0003g0105a0001c0001t0012g0143others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-20580T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941741 | ||||||
| chr17:45941833
|
A | T | 1 | a0003c0004t0004g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-17-20488A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941833 | ||||||
| chr17:45941889
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-20432T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45941889 | ||||||
| chr17:45942113
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-20208C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942113 | ||||||
| chr17:45942277
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-20044G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942277 | ||||||
| chr17:45942298
|
G | C | 1 | a0001c0001t0001g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-17-20023G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942298 | ||||||
| chr17:45942306
|
G | A | 4 | a0001c0001t0003g0248a0001c0001t0003g0253a0002c0003t0019g0044others(1): Show | 4 | HG01123.hp1 HG01358.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-20015G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942306 | ||||||
| chr17:45942314
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-20007T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942314 | ||||||
| chr17:45942346
|
G | A | 84 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0134others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-19975G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942346 | ||||||
| chr17:45942472
|
G | A | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-19849G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942472 | ||||||
| chr17:45942542
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-19779C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942542 | ||||||
| chr17:45942625
|
C | A | 1 | a0002c0003t0002g0146 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-17-19696C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942625 | ||||||
| chr17:45942916
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-19405G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942916 | ||||||
| chr17:45942948
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-19373C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942948 | ||||||
| chr17:45942981
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0003g0105 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-19340G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45942981 | ||||||
| chr17:45943179
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-19142A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943179 | ||||||
| chr17:45943412
|
C | T | 1 | a0002c0002t0003g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-17-18909C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943412 | ||||||
| chr17:45943491
|
A | G | 1 | a0006c0006t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-18830A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943491 | ||||||
| chr17:45943530
|
A | G | 7 | a0001c0001t0002g0053a0001c0001t0009g0034a0001c0001t0010g0052others(4): Show | 7 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-18791A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943530 | ||||||
| chr17:45943682
|
C | T | 1 | a0006c0006t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-18639C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943682 | ||||||
| chr17:45943695
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-18626C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943695 | ||||||
| chr17:45943767
|
T | C | 1 | a0002c0002t0003g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-17-18554T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943767 | ||||||
| chr17:45943800
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-17-18521G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943800 | ||||||
| chr17:45943852
|
C | T | 22 | a0001c0001t0008g0029a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-18469C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45943852 | ||||||
| chr17:45944097
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-18224T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944097 | ||||||
| chr17:45944333
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17988G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944333 | ||||||
| chr17:45944351
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17970G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944351 | ||||||
| chr17:45944364
|
C | T | 5 | a0002c0003t0002g0023a0004c0005t0005g0025a0007c0008t0014g0026others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-17957C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944364 | ||||||
| chr17:45944378
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17943T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944378 | ||||||
| chr17:45944460
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0003g0105 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-17861G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944460 | ||||||
| chr17:45944501
|
C | T | 2 | a0001c0001t0027g0093a0002c0002t0002g0171 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-17-17820C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944501 | ||||||
| chr17:45944594
|
G | A | 14 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-17727G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944594 | ||||||
| chr17:45944595
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-17726G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944595 | ||||||
| chr17:45944677
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17644A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944677 | ||||||
| chr17:45944702
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17619G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944702 | ||||||
| chr17:45944797
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-17-17524G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944797 | ||||||
| chr17:45944953
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17368G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45944953 | ||||||
| chr17:45945010
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17311C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945010 | ||||||
| chr17:45945067
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17254T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945067 | ||||||
| chr17:45945068
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17253G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945068 | ||||||
| chr17:45945162
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17159A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945162 | ||||||
| chr17:45945211
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17110A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945211 | ||||||
| chr17:45945227
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17094C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945227 | ||||||
| chr17:45945266
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-17055G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945266 | ||||||
| chr17:45945369
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-16952G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945369 | ||||||
| chr17:45945459
|
G | A | 1 | a0001c0001t0003g0157 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-17-16862G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945459 | ||||||
| chr17:45945528
|
A | C | 1 | a0002c0002t0003g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-17-16793A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945528 | ||||||
| chr17:45945721
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-16600G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945721 | ||||||
| chr17:45945768
|
G | A | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-16553G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945768 | ||||||
| chr17:45945812
|
CA | C | 245 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-17-16500delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45945812 | |||||
| chr17:45945931
|
A | G | 7 | a0001c0001t0010g0109a0001c0001t0026g0192a0001c0001t0027g0093others(4): Show | 7 | HG01109.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-16390A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945931 | ||||||
| chr17:45945983
|
T | G | 1 | a0015c0019t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-16338T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45945983 | ||||||
| chr17:45946152
|
G | C | 245 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-17-16169G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946152 | ||||||
| chr17:45946154
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-16167T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946154 | ||||||
| chr17:45946183
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-17-16138G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946183 | ||||||
| chr17:45946226
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0003g0105 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-16095G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946226 | ||||||
| chr17:45946400
|
G | A | 1 | a0002c0003t0002g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-17-15921G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946400 | ||||||
| chr17:45946462
|
C | CGTG | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-15854_-17-1585 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946462 | |||||
| chr17:45946476
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-15845G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946476 | ||||||
| chr17:45946500
|
G | A | 1 | a0003c0004t0015g0014 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-17-15821G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946500 | ||||||
| chr17:45946582
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-15739G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946582 | ||||||
| chr17:45946598
|
T | TA | 20 | a0001c0001t0001g0164a0001c0001t0001g0187a0001c0001t0002g0078others(17): Show | 20 | HG01106.hp2 HG01109.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-15705dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946598 | |||||
| chr17:45946598
|
T | TAA | 11 | a0001c0001t0002g0037a0001c0001t0002g0161a0001c0001t0002g0162others(8): Show | 11 | HG00558.hp2 HG00621.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-15706_-17-1570 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946598 | |||||
| chr17:45946615
|
A | AAAAAAAA others(19): Show |
1 | a0003c0004t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(30): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(16): Show |
4 | a0003c0004t0004g0003a0003c0004t0004g0009a0003c0004t0004g0010others(1): Show | 4 | HG01123.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(27): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(15): Show |
1 | a0003c0004t0004g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(17): Show |
1 | a0003c0004t0004g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(19): Show |
1 | a0003c0004t0004g0006 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(30): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(14): Show |
1 | a0003c0004t0011g0015 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(25): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(16): Show |
1 | a0003c0004t0004g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(27): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(18): Show |
2 | a0003c0004t0004g0005a0003c0004t0004g0011 | 2 | HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(20): Show |
1 | a0003c0004t0004g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(31): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(22): Show |
2 | a0003c0004t0004g0019a0003c0004t0016g0007 | 2 | HG00280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(33): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(24): Show |
1 | a0003c0004t0004g0004 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(35): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(5): Show |
2 | a0002c0003t0002g0023a0011c0012t0022g0022 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(15): Show |
1 | a0003c0004t0004g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0228a0004c0005t0005g0025 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(6): Show |
2 | a0007c0008t0014g0026a0009c0011t0002g0030 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(17): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(12): Show |
1 | a0003c0004t0004g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(23): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(18): Show |
1 | a0003c0004t0015g0014 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(20): Show |
2 | a0003c0004t0004g0001a0003c0004t0004g0013 | 2 | HG01099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(31): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAAAT others(4): Show |
4 | a0001c0001t0002g0096a0001c0001t0009g0034a0001c0001t0010g0052others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAATA others(3): Show |
3 | a0002c0002t0008g0035a0008c0009t0009g0032a0008c0009t0009g0033 | 3 | HG02976.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-17-15705_-17-1570 others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0007g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-15705_-17-1570 others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45946615 | |||||
| chr17:45946615
|
A | T | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-15706A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946615 | ||||||
| chr17:45946616
|
AT | A | 26 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG00544.hp2 HG00558.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17-15704delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946616 | ||||||
| chr17:45946616
|
ATAT | A | 5 | a0001c0001t0002g0178a0001c0001t0003g0144a0002c0002t0002g0154others(2): Show | 5 | HG01928.hp2 HG03195.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-15704_-17-1570 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946616 | ||||||
| chr17:45946617
|
T | A | 169 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-17-15704T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946617 | ||||||
| chr17:45946619
|
T | A | 178 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-17-15702T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946619 | ||||||
| chr17:45946621
|
T | A | 75 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0134others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.-17-15700T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946621 | ||||||
| chr17:45946623
|
T | A | 3 | a0001c0001t0023g0088a0002c0003t0001g0075a0002c0018t0002g0081 | 3 | HG02273.hp2 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-15698T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45946623 | ||||||
| chr17:45947133
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-15188A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947133 | ||||||
| chr17:45947186
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-15135C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947186 | ||||||
| chr17:45947196
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-15125G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947196 | ||||||
| chr17:45947294
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-15027G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947294 | ||||||
| chr17:45947383
|
C | CT | 5 | a0001c0001t0003g0156a0001c0001t0003g0243a0002c0002t0003g0064others(2): Show | 5 | HG01109.hp2 HG02074.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-14921dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45947383 | |||||
| chr17:45947383
|
C | T | 1 | a0002c0002t0001g0188 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-17-14938C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947383 | ||||||
| chr17:45947383
|
CTT | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14922_-17-1492 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45947383 | |||||
| chr17:45947471
|
A | C | 6 | a0001c0001t0003g0197a0001c0001t0003g0202a0002c0002t0001g0130others(3): Show | 6 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-14850A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947471 | ||||||
| chr17:45947499
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14822T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947499 | ||||||
| chr17:45947540
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14781A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947540 | ||||||
| chr17:45947667
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14654T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947667 | ||||||
| chr17:45947679
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14642C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947679 | ||||||
| chr17:45947907
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14414G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947907 | ||||||
| chr17:45947981
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14340T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45947981 | ||||||
| chr17:45947993
|
TTTG | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14319_-17-1431 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45947993 | |||||
| chr17:45948041
|
C | CT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14279dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45948041 | |||||
| chr17:45948226
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14095G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948226 | ||||||
| chr17:45948239
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-17-14082C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948239 | ||||||
| chr17:45948284
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14037T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948284 | ||||||
| chr17:45948312
|
G | GCT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-14006_-17-1400 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45948312 | |||||
| chr17:45948395
|
G | T | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-13926G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948395 | ||||||
| chr17:45948510
|
A | G | 1 | a0006c0006t0002g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-17-13811A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948510 | ||||||
| chr17:45948522
|
C | A | 188 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-17-13799C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948522 | ||||||
| chr17:45948646
|
A | G | 1 | a0006c0006t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-17-13675A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948646 | ||||||
| chr17:45948742
|
G | T | 17 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0096others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-13579G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948742 | ||||||
| chr17:45948782
|
T | C | 1 | a0002c0003t0002g0219 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-17-13539T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948782 | ||||||
| chr17:45948907
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-17-13414C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948907 | ||||||
| chr17:45948955
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-13366T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948955 | ||||||
| chr17:45948965
|
G | A | 4 | a0002c0002t0003g0064a0002c0002t0003g0094a0002c0002t0003g0251others(1): Show | 4 | HG02071.hp1 HG02074.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-13356G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45948965 | ||||||
| chr17:45949028
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-13293A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949028 | ||||||
| chr17:45949112
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-13209A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949112 | ||||||
| chr17:45949124
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-13197A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949124 | ||||||
| chr17:45949125
|
A | G | 1 | a0005c0007t0003g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-17-13196A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949125 | ||||||
| chr17:45949129
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-13192A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949129 | ||||||
| chr17:45949182
|
T | C | 224 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.-17-13139T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949182 | ||||||
| chr17:45949373
|
G | A | 82 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-17-12948G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949373 | ||||||
| chr17:45949724
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-12597C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949724 | ||||||
| chr17:45949950
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-12371G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45949950 | ||||||
| chr17:45950000
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-12321T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950000 | ||||||
| chr17:45950017
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-12304A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950017 | ||||||
| chr17:45950155
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-12166G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950155 | ||||||
| chr17:45950330
|
G | A | 21 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0096others(18): Show | 21 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-11991G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950330 | ||||||
| chr17:45950387
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-11934A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950387 | ||||||
| chr17:45950470
|
GC | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-11847delC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45950470 | |||||
| chr17:45950645
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-11676T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950645 | ||||||
| chr17:45950653
|
A | T | 2 | a0004c0005t0005g0038a0004c0005t0005g0039 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-11668A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950653 | ||||||
| chr17:45950679
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-11642G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950679 | ||||||
| chr17:45950817
|
T | C | 22 | a0002c0002t0006g0214a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-11504T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950817 | ||||||
| chr17:45950827
|
T | G | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-17-11494T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45950827 | ||||||
| chr17:45951103
|
CA | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-11217delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951103 | ||||||
| chr17:45951189
|
T | C | 4 | a0001c0001t0010g0109a0001c0001t0026g0192a0001c0001t0027g0093others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-11132T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951189 | ||||||
| chr17:45951341
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-10980G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951341 | ||||||
| chr17:45951430
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-10891T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951430 | ||||||
| chr17:45951460
|
C | T | 3 | a0004c0005t0001g0104a0004c0005t0005g0038a0004c0005t0005g0039 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-10861C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951460 | ||||||
| chr17:45951554
|
A | G | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-10767A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951554 | ||||||
| chr17:45951594
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-10727C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951594 | ||||||
| chr17:45951690
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-17-10631A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951690 | ||||||
| chr17:45951812
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-10509G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951812 | ||||||
| chr17:45951911
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-10410A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45951911 | ||||||
| chr17:45952050
|
T | G | 2 | a0001c0001t0003g0248a0002c0003t0019g0044 | 2 | HG01358.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-17-10271T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952050 | ||||||
| chr17:45952144
|
TGATG | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-10176_-17-1017 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952144 | ||||||
| chr17:45952723
|
G | T | 1 | a0001c0001t0003g0232 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-17-9598G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952723 | ||||||
| chr17:45952749
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-9572C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952749 | ||||||
| chr17:45952770
|
A | G | 4 | a0002c0002t0003g0213a0002c0002t0003g0244a0002c0002t0006g0214others(1): Show | 4 | HG00099.hp1 HG01192.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-9551A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952770 | ||||||
| chr17:45952829
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-9492A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952829 | ||||||
| chr17:45952865
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-9456T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952865 | ||||||
| chr17:45952897
|
A | AC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-9424_-17-9423i others(3): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952897 | ||||||
| chr17:45952945
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-9376T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45952945 | ||||||
| chr17:45953003
|
T | TATGATG | 161 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.-17-9292_-17-9287d others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45953003 | |||||
| chr17:45953003
|
T | TATGATGA others(2): Show |
56 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0139others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.-17-9295_-17-9287d others(11): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45953003 | |||||
| chr17:45953003
|
T | TATGATGA others(5): Show |
1 | a0001c0001t0003g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-17-9298_-17-9287d others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45953003 | |||||
| chr17:45953003
|
TATG | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0227a0001c0001t0003g0252 | 3 | HG00642.hp2 HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-9289_-17-9287d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45953003 | |||||
| chr17:45953407
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-8914A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45953407 | ||||||
| chr17:45953589
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-8732T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45953589 | ||||||
| chr17:45953734
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-8587A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45953734 | ||||||
| chr17:45954019
|
C | T | 37 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0148others(34): Show | 37 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.-17-8302C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954019 | ||||||
| chr17:45954054
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-8267G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954054 | ||||||
| chr17:45954098
|
G | T | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-8223G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954098 | ||||||
| chr17:45954136
|
T | C | 4 | a0001c0001t0002g0178a0001c0001t0008g0029a0001c0010t0013g0129others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8185T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954136 | ||||||
| chr17:45954174
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-8147G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954174 | ||||||
| chr17:45954230
|
A | G | 48 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0139others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-17-8091A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954230 | ||||||
| chr17:45954270
|
G | A | 17 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0096others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-8051G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954270 | ||||||
| chr17:45954328
|
G | A | 21 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0096others(18): Show | 21 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-7993G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954328 | ||||||
| chr17:45954378
|
T | C | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-7943T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954378 | ||||||
| chr17:45954479
|
C | G | 2 | a0001c0001t0002g0168a0001c0001t0003g0105 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-7842C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954479 | ||||||
| chr17:45954580
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-7741A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954580 | ||||||
| chr17:45954707
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-7614A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954707 | ||||||
| chr17:45954834
|
A | G | 2 | a0001c0001t0002g0168a0001c0001t0003g0105 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-7487A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954834 | ||||||
| chr17:45954963
|
C | T | 1 | a0001c0015t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-17-7358C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45954963 | ||||||
| chr17:45955008
|
CAAAAAA | C | 5 | a0001c0001t0010g0109a0001c0001t0026g0192a0001c0001t0027g0093others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-7309_-17-7304d others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45955008 | |||||
| chr17:45955014
|
A | C | 1 | a0007c0008t0014g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-7307A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955014 | ||||||
| chr17:45955104
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-7217C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955104 | ||||||
| chr17:45955230
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-17-7091C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955230 | ||||||
| chr17:45955231
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-7090G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955231 | ||||||
| chr17:45955402
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6919T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955402 | ||||||
| chr17:45955423
|
T | A | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-6898T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955423 | ||||||
| chr17:45955475
|
G | A | 2 | a0001c0001t0002g0079a0004c0005t0007g0077 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-6846G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955475 | ||||||
| chr17:45955513
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6808A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955513 | ||||||
| chr17:45955549
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6772T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955549 | ||||||
| chr17:45955590
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6731G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955590 | ||||||
| chr17:45955636
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6685T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955636 | ||||||
| chr17:45955731
|
T | TTTTTTTT others(4): Show |
21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6584_-17-6574d others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45955731 | |||||
| chr17:45955766
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6555C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955766 | ||||||
| chr17:45955803
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6518T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955803 | ||||||
| chr17:45955822
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6499G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45955822 | ||||||
| chr17:45956028
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6293G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956028 | ||||||
| chr17:45956035
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6286C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956035 | ||||||
| chr17:45956066
|
C | T | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-6255C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956066 | ||||||
| chr17:45956102
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6219G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956102 | ||||||
| chr17:45956122
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-6199C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956122 | ||||||
| chr17:45956334
|
C | A | 1 | a0003c0004t0004g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-5987C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956334 | ||||||
| chr17:45956436
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5885T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956436 | ||||||
| chr17:45956548
|
TTATATAT others(9): Show |
T | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-5735_-17-5720d others(18): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-17-5737_-17-5720d others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-5739_-17-5720d others(22): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(15): Show |
T | 4 | a0001c0001t0003g0105a0002c0002t0017g0112a0002c0018t0002g0081others(1): Show | 4 | HG03139.hp1 HG03453.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-5741_-17-5720d others(24): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(17): Show |
T | 9 | a0001c0001t0002g0071a0001c0001t0002g0096a0001c0001t0002g0116others(6): Show | 9 | HG00733.hp1 HG01258.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-5743_-17-5720d others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(19): Show |
T | 26 | a0001c0001t0002g0031a0001c0001t0002g0046a0001c0001t0002g0047others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17-5745_-17-5720d others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(21): Show |
T | 140 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0099others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-17-5747_-17-5720d others(30): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(25): Show |
T | 19 | a0003c0004t0004g0003a0003c0004t0004g0004a0003c0004t0004g0005others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-5751_-17-5720d others(34): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956548
|
TTATATAT others(27): Show |
T | 2 | a0003c0004t0004g0001a0003c0004t0004g0018 | 2 | HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-17-5753_-17-5720d others(36): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956548 | |||||
| chr17:45956565
|
TATATATA others(20): Show |
T | 1 | a0002c0002t0003g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-17-5755_-17-5729d others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956565 | ||||||
| chr17:45956565
|
TATATATA others(22): Show |
T | 20 | a0001c0001t0001g0074a0001c0001t0001g0148a0001c0001t0001g0165others(17): Show | 20 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-5755_-17-5727d others(31): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956565 | ||||||
| chr17:45956567
|
TATATATA others(20): Show |
T | 5 | a0001c0001t0002g0037a0001c0001t0009g0034a0001c0001t0010g0052others(2): Show | 5 | HG02818.hp1 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5753_-17-5727d others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956567 | ||||||
| chr17:45956567
|
TATATATA others(22): Show |
T | 2 | a0001c0001t0001g0249a0002c0003t0019g0044 | 2 | HG01934.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-17-5753_-17-5725d others(31): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956567 | ||||||
| chr17:45956569
|
TATATATA others(20): Show |
T | 4 | a0001c0001t0002g0142a0002c0002t0001g0045a0008c0009t0009g0032others(1): Show | 4 | HG01070.hp1 HG01070.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-5751_-17-5725d others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956569 | ||||||
| chr17:45956573
|
TATATATA others(20): Show |
T | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-17-5747_-17-5721d others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956573 | ||||||
| chr17:45956578
|
ATATATAT others(17): Show |
A | 2 | a0002c0002t0002g0154a0004c0005t0005g0124 | 2 | NA18522.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-17-5741_-17-5718d others(26): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956578 | |||||
| chr17:45956582
|
ATATATAT others(13): Show |
A | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-5737_-17-5718d others(22): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956582 | |||||
| chr17:45956592
|
A | T | 1 | a0001c0001t0006g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-17-5729A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956592 | ||||||
| chr17:45956592
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0010g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-17-5727_-17-5718d others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956592 | |||||
| chr17:45956594
|
A | T | 14 | a0001c0001t0001g0065a0001c0001t0001g0153a0001c0001t0001g0164others(11): Show | 14 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-5727A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956594 | ||||||
| chr17:45956596
|
A | T | 78 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0139others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-5725A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956596 | ||||||
| chr17:45956598
|
A | T | 113 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-17-5723A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956598 | ||||||
| chr17:45956598
|
ATATT | A | 3 | a0001c0001t0026g0192a0001c0001t0027g0093a0004c0005t0005g0190 | 3 | HG02615.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-17-5721_-17-5718d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45956598 | |||||
| chr17:45956600
|
A | T | 143 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-17-5721A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956600 | ||||||
| chr17:45956604
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5717T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956604 | ||||||
| chr17:45956697
|
T | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0128 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.-17-5624T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956697 | ||||||
| chr17:45956726
|
C | T | 2 | a0004c0005t0025g0121a0012c0016t0002g0111 | 2 | HG01071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-17-5595C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956726 | ||||||
| chr17:45956828
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5493C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956828 | ||||||
| chr17:45956843
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5478T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956843 | ||||||
| chr17:45956866
|
C | T | 2 | a0001c0001t0010g0106a0007c0008t0014g0191 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-5455C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956866 | ||||||
| chr17:45956925
|
A | T | 7 | a0001c0001t0002g0053a0001c0001t0009g0034a0001c0001t0010g0052others(4): Show | 7 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-5396A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956925 | ||||||
| chr17:45956974
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5347C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956974 | ||||||
| chr17:45956975
|
A | C | 2 | a0001c0001t0002g0162a0001c0001t0005g0160 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-17-5346A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45956975 | ||||||
| chr17:45957120
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5201A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957120 | ||||||
| chr17:45957209
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5112T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957209 | ||||||
| chr17:45957307
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-5014T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957307 | ||||||
| chr17:45957370
|
G | A | 239 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-17-4951G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957370 | ||||||
| chr17:45957419
|
A | G | 17 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0096others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4902A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957419 | ||||||
| chr17:45957467
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4854G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957467 | ||||||
| chr17:45957493
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4828A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957493 | ||||||
| chr17:45957612
|
C | T | 2 | a0001c0001t0003g0197a0001c0001t0003g0202 | 2 | HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-17-4709C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957612 | ||||||
| chr17:45957653
|
G | A | 1 | a0004c0005t0005g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-4668G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957653 | ||||||
| chr17:45957856
|
GAA | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4455_-17-4454d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45957856 | |||||
| chr17:45957857
|
A | G | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-4464A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957857 | ||||||
| chr17:45957867
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4454A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957867 | ||||||
| chr17:45957906
|
T | C | 1 | a0004c0005t0005g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-4415T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957906 | ||||||
| chr17:45957912
|
A | C | 2 | a0001c0001t0010g0109a0001c0001t0026g0192 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-4409A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45957912 | ||||||
| chr17:45958001
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4320A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958001 | ||||||
| chr17:45958051
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-17-4270T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958051 | ||||||
| chr17:45958150
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-4171G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958150 | ||||||
| chr17:45958271
|
A | G | 1 | a0002c0002t0003g0225 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-17-4050A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958271 | ||||||
| chr17:45958340
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-3981A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958340 | ||||||
| chr17:45958494
|
C | T | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-3827C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958494 | ||||||
| chr17:45958546
|
C | T | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-17-3775C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958546 | ||||||
| chr17:45958681
|
G | A | 23 | a0001c0001t0027g0093a0002c0002t0002g0171a0003c0004t0004g0001others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-3640G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958681 | ||||||
| chr17:45958721
|
AAAAG | A | 19 | a0003c0004t0004g0001a0003c0004t0004g0004a0003c0004t0004g0005others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-3596_-17-3593d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45958721 | |||||
| chr17:45958725
|
G | GA | 8 | a0001c0001t0002g0053a0001c0001t0009g0034a0001c0001t0010g0052others(5): Show | 8 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-3581dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45958725 | |||||
| chr17:45958725
|
GA | G | 7 | a0001c0001t0001g0245a0001c0001t0002g0043a0001c0001t0002g0050others(4): Show | 7 | HG01515.hp1 HG02273.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-3581delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45958725 | |||||
| chr17:45958741
|
G | A | 2 | a0003c0004t0004g0003a0003c0004t0011g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-17-3580G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958741 | ||||||
| chr17:45958763
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-3558C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958763 | ||||||
| chr17:45958891
|
C | G | 1 | a0002c0002t0001g0220 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-17-3430C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958891 | ||||||
| chr17:45958916
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-17-3405C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958916 | ||||||
| chr17:45958921
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-3400A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45958921 | ||||||
| chr17:45959021
|
C | T | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-17-3300C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959021 | ||||||
| chr17:45959042
|
T | G | 31 | a0001c0001t0002g0178a0001c0001t0008g0029a0001c0001t0010g0109others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-3279T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959042 | ||||||
| chr17:45959096
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-3225T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959096 | ||||||
| chr17:45959421
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2900T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959421 | ||||||
| chr17:45959548
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2773C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959548 | ||||||
| chr17:45959570
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2751G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959570 | ||||||
| chr17:45959713
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2608G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959713 | ||||||
| chr17:45959740
|
C | CA | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2580dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45959740 | |||||
| chr17:45959933
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2388G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959933 | ||||||
| chr17:45959971
|
A | C | 1 | a0001c0001t0003g0157 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-17-2350A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959971 | ||||||
| chr17:45959977
|
C | T | 1 | a0001c0015t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-17-2344C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45959977 | ||||||
| chr17:45960125
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-2196A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45960125 | ||||||
| chr17:45960524
|
G | A | 1 | a0002c0002t0003g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-17-1797G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45960524 | ||||||
| chr17:45960778
|
C | T | 35 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0139others(32): Show | 35 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17-1543C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45960778 | ||||||
| chr17:45960841
|
CA | C | 20 | a0001c0001t0002g0193a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-1463delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45960841 | |||||
| chr17:45960841
|
CAA | C | 124 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-17-1464_-17-1463d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45960841 | |||||
| chr17:45960841
|
CAAA | C | 84 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0138others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17-1465_-17-1463d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45960841 | |||||
| chr17:45960873
|
A | C | 2 | a0004c0005t0005g0190a0008c0009t0009g0033 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-17-1448A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45960873 | ||||||
| chr17:45960929
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-17-1392G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45960929 | ||||||
| chr17:45961016
|
A | G | 2 | a0001c0001t0003g0083a0002c0002t0001g0158 | 2 | HG00597.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-17-1305A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961016 | ||||||
| chr17:45961158
|
G | A | 1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-1163G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961158 | ||||||
| chr17:45961170
|
CA | C | 20 | a0003c0004t0004g0003a0003c0004t0004g0004a0003c0004t0004g0005others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-1139delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45961170 | |||||
| chr17:45961411
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-17-910G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961411 | ||||||
| chr17:45961419
|
A | G | 23 | a0001c0001t0007g0184a0001c0001t0027g0093a0003c0004t0004g0003others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-902A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961419 | ||||||
| chr17:45961642
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-679G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961642 | ||||||
| chr17:45961677
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-644G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961677 | ||||||
| chr17:45961775
|
G | A | 1 | a0002c0002t0021g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-17-546G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961775 | ||||||
| chr17:45961775
|
G | GT | 33 | a0001c0001t0001g0148a0001c0001t0002g0067a0001c0001t0002g0078others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-533dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 45961775 | |||||
| chr17:45961780
|
T | G | 2 | a0001c0001t0001g0247a0002c0002t0003g0173 | 2 | HG03688.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-17-541T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961780 | ||||||
| chr17:45961785
|
T | G | 1 | a0001c0001t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-17-536T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961785 | ||||||
| chr17:45961786
|
T | G | 1 | a0001c0001t0002g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-17-535T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961786 | ||||||
| chr17:45961959
|
G | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0153a0001c0001t0001g0164others(3): Show | 6 | HG00597.hp2 HG03942.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-362G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961959 | ||||||
| chr17:45961999
|
C | T | 84 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0002g0046others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17-322C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45961999 | ||||||
| chr17:45962044
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-277A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45962044 | ||||||
| chr17:45962150
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-171G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45962150 | ||||||
| chr17:45962250
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-17-71C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45962250 | ||||||
| chr17:45962292
|
G | A | 1 | a0002c0002t0003g0244 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-17-29G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | chr17 | 45962292 | ||||||
| chr17:45962654
|
G | A | 1 | a0002c0002t0003g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.133+184G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45962654 | ||||||
| chr17:45962754
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+284C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45962754 | ||||||
| chr17:45962818
|
A | G | 54 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0133others(51): Show | 54 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.133+348A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45962818 | ||||||
| chr17:45962922
|
C | CA | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+462dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45962922 | |||||
| chr17:45963031
|
G | A | 1 | a0002c0002t0006g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.133+561G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963031 | ||||||
| chr17:45963037
|
T | C | 1 | a0003c0004t0016g0007 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.133+567T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963037 | ||||||
| chr17:45963155
|
C | A | 9 | a0001c0001t0002g0024a0001c0001t0002g0037a0001c0001t0002g0079others(6): Show | 9 | HG01167.hp1 HG02257.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.133+685C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963155 | ||||||
| chr17:45963260
|
C | T | 52 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0152others(49): Show | 52 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.133+790C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963260 | ||||||
| chr17:45963361
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.133+891A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963361 | ||||||
| chr17:45963454
|
C | T | 2 | a0001c0001t0002g0125a0011c0012t0022g0022 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.133+984C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963454 | ||||||
| chr17:45963457
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+987C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963457 | ||||||
| chr17:45963506
|
G | T | 1 | a0001c0001t0003g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.133+1036G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963506 | ||||||
| chr17:45963519
|
G | C | 1 | a0002c0002t0003g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.133+1049G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963519 | ||||||
| chr17:45963582
|
T | A | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.133+1112T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963582 | ||||||
| chr17:45963735
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+1265T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963735 | ||||||
| chr17:45963741
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+1271G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963741 | ||||||
| chr17:45963797
|
C | G | 1 | a0001c0001t0003g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.133+1327C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963797 | ||||||
| chr17:45963828
|
G | C | 1 | a0001c0001t0003g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.133+1358G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45963828 | ||||||
| chr17:45964187
|
C | CTTTGT | 3 | a0001c0001t0002g0031a0001c0001t0002g0178a0012c0016t0002g0111 | 3 | HG01071.hp2 HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.133+1726_133+1730d others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45964187 | |||||
| chr17:45964187
|
C | CTTTGTTT others(3): Show |
1 | a0001c0001t0008g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+1721_133+1730d others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45964187 | |||||
| chr17:45964196
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+1726G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964196 | ||||||
| chr17:45964201
|
T | G | 11 | a0001c0001t0002g0031a0001c0001t0002g0178a0001c0001t0008g0029others(8): Show | 11 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+1731T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964201 | ||||||
| chr17:45964396
|
G | A | 1 | a0001c0015t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.133+1926G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964396 | ||||||
| chr17:45964405
|
C | T | 73 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0187others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.133+1935C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964405 | ||||||
| chr17:45964451
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+1981A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964451 | ||||||
| chr17:45964621
|
T | C | 13 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.133+2151T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964621 | ||||||
| chr17:45964626
|
G | T | 13 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.133+2156G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964626 | ||||||
| chr17:45964627
|
T | A | 3 | a0001c0001t0002g0193a0001c0001t0007g0184a0001c0001t0027g0093 | 3 | HG01167.hp1 HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.133+2157T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964627 | ||||||
| chr17:45964662
|
C | T | 1 | a0002c0002t0003g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.133+2192C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964662 | ||||||
| chr17:45964855
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+2385A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964855 | ||||||
| chr17:45964995
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+2525T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45964995 | ||||||
| chr17:45965000
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+2530G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965000 | ||||||
| chr17:45965154
|
G | A | 1 | a0002c0002t0003g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.133+2684G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965154 | ||||||
| chr17:45965159
|
C | T | 4 | a0001c0001t0002g0031a0001c0001t0002g0178a0001c0001t0008g0029others(1): Show | 4 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+2689C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965159 | ||||||
| chr17:45965227
|
C | T | 4 | a0002c0002t0003g0041a0004c0005t0002g0180a0004c0005t0005g0195others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+2757C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965227 | ||||||
| chr17:45965416
|
T | C | 199 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.133+2946T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965416 | ||||||
| chr17:45965417
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+2947G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965417 | ||||||
| chr17:45965502
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3032G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965502 | ||||||
| chr17:45965549
|
A | G | 4 | a0001c0001t0002g0031a0001c0001t0002g0178a0001c0001t0008g0029others(1): Show | 4 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+3079A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965549 | ||||||
| chr17:45965573
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3103G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965573 | ||||||
| chr17:45965576
|
T | C | 199 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.133+3106T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965576 | ||||||
| chr17:45965585
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3115C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965585 | ||||||
| chr17:45965726
|
CA | C | 126 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(123): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.133+3269delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45965726 | |||||
| chr17:45965726
|
CAA | C | 21 | a0001c0001t0003g0233a0003c0004t0004g0001a0003c0004t0004g0003others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3268_133+3269d others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45965726 | |||||
| chr17:45965899
|
C | T | 1 | a0002c0002t0006g0214 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.133+3429C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965899 | ||||||
| chr17:45965936
|
G | A | 1 | a0002c0002t0003g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.133+3466G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45965936 | ||||||
| chr17:45966012
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3542T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966012 | ||||||
| chr17:45966270
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3800C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966270 | ||||||
| chr17:45966288
|
T | C | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.133+3818T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966288 | ||||||
| chr17:45966351
|
G | C | 12 | a0001c0001t0002g0027a0001c0001t0002g0161a0001c0001t0002g0162others(9): Show | 12 | HG00642.hp2 HG01081.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.133+3881G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966351 | ||||||
| chr17:45966404
|
A | G | 1 | a0002c0003t0001g0182 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.133+3934A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966404 | ||||||
| chr17:45966453
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3983G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966453 | ||||||
| chr17:45966483
|
C | T | 7 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0003g0082others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+4013C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966483 | ||||||
| chr17:45966692
|
C | A | 4 | a0002c0002t0003g0213a0002c0002t0003g0244a0002c0002t0006g0214others(1): Show | 4 | HG00099.hp1 HG01192.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+4222C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966692 | ||||||
| chr17:45966791
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+4321G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966791 | ||||||
| chr17:45966793
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.133+4323A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966793 | ||||||
| chr17:45966854
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+4384A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45966854 | ||||||
| chr17:45967065
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+4595C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967065 | ||||||
| chr17:45967084
|
C | G | 1 | a0001c0001t0008g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+4614C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967084 | ||||||
| chr17:45967132
|
A | G | 3 | a0001c0010t0013g0129a0001c0010t0013g0208a0014c0013t0007g0040 | 3 | HG02965.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.133+4662A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967132 | ||||||
| chr17:45967142
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+4672A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967142 | ||||||
| chr17:45967362
|
A | C | 1 | a0002c0002t0006g0070 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.134-4497A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967362 | ||||||
| chr17:45967457
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-4402T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967457 | ||||||
| chr17:45967463
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.134-4396T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967463 | ||||||
| chr17:45967468
|
A | C | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.134-4391A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967468 | ||||||
| chr17:45967574
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-4285T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967574 | ||||||
| chr17:45967619
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-4240A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967619 | ||||||
| chr17:45967728
|
G | A | 11 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-4131G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45967728 | ||||||
| chr17:45968064
|
T | C | 7 | a0001c0001t0009g0034a0001c0001t0010g0052a0001c0001t0010g0106others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-3795T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968064 | ||||||
| chr17:45968096
|
G | A | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.134-3763G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968096 | ||||||
| chr17:45968108
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-3751A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968108 | ||||||
| chr17:45968208
|
AC | A | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.134-3650delC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968208 | ||||||
| chr17:45968209
|
C | CA | 18 | a0001c0001t0001g0136a0001c0001t0002g0024a0001c0001t0002g0036others(15): Show | 18 | HG01167.hp1 HG01243.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.134-3641dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45968209 | |||||
| chr17:45968219
|
C | A | 22 | a0002c0002t0021g0069a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.134-3640C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968219 | ||||||
| chr17:45968237
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.134-3622G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968237 | ||||||
| chr17:45968608
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-3251C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968608 | ||||||
| chr17:45968694
|
C | T | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.134-3165C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968694 | ||||||
| chr17:45968826
|
T | C | 12 | a0001c0001t0002g0027a0001c0001t0002g0161a0001c0001t0002g0162others(9): Show | 12 | HG00642.hp2 HG01081.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.134-3033T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968826 | ||||||
| chr17:45968836
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-3023C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968836 | ||||||
| chr17:45968946
|
G | T | 2 | a0009c0011t0002g0030a0009c0011t0008g0097 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.134-2913G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45968946 | ||||||
| chr17:45969322
|
T | C | 7 | a0001c0001t0009g0034a0001c0001t0010g0052a0001c0001t0010g0106others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-2537T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45969322 | ||||||
| chr17:45969408
|
C | G | 1 | a0001c0001t0002g0228 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.134-2451C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45969408 | ||||||
| chr17:45969502
|
ACATCCAA others(96): Show |
A | 22 | a0001c0001t0003g0085a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.134-2241_134-2139d others(2): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45969502 | |||||
| chr17:45969600
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.134-2259A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45969600 | ||||||
| chr17:45969671
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-2188T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45969671 | ||||||
| chr17:45969744
|
A | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0152others(7): Show | 10 | HG00544.hp2 HG02300.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-2115A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45969744 | ||||||
| chr17:45969850
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-2009T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45969850 | ||||||
| chr17:45970083
|
C | CCCAT | 16 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0036others(13): Show | 16 | HG01071.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-1747_134-1744d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45970083 | |||||
| chr17:45970083
|
CCCAT | C | 22 | a0002c0003t0002g0146a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.134-1747_134-1744d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45970083 | |||||
| chr17:45970243
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-1616C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970243 | ||||||
| chr17:45970436
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-1423A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970436 | ||||||
| chr17:45970660
|
G | A | 9 | a0001c0001t0002g0043a0001c0001t0002g0224a0004c0005t0005g0025others(6): Show | 9 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-1199G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970660 | ||||||
| chr17:45970672
|
T | G | 16 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-1187T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970672 | ||||||
| chr17:45970770
|
G | C | 4 | a0001c0001t0002g0031a0001c0001t0002g0178a0001c0001t0008g0029others(1): Show | 4 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-1089G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970770 | ||||||
| chr17:45970847
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.134-1012G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970847 | ||||||
| chr17:45970881
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.134-978C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970881 | ||||||
| chr17:45970957
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-902G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970957 | ||||||
| chr17:45970970
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-889T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970970 | ||||||
| chr17:45970984
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-875T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45970984 | ||||||
| chr17:45971077
|
A | G | 1 | a0004c0005t0005g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.134-782A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971077 | ||||||
| chr17:45971136
|
G | A | 4 | a0001c0001t0002g0031a0001c0001t0002g0178a0001c0001t0008g0029others(1): Show | 4 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-723G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971136 | ||||||
| chr17:45971136
|
GA | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-722delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971136 | ||||||
| chr17:45971362
|
C | A | 1 | a0002c0002t0003g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.134-497C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971362 | ||||||
| chr17:45971570
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-289C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971570 | ||||||
| chr17:45971571
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-288T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971571 | ||||||
| chr17:45971573
|
AG | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-284delG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 45971573 | |||||
| chr17:45971575
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-284G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971575 | ||||||
| chr17:45971577
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-282G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971577 | ||||||
| chr17:45971731
|
G | A | 1 | a0002c0002t0003g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.134-128G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971731 | ||||||
| chr17:45971767
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-92T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 2/12 | chr17 | 45971767 | ||||||
| chr17:45971963
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+18C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45971963 | ||||||
| chr17:45972101
|
C | T | 1 | a0002c0003t0001g0075 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.220+156C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972101 | ||||||
| chr17:45972184
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+239G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972184 | ||||||
| chr17:45972199
|
A | G | 1 | a0002c0003t0002g0200 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.220+254A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972199 | ||||||
| chr17:45972277
|
T | C | 1 | a0002c0003t0024g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.220+332T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972277 | ||||||
| chr17:45972301
|
G | A | 1 | a0002c0002t0002g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.220+356G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972301 | ||||||
| chr17:45972393
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.220+448G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972393 | ||||||
| chr17:45972501
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+556A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972501 | ||||||
| chr17:45972534
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+589A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972534 | ||||||
| chr17:45972560
|
A | G | 4 | a0001c0001t0002g0031a0001c0001t0002g0178a0001c0001t0008g0029others(1): Show | 4 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+615A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972560 | ||||||
| chr17:45972916
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+971G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972916 | ||||||
| chr17:45972955
|
A | G | 4 | a0007c0008t0003g0185a0007c0008t0014g0026a0007c0008t0014g0191others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+1010A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972955 | ||||||
| chr17:45972974
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+1029G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972974 | ||||||
| chr17:45972976
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.220+1031G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45972976 | ||||||
| chr17:45973029
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+1084C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973029 | ||||||
| chr17:45973097
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+1152T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973097 | ||||||
| chr17:45973197
|
C | T | 1 | a0004c0005t0007g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.220+1252C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973197 | ||||||
| chr17:45973221
|
T | C | 16 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(13): Show | 16 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+1276T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973221 | ||||||
| chr17:45973372
|
C | G | 1 | a0001c0001t0003g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.220+1427C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973372 | ||||||
| chr17:45973457
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+1512G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973457 | ||||||
| chr17:45973462
|
G | C | 85 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0002g0046others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.220+1517G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973462 | ||||||
| chr17:45973484
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+1539A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973484 | ||||||
| chr17:45973648
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+1703A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973648 | ||||||
| chr17:45973862
|
T | C | 13 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(10): Show | 13 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+1917T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45973862 | ||||||
| chr17:45974038
|
G | A | 71 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0002g0046others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.220+2093G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974038 | ||||||
| chr17:45974043
|
T | A | 197 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.220+2098T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974043 | ||||||
| chr17:45974147
|
G | A | 6 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109others(3): Show | 6 | HG02895.hp1 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+2202G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974147 | ||||||
| chr17:45974222
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2277C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974222 | ||||||
| chr17:45974223
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2278T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974223 | ||||||
| chr17:45974246
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2301A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974246 | ||||||
| chr17:45974480
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2535A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974480 | ||||||
| chr17:45974558
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2613G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974558 | ||||||
| chr17:45974573
|
TG | T | 3 | a0001c0010t0013g0129a0001c0010t0013g0208a0014c0013t0007g0040 | 3 | HG02965.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.220+2632delG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 45974573 | |||||
| chr17:45974643
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2698T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974643 | ||||||
| chr17:45974787
|
G | A | 2 | a0001c0001t0002g0125a0011c0012t0022g0022 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.220+2842G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974787 | ||||||
| chr17:45974851
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.220+2906C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974851 | ||||||
| chr17:45974882
|
G | A | 13 | a0001c0001t0002g0043a0001c0001t0002g0224a0004c0005t0002g0180others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+2937G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974882 | ||||||
| chr17:45974918
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2973G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45974918 | ||||||
| chr17:45975023
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.220+3078G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45975023 | ||||||
| chr17:45975367
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-3008A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45975367 | ||||||
| chr17:45975805
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-2570A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45975805 | ||||||
| chr17:45975901
|
C | T | 2 | a0002c0002t0003g0094a0002c0002t0006g0070 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.221-2474C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45975901 | ||||||
| chr17:45975925
|
C | T | 14 | a0001c0001t0002g0043a0001c0001t0002g0224a0004c0005t0001g0104others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-2450C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45975925 | ||||||
| chr17:45975941
|
T | TAG | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-2433_221-2432i others(4): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 45975941 | |||||
| chr17:45976007
|
C | A | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.221-2368C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976007 | ||||||
| chr17:45976082
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-2293A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976082 | ||||||
| chr17:45976171
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.221-2204C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976171 | ||||||
| chr17:45976274
|
C | T | 16 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-2101C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976274 | ||||||
| chr17:45976438
|
C | T | 16 | a0001c0001t0002g0043a0001c0001t0002g0224a0001c0001t0007g0184others(13): Show | 16 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-1937C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976438 | ||||||
| chr17:45976623
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-1752G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976623 | ||||||
| chr17:45976631
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.221-1744G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976631 | ||||||
| chr17:45976773
|
C | T | 1 | a0007c0008t0003g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.221-1602C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976773 | ||||||
| chr17:45976846
|
C | T | 1 | a0006c0006t0002g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221-1529C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976846 | ||||||
| chr17:45976871
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-1504G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976871 | ||||||
| chr17:45976990
|
C | G | 1 | a0002c0002t0001g0045 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.221-1385C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45976990 | ||||||
| chr17:45977022
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-1353T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977022 | ||||||
| chr17:45977067
|
A | G | 202 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.221-1308A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977067 | ||||||
| chr17:45977100
|
C | T | 1 | a0002c0003t0024g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.221-1275C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977100 | ||||||
| chr17:45977230
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-1145T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977230 | ||||||
| chr17:45977305
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-1070C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977305 | ||||||
| chr17:45977330
|
G | A | 144 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.221-1045G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977330 | ||||||
| chr17:45977368
|
A | G | 1 | a0002c0002t0003g0251 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-1007A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977368 | ||||||
| chr17:45977473
|
C | T | 1 | a0002c0002t0008g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221-902C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45977473 | ||||||
| chr17:45978019
|
A | C | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.221-356A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45978019 | ||||||
| chr17:45978020
|
C | A | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.221-355C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45978020 | ||||||
| chr17:45978021
|
A | G | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.221-354A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45978021 | ||||||
| chr17:45978024
|
C | A | 1 | a0006c0006t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221-351C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45978024 | ||||||
| chr17:45978272
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-103T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45978272 | ||||||
| chr17:45978281
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-94A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 3/12 | chr17 | 45978281 | ||||||
| chr17:45978677
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.286+237C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45978677 | ||||||
| chr17:45978731
|
C | G | 201 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.286+291C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45978731 | ||||||
| chr17:45978872
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+432A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45978872 | ||||||
| chr17:45978917
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.286+477C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45978917 | ||||||
| chr17:45979067
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+627T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979067 | ||||||
| chr17:45979068
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+628G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979068 | ||||||
| chr17:45979257
|
A | G | 2 | a0004c0005t0007g0077a0010c0020t0007g0117 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.286+817A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979257 | ||||||
| chr17:45979401
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+961G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979401 | ||||||
| chr17:45979467
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+1027G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979467 | ||||||
| chr17:45979503
|
C | T | 1 | a0002c0003t0002g0073 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.286+1063C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979503 | ||||||
| chr17:45979751
|
C | A | 1 | a0005c0007t0003g0051 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.286+1311C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979751 | ||||||
| chr17:45979815
|
T | A | 3 | a0001c0010t0013g0129a0001c0010t0013g0208a0014c0013t0007g0040 | 3 | HG02965.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.286+1375T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979815 | ||||||
| chr17:45979832
|
C | T | 3 | a0001c0001t0009g0034a0008c0009t0009g0032a0008c0009t0009g0033 | 3 | HG02818.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286+1392C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45979832 | ||||||
| chr17:45980228
|
C | T | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.286+1788C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980228 | ||||||
| chr17:45980229
|
G | A | 29 | a0002c0002t0001g0059a0002c0002t0001g0100a0002c0002t0001g0158others(26): Show | 29 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.286+1789G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980229 | ||||||
| chr17:45980272
|
A | G | 1 | a0001c0001t0010g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+1832A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980272 | ||||||
| chr17:45980369
|
T | C | 9 | a0001c0001t0009g0034a0001c0001t0010g0052a0001c0001t0010g0106others(6): Show | 9 | HG02818.hp1 HG02895.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.286+1929T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980369 | ||||||
| chr17:45980404
|
G | GGAGGCAG others(13): Show |
21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+1979_286+1980i others(22): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45980404 | |||||
| chr17:45980505
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+2065T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980505 | ||||||
| chr17:45980506
|
T | TA | 154 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0133others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.286+2083dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45980506 | |||||
| chr17:45980506
|
T | TAAA | 13 | a0001c0001t0007g0184a0001c0001t0027g0093a0004c0005t0001g0104others(10): Show | 13 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.286+2081_286+2083d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45980506 | |||||
| chr17:45980507
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+2067A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980507 | ||||||
| chr17:45980589
|
T | TACACACA others(5): Show |
21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+2154_286+2165d others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45980589 | |||||
| chr17:45980638
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+2198A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980638 | ||||||
| chr17:45980651
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+2211G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980651 | ||||||
| chr17:45980745
|
C | T | 67 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-2121C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980745 | ||||||
| chr17:45980955
|
T | C | 5 | a0004c0005t0007g0077a0004c0005t0007g0170a0009c0011t0002g0030others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-1911T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45980955 | ||||||
| chr17:45981217
|
C | A | 1 | a0011c0012t0022g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.287-1649C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981217 | ||||||
| chr17:45981263
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1603T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981263 | ||||||
| chr17:45981274
|
A | G | 192 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.287-1592A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981274 | ||||||
| chr17:45981325
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1541G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981325 | ||||||
| chr17:45981333
|
TAGG | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1530_287-1528d others(5): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45981333 | |||||
| chr17:45981350
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1516G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981350 | ||||||
| chr17:45981495
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1371C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981495 | ||||||
| chr17:45981562
|
G | A | 67 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-1304G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981562 | ||||||
| chr17:45981601
|
G | A | 1 | a0005c0007t0003g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.287-1265G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981601 | ||||||
| chr17:45981644
|
A | T | 40 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0152others(37): Show | 40 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.287-1222A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981644 | ||||||
| chr17:45981849
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1017C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981849 | ||||||
| chr17:45981918
|
G | T | 1 | a0003c0004t0004g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.287-948G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45981918 | ||||||
| chr17:45982018
|
C | CAA | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.287-834_287-833dup others(2): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45982018 | |||||
| chr17:45982018
|
CA | C | 6 | a0001c0001t0009g0034a0002c0002t0008g0035a0002c0003t0002g0073others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-833delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 45982018 | |||||
| chr17:45982034
|
G | A | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.287-832G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982034 | ||||||
| chr17:45982042
|
G | A | 190 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.287-824G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982042 | ||||||
| chr17:45982131
|
G | A | 57 | a0002c0002t0001g0045a0002c0002t0001g0055a0002c0002t0001g0059others(54): Show | 57 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.287-735G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982131 | ||||||
| chr17:45982178
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.287-688C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982178 | ||||||
| chr17:45982215
|
G | A | 12 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(9): Show | 12 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-651G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982215 | ||||||
| chr17:45982291
|
C | T | 1 | a0003c0004t0004g0001 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.287-575C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982291 | ||||||
| chr17:45982300
|
C | T | 16 | a0001c0001t0002g0024a0001c0001t0002g0036a0001c0001t0002g0037others(13): Show | 16 | HG00323.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.287-566C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982300 | ||||||
| chr17:45982301
|
G | A | 3 | a0001c0001t0009g0034a0008c0009t0009g0032a0008c0009t0009g0033 | 3 | HG02818.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.287-565G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982301 | ||||||
| chr17:45982345
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0128 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.287-521G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982345 | ||||||
| chr17:45982347
|
G | C | 1 | a0002c0003t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.287-519G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982347 | ||||||
| chr17:45982409
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-457A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982409 | ||||||
| chr17:45982616
|
T | G | 1 | a0002c0002t0003g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.287-250T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982616 | ||||||
| chr17:45982651
|
G | A | 1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.287-215G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982651 | ||||||
| chr17:45982675
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.287-191C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 4/12 | chr17 | 45982675 | ||||||
| chr17:45983951
|
C | T | 3 | a0008c0009t0009g0032a0008c0009t0009g0033a0008c0009t0009g0107 | 3 | HG03225.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1351+21C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45983951 | ||||||
| chr17:45984179
|
A | C | 249 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1351+249A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984179 | ||||||
| chr17:45984235
|
A | G | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1351+305A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984235 | ||||||
| chr17:45984242
|
GT | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1351+315delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 45984242 | |||||
| chr17:45984330
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1351+400C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984330 | ||||||
| chr17:45984527
|
G | T | 67 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1351+597G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984527 | ||||||
| chr17:45984528
|
C | T | 67 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1351+598C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984528 | ||||||
| chr17:45984532
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1351+602T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984532 | ||||||
| chr17:45984611
|
T | C | 5 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0178others(2): Show | 5 | HG01071.hp2 HG01884.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351+681T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984611 | ||||||
| chr17:45984848
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0007g0205 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1351+918C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984848 | ||||||
| chr17:45984971
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1351+1041G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45984971 | ||||||
| chr17:45985064
|
G | T | 2 | a0009c0011t0002g0030a0009c0011t0008g0097 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1351+1134G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985064 | ||||||
| chr17:45985237
|
A | G | 94 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1351+1307A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985237 | ||||||
| chr17:45985246
|
A | G | 5 | a0001c0001t0003g0082a0001c0001t0003g0105a0001c0001t0003g0113others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351+1316A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985246 | ||||||
| chr17:45985323
|
A | C | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1351+1393A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985323 | ||||||
| chr17:45985549
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-1491G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985549 | ||||||
| chr17:45985627
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-1413A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985627 | ||||||
| chr17:45985679
|
C | T | 2 | a0001c0001t0003g0232a0001c0001t0003g0238 | 2 | NA19011.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1352-1361C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985679 | ||||||
| chr17:45985757
|
C | T | 1 | a0001c0001t0005g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1352-1283C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985757 | ||||||
| chr17:45985774
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-1266A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985774 | ||||||
| chr17:45985878
|
C | T | 65 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1352-1162C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985878 | ||||||
| chr17:45985965
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1352-1075G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45985965 | ||||||
| chr17:45986027
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-1013G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986027 | ||||||
| chr17:45986197
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-843T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986197 | ||||||
| chr17:45986357
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-683A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986357 | ||||||
| chr17:45986357
|
A | G | 12 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0178others(9): Show | 12 | HG01071.hp2 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1352-683A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986357 | ||||||
| chr17:45986400
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-640A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986400 | ||||||
| chr17:45986408
|
G | A | 1 | a0002c0003t0002g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1352-632G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986408 | ||||||
| chr17:45986421
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-619A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986421 | ||||||
| chr17:45986473
|
C | T | 2 | a0002c0002t0001g0045a0002c0002t0001g0055 | 2 | HG01070.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1352-567C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986473 | ||||||
| chr17:45986521
|
C | A | 1 | a0001c0001t0002g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1352-519C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986521 | ||||||
| chr17:45986546
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1352-494G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986546 | ||||||
| chr17:45986842
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-198G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986842 | ||||||
| chr17:45986937
|
C | T | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1352-103C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986937 | ||||||
| chr17:45986968
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-72T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 5/12 | chr17 | 45986968 | ||||||
| chr17:45987361
|
T | TGACAGTA others(30): Show |
21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+297_1407+298i others(39): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 45987361 | |||||
| chr17:45987393
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+298A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45987393 | ||||||
| chr17:45987462
|
T | G | 1 | a0002c0002t0006g0214 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1407+367T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45987462 | ||||||
| chr17:45987485
|
C | T | 200 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1407+390C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45987485 | ||||||
| chr17:45987731
|
C | T | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1407+636C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45987731 | ||||||
| chr17:45987897
|
T | C | 129 | a0001c0001t0005g0160a0001c0001t0007g0184a0001c0001t0009g0034others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1407+802T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45987897 | ||||||
| chr17:45987955
|
CTTCA | C | 4 | a0002c0002t0001g0140a0002c0002t0003g0041a0002c0002t0003g0076others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1407+873_1407+876d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 45987955 | |||||
| chr17:45988044
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+949G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988044 | ||||||
| chr17:45988103
|
G | A | 1 | a0004c0005t0002g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1407+1008G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988103 | ||||||
| chr17:45988148
|
C | A | 19 | a0001c0001t0005g0160a0001c0001t0007g0184a0001c0001t0027g0093others(16): Show | 19 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+1053C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988148 | ||||||
| chr17:45988303
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1208A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988303 | ||||||
| chr17:45988342
|
A | C | 21 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0178others(18): Show | 21 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1407+1247A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988342 | ||||||
| chr17:45988342
|
A | T | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1407+1247A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988342 | ||||||
| chr17:45988374
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1279C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988374 | ||||||
| chr17:45988375
|
G | A | 61 | a0002c0002t0001g0045a0002c0002t0001g0055a0002c0002t0001g0059others(58): Show | 61 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1407+1280G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988375 | ||||||
| chr17:45988396
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1407+1301C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988396 | ||||||
| chr17:45988422
|
C | T | 1 | a0001c0001t0003g0157 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1407+1327C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988422 | ||||||
| chr17:45988524
|
A | G | 3 | a0002c0002t0008g0035a0009c0011t0002g0030a0009c0011t0008g0097 | 3 | HG02622.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1408-1354A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988524 | ||||||
| chr17:45988535
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-1343C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988535 | ||||||
| chr17:45988722
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-1156T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988722 | ||||||
| chr17:45988765
|
A | G | 3 | a0002c0002t0008g0035a0009c0011t0002g0030a0009c0011t0008g0097 | 3 | HG02622.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1408-1113A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988765 | ||||||
| chr17:45988806
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-1072A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45988806 | ||||||
| chr17:45988886
|
A | AAAAC | 12 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109others(9): Show | 12 | HG01081.hp2 HG01175.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408-968_1408-965d others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 45988886 | |||||
| chr17:45988886
|
AAAACAAA others(1): Show |
A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-972_1408-965d others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 45988886 | |||||
| chr17:45988947
|
ATAGTG | A | 10 | a0002c0003t0001g0075a0002c0003t0002g0073a0002c0003t0002g0103others(7): Show | 10 | HG01106.hp1 HG01928.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408-929_1408-925d others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 45988947 | |||||
| chr17:45989098
|
G | A | 61 | a0002c0002t0001g0045a0002c0002t0001g0055a0002c0002t0001g0059others(58): Show | 61 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1408-780G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989098 | ||||||
| chr17:45989169
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1408-709C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989169 | ||||||
| chr17:45989268
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-610C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989268 | ||||||
| chr17:45989379
|
G | A | 1 | a0005c0007t0003g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1408-499G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989379 | ||||||
| chr17:45989494
|
C | CA | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-377dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 45989494 | |||||
| chr17:45989500
|
A | C | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1408-378A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989500 | ||||||
| chr17:45989502
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-376C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989502 | ||||||
| chr17:45989502
|
C | T | 1 | a0001c0001t0003g0232 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1408-376C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989502 | ||||||
| chr17:45989508
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-370G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989508 | ||||||
| chr17:45989629
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-249C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989629 | ||||||
| chr17:45989646
|
G | A | 1 | a0007c0008t0014g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1408-232G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989646 | ||||||
| chr17:45989680
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-198G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 6/12 | chr17 | 45989680 | ||||||
| chr17:45990142
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1605+67A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990142 | ||||||
| chr17:45990174
|
A | G | 1 | a0002c0002t0003g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1605+99A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990174 | ||||||
| chr17:45990180
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1605+105T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990180 | ||||||
| chr17:45990316
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1605+241G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990316 | ||||||
| chr17:45990465
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1605+390T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990465 | ||||||
| chr17:45990481
|
G | T | 74 | a0002c0002t0001g0045a0002c0002t0001g0055a0002c0002t0001g0059others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1605+406G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990481 | ||||||
| chr17:45990579
|
A | G | 1 | a0002c0003t0020g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1605+504A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990579 | ||||||
| chr17:45990696
|
C | G | 1 | a0003c0004t0004g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1605+621C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990696 | ||||||
| chr17:45990746
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1605+671C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990746 | ||||||
| chr17:45990835
|
C | T | 1 | a0002c0002t0017g0112 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1606-625C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990835 | ||||||
| chr17:45990872
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1606-588C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990872 | ||||||
| chr17:45990923
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1606-537G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990923 | ||||||
| chr17:45990928
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1606-532G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990928 | ||||||
| chr17:45990973
|
G | A | 44 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(41): Show | 44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1606-487G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990973 | ||||||
| chr17:45990990
|
C | T | 1 | a0001c0001t0012g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1606-470C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45990990 | ||||||
| chr17:45991114
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1606-346T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45991114 | ||||||
| chr17:45991115
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1606-345G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45991115 | ||||||
| chr17:45991126
|
A | G | 18 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(15): Show | 18 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1606-334A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45991126 | ||||||
| chr17:45991177
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1606-283G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45991177 | ||||||
| chr17:45991361
|
C | T | 1 | a0001c0001t0003g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1606-99C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 7/12 | chr17 | 45991361 | ||||||
| chr17:45991814
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+228C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45991814 | ||||||
| chr17:45991832
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+246C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45991832 | ||||||
| chr17:45992010
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+424G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992010 | ||||||
| chr17:45992193
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1732+607T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992193 | ||||||
| chr17:45992268
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1732+682G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992268 | ||||||
| chr17:45992286
|
A | G | 5 | a0001c0001t0002g0024a0001c0001t0002g0037a0001c0001t0002g0079others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1732+700A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992286 | ||||||
| chr17:45992321
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+735A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992321 | ||||||
| chr17:45992402
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+816A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992402 | ||||||
| chr17:45992474
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+888G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992474 | ||||||
| chr17:45992487
|
C | T | 23 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(20): Show | 23 | HG00558.hp1 HG00597.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1732+901C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992487 | ||||||
| chr17:45992538
|
A | G | 16 | a0001c0001t0005g0160a0004c0005t0001g0104a0004c0005t0002g0180others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1732+952A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992538 | ||||||
| chr17:45992552
|
A | T | 1 | a0003c0004t0004g0006 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1732+966A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992552 | ||||||
| chr17:45992604
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+1018C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992604 | ||||||
| chr17:45992693
|
A | G | 1 | a0006c0006t0002g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1732+1107A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992693 | ||||||
| chr17:45992745
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+1159G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992745 | ||||||
| chr17:45992866
|
G | A | 1 | a0003c0004t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1732+1280G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45992866 | ||||||
| chr17:45992891
|
C | CA | 21 | a0001c0001t0001g0128a0001c0001t0001g0210a0001c0001t0001g0236others(18): Show | 21 | HG00597.hp1 HG00609.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+1324dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 45992891 | |||||
| chr17:45992891
|
CA | C | 51 | a0001c0001t0002g0217a0001c0001t0003g0229a0001c0001t0005g0160others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1732+1324delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 45992891 | |||||
| chr17:45993046
|
TCCTTGGT others(18): Show |
T | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1732+1462_1732+148 others(29): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 45993046 | |||||
| chr17:45993179
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+1593G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993179 | ||||||
| chr17:45993217
|
A | G | 112 | a0001c0001t0005g0160a0001c0001t0007g0184a0001c0001t0010g0052others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1732+1631A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993217 | ||||||
| chr17:45993435
|
A | T | 2 | a0002c0002t0001g0220a0002c0002t0003g0151 | 2 | HG00438.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1732+1849A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993435 | ||||||
| chr17:45993584
|
T | G | 2 | a0009c0011t0002g0030a0009c0011t0008g0097 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1732+1998T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993584 | ||||||
| chr17:45993590
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+2004T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993590 | ||||||
| chr17:45993594
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1732+2008A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993594 | ||||||
| chr17:45993723
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+2137C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993723 | ||||||
| chr17:45993837
|
G | C | 1 | a0002c0003t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1732+2251G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993837 | ||||||
| chr17:45993928
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1732+2342T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45993928 | ||||||
| chr17:45994308
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-2091A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994308 | ||||||
| chr17:45994340
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1733-2059C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994340 | ||||||
| chr17:45994445
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1733-1954C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994445 | ||||||
| chr17:45994485
|
G | A | 104 | a0001c0001t0005g0160a0001c0001t0007g0184a0001c0001t0027g0093others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1733-1914G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994485 | ||||||
| chr17:45994506
|
C | T | 4 | a0001c0001t0009g0034a0008c0009t0009g0032a0008c0009t0009g0033others(1): Show | 4 | HG02818.hp1 HG03225.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733-1893C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994506 | ||||||
| chr17:45994545
|
G | A | 1 | a0001c0001t0007g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1733-1854G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994545 | ||||||
| chr17:45994560
|
C | T | 1 | a0011c0012t0022g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1733-1839C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994560 | ||||||
| chr17:45994651
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-1748C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994651 | ||||||
| chr17:45994675
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-1724T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45994675 | ||||||
| chr17:45995057
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-1342A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995057 | ||||||
| chr17:45995104
|
T | C | 1 | a0003c0004t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1733-1295T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995104 | ||||||
| chr17:45995222
|
G | A | 13 | a0001c0001t0005g0160a0004c0005t0002g0180a0004c0005t0005g0025others(10): Show | 13 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1733-1177G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995222 | ||||||
| chr17:45995395
|
G | A | 1 | a0001c0001t0003g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1733-1004G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995395 | ||||||
| chr17:45995433
|
C | T | 10 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1733-966C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995433 | ||||||
| chr17:45995488
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-911T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995488 | ||||||
| chr17:45995501
|
G | A | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1733-898G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995501 | ||||||
| chr17:45995515
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-884C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995515 | ||||||
| chr17:45995548
|
G | A | 1 | a0002c0002t0003g0251 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1733-851G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995548 | ||||||
| chr17:45995618
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-781A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995618 | ||||||
| chr17:45995625
|
C | T | 1 | a0002c0002t0003g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1733-774C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995625 | ||||||
| chr17:45995661
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-738G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995661 | ||||||
| chr17:45995696
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-703T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995696 | ||||||
| chr17:45995756
|
G | A | 2 | a0001c0001t0002g0217a0001c0001t0003g0229 | 2 | HG00323.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1733-643G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995756 | ||||||
| chr17:45995779
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-620G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45995779 | ||||||
| chr17:45996092
|
C | T | 1 | a0001c0001t0023g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1733-307C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45996092 | ||||||
| chr17:45996193
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1733-206G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45996193 | ||||||
| chr17:45996243
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1733-156G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45996243 | ||||||
| chr17:45996368
|
T | C | 4 | a0001c0001t0009g0034a0008c0009t0009g0032a0008c0009t0009g0033others(1): Show | 4 | HG02818.hp1 HG03225.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733-31T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45996368 | ||||||
| chr17:45996373
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1733-26G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 8/12 | chr17 | 45996373 | ||||||
| chr17:45996699
|
G | A | 1 | a0004c0005t0005g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1998+35G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45996699 | ||||||
| chr17:45996767
|
G | A | 3 | a0001c0001t0002g0217a0001c0001t0003g0229a0001c0001t0012g0143 | 3 | HG00323.hp1 HG01891.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1998+103G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45996767 | ||||||
| chr17:45996811
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0227 | 2 | HG00642.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1998+147C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45996811 | ||||||
| chr17:45996992
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA18991.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1998+328C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45996992 | ||||||
| chr17:45997069
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+405C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997069 | ||||||
| chr17:45997215
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+551A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997215 | ||||||
| chr17:45997220
|
G | A | 39 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0152others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1998+556G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997220 | ||||||
| chr17:45997247
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+583A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997247 | ||||||
| chr17:45997253
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+589G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997253 | ||||||
| chr17:45997675
|
G | A | 1 | a0002c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1998+1011G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997675 | ||||||
| chr17:45997733
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+1069T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997733 | ||||||
| chr17:45997744
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+1080A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45997744 | ||||||
| chr17:45998108
|
G | T | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1998+1444G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998108 | ||||||
| chr17:45998140
|
C | G | 30 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(27): Show | 30 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1998+1476C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998140 | ||||||
| chr17:45998169
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+1505T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998169 | ||||||
| chr17:45998247
|
C | A | 14 | a0001c0001t0005g0160a0001c0001t0026g0192a0004c0005t0001g0104others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1998+1583C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998247 | ||||||
| chr17:45998390
|
G | A | 1 | a0006c0006t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1998+1726G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998390 | ||||||
| chr17:45998471
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+1807T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998471 | ||||||
| chr17:45998535
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+1871A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998535 | ||||||
| chr17:45998605
|
G | T | 1 | a0003c0004t0004g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1998+1941G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998605 | ||||||
| chr17:45998697
|
C | T | 51 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0099others(48): Show | 51 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1998+2033C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998697 | ||||||
| chr17:45998713
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1998+2049G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998713 | ||||||
| chr17:45998808
|
C | T | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1998+2144C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998808 | ||||||
| chr17:45998821
|
C | T | 2 | a0001c0001t0026g0192a0004c0005t0005g0190 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1998+2157C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998821 | ||||||
| chr17:45998883
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1998+2219C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45998883 | ||||||
| chr17:45999003
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0227 | 2 | HG00642.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1998+2339C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999003 | ||||||
| chr17:45999100
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+2436A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999100 | ||||||
| chr17:45999299
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+2635A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999299 | ||||||
| chr17:45999345
|
G | A | 13 | a0001c0001t0005g0160a0001c0001t0026g0192a0004c0005t0002g0180others(10): Show | 13 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1998+2681G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999345 | ||||||
| chr17:45999352
|
A | G | 1 | a0003c0004t0016g0007 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1998+2688A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999352 | ||||||
| chr17:45999655
|
T | C | 1 | a0002c0002t0003g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1998+2991T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999655 | ||||||
| chr17:45999678
|
T | C | 241 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1998+3014T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 45999678 | ||||||
| chr17:46000067
|
G | T | 1 | a0006c0006t0002g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1998+3403G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000067 | ||||||
| chr17:46000224
|
G | A | 2 | a0001c0001t0002g0217a0001c0001t0003g0229 | 2 | HG00323.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1998+3560G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000224 | ||||||
| chr17:46000342
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+3678G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000342 | ||||||
| chr17:46000366
|
AT | A | 3 | a0004c0005t0002g0180a0004c0005t0005g0195a0004c0005t0005g0204 | 3 | HG02280.hp2 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1998+3704delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46000366 | |||||
| chr17:46000484
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+3820G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000484 | ||||||
| chr17:46000485
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+3821T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000485 | ||||||
| chr17:46000581
|
C | G | 1 | a0002c0002t0008g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1998+3917C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000581 | ||||||
| chr17:46000719
|
C | T | 3 | a0001c0001t0009g0034a0008c0009t0009g0032a0008c0009t0009g0033 | 3 | HG02818.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1998+4055C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000719 | ||||||
| chr17:46000847
|
A | G | 22 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0036others(19): Show | 22 | HG00323.hp1 HG01071.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1998+4183A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000847 | ||||||
| chr17:46000986
|
G | A | 1 | a0002c0003t0020g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1998+4322G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46000986 | ||||||
| chr17:46001250
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+4586G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001250 | ||||||
| chr17:46001252
|
T | C | 1 | a0003c0004t0016g0007 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1998+4588T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001252 | ||||||
| chr17:46001314
|
T | TA | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+4656dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46001314 | |||||
| chr17:46001450
|
TA | T | 24 | a0002c0002t0003g0251a0003c0004t0004g0001a0003c0004t0004g0003others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1998+4797delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46001450 | |||||
| chr17:46001466
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+4802G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001466 | ||||||
| chr17:46001526
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+4862G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001526 | ||||||
| chr17:46001616
|
T | A | 127 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1998+4952T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001616 | ||||||
| chr17:46001638
|
G | A | 1 | a0006c0006t0002g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1998+4974G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001638 | ||||||
| chr17:46001664
|
A | G | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1998+5000A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46001664 | ||||||
| chr17:46002201
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+5537C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002201 | ||||||
| chr17:46002270
|
G | A | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1998+5606G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002270 | ||||||
| chr17:46002355
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+5691A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002355 | ||||||
| chr17:46002461
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1998+5797C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002461 | ||||||
| chr17:46002526
|
C | A | 1 | a0002c0002t0003g0064 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1998+5862C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002526 | ||||||
| chr17:46002673
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+6009T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002673 | ||||||
| chr17:46002678
|
C | CG | 15 | a0001c0001t0005g0160a0001c0001t0026g0192a0004c0005t0001g0104others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1998+6020dupG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46002678 | |||||
| chr17:46002844
|
G | A | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1998+6180G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002844 | ||||||
| chr17:46002988
|
C | T | 154 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1998+6324C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46002988 | ||||||
| chr17:46003042
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1998+6378G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003042 | ||||||
| chr17:46003099
|
C | CGT | 6 | a0001c0001t0003g0231a0002c0002t0012g0058a0003c0004t0004g0012others(3): Show | 6 | HG01123.hp1 HG01515.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1998+6457_1998+645 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46003099 | |||||
| chr17:46003099
|
C | CGTGTGT | 19 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1998+6453_1998+645 others(10): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46003099 | |||||
| chr17:46003099
|
C | CGTGTGTG others(1): Show |
3 | a0003c0004t0004g0008a0003c0004t0004g0018a0003c0004t0004g0020 | 3 | HG01433.hp2 HG02257.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1998+6451_1998+645 others(12): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46003099 | |||||
| chr17:46003360
|
C | G | 6 | a0001c0001t0026g0192a0004c0005t0002g0180a0004c0005t0005g0190others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1998+6696C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003360 | ||||||
| chr17:46003470
|
G | A | 40 | a0001c0001t0001g0042a0001c0001t0001g0074a0001c0001t0001g0128others(37): Show | 40 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1998+6806G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003470 | ||||||
| chr17:46003570
|
C | T | 4 | a0004c0005t0007g0077a0004c0005t0007g0170a0007c0008t0003g0185others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999-6740C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003570 | ||||||
| chr17:46003698
|
A | G | 29 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109others(26): Show | 29 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1999-6612A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003698 | ||||||
| chr17:46003812
|
T | C | 17 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0043others(14): Show | 17 | HG00323.hp1 HG01071.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1999-6498T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003812 | ||||||
| chr17:46003817
|
G | A | 1 | a0001c0010t0013g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1999-6493G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003817 | ||||||
| chr17:46003852
|
C | CT | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-6457dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46003852 | |||||
| chr17:46003858
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-6452G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003858 | ||||||
| chr17:46003902
|
G | A | 15 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0043others(12): Show | 15 | HG00323.hp1 HG01071.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1999-6408G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46003902 | ||||||
| chr17:46004062
|
C | CG | 4 | a0002c0003t0001g0061a0002c0003t0001g0132a0002c0003t0001g0177others(1): Show | 4 | HG00738.hp1 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999-6245dupG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46004062 | |||||
| chr17:46004096
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-6214T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004096 | ||||||
| chr17:46004130
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1999-6180G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004130 | ||||||
| chr17:46004161
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-6149T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004161 | ||||||
| chr17:46004305
|
A | C | 1 | a0001c0001t0009g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1999-6005A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004305 | ||||||
| chr17:46004422
|
A | C | 1 | a0001c0001t0003g0054 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1999-5888A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004422 | ||||||
| chr17:46004605
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1999-5705C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004605 | ||||||
| chr17:46004815
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5495A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004815 | ||||||
| chr17:46004883
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5427A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46004883 | ||||||
| chr17:46005036
|
G | A | 5 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0193others(2): Show | 5 | HG00642.hp2 HG01167.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999-5274G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005036 | ||||||
| chr17:46005066
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5244G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005066 | ||||||
| chr17:46005075
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5235T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005075 | ||||||
| chr17:46005080
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5230G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005080 | ||||||
| chr17:46005113
|
A | G | 1 | a0002c0002t0002g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1999-5197A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005113 | ||||||
| chr17:46005148
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5162T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005148 | ||||||
| chr17:46005162
|
A | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5148A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005162 | ||||||
| chr17:46005237
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-5073A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005237 | ||||||
| chr17:46005589
|
A | AT | 22 | a0001c0001t0003g0202a0003c0004t0004g0001a0003c0004t0004g0003others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1999-4712dupT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46005589 | |||||
| chr17:46005615
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-4695G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005615 | ||||||
| chr17:46005715
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-4595G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005715 | ||||||
| chr17:46005931
|
T | C | 79 | a0001c0001t0001g0042a0001c0001t0001g0241a0001c0001t0003g0028others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1999-4379T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005931 | ||||||
| chr17:46005957
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-4353C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005957 | ||||||
| chr17:46005998
|
G | A | 4 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109others(1): Show | 4 | HG02895.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999-4312G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46005998 | ||||||
| chr17:46006036
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-4274G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006036 | ||||||
| chr17:46006133
|
C | T | 1 | a0003c0004t0004g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1999-4177C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006133 | ||||||
| chr17:46006435
|
G | T | 4 | a0001c0001t0007g0205a0004c0005t0007g0077a0004c0005t0007g0170others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999-3875G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006435 | ||||||
| chr17:46006447
|
C | T | 18 | a0001c0001t0005g0160a0001c0001t0005g0194a0001c0001t0007g0205others(15): Show | 18 | HG01358.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1999-3863C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006447 | ||||||
| chr17:46006582
|
T | C | 88 | a0001c0001t0001g0241a0001c0001t0003g0028a0001c0001t0003g0054others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1999-3728T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006582 | ||||||
| chr17:46006636
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-3674T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006636 | ||||||
| chr17:46006642
|
T | C | 124 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1999-3668T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006642 | ||||||
| chr17:46006743
|
T | C | 1 | a0002c0002t0021g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1999-3567T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006743 | ||||||
| chr17:46006780
|
G | A | 1 | a0004c0005t0005g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1999-3530G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006780 | ||||||
| chr17:46006791
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-3519T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006791 | ||||||
| chr17:46006815
|
C | T | 2 | a0001c0001t0007g0184a0001c0001t0027g0093 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1999-3495C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006815 | ||||||
| chr17:46006880
|
G | A | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1999-3430G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006880 | ||||||
| chr17:46006951
|
TAATAA | T | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1999-3332_1999-332 others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46006951 | |||||
| chr17:46006969
|
TAAAATAA others(8): Show |
T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-3337_1999-332 others(19): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46006969 | |||||
| chr17:46006970
|
AAAATAAA others(2): Show |
A | 3 | a0001c0001t0005g0194a0004c0005t0005g0195a0004c0005t0005g0204 | 3 | HG02280.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1999-3327_1999-331 others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46006970 | |||||
| chr17:46006974
|
TAAAATAA others(3): Show |
T | 1 | a0001c0001t0026g0192 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1999-3332_1999-332 others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46006974 | |||||
| chr17:46006979
|
TAAATA | T | 63 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(60): Show | 63 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1999-3316_1999-331 others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46006979 | |||||
| chr17:46006983
|
T | A | 74 | a0001c0001t0003g0054a0001c0001t0003g0082a0001c0001t0003g0083others(71): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1999-3327T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006983 | ||||||
| chr17:46006984
|
A | T | 74 | a0001c0001t0003g0054a0001c0001t0003g0082a0001c0001t0003g0083others(71): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1999-3326A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46006984 | ||||||
| chr17:46007037
|
G | C | 71 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0036others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1999-3273G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007037 | ||||||
| chr17:46007167
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-3143T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007167 | ||||||
| chr17:46007214
|
G | A | 1 | a0006c0006t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1999-3096G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007214 | ||||||
| chr17:46007289
|
G | A | 2 | a0001c0001t0007g0184a0001c0001t0027g0093 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1999-3021G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007289 | ||||||
| chr17:46007310
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-3000C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007310 | ||||||
| chr17:46007407
|
A | C | 2 | a0001c0001t0007g0184a0001c0001t0027g0093 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1999-2903A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007407 | ||||||
| chr17:46007411
|
C | T | 1 | a0001c0001t0003g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1999-2899C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007411 | ||||||
| chr17:46007478
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-2832G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007478 | ||||||
| chr17:46007851
|
C | A | 1 | a0002c0003t0019g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1999-2459C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46007851 | ||||||
| chr17:46008190
|
G | A | 4 | a0001c0001t0007g0205a0004c0005t0007g0077a0004c0005t0007g0170others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999-2120G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008190 | ||||||
| chr17:46008199
|
C | T | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1999-2111C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008199 | ||||||
| chr17:46008201
|
A | C | 1 | a0004c0005t0025g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1999-2109A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008201 | ||||||
| chr17:46008244
|
C | T | 43 | a0001c0001t0003g0028a0001c0001t0003g0083a0001c0001t0003g0085others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.1999-2066C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008244 | ||||||
| chr17:46008377
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-1933T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008377 | ||||||
| chr17:46008401
|
C | T | 1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1999-1909C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008401 | ||||||
| chr17:46008486
|
T | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-1824T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008486 | ||||||
| chr17:46008528
|
T | G | 1 | a0002c0002t0003g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1999-1782T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008528 | ||||||
| chr17:46008530
|
G | A | 1 | a0002c0002t0003g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1999-1780G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008530 | ||||||
| chr17:46008605
|
T | C | 1 | a0005c0007t0003g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1999-1705T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008605 | ||||||
| chr17:46008698
|
A | G | 23 | a0001c0001t0005g0160a0001c0001t0005g0194a0001c0001t0007g0205others(20): Show | 23 | HG01358.hp1 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1999-1612A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008698 | ||||||
| chr17:46008734
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-1576T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008734 | ||||||
| chr17:46008829
|
C | T | 1 | a0002c0002t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1999-1481C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008829 | ||||||
| chr17:46008901
|
A | G | 9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(6): Show | 9 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1999-1409A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008901 | ||||||
| chr17:46008939
|
C | T | 1 | a0002c0002t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1999-1371C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46008939 | ||||||
| chr17:46009155
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-1155G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46009155 | ||||||
| chr17:46009278
|
C | T | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1999-1032C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46009278 | ||||||
| chr17:46009357
|
TCATAGTT others(231): Show |
T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-950_1999-713d others(2): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 46009357 | |||||
| chr17:46009388
|
T | A | 1 | a0002c0002t0003g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1999-922T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46009388 | ||||||
| chr17:46009541
|
G | A | 1 | a0002c0002t0006g0070 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1999-769G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46009541 | ||||||
| chr17:46009770
|
G | C | 1 | a0003c0004t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1999-540G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46009770 | ||||||
| chr17:46010036
|
G | A | 1 | a0002c0003t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1999-274G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46010036 | ||||||
| chr17:46010131
|
C | G | 1 | a0001c0001t0010g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1999-179C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46010131 | ||||||
| chr17:46010134
|
A | G | 184 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1999-176A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46010134 | ||||||
| chr17:46010263
|
C | A | 42 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1999-47C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 9/12 | chr17 | 46010263 | ||||||
| chr17:46010550
|
G | A | 1 | a0003c0004t0004g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2091+148G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46010550 | ||||||
| chr17:46010777
|
T | C | 3 | a0001c0001t0010g0052a0001c0001t0010g0106a0001c0001t0010g0109 | 3 | HG03225.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2091+375T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46010777 | ||||||
| chr17:46011058
|
G | A | 3 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0224 | 3 | HG02818.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2091+656G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011058 | ||||||
| chr17:46011381
|
G | A | 1 | a0002c0002t0002g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2091+979G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011381 | ||||||
| chr17:46011406
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2091+1004C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011406 | ||||||
| chr17:46011490
|
G | A | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2091+1088G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011490 | ||||||
| chr17:46011497
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2091+1095G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011497 | ||||||
| chr17:46011560
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2091+1158C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011560 | ||||||
| chr17:46011571
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2091+1169G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011571 | ||||||
| chr17:46011742
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2091+1340T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011742 | ||||||
| chr17:46011780
|
C | A | 1 | a0002c0002t0008g0172 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2091+1378C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011780 | ||||||
| chr17:46011915
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2091+1513G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011915 | ||||||
| chr17:46011968
|
C | T | 12 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0036others(9): Show | 12 | HG01243.hp2 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2091+1566C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46011968 | ||||||
| chr17:46012121
|
C | T | 7 | a0002c0003t0002g0073a0002c0003t0002g0103a0002c0003t0002g0146others(4): Show | 7 | HG01106.hp1 HG01928.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2091+1719C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012121 | ||||||
| chr17:46012197
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2091+1795C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012197 | ||||||
| chr17:46012324
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1919T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012324 | ||||||
| chr17:46012349
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1894C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012349 | ||||||
| chr17:46012361
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1882G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012361 | ||||||
| chr17:46012555
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1688C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012555 | ||||||
| chr17:46012669
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1574C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012669 | ||||||
| chr17:46012674
|
C | T | 4 | a0001c0001t0026g0192a0007c0008t0014g0026a0007c0008t0014g0191others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2092-1569C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012674 | ||||||
| chr17:46012782
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1461A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012782 | ||||||
| chr17:46012830
|
T | C | 6 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0178others(3): Show | 6 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2092-1413T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012830 | ||||||
| chr17:46012870
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1373T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012870 | ||||||
| chr17:46012973
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1270T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46012973 | ||||||
| chr17:46013027
|
T | C | 9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(6): Show | 9 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.2092-1216T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013027 | ||||||
| chr17:46013089
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1154T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013089 | ||||||
| chr17:46013143
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2092-1100C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013143 | ||||||
| chr17:46013170
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1073G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013170 | ||||||
| chr17:46013172
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-1071T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013172 | ||||||
| chr17:46013180
|
C | T | 1 | a0002c0003t0001g0150 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2092-1063C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013180 | ||||||
| chr17:46013280
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-963A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013280 | ||||||
| chr17:46013319
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-924G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013319 | ||||||
| chr17:46013338
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-905A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013338 | ||||||
| chr17:46013412
|
T | A | 67 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0003g0082others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.2092-831T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013412 | ||||||
| chr17:46013413
|
C | A | 67 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0003g0082others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.2092-830C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013413 | ||||||
| chr17:46013430
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-813T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013430 | ||||||
| chr17:46013488
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-755C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013488 | ||||||
| chr17:46013492
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-751C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013492 | ||||||
| chr17:46013497
|
G | A | 1 | a0002c0002t0003g0213 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2092-746G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013497 | ||||||
| chr17:46013669
|
G | A | 1 | a0006c0006t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2092-574G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013669 | ||||||
| chr17:46013726
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2092-517G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013726 | ||||||
| chr17:46013829
|
T | C | 22 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2092-414T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 10/12 | chr17 | 46013829 | ||||||
| chr17:46014358
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+34G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014358 | ||||||
| chr17:46014414
|
G | A | 61 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0003g0082others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.2173+90G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014414 | ||||||
| chr17:46014520
|
C | T | 43 | a0001c0001t0005g0160a0001c0001t0005g0194a0001c0001t0007g0205others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2173+196C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014520 | ||||||
| chr17:46014559
|
A | G | 1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2173+235A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014559 | ||||||
| chr17:46014622
|
T | C | 77 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(74): Show | 77 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2173+298T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014622 | ||||||
| chr17:46014742
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+418T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014742 | ||||||
| chr17:46014784
|
A | G | 2 | a0002c0003t0020g0114a0013c0014t0002g0049 | 2 | HG01123.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2173+460A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014784 | ||||||
| chr17:46014877
|
C | T | 20 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2173+553C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46014877 | ||||||
| chr17:46014882
|
C | CA | 7 | a0001c0001t0003g0243a0001c0001t0023g0088a0001c0001t0026g0192others(4): Show | 7 | HG02717.hp1 HG02723.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173+569dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46014882 | |||||
| chr17:46014882
|
C | CAAAAAAA others(6): Show |
2 | a0003c0004t0004g0012a0003c0004t0004g0013 | 2 | HG02602.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2173+569_2173+570i others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46014882 | |||||
| chr17:46014882
|
C | CAAAAAAA others(7): Show |
16 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2173+569_2173+570i others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46014882 | |||||
| chr17:46014882
|
C | CAAAAAAA others(8): Show |
3 | a0003c0004t0004g0011a0003c0004t0004g0017a0003c0004t0015g0014 | 3 | HG01074.hp1 HG01361.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2173+569_2173+570i others(17): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46014882 | |||||
| chr17:46015131
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+807T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015131 | ||||||
| chr17:46015363
|
TAAA | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+1042_2173+104 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46015363 | |||||
| chr17:46015378
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+1054A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015378 | ||||||
| chr17:46015435
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+1111G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015435 | ||||||
| chr17:46015500
|
A | G | 56 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(53): Show | 56 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.2173+1176A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015500 | ||||||
| chr17:46015511
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2173+1187T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015511 | ||||||
| chr17:46015536
|
A | G | 4 | a0001c0001t0007g0205a0004c0005t0007g0077a0004c0005t0007g0170others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+1212A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015536 | ||||||
| chr17:46015926
|
G | A | 25 | a0001c0001t0005g0160a0001c0001t0005g0194a0001c0001t0007g0184others(22): Show | 25 | HG01358.hp1 HG01884.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2173+1602G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015926 | ||||||
| chr17:46015953
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+1629G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46015953 | ||||||
| chr17:46016130
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+1806A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016130 | ||||||
| chr17:46016158
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2173+1834G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016158 | ||||||
| chr17:46016261
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+1937A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016261 | ||||||
| chr17:46016263
|
A | G | 7 | a0002c0003t0002g0073a0002c0003t0002g0103a0002c0003t0002g0146others(4): Show | 7 | HG01106.hp1 HG01928.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173+1939A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016263 | ||||||
| chr17:46016387
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2173+2063T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016387 | ||||||
| chr17:46016390
|
C | CA | 16 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0178others(13): Show | 16 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2173+2081dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46016390 | |||||
| chr17:46016390
|
CA | C | 7 | a0001c0001t0001g0152a0001c0001t0002g0047a0001c0001t0003g0122others(4): Show | 7 | HG01516.hp2 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173+2081delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46016390 | |||||
| chr17:46016494
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-2124A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016494 | ||||||
| chr17:46016569
|
A | G | 1 | a0002c0002t0003g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2174-2049A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016569 | ||||||
| chr17:46016598
|
T | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-2020T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016598 | ||||||
| chr17:46016627
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1991C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016627 | ||||||
| chr17:46016728
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2174-1890G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016728 | ||||||
| chr17:46016746
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1872A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016746 | ||||||
| chr17:46016767
|
CA | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1844delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46016767 | |||||
| chr17:46016822
|
G | C | 1 | a0004c0005t0005g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2174-1796G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46016822 | ||||||
| chr17:46017008
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1610A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017008 | ||||||
| chr17:46017105
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1513G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017105 | ||||||
| chr17:46017147
|
C | T | 244 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2174-1471C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017147 | ||||||
| chr17:46017301
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1317C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017301 | ||||||
| chr17:46017434
|
T | C | 244 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2174-1184T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017434 | ||||||
| chr17:46017440
|
A | ATTTTTTT others(3): Show |
6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 6 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.2174-1157_2174-114 others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(4): Show |
7 | a0001c0001t0001g0135a0003c0004t0004g0001a0003c0004t0004g0003others(4): Show | 7 | HG00280.hp1 HG01099.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2174-1158_2174-114 others(15): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(5): Show |
8 | a0003c0004t0004g0004a0003c0004t0004g0008a0003c0004t0004g0009others(5): Show | 8 | HG01074.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2174-1159_2174-114 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(6): Show |
3 | a0001c0010t0013g0208a0003c0004t0004g0017a0012c0016t0002g0111 | 3 | HG01071.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2174-1160_2174-114 others(17): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(7): Show |
2 | a0001c0010t0013g0129a0004c0005t0005g0167 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2174-1161_2174-114 others(18): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0008g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2174-1162_2174-114 others(19): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(9): Show |
5 | a0001c0001t0007g0184a0001c0001t0027g0093a0002c0002t0008g0035others(2): Show | 5 | HG02615.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174-1163_2174-114 others(20): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(10): Show |
4 | a0003c0004t0004g0019a0003c0004t0004g0021a0003c0004t0011g0015others(1): Show | 4 | HG01167.hp2 HG02735.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2174-1164_2174-114 others(21): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(11): Show |
5 | a0001c0001t0002g0178a0003c0004t0004g0006a0003c0004t0004g0016others(2): Show | 5 | HG00140.hp1 HG02258.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2174-1165_2174-114 others(22): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(12): Show |
3 | a0001c0001t0002g0031a0003c0004t0004g0005a0004c0005t0007g0077 | 3 | HG01255.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2174-1166_2174-114 others(23): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0005g0160a0002c0002t0021g0069 | 2 | HG01358.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2174-1167_2174-114 others(24): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(14): Show |
1 | a0004c0005t0007g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2174-1168_2174-114 others(25): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0007g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2174-1170_2174-114 others(27): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0002g0043 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2174-1171_2174-114 others(28): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(20): Show |
1 | a0014c0013t0007g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2174-1174_2174-114 others(31): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(23): Show |
1 | a0009c0011t0008g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2174-1177_2174-114 others(34): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(25): Show |
2 | a0004c0005t0005g0195a0004c0005t0005g0204 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2174-1148_2174-114 others(36): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
A | ATTTTTTT others(26): Show |
1 | a0001c0001t0005g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2174-1148_2174-114 others(37): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
AT | A | 9 | a0001c0001t0003g0028a0001c0001t0003g0223a0001c0001t0009g0034others(6): Show | 9 | HG02074.hp2 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2174-1148delT | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATT | A | 38 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0003g0085others(35): Show | 38 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2174-1149_2174-114 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATTT | A | 20 | a0001c0001t0003g0054a0001c0001t0003g0105a0001c0001t0003g0113others(17): Show | 20 | HG00280.hp2 HG00323.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.2174-1150_2174-114 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATTTT | A | 6 | a0001c0001t0002g0087a0002c0003t0001g0101a0002c0003t0002g0146others(3): Show | 6 | HG02109.hp2 HG02738.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.2174-1151_2174-114 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATTTTT | A | 65 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0036others(62): Show | 65 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2174-1152_2174-114 others(9): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATTTTTTT others(2): Show |
A | 40 | a0001c0001t0001g0042a0001c0001t0001g0099a0001c0001t0001g0128others(37): Show | 40 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.2174-1156_2174-114 others(13): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0065a0001c0001t0001g0074 | 2 | HG02300.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2174-1157_2174-114 others(14): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017440
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2174-1159_2174-114 others(16): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46017440 | |||||
| chr17:46017505
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-1113A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017505 | ||||||
| chr17:46017689
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-929C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017689 | ||||||
| chr17:46017950
|
C | G | 42 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.2174-668C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017950 | ||||||
| chr17:46017969
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-649C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46017969 | ||||||
| chr17:46018101
|
T | C | 63 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2174-517T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46018101 | ||||||
| chr17:46018123
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2174-495C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46018123 | ||||||
| chr17:46018147
|
GA | G | 168 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.2174-455delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46018147 | |||||
| chr17:46018195
|
A | T | 1 | a0002c0003t0024g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2174-423A>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46018195 | ||||||
| chr17:46018204
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-414G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46018204 | ||||||
| chr17:46018295
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2174-323T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | chr17 | 46018295 | ||||||
| chr17:46018358
|
T | TA | 9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(6): Show | 9 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.2174-257dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 46018358 | |||||
| chr17:46018839
|
G | C | 3 | a0007c0008t0014g0026a0007c0008t0014g0191a0007c0008t0029g0060 | 3 | HG02717.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2286+109G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46018839 | ||||||
| chr17:46019120
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2286+390C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019120 | ||||||
| chr17:46019148
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0026g0192a0002c0002t0003g0145 | 3 | HG02895.hp1 HG04204.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.2286+418C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019148 | ||||||
| chr17:46019175
|
T | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2286+445T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019175 | ||||||
| chr17:46019187
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2286+457G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019187 | ||||||
| chr17:46019243
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2286+513T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019243 | ||||||
| chr17:46019249
|
T | G | 1 | a0001c0001t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2286+519T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019249 | ||||||
| chr17:46019285
|
G | A | 1 | a0001c0001t0026g0192 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2286+555G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019285 | ||||||
| chr17:46019298
|
AG | A | 59 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0003g0082others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.2286+569delG | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019298 | ||||||
| chr17:46019485
|
G | C | 1 | a0002c0003t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2286+755G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019485 | ||||||
| chr17:46019638
|
G | C | 1 | a0002c0003t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2286+908G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019638 | ||||||
| chr17:46019869
|
G | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2286+1139G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019869 | ||||||
| chr17:46019883
|
G | A | 61 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0003g0082others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.2286+1153G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46019883 | ||||||
| chr17:46020011
|
CACA | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2286+1283_2286+128 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46020011 | |||||
| chr17:46020013
|
CA | C | 14 | a0001c0001t0003g0233a0001c0001t0009g0034a0001c0001t0010g0052others(11): Show | 14 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.2286+1299delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46020013 | |||||
| chr17:46020013
|
CAA | C | 198 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.2286+1298_2286+129 others(6): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46020013 | |||||
| chr17:46020013
|
CAAA | C | 13 | a0001c0001t0001g0152a0001c0001t0002g0096a0002c0003t0001g0075others(10): Show | 13 | HG01106.hp1 HG01123.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.2286+1297_2286+129 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46020013 | |||||
| chr17:46020051
|
C | T | 1 | a0006c0006t0002g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2286+1321C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46020051 | ||||||
| chr17:46020105
|
C | T | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2286+1375C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46020105 | ||||||
| chr17:46020962
|
G | A | 1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2286+2232G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46020962 | ||||||
| chr17:46021135
|
C | A | 1 | a0001c0001t0008g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2286+2405C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021135 | ||||||
| chr17:46021294
|
G | C | 2 | a0001c0001t0008g0029a0009c0011t0008g0097 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2286+2564G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021294 | ||||||
| chr17:46021383
|
A | AC | 5 | a0001c0001t0026g0192a0004c0005t0025g0121a0007c0008t0014g0026others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2287-2569dupC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46021383 | |||||
| chr17:46021431
|
C | T | 57 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0036others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2287-2525C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021431 | ||||||
| chr17:46021495
|
G | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-2461G>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021495 | ||||||
| chr17:46021496
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-2460A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021496 | ||||||
| chr17:46021517
|
G | A | 1 | a0003c0004t0004g0005 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2287-2439G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021517 | ||||||
| chr17:46021601
|
G | A | 24 | a0001c0001t0002g0123a0001c0001t0007g0184a0001c0001t0027g0093others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.2287-2355G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021601 | ||||||
| chr17:46021716
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-2240C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021716 | ||||||
| chr17:46021763
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-2193C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021763 | ||||||
| chr17:46021884
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2287-2072T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021884 | ||||||
| chr17:46021943
|
C | G | 58 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(55): Show | 58 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.2287-2013C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021943 | ||||||
| chr17:46021991
|
T | G | 2 | a0001c0010t0013g0129a0001c0010t0013g0208 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2287-1965T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46021991 | ||||||
| chr17:46022051
|
C | T | 63 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0003g0082others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.2287-1905C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022051 | ||||||
| chr17:46022081
|
A | G | 1 | a0009c0011t0008g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2287-1875A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022081 | ||||||
| chr17:46022302
|
T | C | 235 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2287-1654T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022302 | ||||||
| chr17:46022303
|
G | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-1653G>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022303 | ||||||
| chr17:46022353
|
C | CA | 107 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0074others(104): Show | 107 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2287-1583dupA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46022353 | |||||
| chr17:46022353
|
CA | C | 9 | a0001c0001t0002g0161a0001c0001t0007g0205a0001c0001t0009g0034others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2287-1583delA | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46022353 | |||||
| chr17:46022353
|
CAAA | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-1585_2287-158 others(7): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46022353 | |||||
| chr17:46022443
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-1513A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022443 | ||||||
| chr17:46022447
|
A | G | 4 | a0001c0001t0026g0192a0007c0008t0014g0026a0007c0008t0014g0191others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2287-1509A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022447 | ||||||
| chr17:46022461
|
C | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-1495C>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022461 | ||||||
| chr17:46022490
|
G | GC | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-1462dupC | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46022490 | |||||
| chr17:46022506
|
C | T | 1 | a0002c0002t0003g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2287-1450C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022506 | ||||||
| chr17:46022617
|
T | C | 1 | a0001c0001t0026g0192 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2287-1339T>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022617 | ||||||
| chr17:46022766
|
A | C | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2287-1190A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46022766 | ||||||
| chr17:46022897
|
T | TGATA | 6 | a0001c0001t0007g0205a0004c0005t0007g0077a0004c0005t0007g0170others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2287-1042_2287-103 others(8): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 46022897 | |||||
| chr17:46023187
|
C | A | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-769C>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023187 | ||||||
| chr17:46023300
|
A | C | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-656A>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023300 | ||||||
| chr17:46023338
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2287-618A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023338 | ||||||
| chr17:46023351
|
T | G | 1 | a0008c0009t0009g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2287-605T>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023351 | ||||||
| chr17:46023540
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-416A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023540 | ||||||
| chr17:46023550
|
C | T | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-406C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023550 | ||||||
| chr17:46023638
|
A | G | 21 | a0003c0004t0004g0001a0003c0004t0004g0003a0003c0004t0004g0004others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2287-318A>G | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023638 | ||||||
| chr17:46023703
|
T | A | 1 | a0001c0001t0002g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2287-253T>A | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023703 | ||||||
| chr17:46023840
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA18991.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2287-116C>T | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023840 | ||||||
| chr17:46023879
|
G | C | 1 | a0002c0003t0002g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2287-77G>C | MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 12/12 | chr17 | 46023879 |