| geneid | 4133 |
|---|---|
| ensemblid | ENSG00000078018.22 |
| hgncid | 6839 |
| symbol | MAP2 |
| name | microtubule associated protein 2 |
| refseq_nuc | NM_001375505.1 |
| refseq_prot | NP_001362434.1 |
| ensembl_nuc | ENST00000682079.1 |
| ensembl_prot | ENSP00000507035.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 209424047 |
| end | 209734112 |
| strand | + |
| ver | v1.2 |
| region | chr2:209424047-209734112 |
| region5000 | chr2:209419047-209739112 |
| regionname0 | MAP2_chr2_209424047_209734112 |
| regionname5000 | MAP2_chr2_209419047_209739112 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1827 | 84 | 39 | 10 | 22 | 3 | 8 | 20 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002 | 0/0 | 1827 | 43 | 15 | 4 | 22 | 1 | 1 | 19 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003 | 0/0 | 1827 | 9 | 7 | 1 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0004 | 0/0 | 1827 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0005 | 0/0 | 1827 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0006 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0007 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0008 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0009 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0010 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0011 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0012 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5484 | 68 | 24 | 10 | 21 | 3 | 8 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0002 | 0/0 | 5484 | 34 | 6 | 4 | 22 | 1 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0003 | 0/0 | 5484 | 9 | 9 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0004 | 0/0 | 5484 | 9 | 7 | 1 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0005 | 0/0 | 5484 | 7 | 7 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0006 | 0/0 | 5484 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0007 | 0/0 | 5484 | 3 | 2 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0008 | 0/0 | 5484 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0009 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0010 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0011 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0012 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0013 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0014 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0015 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0016 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0017 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0018 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0019 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| c0020 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| 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 | 4163 | 34 | 5 | 6 | 19 | 1 | 3 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0002 | 0/1 | 4162 | 34 | 25 | 4 | 0 | 2 | 2 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0003 | 0/0 | 4164 | 11 | 7 | 1 | 0 | 0 | 3 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0004 | 0/0 | 4184 | 5 | 0 | 0 | 5 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0005 | 0/0 | 4179 | 5 | 0 | 0 | 4 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0006 | 0/0 | 4161 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0007 | 0/0 | 4162 | 4 | 0 | 0 | 4 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0008 | 0/0 | 4172 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0009 | 0/0 | 4180 | 3 | 1 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0010 | 1/0 | 4167 | 3 | 2 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0011 | 0/0 | 4166 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0012 | 0/0 | 4185 | 3 | 0 | 1 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0013 | 0/0 | 4178 | 2 | 0 | 0 | 1 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0014 | 0/0 | 4184 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0015 | 0/0 | 4184 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0016 | 0/0 | 4183 | 2 | 0 | 1 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0017 | 0/0 | 4166 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0018 | 0/0 | 4160 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0019 | 0/0 | 4183 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0020 | 0/0 | 4181 | 2 | 0 | 1 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0021 | 0/0 | 4163 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0022 | 0/0 | 4180 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0023 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0024 | 0/0 | 4180 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0025 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0026 | 0/0 | 4163 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0027 | 0/0 | 4166 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0028 | 0/0 | 4185 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0029 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0030 | 0/0 | 4180 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0031 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0032 | 0/0 | 4178 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0033 | 0/0 | 4162 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0034 | 0/0 | 4160 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0035 | 0/0 | 4162 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0036 | 0/0 | 4160 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0037 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0038 | 0/0 | 4187 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0039 | 0/0 | 4183 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| t0040 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5484 | 68 | 24 | 10 | 21 | 3 | 8 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0003 | 0/0 | 5484 | 9 | 9 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0006 | 0/0 | 5484 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0013 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0014 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0017 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002 | 0/0 | 5484 | 34 | 6 | 4 | 22 | 1 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0005 | 0/0 | 5484 | 7 | 7 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0010 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0011 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003c0004 | 0/0 | 5484 | 9 | 7 | 1 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0004c0007 | 0/0 | 5484 | 3 | 2 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0005c0008 | 0/0 | 5484 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0006c0018 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0007c0009 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0008c0015 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0009c0019 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0010c0012 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0011c0016 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0012c0020 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9646 | 30 | 3 | 5 | 18 | 1 | 3 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0002 | 0/1 | 9645 | 24 | 15 | 4 | 0 | 2 | 2 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0003 | 0/0 | 9647 | 6 | 2 | 1 | 0 | 0 | 3 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0007 | 0/0 | 9645 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0010 | 1/0 | 9650 | 2 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0021 | 0/0 | 9646 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0025 | 0/0 | 9648 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0033 | 0/0 | 9645 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0001t0034 | 0/0 | 9643 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0003t0002 | 0/0 | 9645 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0003t0006 | 0/0 | 9644 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0003t0018 | 0/0 | 9643 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0003t0036 | 0/0 | 9643 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0006t0002 | 0/0 | 9645 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0013t0006 | 0/0 | 9644 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0014t0001 | 0/0 | 9646 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0001c0017t0007 | 0/0 | 9645 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0004 | 0/0 | 9667 | 5 | 0 | 0 | 5 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0005 | 0/0 | 9662 | 5 | 0 | 0 | 4 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0009 | 0/0 | 9663 | 3 | 1 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0012 | 0/0 | 9668 | 3 | 0 | 1 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0013 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0014 | 0/0 | 9667 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0015 | 0/0 | 9667 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0016 | 0/0 | 9666 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0019 | 0/0 | 9666 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0020 | 0/0 | 9664 | 2 | 0 | 1 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0022 | 0/0 | 9663 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0023 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0024 | 0/0 | 9663 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0028 | 0/0 | 9668 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0029 | 0/0 | 9665 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0030 | 0/0 | 9663 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0031 | 0/0 | 9662 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0032 | 0/0 | 9661 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0002t0039 | 0/0 | 9666 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0005t0008 | 0/0 | 9655 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0005t0011 | 0/0 | 9649 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0005t0027 | 0/0 | 9649 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0010t0015 | 0/0 | 9667 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0002c0011t0037 | 0/0 | 9666 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003c0004t0001 | 0/0 | 9646 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003c0004t0002 | 0/0 | 9645 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003c0004t0003 | 0/0 | 9647 | 5 | 5 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003c0004t0026 | 0/0 | 9646 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0003c0004t0035 | 0/0 | 9645 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0004c0007t0010 | 0/0 | 9650 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0004c0007t0017 | 0/0 | 9649 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0005c0008t0013 | 0/0 | 9661 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0005c0008t0016 | 0/0 | 9666 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0006c0018t0001 | 0/0 | 9646 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0007c0009t0002 | 0/0 | 9645 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0008c0015t0002 | 0/0 | 9645 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0009c0019t0007 | 0/0 | 9645 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0010c0012t0038 | 0/0 | 9670 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0011c0016t0001 | 0/0 | 9646 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| a0012c0020t0040 | 0/0 | 9646 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | copy fasta | chr2 | 209419047 | 209739112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0010g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0021g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0025g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0033g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0001t0034g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0018g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0003t0036g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0006t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0006t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0006t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0013t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0014t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0001c0017t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0012g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0012g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0013g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0014g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0015g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0016g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0019g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0020g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0022g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0023g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0024g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0028g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0029g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0030g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0031g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0032g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0002t0039g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0005t0027g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0010t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0002c0011t0037g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0026g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0003c0004t0035g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0004c0007t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0004c0007t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0004c0007t0017g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0005c0008t0013g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0005c0008t0016g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0006c0018t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0007c0009t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0008c0015t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0009c0019t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0010c0012t0038g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0011c0016t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| a0012c0020t0040g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00099 | hp2 | a0002 | c0002 | t0005 | g0046 | EUR | GBR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00408 | hp1 | a0002 | c0002 | t0013 | g0102 | EAS | CHS | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00597 | hp1 | a0002 | c0002 | t0009 | g0112 | EAS | CHS | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00597 | hp2 | a0001 | c0017 | t0007 | g0036 | EAS | CHS | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG00733 | hp2 | a0010 | c0012 | t0038 | g0045 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01109 | hp1 | a0006 | c0018 | t0001 | g0123 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01192 | hp1 | a0002 | c0002 | t0020 | g0048 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01243 | hp2 | a0004 | c0007 | t0017 | g0147 | AMR | PUR | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01261 | hp2 | a0002 | c0002 | t0016 | g0031 | AMR | CLM | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01358 | hp1 | a0003 | c0004 | t0026 | g0109 | AMR | CLM | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01433 | hp1 | a0002 | c0002 | t0031 | g0080 | AMR | CLM | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01884 | hp2 | a0003 | c0004 | t0003 | g0090 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01891 | hp1 | a0002 | c0005 | t0027 | g0070 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01891 | hp2 | a0001 | c0001 | t0025 | g0141 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01975 | hp2 | a0002 | c0002 | t0012 | g0034 | AMR | PEL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02055 | hp1 | a0002 | c0005 | t0008 | g0134 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02080 | hp1 | a0009 | c0019 | t0007 | g0042 | EAS | KHV | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02080 | hp2 | a0002 | c0002 | t0004 | g0145 | EAS | KHV | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02257 | hp1 | a0001 | c0001 | t0033 | g0007 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02258 | hp1 | a0003 | c0004 | t0003 | g0089 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02258 | hp2 | a0001 | c0001 | t0034 | g0096 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02280 | hp1 | a0001 | c0014 | t0001 | g0101 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02280 | hp2 | a0002 | c0002 | t0015 | g0066 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0099 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02451 | hp2 | a0004 | c0007 | t0017 | g0058 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02572 | hp1 | a0001 | c0003 | t0036 | g0006 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02572 | hp2 | a0002 | c0002 | t0028 | g0067 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02615 | hp1 | a0002 | c0002 | t0032 | g0069 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02622 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0004 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02683 | hp1 | a0003 | c0004 | t0035 | g0021 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02886 | hp1 | a0003 | c0004 | t0003 | g0088 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02886 | hp2 | a0002 | c0002 | t0029 | g0061 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02895 | hp1 | a0003 | c0004 | t0002 | g0062 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02895 | hp2 | a0001 | c0006 | t0002 | g0057 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02922 | hp1 | a0001 | c0013 | t0006 | g0073 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02965 | hp2 | a0003 | c0004 | t0003 | g0091 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03041 | hp2 | a0001 | c0006 | t0002 | g0093 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03098 | hp1 | a0002 | c0005 | t0011 | g0072 | AFR | MSL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0059 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03130 | hp2 | a0002 | c0005 | t0011 | g0094 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03139 | hp1 | a0002 | c0010 | t0015 | g0065 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03195 | hp1 | a0007 | c0009 | t0002 | g0060 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03195 | hp2 | a0002 | c0005 | t0011 | g0071 | AFR | ESN | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03225 | hp1 | a0001 | c0003 | t0006 | g0023 | AFR | MSL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03239 | hp2 | a0005 | c0008 | t0016 | g0024 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03540 | hp2 | a0001 | c0003 | t0018 | g0005 | AFR | GWD | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03579 | hp1 | a0008 | c0015 | t0002 | g0075 | AFR | MSL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03579 | hp2 | a0002 | c0005 | t0008 | g0136 | AFR | MSL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03710 | hp1 | a0005 | c0008 | t0013 | g0131 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | BEB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG04204 | hp1 | a0002 | c0002 | t0022 | g0100 | SAS | STU | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | STU | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18522 | hp1 | a0002 | c0005 | t0008 | g0135 | AFR | YRI | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0055 | AFR | YRI | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18906 | hp1 | a0002 | c0002 | t0030 | g0068 | AFR | YRI | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18906 | hp2 | a0004 | c0007 | t0010 | g0148 | AFR | YRI | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18942 | hp1 | a0002 | c0002 | t0039 | g0051 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18943 | hp1 | a0002 | c0002 | t0014 | g0113 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18954 | hp1 | a0002 | c0002 | t0020 | g0047 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18959 | hp1 | a0001 | c0001 | t0021 | g0104 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18959 | hp2 | a0002 | c0002 | t0004 | g0119 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18963 | hp2 | a0002 | c0002 | t0023 | g0124 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18982 | hp1 | a0011 | c0016 | t0001 | g0009 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18982 | hp2 | a0002 | c0002 | t0009 | g0108 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18983 | hp2 | a0002 | c0002 | t0012 | g0038 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18984 | hp2 | a0002 | c0002 | t0005 | g0039 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18986 | hp1 | a0002 | c0002 | t0024 | g0121 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18995 | hp1 | a0002 | c0002 | t0012 | g0043 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19002 | hp1 | a0002 | c0002 | t0005 | g0041 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0049 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19007 | hp1 | a0002 | c0002 | t0019 | g0040 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19043 | hp2 | a0001 | c0006 | t0002 | g0056 | AFR | LWK | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19056 | hp1 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0050 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19066 | hp2 | a0002 | c0002 | t0005 | g0035 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19074 | hp2 | a0002 | c0002 | t0014 | g0143 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19079 | hp1 | a0002 | c0002 | t0004 | g0118 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19080 | hp2 | a0002 | c0002 | t0019 | g0044 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19083 | hp1 | a0002 | c0002 | t0005 | g0033 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19088 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02486 | hp2 | a0003 | c0004 | t0003 | g0097 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02559 | hp1 | a0001 | c0003 | t0018 | g0016 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG02559 | hp2 | a0001 | c0006 | t0002 | g0092 | AFR | ACB | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG06807 | hp1 | a0002 | c0002 | t0009 | g0098 | AFR | USA | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| HG06807 | hp2 | a0012 | c0020 | t0040 | g0084 | AFR | USA | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | USA | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA21309 | hp1 | a0002 | c0011 | t0037 | g0037 | AFR | LWK | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | LWK | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0013 | REF | REF | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0117 | REF | REF | MAP2_chr2_209419047_209739112 | MAP2 | chr2 | 209419047 | 209739112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:209692696
|
G | A | 1 | a0005 | 2 | HG03239.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.526G>A | p.Asp176Asn | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 977/9650 | 526/5484 | 176/1827 | chr2 | 209692696 | ||
| chr2:209692706
|
A | G | 1 | a0004 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.536A>G | p.Glu179Gly | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 987/9650 | 536/5484 | 179/1827 | chr2 | 209692706 | ||
| chr2:209692997
|
A | T | 1 | a0012 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.827A>T | p.Asp276Val | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1278/9650 | 827/5484 | 276/1827 | chr2 | 209692997 | ||
| chr2:209693147
|
T | C | 1 | a0011 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.977T>C | p.Leu326Ser | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1428/9650 | 977/5484 | 326/1827 | chr2 | 209693147 | ||
| chr2:209693155
|
A | G | 1 | a0010 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.985A>G | p.Met329Val | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1436/9650 | 985/5484 | 329/1827 | chr2 | 209693155 | ||
| chr2:209693438
|
G | A | 4 | a0002a0004a0005others(1): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
missense_variant | MODERATE | c.1268G>A | p.Arg423Lys | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1719/9650 | 1268/5484 | 423/1827 | chr2 | 209693438 | ||
| chr2:209694515
|
C | T | 1 | a0009 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.2345C>T | p.Ala782Val | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 2796/9650 | 2345/5484 | 782/1827 | chr2 | 209694515 | ||
| chr2:209695097
|
A | T | 1 | a0004 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2927A>T | p.His976Leu | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 3378/9650 | 2927/5484 | 976/1827 | chr2 | 209695097 | ||
| chr2:209695228
|
A | G | 1 | a0006 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.3058A>G | p.Ser1020Gly | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 3509/9650 | 3058/5484 | 1020/1827 | chr2 | 209695228 | ||
| chr2:209695465
|
A | G | 1 | a0003 | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
missense_variant | MODERATE | c.3295A>G | p.Met1099Val | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 3746/9650 | 3295/5484 | 1099/1827 | chr2 | 209695465 | ||
| chr2:209695699
|
C | T | 1 | a0008 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.3529C>T | p.Pro1177Ser | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 3980/9650 | 3529/5484 | 1177/1827 | chr2 | 209695699 | ||
| chr2:209696201
|
A | C | 1 | a0007 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.4031A>C | p.Lys1344Thr | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 4482/9650 | 4031/5484 | 1344/1827 | chr2 | 209696201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:209653191
|
T | C | 12 | a0001c0003a0001c0006a0001c0013others(9): Show | 73 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(70): Show |
synonymous_variant | LOW | c.21T>C | p.Asp7Asp | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/16 | 472/9650 | 21/5484 | 7/1827 | chr2 | 209653191 | ||
| chr2:209653302
|
C | T | 1 | a0001c0013 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.132C>T | p.Ser44Ser | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/16 | 583/9650 | 132/5484 | 44/1827 | chr2 | 209653302 | ||
| chr2:209692656
|
C | T | 7 | a0002c0002a0002c0005a0002c0010others(4): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
synonymous_variant | LOW | c.486C>T | p.His162His | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 937/9650 | 486/5484 | 162/1827 | chr2 | 209692656 | ||
| chr2:209692728
|
T | C | 1 | a0001c0013 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.558T>C | p.Ser186Ser | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1009/9650 | 558/5484 | 186/1827 | chr2 | 209692728 | ||
| chr2:209692818
|
G | A | 14 | a0001c0003a0001c0006a0001c0013others(11): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.648G>A | p.Thr216Thr | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1099/9650 | 648/5484 | 216/1827 | chr2 | 209692818 | ||
| chr2:209693643
|
A | T | 1 | a0002c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1473A>T | p.Thr491Thr | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 1924/9650 | 1473/5484 | 491/1827 | chr2 | 209693643 | ||
| chr2:209694207
|
T | C | 1 | a0002c0005 | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
synonymous_variant | LOW | c.2037T>C | p.Asp679Asp | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 2488/9650 | 2037/5484 | 679/1827 | chr2 | 209694207 | ||
| chr2:209694450
|
T | C | 1 | a0001c0006 | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.2280T>C | p.Pro760Pro | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 2731/9650 | 2280/5484 | 760/1827 | chr2 | 209694450 | ||
| chr2:209695236
|
G | T | 5 | a0002c0002a0002c0010a0002c0011others(2): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
synonymous_variant | LOW | c.3066G>T | p.Val1022Val | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 3517/9650 | 3066/5484 | 1022/1827 | chr2 | 209695236 | ||
| chr2:209695557
|
G | A | 1 | a0002c0010 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.3387G>A | p.Glu1129Glu | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 8/16 | 3838/9650 | 3387/5484 | 1129/1827 | chr2 | 209695557 | ||
| chr2:209705582
|
C | T | 1 | a0001c0017 | 1 | HG00597.hp2 | splice_region_variant&synonymous_variant | LOW | c.4587C>T | p.Asp1529Asp | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/16 | 5038/9650 | 4587/5484 | 1529/1827 | chr2 | 209705582 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:209424160
|
T | C | 1 | a0001c0001t0021 | 1 | NA18959.hp1 | 5_prime_UTR_variant | MODIFIER | c.-338T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/16 | 229011 | chr2 | 209424160 | |||||
| chr2:209424160
|
TC | T | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(35): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
5_prime_UTR_variant | MODIFIER | c.-330delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/16 | 229003 | INFO_REALIGN_3_PRIME | chr2 | 209424160 | ||||
| chr2:209424162
|
C | T | 11 | a0001c0001t0007a0001c0017t0007a0002c0002t0005others(8): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-336C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/16 | 229009 | chr2 | 209424162 | |||||
| chr2:209730600
|
G | A | 27 | a0002c0002t0004a0002c0002t0005a0002c0002t0009others(24): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 203 | chr2 | 209730600 | |||||
| chr2:209731029
|
G | A | 3 | a0002c0005t0008a0002c0005t0011a0002c0005t0027 | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*632G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 632 | chr2 | 209731029 | |||||
| chr2:209731096
|
G | C | 27 | a0002c0002t0004a0002c0002t0005a0002c0002t0009others(24): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*699G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 699 | chr2 | 209731096 | |||||
| chr2:209731167
|
A | G | 1 | a0001c0003t0036 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*770A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 770 | chr2 | 209731167 | |||||
| chr2:209731611
|
A | AT | 2 | a0001c0003t0006a0001c0013t0006 | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1220dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 209731611 | ||||
| chr2:209731705
|
A | G | 1 | a0002c0005t0027 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1308A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 1308 | chr2 | 209731705 | |||||
| chr2:209731821
|
A | T | 2 | a0002c0002t0014a0002c0002t0039 | 3 | NA18942.hp1 NA18943.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1424A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 1424 | chr2 | 209731821 | |||||
| chr2:209732101
|
T | C | 27 | a0002c0002t0004a0002c0002t0005a0002c0002t0009others(24): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1704T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 1704 | chr2 | 209732101 | |||||
| chr2:209732226
|
A | G | 2 | a0003c0004t0026a0003c0004t0035 | 2 | HG01358.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1829A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 1829 | chr2 | 209732226 | |||||
| chr2:209732454
|
A | T | 2 | a0001c0003t0018a0001c0003t0036 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2057A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2057 | chr2 | 209732454 | |||||
| chr2:209732896
|
CA | C | 2 | a0002c0005t0011a0002c0005t0027 | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2500delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2500 | chr2 | 209732896 | |||||
| chr2:209732948
|
A | G | 1 | a0002c0002t0024 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2551A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2551 | chr2 | 209732948 | |||||
| chr2:209733005
|
G | A | 1 | a0001c0001t0033 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2608G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2608 | chr2 | 209733005 | |||||
| chr2:209733075
|
C | T | 3 | a0002c0005t0008a0002c0005t0011a0002c0005t0027 | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2678C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2678 | chr2 | 209733075 | |||||
| chr2:209733076
|
G | A | 2 | a0003c0004t0026a0003c0004t0035 | 2 | HG01358.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2679G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2679 | chr2 | 209733076 | |||||
| chr2:209733260
|
G | A | 1 | a0002c0011t0037 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2863G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 2863 | chr2 | 209733260 | |||||
| chr2:209733460
|
C | CCACA | 1 | a0002c0005t0008 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3093_*3096dupACAC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
C | CCACACAC others(3): Show |
2 | a0002c0002t0013a0005c0008t0013 | 2 | HG00408.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3087_*3096dupACAC others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
C | CCACACAC others(5): Show |
7 | a0002c0002t0005a0002c0002t0009a0002c0002t0022others(4): Show | 13 | HG00099.hp2 HG00597.hp1 HG01433.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3085_*3096dupACAC others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
C | CCACACAC others(7): Show |
2 | a0002c0002t0020a0002c0002t0030 | 3 | HG01192.hp1 NA18906.hp1 NA18954.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3083_*3096dupACAC others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
C | CCACACAC others(9): Show |
8 | a0002c0002t0004a0002c0002t0014a0002c0002t0016others(5): Show | 14 | HG01261.hp2 HG02080.hp2 HG02886.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3081_*3096dupACAC others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
C | CCACACAC others(11): Show |
4 | a0002c0002t0012a0002c0002t0015a0002c0002t0028others(1): Show | 6 | HG01975.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3079_*3096dupACAC others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
C | CCACACAC others(13): Show |
1 | a0010c0012t0038 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3077_*3096dupACAC others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3097 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
CCA | C | 3 | a0001c0001t0003a0001c0001t0025a0003c0004t0003 | 12 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3095_*3096delAC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3095 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
CCACA | C | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(16): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3093_*3096delACAC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3093 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733460
|
CCACACA | C | 5 | a0001c0001t0034a0001c0003t0006a0001c0003t0018others(2): Show | 8 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3091_*3096delACAC others(2): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3091 | INFO_REALIGN_3_PRIME | chr2 | 209733460 | ||||
| chr2:209733748
|
G | C | 1 | a0004c0007t0017 | 2 | HG01243.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3351G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3351 | chr2 | 209733748 | |||||
| chr2:209733881
|
G | GA | 22 | a0002c0002t0004a0002c0002t0005a0002c0002t0009others(19): Show | 41 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3493dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3494 | INFO_REALIGN_3_PRIME | chr2 | 209733881 | ||||
| chr2:209733925
|
G | A | 1 | a0002c0002t0022 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3528G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 16/16 | 3528 | chr2 | 209733925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:209424397
|
G | A | 1 | a0002c0002t0004g0001 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-222+121G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209424397 | ||||||
| chr2:209424473
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-222+197C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209424473 | ||||||
| chr2:209424533
|
G | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+257G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209424533 | ||||||
| chr2:209424627
|
G | T | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+351G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209424627 | ||||||
| chr2:209424710
|
C | T | 1 | a0004c0007t0017g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-222+434C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209424710 | ||||||
| chr2:209425194
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01192.hp2 HG01993.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+918T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425194 | ||||||
| chr2:209425297
|
G | A | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-222+1021G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425297 | ||||||
| chr2:209425446
|
T | A | 1 | a0001c0001t0001g0014 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-222+1170T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425446 | ||||||
| chr2:209425456
|
T | G | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+1180T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425456 | ||||||
| chr2:209425474
|
T | C | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+1198T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425474 | ||||||
| chr2:209425702
|
T | A | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+1426T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425702 | ||||||
| chr2:209425972
|
G | A | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-222+1696G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425972 | ||||||
| chr2:209425999
|
A | G | 13 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(10): Show | 13 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-222+1723A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209425999 | ||||||
| chr2:209426003
|
G | A | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+1727G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426003 | ||||||
| chr2:209426012
|
C | T | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+1736C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426012 | ||||||
| chr2:209426054
|
G | A | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-222+1778G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426054 | ||||||
| chr2:209426139
|
A | G | 10 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(7): Show | 10 | HG01891.hp2 HG02080.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.-222+1863A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426139 | ||||||
| chr2:209426197
|
T | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-222+1921T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426197 | ||||||
| chr2:209426284
|
T | G | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+2008T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426284 | ||||||
| chr2:209426382
|
A | T | 93 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-222+2106A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426382 | ||||||
| chr2:209426434
|
G | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+2158G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426434 | ||||||
| chr2:209426585
|
C | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+2309C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426585 | ||||||
| chr2:209426649
|
A | G | 44 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-222+2373A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209426649 | ||||||
| chr2:209427091
|
G | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+2815G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209427091 | ||||||
| chr2:209427260
|
T | C | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+2984T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209427260 | ||||||
| chr2:209427348
|
AT | A | 14 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(11): Show | 14 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-222+3079delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209427348 | |||||
| chr2:209427457
|
C | T | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+3181C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209427457 | ||||||
| chr2:209427844
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+3568A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209427844 | ||||||
| chr2:209428104
|
A | C | 8 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+3828A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209428104 | ||||||
| chr2:209428257
|
A | T | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-222+3981A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209428257 | ||||||
| chr2:209428381
|
C | CT | 18 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(15): Show | 18 | HG00733.hp1 HG01884.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-222+4120dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428381 | |||||
| chr2:209428381
|
CT | C | 21 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(18): Show | 21 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-222+4120delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428381 | |||||
| chr2:209428381
|
CTT | C | 8 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(5): Show | 8 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-222+4119_-222+412 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428381 | |||||
| chr2:209428626
|
T | G | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+4350T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209428626 | ||||||
| chr2:209428875
|
C | T | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+4599C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209428875 | ||||||
| chr2:209428923
|
T | TTTTA | 17 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 17 | HG00597.hp1 HG01192.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-222+4691_-222+469 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428923 | |||||
| chr2:209428923
|
T | TTTTATTT others(1): Show |
6 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0021g0104others(3): Show | 6 | HG00408.hp1 HG00408.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+4687_-222+469 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428923 | |||||
| chr2:209428923
|
T | TTTTATTT others(5): Show |
1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-222+4683_-222+469 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428923 | |||||
| chr2:209428923
|
TTTTA | T | 6 | a0001c0001t0001g0132a0001c0001t0001g0133a0002c0002t0009g0098others(3): Show | 6 | HG02451.hp1 HG03579.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+4691_-222+469 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428923 | |||||
| chr2:209428923
|
TTTTATTT others(5): Show |
T | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+4683_-222+469 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428923 | |||||
| chr2:209428923
|
TTTTATTT others(17): Show |
T | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+4671_-222+469 others(28): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209428923 | |||||
| chr2:209429053
|
A | G | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-222+4777A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429053 | ||||||
| chr2:209429164
|
A | G | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-222+4888A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429164 | ||||||
| chr2:209429233
|
A | G | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+4957A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429233 | ||||||
| chr2:209429288
|
A | G | 1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-222+5012A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429288 | ||||||
| chr2:209429383
|
GT | G | 85 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.-222+5119delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209429383 | |||||
| chr2:209429417
|
G | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+5141G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429417 | ||||||
| chr2:209429494
|
T | C | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-222+5218T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429494 | ||||||
| chr2:209429678
|
A | G | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+5402A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429678 | ||||||
| chr2:209429698
|
A | T | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-222+5422A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429698 | ||||||
| chr2:209429800
|
C | T | 94 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-222+5524C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429800 | ||||||
| chr2:209429908
|
A | G | 1 | a0003c0004t0003g0097 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-222+5632A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209429908 | ||||||
| chr2:209430101
|
C | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+5825C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430101 | ||||||
| chr2:209430275
|
G | A | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-222+5999G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430275 | ||||||
| chr2:209430405
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-222+6129A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430405 | ||||||
| chr2:209430440
|
T | A | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+6164T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430440 | ||||||
| chr2:209430564
|
G | A | 1 | a0002c0002t0004g0001 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-222+6288G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430564 | ||||||
| chr2:209430750
|
A | G | 55 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(52): Show | 55 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-222+6474A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430750 | ||||||
| chr2:209430782
|
C | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+6506C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430782 | ||||||
| chr2:209430830
|
CAT | C | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+6556_-222+655 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209430830 | |||||
| chr2:209430844
|
C | A | 11 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-222+6568C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430844 | ||||||
| chr2:209430846
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-222+6570T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430846 | ||||||
| chr2:209430925
|
ATC | A | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+6652_-222+665 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209430925 | |||||
| chr2:209430931
|
G | T | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+6655G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430931 | ||||||
| chr2:209430932
|
A | C | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+6656A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430932 | ||||||
| chr2:209430934
|
T | C | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+6658T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430934 | ||||||
| chr2:209430935
|
AAAGTTTT others(2): Show |
A | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+6660_-222+666 others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209430935 | ||||||
| chr2:209430982
|
GC | G | 8 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+6708delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209430982 | |||||
| chr2:209431303
|
A | G | 94 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-222+7027A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431303 | ||||||
| chr2:209431479
|
G | A | 8 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+7203G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431479 | ||||||
| chr2:209431489
|
C | T | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+7213C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431489 | ||||||
| chr2:209431521
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-222+7245A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431521 | ||||||
| chr2:209431621
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+7345A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431621 | ||||||
| chr2:209431971
|
C | T | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+7695C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431971 | ||||||
| chr2:209431995
|
A | T | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+7719A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209431995 | ||||||
| chr2:209432012
|
G | A | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-222+7736G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432012 | ||||||
| chr2:209432040
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+7764G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432040 | ||||||
| chr2:209432138
|
T | A | 1 | a0002c0002t0012g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-222+7862T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432138 | ||||||
| chr2:209432442
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-222+8166G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432442 | ||||||
| chr2:209432480
|
G | A | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+8204G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432480 | ||||||
| chr2:209432561
|
T | C | 22 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(19): Show | 22 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.-222+8285T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432561 | ||||||
| chr2:209432574
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-222+8298C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432574 | ||||||
| chr2:209432576
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-222+8300A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432576 | ||||||
| chr2:209432648
|
G | A | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-222+8372G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432648 | ||||||
| chr2:209432816
|
G | A | 2 | a0001c0003t0002g0054a0001c0003t0002g0055 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-222+8540G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432816 | ||||||
| chr2:209432843
|
G | A | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-222+8567G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432843 | ||||||
| chr2:209432852
|
T | C | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+8576T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432852 | ||||||
| chr2:209432914
|
A | T | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-222+8638A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209432914 | ||||||
| chr2:209433214
|
A | G | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+8938A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433214 | ||||||
| chr2:209433254
|
A | G | 1 | a0002c0002t0016g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-222+8978A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433254 | ||||||
| chr2:209433353
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-222+9077G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433353 | ||||||
| chr2:209433396
|
A | C | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+9120A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433396 | ||||||
| chr2:209433568
|
A | G | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+9292A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433568 | ||||||
| chr2:209433914
|
A | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+9638A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433914 | ||||||
| chr2:209433993
|
C | T | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+9717C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209433993 | ||||||
| chr2:209434066
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+9790A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434066 | ||||||
| chr2:209434101
|
C | G | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+9825C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434101 | ||||||
| chr2:209434249
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-222+9973T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434249 | ||||||
| chr2:209434314
|
TA | T | 2 | a0001c0006t0002g0056a0001c0006t0002g0057 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-222+10039delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434314 | ||||||
| chr2:209434315
|
A | T | 55 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.-222+10039A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434315 | ||||||
| chr2:209434814
|
C | CCT | 22 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-222+10557_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434814 | |||||
| chr2:209434814
|
C | CCTCT | 25 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(22): Show | 25 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-222+10555_-222+10 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434814 | |||||
| chr2:209434831
|
CTCTA | C | 8 | a0001c0006t0002g0092a0001c0006t0002g0093a0002c0005t0011g0094others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+10557_-222+10 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434831 | |||||
| chr2:209434833
|
C | CTA | 3 | a0001c0006t0002g0056a0005c0008t0016g0024a0008c0015t0002g0075 | 3 | HG03239.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-222+10571_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434833 | |||||
| chr2:209434833
|
C | CTCTCTCT others(16): Show |
4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+10558_-222+10 others(29): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434833 | |||||
| chr2:209434833
|
CTA | C | 2 | a0001c0001t0010g0116a0001c0003t0036g0006 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-222+10571_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434833 | |||||
| chr2:209434833
|
CTATATAT others(10): Show |
C | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-222+10569_-222+10 others(23): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434833 | |||||
| chr2:209434835
|
A | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-222+10559A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434835 | ||||||
| chr2:209434837
|
A | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(67): Show | 70 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.-222+10561A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434837 | ||||||
| chr2:209434839
|
A | ATGT | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+10564_-222+10 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434839 | |||||
| chr2:209434839
|
A | C | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0105others(28): Show | 31 | HG01192.hp2 HG01261.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-222+10563A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434839 | ||||||
| chr2:209434841
|
A | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0138a0001c0001t0001g0146 | 3 | HG01261.hp1 NA18986.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-222+10565A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434841 | ||||||
| chr2:209434843
|
ATATATGT others(35): Show |
A | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+10573_-222+10 others(48): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434843 | |||||
| chr2:209434845
|
A | G | 23 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(20): Show | 23 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-222+10569A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434845 | ||||||
| chr2:209434846
|
TATGTTA | T | 23 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(20): Show | 23 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-222+10571_-222+10 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434846 | ||||||
| chr2:209434850
|
TTA | T | 9 | a0001c0006t0002g0092a0001c0006t0002g0093a0002c0002t0014g0113others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+10584_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434850 | |||||
| chr2:209434852
|
A | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-222+10576A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434852 | ||||||
| chr2:209434854
|
A | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-222+10578A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434854 | ||||||
| chr2:209434860
|
A | ATGTTATA others(26): Show |
1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+10616_-222+10 others(39): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434860 | |||||
| chr2:209434863
|
T | TTA | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+10595_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434863 | |||||
| chr2:209434865
|
ATATATAT others(13): Show |
A | 3 | a0001c0001t0033g0007a0001c0003t0018g0005a0001c0003t0036g0006 | 3 | HG02257.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-222+10597_-222+10 others(26): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434865 | |||||
| chr2:209434873
|
G | A | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-222+10597G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434873 | ||||||
| chr2:209434874
|
T | TGTTA | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-222+10598_-222+10 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434874 | ||||||
| chr2:209434874
|
T | TTA | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+10606_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434874 | |||||
| chr2:209434874
|
T | TTATATAT others(47): Show |
1 | a0002c0002t0005g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-222+10607_-222+10 others(60): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434874 | |||||
| chr2:209434874
|
T | TTATATAT others(45): Show |
18 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(15): Show | 18 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-222+10607_-222+10 others(58): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434874 | |||||
| chr2:209434874
|
T | TTATATAT others(43): Show |
1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+10607_-222+10 others(56): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434874 | |||||
| chr2:209434874
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-222+10645_-222+10 others(30): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434874 | |||||
| chr2:209434876
|
ATATATAT others(2): Show |
A | 16 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.-222+10608_-222+10 others(15): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434876 | |||||
| chr2:209434878
|
ATATATGT | A | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+10608_-222+10 others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434878 | |||||
| chr2:209434882
|
A | G | 30 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(27): Show | 30 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-222+10606A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434882 | ||||||
| chr2:209434884
|
G | T | 30 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(27): Show | 30 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-222+10608G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434884 | ||||||
| chr2:209434885
|
T | A | 30 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(27): Show | 30 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-222+10609T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434885 | ||||||
| chr2:209434885
|
T | TTA | 6 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(3): Show | 6 | HG02622.hp2 HG02647.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+10617_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434885 | |||||
| chr2:209434885
|
TTA | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-222+10617_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434885 | |||||
| chr2:209434885
|
TTATATAT others(6): Show |
T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+10630_-222+10 others(19): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434885 | |||||
| chr2:209434893
|
A | G | 3 | a0001c0001t0001g0140a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-222+10617A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434893 | ||||||
| chr2:209434895
|
G | T | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+10619G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434895 | ||||||
| chr2:209434896
|
T | A | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+10620T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434896 | ||||||
| chr2:209434909
|
T | TTA | 6 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(3): Show | 6 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+10641_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434909 | |||||
| chr2:209434917
|
A | ATATG | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+10642_-222+10 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434917 | |||||
| chr2:209434920
|
TTA | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+10654_-222+10 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434920 | |||||
| chr2:209434922
|
A | ATATATAT others(106): Show |
1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-222+10666_-222+10 others(119): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434922 | |||||
| chr2:209434922
|
A | ATATATAT others(54): Show |
4 | a0001c0013t0006g0073a0002c0005t0011g0071a0002c0005t0011g0072others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+10666_-222+10 others(67): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434922 | |||||
| chr2:209434922
|
A | ATATATAT others(41): Show |
2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+10666_-222+10 others(54): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209434922 | |||||
| chr2:209434935
|
A | T | 1 | a0001c0017t0007g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-222+10659A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434935 | ||||||
| chr2:209434943
|
G | A | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+10667G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209434943 | ||||||
| chr2:209435061
|
T | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+10785T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435061 | ||||||
| chr2:209435260
|
C | A | 7 | a0001c0006t0002g0092a0001c0006t0002g0093a0003c0004t0003g0088others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-222+10984C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435260 | ||||||
| chr2:209435272
|
T | TA | 8 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+11006dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435272 | |||||
| chr2:209435634
|
T | C | 27 | a0001c0001t0002g0020a0001c0001t0002g0052a0001c0001t0002g0053others(24): Show | 27 | HG00733.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-222+11358T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435634 | ||||||
| chr2:209435742
|
T | G | 94 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-222+11466T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435742 | ||||||
| chr2:209435948
|
T | TATATATA others(143): Show |
2 | a0001c0001t0001g0012a0002c0002t0023g0124 | 2 | NA18963.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-222+11695_-222+11 others(156): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(43): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0128others(14): Show | 17 | HG01358.hp1 HG01891.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-222+11720_-222+11 others(56): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(68): Show |
1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-222+11720_-222+11 others(81): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(93): Show |
11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0105others(8): Show | 11 | HG01109.hp1 HG01192.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.-222+11720_-222+11 others(106): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(118): Show |
8 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0115others(5): Show | 8 | HG00140.hp1 HG00597.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-222+11720_-222+11 others(131): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(143): Show |
3 | a0001c0001t0021g0104a0002c0002t0013g0102a0002c0002t0014g0113 | 3 | HG00408.hp1 NA18943.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-222+11720_-222+11 others(156): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(168): Show |
1 | a0005c0008t0013g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-222+11720_-222+11 others(181): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435948
|
T | TATATATA others(18): Show |
1 | a0001c0017t0007g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-222+11680_-222+11 others(31): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435948 | |||||
| chr2:209435957
|
A | C | 19 | a0001c0001t0007g0049a0001c0001t0007g0050a0002c0002t0005g0033others(16): Show | 19 | HG00099.hp2 HG00733.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-222+11681A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435957 | ||||||
| chr2:209435957
|
A | T | 70 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-222+11681A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435957 | ||||||
| chr2:209435973
|
AATATATA others(18): Show |
A | 11 | a0001c0001t0003g0074a0001c0003t0002g0054a0001c0003t0002g0055others(8): Show | 11 | HG01891.hp1 HG02922.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.-222+11721_-222+11 others(31): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435973 | |||||
| chr2:209435982
|
A | T | 14 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-222+11706A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435982 | ||||||
| chr2:209435990
|
T | TTATA | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+11717_-222+11 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435990 | |||||
| chr2:209435992
|
ATATACTA others(16): Show |
A | 46 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(43): Show | 46 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-222+11721_-222+11 others(29): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435992 | |||||
| chr2:209435997
|
C | A | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+11721C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435997 | ||||||
| chr2:209435997
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.-222+11721C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435997 | ||||||
| chr2:209435998
|
T | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.-222+11722T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209435998 | ||||||
| chr2:209435998
|
T | TATATATA others(68): Show |
9 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0125others(6): Show | 9 | HG00408.hp2 HG01358.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.-222+11748_-222+11 others(81): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435998 | |||||
| chr2:209435998
|
T | TATATATA others(93): Show |
1 | a0002c0002t0024g0121 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-222+11748_-222+11 others(106): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209435998 | |||||
| chr2:209436007
|
A | T | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+11731A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209436007 | ||||||
| chr2:209436015
|
T | TTA | 44 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.-222+11746_-222+11 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209436015 | |||||
| chr2:209436015
|
T | TTATATAT others(70): Show |
2 | a0002c0005t0008g0134a0002c0005t0008g0136 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-222+11748_-222+11 others(83): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209436015 | |||||
| chr2:209436015
|
T | TTATATAT others(95): Show |
1 | a0002c0005t0008g0135 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-222+11748_-222+11 others(108): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209436015 | |||||
| chr2:209436015
|
T | TTATATAT others(45): Show |
1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+11748_-222+11 others(58): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209436015 | |||||
| chr2:209436727
|
G | T | 4 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+12451G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209436727 | ||||||
| chr2:209436750
|
C | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+12474C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209436750 | ||||||
| chr2:209436985
|
C | T | 1 | a0001c0006t0002g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-222+12709C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209436985 | ||||||
| chr2:209437098
|
G | T | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+12822G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209437098 | ||||||
| chr2:209437417
|
A | G | 27 | a0001c0001t0002g0020a0001c0001t0002g0052a0001c0001t0002g0053others(24): Show | 27 | HG00733.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-222+13141A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209437417 | ||||||
| chr2:209437436
|
T | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+13160T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209437436 | ||||||
| chr2:209437496
|
T | C | 27 | a0001c0001t0002g0020a0001c0001t0002g0052a0001c0001t0002g0053others(24): Show | 27 | HG00733.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-222+13220T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209437496 | ||||||
| chr2:209437645
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-222+13369A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209437645 | ||||||
| chr2:209437875
|
CT | C | 5 | a0001c0013t0006g0073a0002c0005t0011g0071a0002c0005t0011g0072others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+13600delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209437875 | ||||||
| chr2:209438001
|
C | A | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+13725C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438001 | ||||||
| chr2:209438043
|
A | G | 1 | a0001c0006t0002g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-222+13767A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438043 | ||||||
| chr2:209438053
|
G | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+13777G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438053 | ||||||
| chr2:209438241
|
G | T | 1 | a0002c0002t0032g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-222+13965G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438241 | ||||||
| chr2:209438359
|
G | A | 1 | a0002c0002t0032g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-222+14083G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438359 | ||||||
| chr2:209438467
|
T | C | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+14191T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438467 | ||||||
| chr2:209438532
|
T | A | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+14256T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438532 | ||||||
| chr2:209438558
|
T | G | 1 | a0002c0002t0014g0113 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-222+14282T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438558 | ||||||
| chr2:209438587
|
C | G | 57 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-222+14311C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438587 | ||||||
| chr2:209438656
|
A | G | 57 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-222+14380A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438656 | ||||||
| chr2:209438956
|
C | T | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+14680C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438956 | ||||||
| chr2:209438988
|
C | T | 1 | a0006c0018t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-222+14712C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209438988 | ||||||
| chr2:209439028
|
A | G | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+14752A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439028 | ||||||
| chr2:209439117
|
C | T | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00733.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-222+14841C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439117 | ||||||
| chr2:209439258
|
T | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+14982T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439258 | ||||||
| chr2:209439259
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-222+14983A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439259 | ||||||
| chr2:209439347
|
A | G | 22 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(19): Show | 22 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.-222+15071A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439347 | ||||||
| chr2:209439361
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-222+15085A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439361 | ||||||
| chr2:209439448
|
A | G | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+15172A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439448 | ||||||
| chr2:209439654
|
T | C | 8 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+15378T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439654 | ||||||
| chr2:209439733
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+15457C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439733 | ||||||
| chr2:209439734
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-222+15458G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209439734 | ||||||
| chr2:209440188
|
A | T | 1 | a0002c0002t0039g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-222+15912A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209440188 | ||||||
| chr2:209440274
|
G | A | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-222+15998G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209440274 | ||||||
| chr2:209440557
|
G | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+16281G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209440557 | ||||||
| chr2:209440656
|
G | A | 1 | a0004c0007t0017g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-222+16380G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209440656 | ||||||
| chr2:209441004
|
A | C | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+16728A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441004 | ||||||
| chr2:209441239
|
C | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+16963C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441239 | ||||||
| chr2:209441308
|
G | A | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+17032G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441308 | ||||||
| chr2:209441335
|
T | TAAAAC | 60 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(57): Show | 60 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.-222+17061_-222+17 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209441335 | |||||
| chr2:209441340
|
C | A | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+17064C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441340 | ||||||
| chr2:209441347
|
C | T | 2 | a0001c0006t0002g0056a0001c0006t0002g0057 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-222+17071C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441347 | ||||||
| chr2:209441358
|
A | G | 8 | a0001c0001t0002g0077a0001c0001t0002g0079a0001c0001t0002g0081others(5): Show | 8 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+17082A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441358 | ||||||
| chr2:209441531
|
C | T | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+17255C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209441531 | ||||||
| chr2:209442156
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-222+17880G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209442156 | ||||||
| chr2:209442594
|
C | T | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-222+18318C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209442594 | ||||||
| chr2:209442706
|
C | G | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-222+18430C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209442706 | ||||||
| chr2:209443175
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0146a0002c0002t0004g0145 | 3 | HG02080.hp2 NA18986.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-222+18899A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443175 | ||||||
| chr2:209443216
|
GT | G | 11 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-222+18952delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209443216 | |||||
| chr2:209443421
|
G | A | 1 | a0001c0001t0025g0141 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-222+19145G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443421 | ||||||
| chr2:209443558
|
C | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00733.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-222+19282C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443558 | ||||||
| chr2:209443570
|
CG | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-222+19295delG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443570 | ||||||
| chr2:209443605
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-222+19329C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443605 | ||||||
| chr2:209443819
|
C | T | 54 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(51): Show | 54 | HG01243.hp1 HG01243.hp2 HG01433.hp1 others(51): Show |
intron_variant | MODIFIER | c.-222+19543C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443819 | ||||||
| chr2:209443959
|
A | G | 5 | a0001c0013t0006g0073a0002c0005t0011g0071a0002c0005t0011g0072others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+19683A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209443959 | ||||||
| chr2:209444150
|
G | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+19874G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209444150 | ||||||
| chr2:209444277
|
C | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+20001C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209444277 | ||||||
| chr2:209444530
|
C | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+20254C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209444530 | ||||||
| chr2:209444847
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-222+20571T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209444847 | ||||||
| chr2:209444970
|
A | G | 13 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(10): Show | 13 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-222+20694A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209444970 | ||||||
| chr2:209445486
|
AT | A | 32 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.-222+21213delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209445486 | |||||
| chr2:209445813
|
T | G | 32 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.-222+21537T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209445813 | ||||||
| chr2:209445888
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00733.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-222+21612A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209445888 | ||||||
| chr2:209445977
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-222+21701A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209445977 | ||||||
| chr2:209446203
|
A | G | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+21927A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446203 | ||||||
| chr2:209446242
|
C | T | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-222+21966C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446242 | ||||||
| chr2:209446396
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-222+22120G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446396 | ||||||
| chr2:209446521
|
C | T | 8 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(5): Show | 8 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+22245C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446521 | ||||||
| chr2:209446597
|
A | C | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+22321A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446597 | ||||||
| chr2:209446826
|
AC | A | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+22552delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209446826 | |||||
| chr2:209446836
|
C | A | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+22560C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446836 | ||||||
| chr2:209446863
|
A | G | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+22587A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446863 | ||||||
| chr2:209446900
|
C | G | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-222+22624C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209446900 | ||||||
| chr2:209447308
|
C | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+23032C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209447308 | ||||||
| chr2:209447809
|
A | G | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+23533A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209447809 | ||||||
| chr2:209447838
|
A | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+23562A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209447838 | ||||||
| chr2:209447844
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-222+23568A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209447844 | ||||||
| chr2:209447880
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-222+23604A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209447880 | ||||||
| chr2:209448023
|
G | A | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+23747G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209448023 | ||||||
| chr2:209448045
|
A | G | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+23769A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209448045 | ||||||
| chr2:209448064
|
C | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+23788C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209448064 | ||||||
| chr2:209448146
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0126others(1): Show | 4 | HG00408.hp2 HG01358.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+23870A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209448146 | ||||||
| chr2:209448929
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-222+24653C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209448929 | ||||||
| chr2:209449082
|
C | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+24806C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449082 | ||||||
| chr2:209449113
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-222+24837C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449113 | ||||||
| chr2:209449322
|
A | G | 94 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-222+25046A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449322 | ||||||
| chr2:209449499
|
T | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-222+25223T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449499 | ||||||
| chr2:209449565
|
TAA | T | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+25292_-222+25 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209449565 | |||||
| chr2:209449678
|
T | C | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+25402T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449678 | ||||||
| chr2:209449800
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-222+25524G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449800 | ||||||
| chr2:209449833
|
TGC | T | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-222+25558_-222+25 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449833 | ||||||
| chr2:209449837
|
G | C | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-222+25561G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449837 | ||||||
| chr2:209449965
|
A | G | 93 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-222+25689A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209449965 | ||||||
| chr2:209450142
|
A | G | 4 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+25866A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450142 | ||||||
| chr2:209450154
|
C | G | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+25878C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450154 | ||||||
| chr2:209450162
|
G | A | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+25886G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450162 | ||||||
| chr2:209450193
|
C | T | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+25917C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450193 | ||||||
| chr2:209450196
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-222+25920C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450196 | ||||||
| chr2:209450244
|
C | T | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-222+25968C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450244 | ||||||
| chr2:209450302
|
C | T | 8 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0033g0007others(5): Show | 8 | HG01884.hp1 HG01975.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-222+26026C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450302 | ||||||
| chr2:209450315
|
A | C | 15 | a0001c0001t0003g0074a0001c0003t0002g0054a0001c0003t0002g0055others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-222+26039A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450315 | ||||||
| chr2:209450645
|
A | C | 94 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-222+26369A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450645 | ||||||
| chr2:209450645
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-222+26369A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450645 | ||||||
| chr2:209450742
|
T | C | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-222+26466T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450742 | ||||||
| chr2:209450913
|
A | C | 25 | a0001c0001t0002g0020a0001c0001t0002g0052a0001c0001t0002g0053others(22): Show | 25 | HG00733.hp1 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-222+26637A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450913 | ||||||
| chr2:209450954
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-222+26678A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209450954 | ||||||
| chr2:209450975
|
A | AT | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+26707dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209450975 | |||||
| chr2:209451057
|
C | T | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+26781C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451057 | ||||||
| chr2:209451102
|
G | C | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+26826G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451102 | ||||||
| chr2:209451181
|
T | C | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+26905T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451181 | ||||||
| chr2:209451191
|
GA | G | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+26922delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209451191 | |||||
| chr2:209451285
|
G | A | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+27009G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451285 | ||||||
| chr2:209451486
|
G | A | 56 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(53): Show | 56 | HG01243.hp1 HG01243.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.-222+27210G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451486 | ||||||
| chr2:209451504
|
A | G | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-222+27228A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451504 | ||||||
| chr2:209451730
|
G | A | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+27454G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451730 | ||||||
| chr2:209451895
|
A | G | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+27619A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209451895 | ||||||
| chr2:209452496
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-222+28220T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209452496 | ||||||
| chr2:209452665
|
G | A | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+28389G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209452665 | ||||||
| chr2:209452820
|
C | G | 1 | a0001c0003t0002g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-222+28544C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209452820 | ||||||
| chr2:209452831
|
T | A | 1 | a0002c0002t0029g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-222+28555T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209452831 | ||||||
| chr2:209452991
|
T | C | 22 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(19): Show | 22 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.-222+28715T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209452991 | ||||||
| chr2:209453106
|
G | A | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+28830G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209453106 | ||||||
| chr2:209453192
|
G | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+28916G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209453192 | ||||||
| chr2:209453540
|
A | G | 35 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(32): Show | 35 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.-222+29264A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209453540 | ||||||
| chr2:209453779
|
CAT | C | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+29504_-222+29 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209453779 | ||||||
| chr2:209453916
|
C | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+29640C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209453916 | ||||||
| chr2:209454106
|
G | A | 2 | a0002c0002t0005g0035a0002c0002t0019g0040 | 2 | NA19007.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-222+29830G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454106 | ||||||
| chr2:209454124
|
C | T | 8 | a0001c0001t0002g0077a0001c0001t0002g0079a0001c0001t0002g0081others(5): Show | 8 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+29848C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454124 | ||||||
| chr2:209454149
|
CAA | C | 18 | a0001c0001t0001g0111a0001c0001t0002g0052a0001c0001t0002g0053others(15): Show | 18 | HG00733.hp1 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-222+29899_-222+29 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209454149 | |||||
| chr2:209454149
|
CAAA | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.-222+29898_-222+29 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209454149 | |||||
| chr2:209454149
|
CAAAAAAA others(2): Show |
C | 21 | a0001c0001t0002g0020a0001c0001t0003g0074a0001c0001t0033g0007others(18): Show | 21 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-222+29892_-222+29 others(15): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209454149 | |||||
| chr2:209454176
|
A | G | 37 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(34): Show | 37 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.-222+29900A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454176 | ||||||
| chr2:209454211
|
C | A | 1 | a0002c0002t0024g0121 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-222+29935C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454211 | ||||||
| chr2:209454494
|
C | T | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-222+30218C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454494 | ||||||
| chr2:209454633
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+30357G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454633 | ||||||
| chr2:209454798
|
T | TTG | 11 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-222+30536_-222+30 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209454798 | |||||
| chr2:209454849
|
G | A | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+30573G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454849 | ||||||
| chr2:209454912
|
G | A | 1 | a0002c0002t0015g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-222+30636G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454912 | ||||||
| chr2:209454940
|
A | C | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+30664A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209454940 | ||||||
| chr2:209455021
|
G | A | 23 | a0001c0001t0002g0020a0001c0001t0003g0022a0001c0001t0003g0074others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+30745G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455021 | ||||||
| chr2:209455060
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-222+30784T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455060 | ||||||
| chr2:209455116
|
G | A | 5 | a0001c0001t0001g0144a0001c0003t0002g0054a0001c0003t0002g0055others(2): Show | 5 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+30840G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455116 | ||||||
| chr2:209455170
|
A | G | 2 | a0001c0001t0003g0022a0003c0004t0035g0021 | 2 | HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+30894A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455170 | ||||||
| chr2:209455206
|
C | T | 1 | a0001c0003t0006g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-222+30930C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455206 | ||||||
| chr2:209455588
|
A | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-222+31312A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455588 | ||||||
| chr2:209455639
|
C | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+31363C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455639 | ||||||
| chr2:209455728
|
C | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(30): Show | 33 | HG01243.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.-222+31452C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455728 | ||||||
| chr2:209455888
|
T | C | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+31612T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209455888 | ||||||
| chr2:209456200
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-222+31924C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456200 | ||||||
| chr2:209456227
|
G | T | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+31951G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456227 | ||||||
| chr2:209456229
|
A | C | 20 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(17): Show | 20 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-222+31953A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456229 | ||||||
| chr2:209456852
|
T | C | 4 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+32576T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456852 | ||||||
| chr2:209456862
|
G | A | 7 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222+32586G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456862 | ||||||
| chr2:209456975
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-222+32699A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456975 | ||||||
| chr2:209456981
|
A | G | 19 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0017t0007g0036others(16): Show | 19 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-222+32705A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209456981 | ||||||
| chr2:209456988
|
AAC | A | 3 | a0001c0001t0002g0020a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01884.hp1 HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+32716_-222+32 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209456988 | |||||
| chr2:209457016
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-222+32740G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457016 | ||||||
| chr2:209457199
|
G | A | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-222+32923G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457199 | ||||||
| chr2:209457216
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.-222+32940C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457216 | ||||||
| chr2:209457337
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-222+33061G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457337 | ||||||
| chr2:209457488
|
G | C | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+33212G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457488 | ||||||
| chr2:209457549
|
T | C | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-222+33273T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457549 | ||||||
| chr2:209457658
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+33382C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457658 | ||||||
| chr2:209457676
|
T | C | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+33400T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457676 | ||||||
| chr2:209457723
|
A | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+33447A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457723 | ||||||
| chr2:209457750
|
G | A | 5 | a0002c0002t0005g0039a0002c0002t0005g0041a0002c0002t0012g0043others(2): Show | 5 | HG02080.hp1 NA18984.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+33474G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457750 | ||||||
| chr2:209457985
|
T | C | 4 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0085others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+33709T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209457985 | ||||||
| chr2:209458042
|
G | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+33766G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209458042 | ||||||
| chr2:209458716
|
T | C | 3 | a0001c0001t0002g0053a0001c0001t0002g0085a0001c0001t0034g0096 | 3 | HG02258.hp2 HG02698.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+34440T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209458716 | ||||||
| chr2:209458745
|
A | G | 6 | a0001c0001t0033g0007a0001c0003t0018g0005a0001c0003t0036g0006others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+34469A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209458745 | ||||||
| chr2:209458757
|
G | C | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-222+34481G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209458757 | ||||||
| chr2:209458775
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-222+34499G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209458775 | ||||||
| chr2:209458908
|
T | C | 2 | a0001c0001t0002g0015a0002c0002t0005g0041 | 2 | HG02622.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-222+34632T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209458908 | ||||||
| chr2:209459065
|
T | G | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-222+34789T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459065 | ||||||
| chr2:209459120
|
A | G | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+34844A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459120 | ||||||
| chr2:209459129
|
T | C | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+34853T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459129 | ||||||
| chr2:209459142
|
G | A | 3 | a0001c0001t0033g0007a0001c0003t0018g0005a0001c0003t0036g0006 | 3 | HG02257.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-222+34866G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459142 | ||||||
| chr2:209459199
|
C | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.-222+34923C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459199 | ||||||
| chr2:209459205
|
G | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+34929G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459205 | ||||||
| chr2:209459288
|
T | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+35012T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459288 | ||||||
| chr2:209459312
|
G | A | 12 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(9): Show | 12 | HG01243.hp2 HG01433.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-222+35036G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459312 | ||||||
| chr2:209459404
|
T | C | 3 | a0001c0013t0006g0073a0002c0005t0027g0070a0008c0015t0002g0075 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-222+35128T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459404 | ||||||
| chr2:209459421
|
A | G | 3 | a0001c0013t0006g0073a0002c0005t0027g0070a0008c0015t0002g0075 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-222+35145A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459421 | ||||||
| chr2:209459557
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+35281C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459557 | ||||||
| chr2:209459653
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0032 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-222+35377T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459653 | ||||||
| chr2:209459769
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-222+35493C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209459769 | ||||||
| chr2:209460070
|
A | C | 2 | a0001c0001t0003g0022a0003c0004t0035g0021 | 2 | HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-222+35794A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209460070 | ||||||
| chr2:209460281
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+36005T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209460281 | ||||||
| chr2:209460327
|
C | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+36051C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209460327 | ||||||
| chr2:209460353
|
A | G | 1 | a0002c0002t0004g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-222+36077A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209460353 | ||||||
| chr2:209460588
|
T | TTTCC | 3 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0003t0018g0016 | 3 | HG02559.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-222+36332_-222+36 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209460588 | |||||
| chr2:209460588
|
TTTCC | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+36332_-222+36 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209460588 | |||||
| chr2:209460840
|
C | T | 1 | a0002c0002t0014g0113 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-222+36564C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209460840 | ||||||
| chr2:209460877
|
T | G | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-222+36601T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209460877 | ||||||
| chr2:209461089
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-222+36813A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461089 | ||||||
| chr2:209461255
|
G | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+36979G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461255 | ||||||
| chr2:209461256
|
A | C | 2 | a0001c0001t0003g0076a0001c0001t0003g0078 | 2 | HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-222+36980A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461256 | ||||||
| chr2:209461277
|
T | C | 1 | a0011c0016t0001g0009 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-222+37001T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461277 | ||||||
| chr2:209461295
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-222+37019A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461295 | ||||||
| chr2:209461365
|
G | A | 2 | a0002c0002t0005g0033a0002c0002t0005g0039 | 2 | NA18984.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-222+37089G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461365 | ||||||
| chr2:209461473
|
G | A | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-222+37197G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461473 | ||||||
| chr2:209461477
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-222+37201C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461477 | ||||||
| chr2:209461481
|
GT | G | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-222+37209delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209461481 | |||||
| chr2:209461520
|
A | G | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+37244A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461520 | ||||||
| chr2:209461524
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0002g0063 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-222+37248C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461524 | ||||||
| chr2:209461609
|
CT | C | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+37334delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461609 | ||||||
| chr2:209461741
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-222+37465A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461741 | ||||||
| chr2:209461759
|
C | G | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+37483C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209461759 | ||||||
| chr2:209462154
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-222+37878G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462154 | ||||||
| chr2:209462164
|
A | G | 1 | a0002c0002t0032g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-222+37888A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462164 | ||||||
| chr2:209462390
|
A | T | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-222+38114A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462390 | ||||||
| chr2:209462461
|
A | G | 1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-222+38185A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462461 | ||||||
| chr2:209462764
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+38488T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462764 | ||||||
| chr2:209462879
|
T | C | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+38603T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462879 | ||||||
| chr2:209462972
|
C | A | 1 | a0002c0002t0009g0112 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-222+38696C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209462972 | ||||||
| chr2:209462976
|
GCATAATG others(4): Show |
G | 1 | a0003c0004t0003g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-222+38703_-222+38 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209462976 | |||||
| chr2:209463002
|
C | T | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-222+38726C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209463002 | ||||||
| chr2:209463103
|
A | G | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-222+38827A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209463103 | ||||||
| chr2:209463854
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-222+39578G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209463854 | ||||||
| chr2:209463927
|
G | A | 1 | a0002c0002t0005g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-222+39651G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209463927 | ||||||
| chr2:209464001
|
A | G | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-222+39725A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209464001 | ||||||
| chr2:209464240
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-222+39964A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209464240 | ||||||
| chr2:209464306
|
T | A | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-222+40030T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209464306 | ||||||
| chr2:209464418
|
A | G | 3 | a0001c0001t0002g0029a0001c0001t0003g0022a0003c0004t0035g0021 | 3 | HG01975.hp1 HG02683.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-222+40142A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209464418 | ||||||
| chr2:209464648
|
A | G | 1 | a0002c0002t0009g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-222+40372A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209464648 | ||||||
| chr2:209464835
|
T | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+40559T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209464835 | ||||||
| chr2:209465020
|
C | T | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-222+40744C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465020 | ||||||
| chr2:209465436
|
TTCTA | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(46): Show | 49 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-222+41163_-222+41 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209465436 | |||||
| chr2:209465599
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-222+41323G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465599 | ||||||
| chr2:209465643
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-222+41367G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465643 | ||||||
| chr2:209465684
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(47): Show | 50 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-222+41408A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465684 | ||||||
| chr2:209465699
|
A | G | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+41423A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465699 | ||||||
| chr2:209465718
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-222+41442A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465718 | ||||||
| chr2:209465852
|
G | A | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-222+41576G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465852 | ||||||
| chr2:209465937
|
T | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-41655T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465937 | ||||||
| chr2:209465987
|
C | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-221-41605C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209465987 | ||||||
| chr2:209466030
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(79): Show | 82 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-221-41562G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209466030 | ||||||
| chr2:209466163
|
C | T | 1 | a0001c0001t0007g0050 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-221-41429C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209466163 | ||||||
| chr2:209466564
|
A | G | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-41028A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209466564 | ||||||
| chr2:209466722
|
T | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(9): Show | 12 | HG01243.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-40870T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209466722 | ||||||
| chr2:209466809
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-221-40783C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209466809 | ||||||
| chr2:209466855
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-221-40737C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209466855 | ||||||
| chr2:209467304
|
C | T | 3 | a0001c0013t0006g0073a0002c0005t0027g0070a0008c0015t0002g0075 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-221-40288C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209467304 | ||||||
| chr2:209467554
|
C | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-40038C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209467554 | ||||||
| chr2:209467624
|
G | A | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-221-39968G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209467624 | ||||||
| chr2:209467650
|
T | G | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-221-39942T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209467650 | ||||||
| chr2:209467817
|
C | T | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-221-39775C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209467817 | ||||||
| chr2:209468022
|
G | A | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-221-39570G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209468022 | ||||||
| chr2:209468096
|
CTTTT | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-39489_-221-39 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209468096 | |||||
| chr2:209468266
|
G | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-39326G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209468266 | ||||||
| chr2:209468317
|
C | CT | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(64): Show | 67 | HG00140.hp1 HG00733.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.-221-39254dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209468317 | |||||
| chr2:209468317
|
C | CTT | 25 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(22): Show | 25 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-221-39255_-221-39 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209468317 | |||||
| chr2:209468483
|
G | A | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-39109G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209468483 | ||||||
| chr2:209468963
|
A | G | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-221-38629A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209468963 | ||||||
| chr2:209469049
|
A | C | 16 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-221-38543A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469049 | ||||||
| chr2:209469100
|
C | T | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-38492C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469100 | ||||||
| chr2:209469139
|
T | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-38453T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469139 | ||||||
| chr2:209469297
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-221-38295C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469297 | ||||||
| chr2:209469421
|
A | AT | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-38162dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209469421 | |||||
| chr2:209469468
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-38124G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469468 | ||||||
| chr2:209469569
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0002g0063 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-221-38023A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469569 | ||||||
| chr2:209469629
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0115a0006c0018t0001g0123 | 3 | HG01109.hp1 HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-221-37963C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469629 | ||||||
| chr2:209469773
|
T | C | 21 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-221-37819T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469773 | ||||||
| chr2:209469861
|
C | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-37731C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209469861 | ||||||
| chr2:209470198
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-221-37394A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209470198 | ||||||
| chr2:209470238
|
A | T | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-37354A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209470238 | ||||||
| chr2:209470255
|
G | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-37337G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209470255 | ||||||
| chr2:209470480
|
A | T | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-37112A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209470480 | ||||||
| chr2:209470547
|
G | T | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-37045G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209470547 | ||||||
| chr2:209470992
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-36600A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209470992 | ||||||
| chr2:209471607
|
A | C | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-35985A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209471607 | ||||||
| chr2:209471778
|
G | T | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-35814G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209471778 | ||||||
| chr2:209471905
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-221-35687A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209471905 | ||||||
| chr2:209472029
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-35563G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472029 | ||||||
| chr2:209472074
|
T | C | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-35518T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472074 | ||||||
| chr2:209472123
|
G | A | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-221-35469G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472123 | ||||||
| chr2:209472262
|
G | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-35330G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472262 | ||||||
| chr2:209472289
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-221-35303C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472289 | ||||||
| chr2:209472334
|
C | G | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-35258C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472334 | ||||||
| chr2:209472366
|
A | G | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-35226A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472366 | ||||||
| chr2:209472392
|
T | C | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-35200T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472392 | ||||||
| chr2:209472510
|
T | G | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-221-35082T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472510 | ||||||
| chr2:209472512
|
T | C | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-221-35080T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472512 | ||||||
| chr2:209472729
|
C | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-34863C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472729 | ||||||
| chr2:209472734
|
CA | C | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-34848delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209472734 | |||||
| chr2:209472744
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-221-34848A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472744 | ||||||
| chr2:209472791
|
ACAGTCAA others(117): Show |
A | 1 | a0001c0003t0002g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-221-34798_-221-34 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209472791 | |||||
| chr2:209472864
|
G | T | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-34728G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209472864 | ||||||
| chr2:209473213
|
A | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-34379A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209473213 | ||||||
| chr2:209473555
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-34037A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209473555 | ||||||
| chr2:209473628
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-221-33964G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209473628 | ||||||
| chr2:209474014
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-221-33578C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209474014 | ||||||
| chr2:209474134
|
A | AC | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-221-33456dupC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209474134 | |||||
| chr2:209474154
|
T | C | 3 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0120 | 3 | NA18959.hp2 NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-221-33438T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209474154 | ||||||
| chr2:209474466
|
A | G | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-33126A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209474466 | ||||||
| chr2:209474722
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-32870G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209474722 | ||||||
| chr2:209474793
|
T | C | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-221-32799T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209474793 | ||||||
| chr2:209475141
|
G | T | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-32451G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209475141 | ||||||
| chr2:209475305
|
A | C | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-32287A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209475305 | ||||||
| chr2:209475608
|
T | C | 2 | a0002c0002t0004g0118a0002c0002t0004g0119 | 2 | NA18959.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-221-31984T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209475608 | ||||||
| chr2:209475693
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-221-31899G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209475693 | ||||||
| chr2:209475929
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-31663G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209475929 | ||||||
| chr2:209475995
|
T | C | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-31597T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209475995 | ||||||
| chr2:209476225
|
A | C | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-221-31367A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209476225 | ||||||
| chr2:209476243
|
G | A | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-31349G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209476243 | ||||||
| chr2:209476269
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-31323A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209476269 | ||||||
| chr2:209476397
|
G | GT | 71 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.-221-31180dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209476397 | |||||
| chr2:209476599
|
G | C | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-221-30993G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209476599 | ||||||
| chr2:209476705
|
T | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-221-30887T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209476705 | ||||||
| chr2:209476759
|
C | T | 1 | a0002c0002t0019g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-221-30833C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209476759 | ||||||
| chr2:209477019
|
A | G | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-30573A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477019 | ||||||
| chr2:209477144
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0002g0063 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-221-30448G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477144 | ||||||
| chr2:209477240
|
A | C | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-221-30352A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477240 | ||||||
| chr2:209477334
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-30258A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477334 | ||||||
| chr2:209477396
|
T | TA | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-30188dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209477396 | |||||
| chr2:209477528
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-30064A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477528 | ||||||
| chr2:209477541
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-221-30051G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477541 | ||||||
| chr2:209477783
|
G | T | 2 | a0001c0006t0002g0092a0001c0006t0002g0093 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-221-29809G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477783 | ||||||
| chr2:209477808
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-29784G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477808 | ||||||
| chr2:209477842
|
T | TA | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-29735dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209477842 | |||||
| chr2:209477850
|
A | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-29742A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209477850 | ||||||
| chr2:209478043
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-29549C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478043 | ||||||
| chr2:209478059
|
T | G | 6 | a0001c0001t0002g0085a0001c0001t0034g0096a0001c0003t0002g0054others(3): Show | 6 | HG02258.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-221-29533T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478059 | ||||||
| chr2:209478071
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0034g0096a0001c0003t0002g0054others(3): Show | 6 | HG02258.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-221-29521T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478071 | ||||||
| chr2:209478383
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-221-29209G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478383 | ||||||
| chr2:209478626
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-28966T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478626 | ||||||
| chr2:209478770
|
T | C | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-221-28822T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478770 | ||||||
| chr2:209478788
|
T | A | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-221-28804T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209478788 | ||||||
| chr2:209479398
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-221-28194G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209479398 | ||||||
| chr2:209479712
|
A | G | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-27880A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209479712 | ||||||
| chr2:209479840
|
A | T | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-221-27752A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209479840 | ||||||
| chr2:209479850
|
C | T | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-27742C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209479850 | ||||||
| chr2:209480147
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-27445G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480147 | ||||||
| chr2:209480283
|
A | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-221-27309A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480283 | ||||||
| chr2:209480524
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-221-27068T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480524 | ||||||
| chr2:209480528
|
A | G | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-221-27064A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480528 | ||||||
| chr2:209480537
|
A | AGTTT | 29 | a0001c0001t0001g0002a0001c0001t0001g0107a0001c0001t0001g0111others(26): Show | 29 | HG00140.hp1 HG00597.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-221-27030_-221-27 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209480537 | |||||
| chr2:209480537
|
A | AGTTTGTT others(1): Show |
30 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00733.hp1 HG01109.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.-221-27034_-221-27 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209480537 | |||||
| chr2:209480537
|
A | AGTTTGTT others(5): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0128a0002c0002t0022g0100others(1): Show | 4 | HG01358.hp1 HG03239.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-27038_-221-27 others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209480537 | |||||
| chr2:209480537
|
AGTTT | A | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-27030_-221-27 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209480537 | |||||
| chr2:209480550
|
G | GTTTGTTT others(1): Show |
5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-27035_-221-27 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209480550 | |||||
| chr2:209480599
|
G | A | 9 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-26993G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480599 | ||||||
| chr2:209480675
|
A | G | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-221-26917A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480675 | ||||||
| chr2:209480964
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-221-26628A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209480964 | ||||||
| chr2:209481156
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-221-26436A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481156 | ||||||
| chr2:209481209
|
G | T | 1 | a0002c0002t0005g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-221-26383G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481209 | ||||||
| chr2:209481210
|
C | T | 1 | a0002c0002t0005g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-221-26382C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481210 | ||||||
| chr2:209481360
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(74): Show | 77 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-221-26232A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481360 | ||||||
| chr2:209481548
|
A | G | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-221-26044A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481548 | ||||||
| chr2:209481656
|
T | C | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-221-25936T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481656 | ||||||
| chr2:209481892
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-221-25700A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481892 | ||||||
| chr2:209481951
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-25641G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209481951 | ||||||
| chr2:209482012
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(70): Show | 73 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.-221-25580C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482012 | ||||||
| chr2:209482022
|
C | CA | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-25570_-221-25 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482022 | ||||||
| chr2:209482119
|
G | A | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-221-25473G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482119 | ||||||
| chr2:209482211
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-221-25381T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482211 | ||||||
| chr2:209482269
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-25323A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482269 | ||||||
| chr2:209482345
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-221-25247C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482345 | ||||||
| chr2:209482426
|
T | C | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-25166T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482426 | ||||||
| chr2:209482558
|
C | A | 12 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-25034C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482558 | ||||||
| chr2:209482599
|
C | T | 10 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-221-24993C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482599 | ||||||
| chr2:209482775
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(79): Show | 82 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-221-24817A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209482775 | ||||||
| chr2:209483098
|
C | A | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-221-24494C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209483098 | ||||||
| chr2:209483466
|
C | G | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-221-24126C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209483466 | ||||||
| chr2:209483538
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-24054C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209483538 | ||||||
| chr2:209483571
|
C | T | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-24021C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209483571 | ||||||
| chr2:209483638
|
T | C | 5 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-23954T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209483638 | ||||||
| chr2:209484050
|
T | TA | 10 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-221-23539dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209484050 | |||||
| chr2:209484142
|
C | T | 7 | a0001c0001t0003g0064a0002c0002t0015g0066a0002c0002t0029g0061others(4): Show | 7 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-23450C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209484142 | ||||||
| chr2:209484297
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-221-23295T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209484297 | ||||||
| chr2:209484429
|
C | T | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-221-23163C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209484429 | ||||||
| chr2:209484502
|
C | G | 1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-221-23090C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209484502 | ||||||
| chr2:209485038
|
T | A | 1 | a0001c0006t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-221-22554T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209485038 | ||||||
| chr2:209485852
|
G | T | 1 | a0002c0002t0030g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-221-21740G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209485852 | ||||||
| chr2:209485915
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 63 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-221-21677G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209485915 | ||||||
| chr2:209486043
|
C | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-21549C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486043 | ||||||
| chr2:209486155
|
C | T | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-21437C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486155 | ||||||
| chr2:209486234
|
C | CT | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-21354dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209486234 | |||||
| chr2:209486239
|
C | CT | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(46): Show | 49 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-221-21344dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209486239 | |||||
| chr2:209486239
|
C | T | 19 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(16): Show | 19 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-221-21353C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486239 | ||||||
| chr2:209486395
|
T | C | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-21197T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486395 | ||||||
| chr2:209486469
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-21123G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486469 | ||||||
| chr2:209486487
|
G | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-21105G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486487 | ||||||
| chr2:209486511
|
C | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-21081C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486511 | ||||||
| chr2:209486654
|
T | C | 3 | a0001c0001t0001g0128a0002c0002t0022g0100a0003c0004t0026g0109 | 3 | HG01358.hp1 HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-221-20938T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486654 | ||||||
| chr2:209486666
|
G | A | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-20926G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486666 | ||||||
| chr2:209486742
|
G | C | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-221-20850G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486742 | ||||||
| chr2:209486820
|
A | G | 7 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-20772A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486820 | ||||||
| chr2:209486994
|
T | A | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-221-20598T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209486994 | ||||||
| chr2:209487059
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-20533T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487059 | ||||||
| chr2:209487081
|
A | G | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-20511A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487081 | ||||||
| chr2:209487125
|
T | C | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-221-20467T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487125 | ||||||
| chr2:209487275
|
G | C | 2 | a0001c0001t0003g0022a0003c0004t0035g0021 | 2 | HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-221-20317G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487275 | ||||||
| chr2:209487312
|
T | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-20280T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487312 | ||||||
| chr2:209487704
|
G | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-19888G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487704 | ||||||
| chr2:209487813
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-19779T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209487813 | ||||||
| chr2:209488023
|
C | T | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-19569C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488023 | ||||||
| chr2:209488024
|
G | C | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-19568G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488024 | ||||||
| chr2:209488057
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-221-19535G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488057 | ||||||
| chr2:209488291
|
G | A | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-19301G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488291 | ||||||
| chr2:209488323
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-19269A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488323 | ||||||
| chr2:209488358
|
C | T | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-19234C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488358 | ||||||
| chr2:209488707
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-18885A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488707 | ||||||
| chr2:209488868
|
C | T | 1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-221-18724C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488868 | ||||||
| chr2:209488939
|
C | T | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-18653C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209488939 | ||||||
| chr2:209489786
|
G | A | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-221-17806G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209489786 | ||||||
| chr2:209489799
|
C | T | 16 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-221-17793C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209489799 | ||||||
| chr2:209489872
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0115 | 2 | HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-221-17720G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209489872 | ||||||
| chr2:209490045
|
C | T | 4 | a0001c0001t0002g0077a0001c0001t0002g0083a0001c0001t0003g0076others(1): Show | 4 | HG01433.hp2 HG02683.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-17547C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490045 | ||||||
| chr2:209490070
|
A | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-221-17522A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490070 | ||||||
| chr2:209490200
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-17392A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490200 | ||||||
| chr2:209490288
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-221-17304A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490288 | ||||||
| chr2:209490434
|
C | G | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-17158C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490434 | ||||||
| chr2:209490519
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-221-17073G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490519 | ||||||
| chr2:209490605
|
C | CA | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 40 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.-221-16957dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490605
|
C | CAA | 10 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0114others(7): Show | 10 | HG01109.hp1 HG01261.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-221-16958_-221-16 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490605
|
C | CAAA | 6 | a0001c0001t0002g0019a0001c0003t0002g0055a0001c0003t0018g0016others(3): Show | 6 | HG00597.hp1 HG00597.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-16959_-221-16 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490605
|
CA | C | 12 | a0001c0001t0001g0139a0001c0001t0002g0025a0001c0001t0002g0032others(9): Show | 12 | HG01884.hp2 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-16957delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490605
|
CAA | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0026a0001c0001t0002g0027others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-221-16958_-221-16 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490605
|
CAAA | C | 6 | a0001c0001t0002g0081a0001c0001t0003g0078a0001c0001t0034g0096others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-16959_-221-16 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490605
|
CAAAA | C | 5 | a0001c0001t0002g0077a0001c0001t0002g0082a0001c0001t0002g0083others(2): Show | 5 | HG01433.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-16960_-221-16 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209490605 | |||||
| chr2:209490714
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-221-16878G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490714 | ||||||
| chr2:209490959
|
A | G | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-16633A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490959 | ||||||
| chr2:209490976
|
C | G | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-16616C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209490976 | ||||||
| chr2:209491091
|
A | G | 2 | a0001c0001t0003g0076a0001c0001t0003g0078 | 2 | HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-221-16501A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209491091 | ||||||
| chr2:209491423
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-221-16169A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209491423 | ||||||
| chr2:209491518
|
T | C | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-16074T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209491518 | ||||||
| chr2:209491754
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-15838G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209491754 | ||||||
| chr2:209491770
|
C | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-221-15822C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209491770 | ||||||
| chr2:209492067
|
C | T | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-15525C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492067 | ||||||
| chr2:209492079
|
C | G | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-221-15513C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492079 | ||||||
| chr2:209492155
|
A | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0019 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-221-15437A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492155 | ||||||
| chr2:209492159
|
A | G | 1 | a0001c0001t0007g0049 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-221-15433A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492159 | ||||||
| chr2:209492170
|
T | TAAAC | 94 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-221-15419_-221-15 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209492170 | |||||
| chr2:209492182
|
C | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-15410C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492182 | ||||||
| chr2:209492546
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-15046G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492546 | ||||||
| chr2:209492924
|
A | T | 5 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-14668A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209492924 | ||||||
| chr2:209493062
|
G | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-14530G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493062 | ||||||
| chr2:209493164
|
A | T | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-221-14428A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493164 | ||||||
| chr2:209493326
|
C | G | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-14266C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493326 | ||||||
| chr2:209493343
|
G | T | 19 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(16): Show | 19 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-221-14249G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493343 | ||||||
| chr2:209493358
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-221-14234A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493358 | ||||||
| chr2:209493467
|
C | T | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-221-14125C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493467 | ||||||
| chr2:209493667
|
C | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00733.hp1 HG01192.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-221-13925C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493667 | ||||||
| chr2:209493703
|
T | G | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-13889T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493703 | ||||||
| chr2:209493783
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-13809A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493783 | ||||||
| chr2:209493819
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-13773T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493819 | ||||||
| chr2:209493895
|
A | G | 1 | a0005c0008t0013g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-221-13697A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493895 | ||||||
| chr2:209493977
|
T | G | 1 | a0003c0004t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-221-13615T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493977 | ||||||
| chr2:209493984
|
G | C | 1 | a0003c0004t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-221-13608G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209493984 | ||||||
| chr2:209494045
|
A | C | 1 | a0005c0008t0013g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-221-13547A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494045 | ||||||
| chr2:209494191
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-221-13401C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494191 | ||||||
| chr2:209494270
|
G | A | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-13322G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494270 | ||||||
| chr2:209494288
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-13304T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494288 | ||||||
| chr2:209494432
|
T | TA | 9 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(6): Show | 9 | HG01433.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-13146dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209494432 | |||||
| chr2:209494436
|
A | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-13156A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494436 | ||||||
| chr2:209494441
|
A | G | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-13151A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494441 | ||||||
| chr2:209494447
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-13145G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209494447 | ||||||
| chr2:209495023
|
T | C | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-221-12569T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495023 | ||||||
| chr2:209495052
|
C | T | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-221-12540C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495052 | ||||||
| chr2:209495100
|
T | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-12492T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495100 | ||||||
| chr2:209495103
|
C | T | 9 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0006g0003others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-12489C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495103 | ||||||
| chr2:209495104
|
G | A | 3 | a0001c0013t0006g0073a0002c0005t0027g0070a0008c0015t0002g0075 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-221-12488G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495104 | ||||||
| chr2:209495220
|
G | A | 1 | a0002c0002t0004g0001 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-221-12372G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495220 | ||||||
| chr2:209495228
|
A | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-12364A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495228 | ||||||
| chr2:209495249
|
T | A | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-12343T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495249 | ||||||
| chr2:209495302
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0032 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-221-12290C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495302 | ||||||
| chr2:209495597
|
T | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-11995T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495597 | ||||||
| chr2:209495783
|
A | G | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-221-11809A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495783 | ||||||
| chr2:209495889
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-11703A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209495889 | ||||||
| chr2:209496026
|
C | T | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-221-11566C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496026 | ||||||
| chr2:209496041
|
A | G | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-221-11551A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496041 | ||||||
| chr2:209496084
|
G | T | 1 | a0002c0002t0020g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-221-11508G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496084 | ||||||
| chr2:209496085
|
C | T | 1 | a0002c0002t0020g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-221-11507C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496085 | ||||||
| chr2:209496093
|
C | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-221-11499C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496093 | ||||||
| chr2:209496323
|
G | T | 1 | a0005c0008t0013g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-221-11269G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496323 | ||||||
| chr2:209496403
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-11189G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496403 | ||||||
| chr2:209496552
|
C | T | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-11040C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496552 | ||||||
| chr2:209496768
|
C | T | 1 | a0002c0002t0012g0038 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-221-10824C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496768 | ||||||
| chr2:209496808
|
T | G | 1 | a0010c0012t0038g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-221-10784T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496808 | ||||||
| chr2:209496949
|
TA | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00733.hp1 HG01192.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-221-10632delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209496949 | |||||
| chr2:209496987
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.-221-10605C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209496987 | ||||||
| chr2:209497169
|
C | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-221-10423C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497169 | ||||||
| chr2:209497174
|
G | T | 1 | a0002c0010t0015g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-221-10418G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497174 | ||||||
| chr2:209497247
|
T | C | 1 | a0002c0002t0030g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-221-10345T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497247 | ||||||
| chr2:209497260
|
C | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-10332C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497260 | ||||||
| chr2:209497291
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-221-10301A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497291 | ||||||
| chr2:209497380
|
C | T | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-10212C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497380 | ||||||
| chr2:209497476
|
C | A | 1 | a0002c0005t0008g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-221-10116C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497476 | ||||||
| chr2:209497547
|
A | G | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-221-10045A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497547 | ||||||
| chr2:209497861
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(64): Show | 67 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-221-9731G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209497861 | ||||||
| chr2:209498008
|
T | C | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-221-9584T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498008 | ||||||
| chr2:209498356
|
C | G | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-9236C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498356 | ||||||
| chr2:209498388
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.-221-9204T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498388 | ||||||
| chr2:209498659
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-221-8933C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498659 | ||||||
| chr2:209498800
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-221-8792C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498800 | ||||||
| chr2:209498887
|
G | T | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-221-8705G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498887 | ||||||
| chr2:209498937
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-221-8655T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498937 | ||||||
| chr2:209498981
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-8611T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209498981 | ||||||
| chr2:209499111
|
A | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-221-8481A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209499111 | ||||||
| chr2:209499156
|
T | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-221-8436T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209499156 | ||||||
| chr2:209499158
|
C | A | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-221-8434C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209499158 | ||||||
| chr2:209499455
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-8137C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209499455 | ||||||
| chr2:209499705
|
G | A | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-221-7887G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209499705 | ||||||
| chr2:209499935
|
G | T | 9 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0006g0003others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-7657G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209499935 | ||||||
| chr2:209500016
|
T | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-221-7576T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500016 | ||||||
| chr2:209500059
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-7533C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500059 | ||||||
| chr2:209500083
|
T | G | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-221-7509T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500083 | ||||||
| chr2:209500321
|
A | G | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-221-7271A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500321 | ||||||
| chr2:209500408
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-7184T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500408 | ||||||
| chr2:209500458
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-7134A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500458 | ||||||
| chr2:209500528
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-221-7064C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500528 | ||||||
| chr2:209500729
|
T | TAACA | 2 | a0001c0001t0003g0022a0003c0004t0035g0021 | 2 | HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-221-6853_-221-685 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209500729 | |||||
| chr2:209500741
|
A | G | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-6851A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500741 | ||||||
| chr2:209500746
|
C | A | 1 | a0004c0007t0017g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-221-6846C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500746 | ||||||
| chr2:209500844
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-221-6748G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500844 | ||||||
| chr2:209500891
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-6701G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500891 | ||||||
| chr2:209500942
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-6650C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500942 | ||||||
| chr2:209500943
|
G | A | 7 | a0001c0001t0003g0064a0002c0002t0015g0066a0002c0002t0029g0061others(4): Show | 7 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-6649G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209500943 | ||||||
| chr2:209501037
|
C | CA | 20 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0025others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-221-6539dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209501037 | |||||
| chr2:209501037
|
C | CAA | 54 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(51): Show | 54 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-221-6540_-221-653 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209501037 | |||||
| chr2:209501037
|
C | CAAA | 9 | a0001c0001t0001g0115a0001c0001t0002g0063a0001c0001t0002g0081others(6): Show | 9 | HG01261.hp1 HG01261.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-221-6541_-221-653 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209501037 | |||||
| chr2:209501162
|
G | A | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-221-6430G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209501162 | ||||||
| chr2:209501248
|
G | T | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-221-6344G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209501248 | ||||||
| chr2:209501291
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-221-6301T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209501291 | ||||||
| chr2:209501365
|
T | C | 14 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(11): Show | 14 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.-221-6227T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209501365 | ||||||
| chr2:209501397
|
G | C | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-221-6195G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209501397 | ||||||
| chr2:209501647
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-221-5945T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209501647 | ||||||
| chr2:209502011
|
G | GAT | 7 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0018g0005others(4): Show | 7 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-221-5569_-221-556 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502011 | |||||
| chr2:209502116
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-5476C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502116 | ||||||
| chr2:209502252
|
G | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-5340G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502252 | ||||||
| chr2:209502261
|
C | T | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-221-5331C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502261 | ||||||
| chr2:209502290
|
C | T | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-5302C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502290 | ||||||
| chr2:209502301
|
G | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-5291G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502301 | ||||||
| chr2:209502331
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-221-5261G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502331 | ||||||
| chr2:209502340
|
G | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-5252G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502340 | ||||||
| chr2:209502373
|
T | G | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-221-5219T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502373 | ||||||
| chr2:209502457
|
T | G | 9 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0006g0003others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-5135T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502457 | ||||||
| chr2:209502523
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.-221-5069G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502523 | ||||||
| chr2:209502886
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0063 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-221-4706T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502886 | ||||||
| chr2:209502935
|
T | C | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-221-4657T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209502935 | ||||||
| chr2:209502990
|
AT | A | 5 | a0002c0002t0009g0098a0002c0005t0008g0134a0002c0005t0008g0135others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-4594delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502990 | |||||
| chr2:209502997
|
TTC | T | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-4593_-221-459 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502997 | |||||
| chr2:209502999
|
C | CT | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00597.hp2 HG00733.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.-221-4576dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502999 | |||||
| chr2:209502999
|
C | CTT | 5 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-4577_-221-457 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502999 | |||||
| chr2:209502999
|
CT | C | 6 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(3): Show | 6 | HG01884.hp1 HG01975.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-4576delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502999 | |||||
| chr2:209502999
|
CTTTTTTT | C | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-4582_-221-457 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209502999 | |||||
| chr2:209503000
|
T | C | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-4592T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503000 | ||||||
| chr2:209503005
|
T | C | 3 | a0001c0013t0006g0073a0002c0005t0027g0070a0008c0015t0002g0075 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-221-4587T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503005 | ||||||
| chr2:209503330
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-4262A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503330 | ||||||
| chr2:209503362
|
C | G | 9 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0006g0003others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-4230C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503362 | ||||||
| chr2:209503383
|
A | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.-221-4209A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503383 | ||||||
| chr2:209503622
|
A | G | 2 | a0002c0002t0004g0001a0002c0002t0020g0047 | 2 | NA18954.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-221-3970A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503622 | ||||||
| chr2:209503954
|
G | A | 1 | a0002c0002t0005g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-221-3638G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209503954 | ||||||
| chr2:209504098
|
G | GA | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-3479dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209504098 | |||||
| chr2:209504260
|
G | C | 21 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-221-3332G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209504260 | ||||||
| chr2:209504266
|
T | TA | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-221-3315dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209504266 | |||||
| chr2:209504270
|
A | G | 1 | a0001c0003t0018g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-221-3322A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209504270 | ||||||
| chr2:209504372
|
A | G | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-3220A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209504372 | ||||||
| chr2:209504390
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-3202G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209504390 | ||||||
| chr2:209504524
|
TAA | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-3066_-221-306 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209504524 | |||||
| chr2:209504623
|
C | G | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-221-2969C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209504623 | ||||||
| chr2:209504725
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.-221-2867A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209504725 | ||||||
| chr2:209504749
|
A | AT | 11 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(8): Show | 11 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-221-2833dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209504749 | |||||
| chr2:209505032
|
A | G | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-2560A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505032 | ||||||
| chr2:209505041
|
C | CT | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-2549dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 209505041 | |||||
| chr2:209505468
|
G | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-221-2124G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505468 | ||||||
| chr2:209505479
|
T | A | 2 | a0001c0001t0003g0022a0003c0004t0035g0021 | 2 | HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-221-2113T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505479 | ||||||
| chr2:209505632
|
TGGATACT others(117): Show |
T | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-221-1959_-221-183 others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505632 | ||||||
| chr2:209505876
|
G | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-1716G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505876 | ||||||
| chr2:209505907
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-1685G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505907 | ||||||
| chr2:209505942
|
C | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-1650C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505942 | ||||||
| chr2:209505943
|
G | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-1649G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209505943 | ||||||
| chr2:209506001
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-1591C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506001 | ||||||
| chr2:209506032
|
G | A | 1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-221-1560G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506032 | ||||||
| chr2:209506041
|
A | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-1551A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506041 | ||||||
| chr2:209506178
|
C | G | 3 | a0001c0001t0001g0128a0002c0002t0022g0100a0003c0004t0026g0109 | 3 | HG01358.hp1 HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-221-1414C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506178 | ||||||
| chr2:209506217
|
A | C | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-1375A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506217 | ||||||
| chr2:209506345
|
T | G | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-1247T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506345 | ||||||
| chr2:209506427
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(46): Show | 49 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-221-1165C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506427 | ||||||
| chr2:209506619
|
G | A | 1 | a0003c0004t0026g0109 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-221-973G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506619 | ||||||
| chr2:209506720
|
C | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-221-872C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506720 | ||||||
| chr2:209506738
|
T | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-854T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506738 | ||||||
| chr2:209506758
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-834T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506758 | ||||||
| chr2:209506827
|
C | T | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-765C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506827 | ||||||
| chr2:209506893
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-221-699G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506893 | ||||||
| chr2:209506895
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-221-697A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506895 | ||||||
| chr2:209506994
|
G | A | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-221-598G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209506994 | ||||||
| chr2:209507230
|
G | T | 1 | a0001c0001t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-221-362G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209507230 | ||||||
| chr2:209507261
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-331T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209507261 | ||||||
| chr2:209507279
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-313C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209507279 | ||||||
| chr2:209507429
|
T | C | 1 | a0001c0003t0002g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-221-163T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209507429 | ||||||
| chr2:209507445
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-147C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209507445 | ||||||
| chr2:209507501
|
A | C | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-91A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 1/15 | chr2 | 209507501 | ||||||
| chr2:209507908
|
C | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+267C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209507908 | ||||||
| chr2:209507978
|
A | C | 9 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0006g0003others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-172+337A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209507978 | ||||||
| chr2:209508001
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+360G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508001 | ||||||
| chr2:209508053
|
G | A | 9 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-172+412G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508053 | ||||||
| chr2:209508076
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+435G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508076 | ||||||
| chr2:209508194
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+553G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508194 | ||||||
| chr2:209508224
|
A | C | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-172+583A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508224 | ||||||
| chr2:209508224
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+583A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508224 | ||||||
| chr2:209508260
|
T | C | 3 | a0001c0013t0006g0073a0002c0005t0027g0070a0008c0015t0002g0075 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-172+619T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508260 | ||||||
| chr2:209508279
|
GA | G | 13 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.-172+648delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209508279 | |||||
| chr2:209508315
|
CTT | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+677_-172+678d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209508315 | |||||
| chr2:209508390
|
A | G | 1 | a0002c0002t0019g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-172+749A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508390 | ||||||
| chr2:209508442
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+801C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508442 | ||||||
| chr2:209508584
|
CCACA | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(72): Show | 75 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.-172+968_-172+971d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209508584 | |||||
| chr2:209508584
|
CCACACAC others(1): Show |
C | 14 | a0001c0001t0001g0115a0001c0001t0002g0013a0001c0001t0002g0020others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-172+964_-172+971d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209508584 | |||||
| chr2:209508584
|
CCACACAC others(3): Show |
C | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-172+962_-172+971d others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209508584 | |||||
| chr2:209508592
|
A | C | 5 | a0001c0001t0003g0074a0001c0003t0006g0023a0001c0013t0006g0073others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+951A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508592 | ||||||
| chr2:209508655
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-172+1014G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508655 | ||||||
| chr2:209508682
|
C | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-172+1041C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508682 | ||||||
| chr2:209508836
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-172+1195A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508836 | ||||||
| chr2:209508860
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+1219C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508860 | ||||||
| chr2:209508861
|
T | TA | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+1220_-172+122 others(5): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209508861 | ||||||
| chr2:209509328
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-172+1687C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509328 | ||||||
| chr2:209509393
|
T | A | 10 | a0001c0001t0007g0049a0001c0001t0007g0050a0002c0002t0004g0001others(7): Show | 10 | HG01975.hp2 NA18954.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+1752T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509393 | ||||||
| chr2:209509412
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+1771T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509412 | ||||||
| chr2:209509431
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+1790G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509431 | ||||||
| chr2:209509512
|
T | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+1871T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509512 | ||||||
| chr2:209509782
|
A | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+2141A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509782 | ||||||
| chr2:209509861
|
T | C | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+2220T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509861 | ||||||
| chr2:209509920
|
T | C | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-172+2279T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509920 | ||||||
| chr2:209509945
|
T | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(46): Show | 49 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-172+2304T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509945 | ||||||
| chr2:209509957
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+2316C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209509957 | ||||||
| chr2:209510030
|
CA | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.-172+2402delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209510030 | |||||
| chr2:209510055
|
A | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+2414A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510055 | ||||||
| chr2:209510223
|
G | C | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-172+2582G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510223 | ||||||
| chr2:209510330
|
A | G | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-172+2689A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510330 | ||||||
| chr2:209510401
|
T | C | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-172+2760T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510401 | ||||||
| chr2:209510522
|
A | G | 25 | a0001c0001t0007g0049a0001c0001t0007g0050a0002c0002t0004g0001others(22): Show | 25 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.-172+2881A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510522 | ||||||
| chr2:209510564
|
T | C | 1 | a0001c0001t0003g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-172+2923T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510564 | ||||||
| chr2:209510654
|
A | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-172+3013A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510654 | ||||||
| chr2:209510672
|
T | C | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-172+3031T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510672 | ||||||
| chr2:209510722
|
T | C | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+3081T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510722 | ||||||
| chr2:209510864
|
T | G | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-172+3223T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510864 | ||||||
| chr2:209510991
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+3350G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209510991 | ||||||
| chr2:209511098
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+3457C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511098 | ||||||
| chr2:209511152
|
A | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+3511A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511152 | ||||||
| chr2:209511248
|
T | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+3607T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511248 | ||||||
| chr2:209511482
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-172+3841G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511482 | ||||||
| chr2:209511690
|
C | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-172+4049C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511690 | ||||||
| chr2:209511698
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4057T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511698 | ||||||
| chr2:209511712
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4071C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511712 | ||||||
| chr2:209511723
|
C | T | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-172+4082C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511723 | ||||||
| chr2:209511747
|
T | C | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-172+4106T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511747 | ||||||
| chr2:209511749
|
T | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+4108T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511749 | ||||||
| chr2:209511786
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4145T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511786 | ||||||
| chr2:209511810
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4169G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209511810 | ||||||
| chr2:209512030
|
A | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4389A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512030 | ||||||
| chr2:209512067
|
G | A | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-172+4426G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512067 | ||||||
| chr2:209512200
|
C | T | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+4559C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512200 | ||||||
| chr2:209512263
|
C | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4622C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512263 | ||||||
| chr2:209512271
|
T | C | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4630T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512271 | ||||||
| chr2:209512359
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+4718A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512359 | ||||||
| chr2:209512369
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-172+4728G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512369 | ||||||
| chr2:209512371
|
G | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+4730G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512371 | ||||||
| chr2:209512385
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4744T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512385 | ||||||
| chr2:209512391
|
A | AAAAC | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4766_-172+476 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512391 | |||||
| chr2:209512412
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4771T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512412 | ||||||
| chr2:209512534
|
T | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4893T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512534 | ||||||
| chr2:209512556
|
T | TAC | 28 | a0001c0001t0002g0015a0001c0001t0002g0027a0001c0001t0003g0028others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(25): Show |
intron_variant | MODIFIER | c.-172+4959_-172+496 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
T | TACAC | 4 | a0001c0001t0002g0025a0002c0002t0012g0043a0002c0002t0020g0047others(1): Show | 4 | HG02080.hp1 HG04204.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+4957_-172+496 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TAC | T | 10 | a0001c0001t0001g0103a0001c0001t0002g0013a0001c0001t0002g0032others(7): Show | 10 | HG00408.hp2 HG01243.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.-172+4959_-172+496 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACAC | T | 9 | a0001c0001t0001g0127a0001c0001t0002g0017a0001c0001t0002g0018others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-172+4957_-172+496 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACACAC | T | 4 | a0002c0002t0029g0061a0004c0007t0017g0058a0004c0007t0017g0147others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+4955_-172+496 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACACACA others(1): Show |
T | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-172+4953_-172+496 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACACACA others(3): Show |
T | 5 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(2): Show | 5 | HG02055.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+4951_-172+496 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0033g0007a0001c0003t0036g0006a0001c0006t0002g0056others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+4949_-172+496 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACACACA others(7): Show |
T | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(47): Show | 50 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-172+4947_-172+496 others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512556
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-172+4945_-172+496 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512556 | |||||
| chr2:209512584
|
CACACACA others(11): Show |
C | 9 | a0001c0001t0002g0029a0001c0001t0002g0077a0001c0001t0002g0081others(6): Show | 9 | HG01433.hp2 HG01975.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-172+4949_-172+496 others(22): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512584 | |||||
| chr2:209512586
|
CACACACA others(9): Show |
C | 3 | a0001c0001t0002g0020a0001c0001t0002g0085a0001c0001t0034g0096 | 3 | HG01884.hp1 HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-172+4951_-172+496 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209512586 | |||||
| chr2:209512606
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+4965C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512606 | ||||||
| chr2:209512690
|
G | A | 2 | a0001c0001t0003g0022a0003c0004t0035g0021 | 2 | HG01975.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-172+5049G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512690 | ||||||
| chr2:209512692
|
A | G | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-172+5051A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512692 | ||||||
| chr2:209512703
|
A | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5062A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512703 | ||||||
| chr2:209512728
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5087G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512728 | ||||||
| chr2:209512789
|
A | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5148A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512789 | ||||||
| chr2:209512873
|
C | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5232C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512873 | ||||||
| chr2:209512924
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5283G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209512924 | ||||||
| chr2:209513121
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 58 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-172+5480T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513121 | ||||||
| chr2:209513206
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-172+5565G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513206 | ||||||
| chr2:209513324
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5683G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513324 | ||||||
| chr2:209513547
|
C | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+5906C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513547 | ||||||
| chr2:209513562
|
ATGTG | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 55 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-172+5925_-172+592 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209513562 | |||||
| chr2:209513605
|
C | T | 6 | a0001c0001t0002g0077a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01433.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+5964C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513605 | ||||||
| chr2:209513627
|
G | GAAAAAAC | 11 | a0001c0001t0002g0029a0001c0001t0002g0077a0001c0001t0002g0081others(8): Show | 11 | HG01433.hp2 HG01975.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-172+6000_-172+600 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209513627 | |||||
| chr2:209513639
|
A | C | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+5998A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513639 | ||||||
| chr2:209513702
|
G | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+6061G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513702 | ||||||
| chr2:209513751
|
C | T | 1 | a0002c0002t0020g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-172+6110C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513751 | ||||||
| chr2:209513915
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(54): Show | 57 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-172+6274C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513915 | ||||||
| chr2:209513946
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(54): Show | 57 | HG00140.hp1 HG00597.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-172+6305C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209513946 | ||||||
| chr2:209514064
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.-172+6423C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514064 | ||||||
| chr2:209514100
|
G | A | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-172+6459G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514100 | ||||||
| chr2:209514129
|
A | G | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+6488A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514129 | ||||||
| chr2:209514162
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0063 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-172+6521T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514162 | ||||||
| chr2:209514171
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-172+6530G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514171 | ||||||
| chr2:209514177
|
GT | G | 10 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0077others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-172+6543delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209514177 | |||||
| chr2:209514212
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-172+6571A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514212 | ||||||
| chr2:209514520
|
C | G | 1 | a0002c0002t0014g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-172+6879C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514520 | ||||||
| chr2:209514649
|
A | C | 87 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-172+7008A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514649 | ||||||
| chr2:209514659
|
T | A | 87 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-172+7018T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514659 | ||||||
| chr2:209514946
|
T | C | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+7305T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514946 | ||||||
| chr2:209514948
|
C | G | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+7307C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209514948 | ||||||
| chr2:209515050
|
A | G | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+7409A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515050 | ||||||
| chr2:209515134
|
T | TTTTC | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-172+7502_-172+750 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209515134 | |||||
| chr2:209515164
|
T | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+7523T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515164 | ||||||
| chr2:209515325
|
A | G | 10 | a0001c0001t0010g0116a0001c0001t0033g0007a0001c0003t0006g0003others(7): Show | 10 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+7684A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515325 | ||||||
| chr2:209515428
|
G | T | 10 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+7787G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515428 | ||||||
| chr2:209515462
|
G | A | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+7821G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515462 | ||||||
| chr2:209515523
|
A | T | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-172+7882A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515523 | ||||||
| chr2:209515646
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-172+8005G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515646 | ||||||
| chr2:209515665
|
A | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+8024A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515665 | ||||||
| chr2:209515786
|
T | A | 4 | a0001c0001t0002g0077a0001c0001t0002g0083a0001c0001t0003g0076others(1): Show | 4 | HG01433.hp2 HG02683.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+8145T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515786 | ||||||
| chr2:209515995
|
A | G | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-172+8354A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209515995 | ||||||
| chr2:209516071
|
A | G | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+8430A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516071 | ||||||
| chr2:209516084
|
T | C | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-172+8443T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516084 | ||||||
| chr2:209516096
|
G | A | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+8455G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516096 | ||||||
| chr2:209516279
|
TAAAG | T | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+8640_-172+864 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209516279 | |||||
| chr2:209516289
|
G | A | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-172+8648G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516289 | ||||||
| chr2:209516355
|
A | G | 1 | a0002c0002t0014g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-172+8714A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516355 | ||||||
| chr2:209516474
|
T | A | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-172+8833T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516474 | ||||||
| chr2:209516544
|
G | A | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+8903G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516544 | ||||||
| chr2:209516589
|
T | C | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+8948T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516589 | ||||||
| chr2:209516624
|
A | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+8983A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516624 | ||||||
| chr2:209516753
|
T | C | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+9112T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516753 | ||||||
| chr2:209516830
|
G | C | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+9189G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209516830 | ||||||
| chr2:209517183
|
C | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+9542C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517183 | ||||||
| chr2:209517217
|
A | G | 2 | a0001c0001t0003g0074a0001c0003t0006g0023 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-172+9576A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517217 | ||||||
| chr2:209517332
|
T | C | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+9691T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517332 | ||||||
| chr2:209517336
|
A | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+9695A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517336 | ||||||
| chr2:209517351
|
G | A | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+9710G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517351 | ||||||
| chr2:209517434
|
A | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-172+9793A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517434 | ||||||
| chr2:209517466
|
C | T | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+9825C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517466 | ||||||
| chr2:209517711
|
C | T | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+10070C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517711 | ||||||
| chr2:209517843
|
G | A | 4 | a0001c0001t0002g0077a0001c0001t0002g0083a0001c0001t0003g0076others(1): Show | 4 | HG01433.hp2 HG02683.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+10202G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517843 | ||||||
| chr2:209517862
|
AT | A | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+10231delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209517862 | |||||
| chr2:209517866
|
T | G | 30 | a0001c0001t0007g0049a0001c0001t0007g0050a0002c0002t0004g0001others(27): Show | 30 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.-172+10225T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517866 | ||||||
| chr2:209517883
|
A | G | 57 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(54): Show | 57 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.-172+10242A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517883 | ||||||
| chr2:209517985
|
T | C | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+10344T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517985 | ||||||
| chr2:209517994
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-172+10353C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209517994 | ||||||
| chr2:209518090
|
C | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+10449C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209518090 | ||||||
| chr2:209518134
|
T | A | 86 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.-172+10493T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209518134 | ||||||
| chr2:209518194
|
T | G | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+10553T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209518194 | ||||||
| chr2:209518246
|
A | AG | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+10609dupG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209518246 | |||||
| chr2:209518394
|
G | A | 13 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(10): Show | 13 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-172+10753G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209518394 | ||||||
| chr2:209519021
|
A | G | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+11380A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519021 | ||||||
| chr2:209519353
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-172+11712T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519353 | ||||||
| chr2:209519371
|
C | T | 1 | a0002c0002t0030g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-172+11730C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519371 | ||||||
| chr2:209519468
|
A | T | 3 | a0001c0001t0010g0116a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-172+11827A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519468 | ||||||
| chr2:209519534
|
C | T | 4 | a0001c0001t0002g0077a0001c0001t0002g0083a0001c0001t0003g0076others(1): Show | 4 | HG01433.hp2 HG02683.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+11893C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519534 | ||||||
| chr2:209519638
|
A | G | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+11997A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519638 | ||||||
| chr2:209519805
|
AC | A | 63 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-172+12165delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519805 | ||||||
| chr2:209519832
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0132others(1): Show | 4 | HG03710.hp2 HG04184.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+12191A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519832 | ||||||
| chr2:209519866
|
A | G | 3 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0120 | 3 | NA18959.hp2 NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-172+12225A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209519866 | ||||||
| chr2:209520434
|
AGAGG | A | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+12796_-172+12 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209520434 | |||||
| chr2:209520553
|
C | T | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-172+12912C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209520553 | ||||||
| chr2:209520560
|
A | G | 4 | a0001c0001t0002g0077a0001c0001t0002g0083a0001c0001t0003g0076others(1): Show | 4 | HG01433.hp2 HG02683.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+12919A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209520560 | ||||||
| chr2:209521045
|
C | T | 2 | a0002c0002t0004g0118a0002c0002t0004g0119 | 2 | NA18959.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-172+13404C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521045 | ||||||
| chr2:209521086
|
T | C | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-172+13445T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521086 | ||||||
| chr2:209521175
|
A | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+13534A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521175 | ||||||
| chr2:209521323
|
A | C | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-172+13682A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521323 | ||||||
| chr2:209521451
|
C | T | 59 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-172+13810C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521451 | ||||||
| chr2:209521560
|
A | C | 88 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.-172+13919A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521560 | ||||||
| chr2:209521570
|
A | T | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+13929A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521570 | ||||||
| chr2:209521571
|
A | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0107a0001c0001t0001g0140others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-172+13930A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521571 | ||||||
| chr2:209521661
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0003g0022others(1): Show | 4 | HG01884.hp1 HG01975.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+14020G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521661 | ||||||
| chr2:209521679
|
T | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-172+14038T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209521679 | ||||||
| chr2:209522077
|
C | T | 1 | a0001c0006t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-172+14436C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522077 | ||||||
| chr2:209522293
|
T | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+14652T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522293 | ||||||
| chr2:209522296
|
A | T | 1 | a0004c0007t0017g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-172+14655A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522296 | ||||||
| chr2:209522299
|
A | C | 1 | a0002c0002t0032g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-172+14658A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522299 | ||||||
| chr2:209522373
|
G | A | 1 | a0010c0012t0038g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-172+14732G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522373 | ||||||
| chr2:209522503
|
CAAAT | C | 3 | a0001c0001t0002g0083a0001c0001t0003g0076a0001c0001t0003g0078 | 3 | HG01433.hp2 HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-172+14865_-172+14 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209522503 | |||||
| chr2:209522520
|
T | C | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-172+14879T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522520 | ||||||
| chr2:209522629
|
G | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01192.hp2 HG01993.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-172+14988G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522629 | ||||||
| chr2:209522860
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+15219G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522860 | ||||||
| chr2:209522895
|
G | A | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+15254G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209522895 | ||||||
| chr2:209523008
|
G | A | 96 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0017others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-172+15367G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523008 | ||||||
| chr2:209523111
|
T | C | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+15470T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523111 | ||||||
| chr2:209523433
|
C | T | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+15792C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523433 | ||||||
| chr2:209523434
|
G | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-172+15793G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523434 | ||||||
| chr2:209523485
|
C | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+15844C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523485 | ||||||
| chr2:209523529
|
G | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0025a0001c0001t0002g0026others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-172+15888G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523529 | ||||||
| chr2:209523681
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-172+16040C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523681 | ||||||
| chr2:209523974
|
G | C | 61 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-172+16333G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523974 | ||||||
| chr2:209523984
|
G | T | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+16343G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209523984 | ||||||
| chr2:209524179
|
C | T | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+16538C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209524179 | ||||||
| chr2:209524190
|
A | G | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-172+16549A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209524190 | ||||||
| chr2:209524295
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+16654G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209524295 | ||||||
| chr2:209524338
|
T | A | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-172+16697T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209524338 | ||||||
| chr2:209524452
|
G | C | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+16811G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209524452 | ||||||
| chr2:209524538
|
G | T | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-172+16897G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209524538 | ||||||
| chr2:209525054
|
C | T | 1 | a0002c0002t0005g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-172+17413C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525054 | ||||||
| chr2:209525321
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-172+17680G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525321 | ||||||
| chr2:209525437
|
A | G | 61 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-172+17796A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525437 | ||||||
| chr2:209525599
|
T | C | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+17958T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525599 | ||||||
| chr2:209525801
|
C | T | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-172+18160C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525801 | ||||||
| chr2:209525828
|
G | T | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+18187G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525828 | ||||||
| chr2:209525862
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG00408.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-172+18221A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525862 | ||||||
| chr2:209525998
|
A | G | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-172+18357A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209525998 | ||||||
| chr2:209526119
|
A | G | 1 | a0003c0004t0035g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-172+18478A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209526119 | ||||||
| chr2:209526551
|
C | T | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+18910C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209526551 | ||||||
| chr2:209526609
|
T | TG | 99 | a0001c0001t0001g0014a0001c0001t0001g0107a0001c0001t0002g0013others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.-172+18972dupG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209526609 | |||||
| chr2:209526816
|
GAA | G | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+19178_-172+19 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209526816 | |||||
| chr2:209527113
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0107a0001c0001t0002g0013others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-172+19472A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527113 | ||||||
| chr2:209527189
|
A | G | 5 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0085others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+19548A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527189 | ||||||
| chr2:209527240
|
C | G | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-172+19599C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527240 | ||||||
| chr2:209527564
|
G | A | 3 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0120 | 3 | NA18959.hp2 NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-172+19923G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527564 | ||||||
| chr2:209527659
|
G | A | 6 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-172+20018G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527659 | ||||||
| chr2:209527770
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-172+20129A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527770 | ||||||
| chr2:209527779
|
C | T | 14 | a0001c0001t0002g0083a0001c0001t0003g0074a0001c0001t0003g0076others(11): Show | 14 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+20138C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527779 | ||||||
| chr2:209527987
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.-172+20346G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209527987 | ||||||
| chr2:209528023
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-172+20382T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528023 | ||||||
| chr2:209528042
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-172+20401G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528042 | ||||||
| chr2:209528098
|
TC | T | 20 | a0001c0001t0001g0128a0001c0001t0002g0020a0001c0001t0002g0081others(17): Show | 20 | HG01358.hp1 HG01433.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-172+20464delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528098 | |||||
| chr2:209528105
|
CT | C | 20 | a0001c0001t0001g0107a0001c0001t0002g0025a0001c0001t0003g0022others(17): Show | 20 | HG00733.hp2 HG01975.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.-172+20465delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528105 | ||||||
| chr2:209528122
|
T | C | 11 | a0001c0001t0003g0074a0001c0001t0010g0116a0001c0001t0033g0007others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-172+20481T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528122 | ||||||
| chr2:209528183
|
C | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+20542C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528183 | ||||||
| chr2:209528224
|
A | G | 10 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095others(7): Show | 10 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+20583A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528224 | ||||||
| chr2:209528287
|
C | G | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-172+20646C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528287 | ||||||
| chr2:209528340
|
C | T | 4 | a0001c0001t0010g0116a0004c0007t0010g0148a0004c0007t0017g0058others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+20699C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528340 | ||||||
| chr2:209528411
|
C | G | 19 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0002g0083others(16): Show | 19 | HG01433.hp2 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-172+20770C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528411 | ||||||
| chr2:209528500
|
CT | C | 3 | a0001c0001t0002g0083a0001c0001t0003g0076a0001c0001t0003g0078 | 3 | HG01433.hp2 HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-172+20860delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528500 | ||||||
| chr2:209528737
|
CATGTATA others(13): Show |
C | 10 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-172+21110_-172+21 others(26): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528737 | |||||
| chr2:209528742
|
A | ATATATGT others(19): Show |
1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-172+21130_-172+21 others(32): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528742 | |||||
| chr2:209528742
|
A | ATATATGT others(45): Show |
1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-172+21104_-172+21 others(58): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528742 | |||||
| chr2:209528771
|
TATGTACA others(19): Show |
T | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-172+21156_-172+21 others(32): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528771 | |||||
| chr2:209528772
|
A | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(9): Show | 12 | HG01433.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-172+21131A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528772 | ||||||
| chr2:209528782
|
GTA | G | 12 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+21143_-172+21 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528782 | |||||
| chr2:209528797
|
C | T | 71 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.-172+21156C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528797 | ||||||
| chr2:209528797
|
CATGTACA others(19): Show |
C | 1 | a0001c0017t0007g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-172+21179_-172+21 others(32): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528797 | |||||
| chr2:209528840
|
A | G | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-172+21199A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528840 | ||||||
| chr2:209528848
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-172+21207G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528848 | ||||||
| chr2:209528848
|
GTGTGTGT others(5): Show |
G | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-172+21223_-172+21 others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528848 | |||||
| chr2:209528856
|
G | A | 12 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+21215G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528856 | ||||||
| chr2:209528886
|
G | GTA | 9 | a0002c0005t0011g0094a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-172+21250_-172+21 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528886 | |||||
| chr2:209528921
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-172+21280T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209528921 | ||||||
| chr2:209528923
|
CAT | C | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-172+21290_-172+21 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209528923 | |||||
| chr2:209529154
|
G | A | 5 | a0001c0001t0001g0128a0001c0001t0002g0083a0001c0001t0003g0028others(2): Show | 5 | HG01433.hp2 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+21513G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529154 | ||||||
| chr2:209529543
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+21902T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529543 | ||||||
| chr2:209529547
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+21906T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529547 | ||||||
| chr2:209529826
|
T | A | 49 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-172+22185T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529826 | ||||||
| chr2:209529889
|
C | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-172+22248C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529889 | ||||||
| chr2:209529896
|
A | T | 49 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-172+22255A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529896 | ||||||
| chr2:209529904
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(99): Show | 102 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.-172+22263G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209529904 | ||||||
| chr2:209530128
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-172+22487A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530128 | ||||||
| chr2:209530148
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0111 | 2 | NA19007.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-172+22507G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530148 | ||||||
| chr2:209530205
|
CAG | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+22568_-172+22 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209530205 | |||||
| chr2:209530213
|
G | A | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+22572G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530213 | ||||||
| chr2:209530439
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-172+22798G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530439 | ||||||
| chr2:209530445
|
T | C | 2 | a0003c0004t0026g0109a0003c0004t0035g0021 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-172+22804T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530445 | ||||||
| chr2:209530573
|
G | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-172+22932G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530573 | ||||||
| chr2:209530686
|
C | A | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-172+23045C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530686 | ||||||
| chr2:209530692
|
A | G | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-172+23051A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530692 | ||||||
| chr2:209530998
|
T | C | 46 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-172+23357T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209530998 | ||||||
| chr2:209531274
|
A | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+23633A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209531274 | ||||||
| chr2:209531529
|
C | T | 1 | a0001c0003t0006g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-172+23888C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209531529 | ||||||
| chr2:209531538
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-172+23897T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209531538 | ||||||
| chr2:209531556
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-172+23915G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209531556 | ||||||
| chr2:209531906
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+24265T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209531906 | ||||||
| chr2:209531960
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+24319T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209531960 | ||||||
| chr2:209532020
|
C | T | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-172+24379C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532020 | ||||||
| chr2:209532021
|
G | A | 45 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(42): Show | 45 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-172+24380G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532021 | ||||||
| chr2:209532081
|
C | A | 83 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-172+24440C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532081 | ||||||
| chr2:209532240
|
G | GA | 8 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-172+24617dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209532240 | |||||
| chr2:209532240
|
GA | G | 16 | a0001c0001t0001g0128a0001c0001t0021g0104a0001c0001t0033g0007others(13): Show | 16 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-172+24617delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209532240 | |||||
| chr2:209532240
|
GAA | G | 6 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-172+24616_-172+24 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209532240 | |||||
| chr2:209532254
|
A | T | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+24613A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532254 | ||||||
| chr2:209532583
|
C | G | 1 | a0001c0001t0007g0050 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-172+24942C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532583 | ||||||
| chr2:209532606
|
G | A | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+24965G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532606 | ||||||
| chr2:209532670
|
T | C | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-172+25029T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532670 | ||||||
| chr2:209532736
|
T | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+25095T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532736 | ||||||
| chr2:209532990
|
T | G | 2 | a0002c0002t0009g0098a0003c0004t0001g0099 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-172+25349T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209532990 | ||||||
| chr2:209533261
|
G | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+25620G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533261 | ||||||
| chr2:209533496
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-172+25855G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533496 | ||||||
| chr2:209533508
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-172+25867G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533508 | ||||||
| chr2:209533621
|
A | T | 46 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-172+25980A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533621 | ||||||
| chr2:209533628
|
T | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-172+25987T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533628 | ||||||
| chr2:209533696
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-172+26055T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533696 | ||||||
| chr2:209533953
|
G | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+26312G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209533953 | ||||||
| chr2:209534130
|
C | T | 1 | a0003c0004t0026g0109 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-172+26489C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209534130 | ||||||
| chr2:209534169
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-172+26528A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209534169 | ||||||
| chr2:209534350
|
T | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+26709T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209534350 | ||||||
| chr2:209534485
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+26844G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209534485 | ||||||
| chr2:209534740
|
T | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+27099T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209534740 | ||||||
| chr2:209534985
|
C | CA | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-172+27345dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209534985 | |||||
| chr2:209535236
|
C | T | 6 | a0001c0001t0003g0064a0002c0002t0015g0066a0002c0002t0029g0061others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-172+27595C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535236 | ||||||
| chr2:209535417
|
T | C | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+27776T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535417 | ||||||
| chr2:209535546
|
C | CTGGCAAA others(1): Show |
8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-172+27908_-172+27 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209535546 | |||||
| chr2:209535556
|
G | GGCAAAGT others(3): Show |
3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+27915_-172+27 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535556 | ||||||
| chr2:209535557
|
T | G | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+27916T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535557 | ||||||
| chr2:209535558
|
C | CAAAGTGT others(2): Show |
3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+27917_-172+27 others(15): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535558 | ||||||
| chr2:209535558
|
C | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+27917C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535558 | ||||||
| chr2:209535586
|
C | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0002g0015others(69): Show | 72 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-172+27945C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535586 | ||||||
| chr2:209535749
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-172+28108G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535749 | ||||||
| chr2:209535772
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-172+28131A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535772 | ||||||
| chr2:209535941
|
T | A | 5 | a0001c0001t0002g0032a0001c0003t0002g0054a0001c0003t0002g0055others(2): Show | 5 | HG02486.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+28300T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209535941 | ||||||
| chr2:209536567
|
G | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-172+28926G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209536567 | ||||||
| chr2:209536674
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+29033T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209536674 | ||||||
| chr2:209536844
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+29203G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209536844 | ||||||
| chr2:209536972
|
A | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+29331A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209536972 | ||||||
| chr2:209537003
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-172+29362G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537003 | ||||||
| chr2:209537084
|
T | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+29443T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537084 | ||||||
| chr2:209537167
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+29526G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537167 | ||||||
| chr2:209537198
|
C | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+29557C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537198 | ||||||
| chr2:209537424
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-172+29783A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537424 | ||||||
| chr2:209537480
|
AT | A | 11 | a0001c0014t0001g0101a0002c0005t0011g0094a0003c0004t0002g0062others(8): Show | 11 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-172+29840delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537480 | ||||||
| chr2:209537625
|
C | T | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+29984C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537625 | ||||||
| chr2:209537812
|
T | G | 83 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-172+30171T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537812 | ||||||
| chr2:209537954
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-172+30313A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209537954 | ||||||
| chr2:209538112
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+30471G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538112 | ||||||
| chr2:209538292
|
A | G | 1 | a0002c0002t0015g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-172+30651A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538292 | ||||||
| chr2:209538461
|
AT | A | 4 | a0001c0001t0033g0007a0002c0005t0011g0071a0002c0005t0011g0072others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-172+30829delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209538461 | |||||
| chr2:209538509
|
GGTCAGAG others(4): Show |
G | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-172+30869_-172+30 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538509 | ||||||
| chr2:209538522
|
G | A | 9 | a0002c0005t0011g0094a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-172+30881G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538522 | ||||||
| chr2:209538535
|
C | CT | 13 | a0001c0001t0002g0020a0001c0001t0003g0076a0001c0001t0010g0116others(10): Show | 13 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-172+30912dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209538535 | |||||
| chr2:209538553
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-172+30912T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538553 | ||||||
| chr2:209538553
|
T | TC | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+30914dupC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209538553 | |||||
| chr2:209538553
|
T | TTC | 7 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-172+30912_-172+30 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538553 | ||||||
| chr2:209538645
|
T | C | 3 | a0002c0002t0014g0143a0002c0002t0039g0051a0009c0019t0007g0042 | 3 | HG02080.hp1 NA18942.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-172+31004T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538645 | ||||||
| chr2:209538674
|
A | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+31033A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538674 | ||||||
| chr2:209538941
|
C | A | 9 | a0002c0005t0011g0094a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-172+31300C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538941 | ||||||
| chr2:209538978
|
A | T | 46 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-172+31337A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209538978 | ||||||
| chr2:209539014
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-172+31373G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539014 | ||||||
| chr2:209539188
|
A | C | 13 | a0001c0001t0002g0029a0001c0001t0010g0116a0001c0014t0001g0101others(10): Show | 13 | HG01358.hp1 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-172+31547A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539188 | ||||||
| chr2:209539227
|
A | G | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-172+31586A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539227 | ||||||
| chr2:209539276
|
G | T | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+31635G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539276 | ||||||
| chr2:209539277
|
A | T | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+31636A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539277 | ||||||
| chr2:209539297
|
T | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-172+31656T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539297 | ||||||
| chr2:209539344
|
A | G | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+31703A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539344 | ||||||
| chr2:209539471
|
G | A | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+31830G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539471 | ||||||
| chr2:209539500
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-172+31859C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539500 | ||||||
| chr2:209539531
|
C | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-172+31890C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539531 | ||||||
| chr2:209539581
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(14): Show | 17 | HG02258.hp2 HG02486.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.-172+31940C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539581 | ||||||
| chr2:209539680
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32039G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539680 | ||||||
| chr2:209539711
|
CT | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32079delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209539711 | |||||
| chr2:209539720
|
T | TA | 5 | a0001c0001t0003g0064a0002c0002t0029g0061a0002c0002t0030g0068others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+32080dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209539720 | |||||
| chr2:209539833
|
C | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32192C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539833 | ||||||
| chr2:209539934
|
G | GA | 28 | a0001c0001t0002g0020a0001c0001t0002g0029a0001c0001t0010g0116others(25): Show | 28 | HG00597.hp2 HG01243.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.-172+32311dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209539934 | |||||
| chr2:209539934
|
G | GAA | 45 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(42): Show | 45 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-172+32310_-172+32 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209539934 | |||||
| chr2:209539955
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-172+32314G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209539955 | ||||||
| chr2:209540005
|
G | A | 1 | a0002c0002t0019g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-172+32364G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540005 | ||||||
| chr2:209540087
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32446G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540087 | ||||||
| chr2:209540097
|
T | TA | 52 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0115others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-172+32482dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540097 | |||||
| chr2:209540097
|
T | TAA | 7 | a0001c0001t0002g0030a0001c0001t0003g0064a0002c0002t0004g0118others(4): Show | 7 | HG00597.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-172+32481_-172+32 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540097 | |||||
| chr2:209540097
|
TA | T | 12 | a0001c0001t0021g0104a0002c0005t0011g0094a0003c0004t0001g0099others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-172+32482delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540097 | |||||
| chr2:209540097
|
TAAAAAAA others(1): Show |
T | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32475_-172+32 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540097 | |||||
| chr2:209540129
|
A | T | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-172+32488A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540129 | ||||||
| chr2:209540136
|
A | T | 2 | a0001c0001t0002g0029a0001c0001t0010g0116 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-172+32495A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540136 | ||||||
| chr2:209540160
|
CTG | C | 2 | a0001c0001t0002g0029a0001c0001t0010g0116 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-172+32521_-172+32 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540160 | |||||
| chr2:209540171
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0010g0116 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-172+32530A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540171 | ||||||
| chr2:209540216
|
T | TTCTTG | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32575_-172+32 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540216 | ||||||
| chr2:209540295
|
G | A | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-172+32654G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540295 | ||||||
| chr2:209540477
|
C | A | 29 | a0001c0001t0007g0049a0002c0002t0004g0001a0002c0002t0004g0118others(26): Show | 29 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.-172+32836C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540477 | ||||||
| chr2:209540495
|
GTGGCACG others(1133): Show |
G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+32857_-172+33 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540495 | |||||
| chr2:209540630
|
C | CA | 24 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0106others(21): Show | 24 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-172+33021dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540630
|
C | CAA | 12 | a0001c0001t0001g0014a0001c0001t0001g0122a0001c0001t0001g0130others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.-172+33020_-172+33 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540630
|
C | CAAA | 8 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0114others(5): Show | 8 | HG01109.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-172+33019_-172+33 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540630
|
C | CAAAA | 7 | a0001c0001t0001g0129a0001c0001t0002g0013a0001c0001t0003g0074others(4): Show | 7 | HG02080.hp2 HG02258.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-172+33018_-172+33 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540630
|
CAAAAAAA | C | 9 | a0001c0001t0002g0020a0002c0005t0011g0094a0003c0004t0002g0062others(6): Show | 9 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-172+33015_-172+33 others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540630
|
CAAAAAAA others(3): Show |
C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-172+33012_-172+33 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540630
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-172+33009_-172+33 others(19): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540630 | |||||
| chr2:209540660
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-172+33021_-172+33 others(19): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540660 | |||||
| chr2:209540660
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-172+33021_-172+33 others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540660 | |||||
| chr2:209540660
|
A | AAAAAAAA others(4): Show |
8 | a0001c0001t0002g0030a0001c0001t0002g0081a0001c0001t0003g0064others(5): Show | 8 | HG00733.hp2 HG01109.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-172+33021_-172+33 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540660 | |||||
| chr2:209540660
|
A | AAAAAAAA others(3): Show |
23 | a0001c0001t0002g0082a0002c0002t0004g0001a0002c0002t0004g0119others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-172+33021_-172+33 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540660 | |||||
| chr2:209540660
|
A | AAAAAAAA others(2): Show |
11 | a0001c0001t0007g0049a0002c0002t0005g0033a0002c0002t0005g0039others(8): Show | 11 | HG01975.hp2 HG02080.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-172+33021_-172+33 others(15): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209540660 | |||||
| chr2:209540660
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0018 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-172+33019A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209540660 | ||||||
| chr2:209541116
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-172+33475C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209541116 | ||||||
| chr2:209541417
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-172+33776T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209541417 | ||||||
| chr2:209541689
|
C | T | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+34048C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209541689 | ||||||
| chr2:209541882
|
ATTAAG | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-172+34246_-172+34 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209541882 | |||||
| chr2:209542024
|
G | A | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-172+34383G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542024 | ||||||
| chr2:209542303
|
A | G | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-172+34662A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542303 | ||||||
| chr2:209542346
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+34705G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542346 | ||||||
| chr2:209542463
|
G | A | 1 | a0002c0002t0012g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-172+34822G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542463 | ||||||
| chr2:209542533
|
G | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+34892G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542533 | ||||||
| chr2:209542649
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-172+35008C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542649 | ||||||
| chr2:209542672
|
A | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+35031A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542672 | ||||||
| chr2:209542726
|
G | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-172+35085G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542726 | ||||||
| chr2:209542821
|
T | G | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-172+35180T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209542821 | ||||||
| chr2:209543232
|
T | C | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-172+35591T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543232 | ||||||
| chr2:209543692
|
A | G | 77 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-172+36051A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543692 | ||||||
| chr2:209543735
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+36094G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543735 | ||||||
| chr2:209543753
|
G | A | 77 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-172+36112G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543753 | ||||||
| chr2:209543880
|
A | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-36156A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543880 | ||||||
| chr2:209543907
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-171-36129G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543907 | ||||||
| chr2:209543931
|
T | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-36105T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209543931 | ||||||
| chr2:209544005
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG01433.hp2 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-171-36031G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209544005 | ||||||
| chr2:209544304
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-35732T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209544304 | ||||||
| chr2:209544538
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-171-35498A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209544538 | ||||||
| chr2:209544630
|
G | A | 46 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-171-35406G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209544630 | ||||||
| chr2:209544690
|
T | C | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-171-35346T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209544690 | ||||||
| chr2:209544776
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-35260T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209544776 | ||||||
| chr2:209545078
|
T | C | 2 | a0001c0001t0002g0025a0001c0001t0003g0022 | 2 | HG01975.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-171-34958T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209545078 | ||||||
| chr2:209545108
|
G | T | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-34928G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209545108 | ||||||
| chr2:209545583
|
G | A | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-34453G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209545583 | ||||||
| chr2:209545609
|
A | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-171-34427A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209545609 | ||||||
| chr2:209545813
|
T | A | 1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-171-34223T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209545813 | ||||||
| chr2:209546154
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-171-33882T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209546154 | ||||||
| chr2:209546344
|
A | AT | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-171-33691dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209546344 | |||||
| chr2:209546346
|
G | T | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-171-33690G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209546346 | ||||||
| chr2:209547183
|
C | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-32853C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547183 | ||||||
| chr2:209547324
|
C | CT | 79 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(76): Show | 79 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-171-32702dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209547324 | |||||
| chr2:209547335
|
A | T | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-32701A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547335 | ||||||
| chr2:209547339
|
A | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-32697A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547339 | ||||||
| chr2:209547392
|
T | C | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-32644T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547392 | ||||||
| chr2:209547442
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-32594A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547442 | ||||||
| chr2:209547570
|
A | G | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-171-32466A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547570 | ||||||
| chr2:209547616
|
A | G | 1 | a0010c0012t0038g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-171-32420A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547616 | ||||||
| chr2:209547898
|
C | G | 14 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-32138C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209547898 | ||||||
| chr2:209548213
|
T | A | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-171-31823T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548213 | ||||||
| chr2:209548461
|
A | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-31575A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548461 | ||||||
| chr2:209548566
|
A | G | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-171-31470A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548566 | ||||||
| chr2:209548726
|
G | A | 17 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(14): Show | 17 | HG00733.hp2 HG02055.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-171-31310G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548726 | ||||||
| chr2:209548775
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-171-31261A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548775 | ||||||
| chr2:209548840
|
G | T | 1 | a0001c0006t0002g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-171-31196G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548840 | ||||||
| chr2:209548996
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-31040C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209548996 | ||||||
| chr2:209549010
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-31026T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549010 | ||||||
| chr2:209549257
|
G | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-30779G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549257 | ||||||
| chr2:209549312
|
A | G | 1 | a0002c0002t0020g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-171-30724A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549312 | ||||||
| chr2:209549538
|
T | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-30498T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549538 | ||||||
| chr2:209549703
|
C | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-30333C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549703 | ||||||
| chr2:209549798
|
C | T | 1 | a0001c0001t0025g0141 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-171-30238C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549798 | ||||||
| chr2:209549809
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-171-30227A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549809 | ||||||
| chr2:209549875
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-171-30161C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549875 | ||||||
| chr2:209549891
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-30145C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549891 | ||||||
| chr2:209549906
|
A | G | 1 | a0002c0002t0012g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-171-30130A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209549906 | ||||||
| chr2:209550051
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-171-29985A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550051 | ||||||
| chr2:209550096
|
A | G | 3 | a0001c0001t0003g0074a0001c0014t0001g0101a0008c0015t0002g0075 | 3 | HG02280.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-171-29940A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550096 | ||||||
| chr2:209550222
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0010 | 2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-171-29814T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550222 | ||||||
| chr2:209550262
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-29774C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550262 | ||||||
| chr2:209550278
|
T | G | 2 | a0003c0004t0026g0109a0003c0004t0035g0021 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-171-29758T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550278 | ||||||
| chr2:209550803
|
G | A | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-171-29233G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550803 | ||||||
| chr2:209550816
|
A | G | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-171-29220A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550816 | ||||||
| chr2:209550886
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-29150C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209550886 | ||||||
| chr2:209551047
|
T | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-28989T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209551047 | ||||||
| chr2:209551455
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-171-28581A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209551455 | ||||||
| chr2:209551664
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-28372A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209551664 | ||||||
| chr2:209551872
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-28164A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209551872 | ||||||
| chr2:209551964
|
C | T | 2 | a0001c0001t0003g0076a0001c0001t0003g0078 | 2 | HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-171-28072C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209551964 | ||||||
| chr2:209552633
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-27403C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552633 | ||||||
| chr2:209552637
|
T | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-27399T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552637 | ||||||
| chr2:209552644
|
C | T | 56 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-171-27392C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552644 | ||||||
| chr2:209552667
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-27369T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552667 | ||||||
| chr2:209552759
|
G | C | 4 | a0002c0002t0009g0108a0002c0002t0009g0112a0002c0002t0013g0102others(1): Show | 4 | HG00408.hp1 HG00597.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-27277G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552759 | ||||||
| chr2:209552785
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-171-27251C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552785 | ||||||
| chr2:209552926
|
G | A | 56 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-171-27110G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209552926 | ||||||
| chr2:209553018
|
G | GTT | 6 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(3): Show | 6 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-171-27008_-171-27 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209553018 | |||||
| chr2:209553021
|
T | G | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-171-27015T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553021 | ||||||
| chr2:209553146
|
G | A | 56 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-171-26890G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553146 | ||||||
| chr2:209553168
|
C | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-26868C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553168 | ||||||
| chr2:209553172
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-26864C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553172 | ||||||
| chr2:209553343
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-171-26693T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553343 | ||||||
| chr2:209553412
|
A | T | 1 | a0001c0003t0002g0054 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-171-26624A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553412 | ||||||
| chr2:209553482
|
T | C | 1 | a0002c0002t0014g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-171-26554T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553482 | ||||||
| chr2:209553683
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-26353A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553683 | ||||||
| chr2:209553735
|
C | G | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-171-26301C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553735 | ||||||
| chr2:209553741
|
G | A | 1 | a0003c0004t0003g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-171-26295G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553741 | ||||||
| chr2:209553762
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-26274T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553762 | ||||||
| chr2:209553769
|
C | T | 1 | a0010c0012t0038g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-171-26267C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209553769 | ||||||
| chr2:209554154
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-171-25882C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554154 | ||||||
| chr2:209554388
|
G | A | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-171-25648G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554388 | ||||||
| chr2:209554711
|
T | C | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-25325T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554711 | ||||||
| chr2:209554748
|
CA | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-25279delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209554748 | |||||
| chr2:209554786
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-25250G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554786 | ||||||
| chr2:209554855
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-25181G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554855 | ||||||
| chr2:209554932
|
T | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0111 | 2 | NA19007.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-171-25104T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554932 | ||||||
| chr2:209554949
|
TATTA | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-25086_-171-25 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554949 | ||||||
| chr2:209554955
|
T | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-25081T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554955 | ||||||
| chr2:209554957
|
T | A | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-171-25079T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209554957 | ||||||
| chr2:209555087
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-24949G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555087 | ||||||
| chr2:209555115
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-24921A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555115 | ||||||
| chr2:209555151
|
T | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-24885T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555151 | ||||||
| chr2:209555241
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-24795A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555241 | ||||||
| chr2:209555659
|
A | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-24377A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555659 | ||||||
| chr2:209555895
|
G | A | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-171-24141G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555895 | ||||||
| chr2:209555970
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-24066G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209555970 | ||||||
| chr2:209556024
|
C | CT | 126 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0105others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-171-24000dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556024 | |||||
| chr2:209556042
|
C | CT | 18 | a0001c0001t0001g0128a0001c0001t0002g0029a0001c0001t0002g0032others(15): Show | 18 | HG02258.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-171-23978dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556042 | |||||
| chr2:209556042
|
CT | C | 13 | a0001c0001t0002g0020a0001c0001t0010g0116a0001c0003t0018g0005others(10): Show | 13 | HG01243.hp2 HG01358.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-171-23978delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556042 | |||||
| chr2:209556042
|
CTT | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23979_-171-23 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556042 | |||||
| chr2:209556068
|
CTCTTGCT | C | 4 | a0001c0001t0002g0020a0002c0005t0008g0134a0002c0005t0008g0135others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-23967_-171-23 others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556068 | ||||||
| chr2:209556095
|
G | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23941G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556095 | ||||||
| chr2:209556199
|
C | A | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-171-23837C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556199 | ||||||
| chr2:209556218
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(97): Show | 100 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-171-23818A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556218 | ||||||
| chr2:209556312
|
G | A | 1 | a0010c0012t0038g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-171-23724G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556312 | ||||||
| chr2:209556448
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23588G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556448 | ||||||
| chr2:209556540
|
A | G | 9 | a0002c0005t0011g0094a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-171-23496A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556540 | ||||||
| chr2:209556662
|
TA | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-171-23355delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556662 | |||||
| chr2:209556662
|
TAA | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-171-23356_-171-23 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556662 | |||||
| chr2:209556662
|
TAAAAA | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23359_-171-23 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209556662 | |||||
| chr2:209556705
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23331C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556705 | ||||||
| chr2:209556716
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23320G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556716 | ||||||
| chr2:209556735
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(96): Show | 99 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-171-23301G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556735 | ||||||
| chr2:209556745
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23291A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556745 | ||||||
| chr2:209556992
|
G | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-23044G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209556992 | ||||||
| chr2:209557027
|
T | A | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-171-23009T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557027 | ||||||
| chr2:209557195
|
G | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-22841G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557195 | ||||||
| chr2:209557390
|
T | C | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-171-22646T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557390 | ||||||
| chr2:209557400
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-22636C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557400 | ||||||
| chr2:209557415
|
G | A | 1 | a0003c0004t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-171-22621G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557415 | ||||||
| chr2:209557417
|
G | GT | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-22619_-171-22 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557417 | ||||||
| chr2:209557418
|
G | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-22618G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557418 | ||||||
| chr2:209557571
|
T | C | 1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-171-22465T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557571 | ||||||
| chr2:209557582
|
G | A | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-171-22454G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557582 | ||||||
| chr2:209557669
|
T | G | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-171-22367T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557669 | ||||||
| chr2:209557744
|
G | A | 60 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(57): Show | 60 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-171-22292G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557744 | ||||||
| chr2:209557904
|
A | T | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-171-22132A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209557904 | ||||||
| chr2:209558017
|
C | T | 1 | a0002c0002t0014g0113 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-171-22019C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558017 | ||||||
| chr2:209558188
|
ATTTC | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21840_-171-21 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209558188 | |||||
| chr2:209558228
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21808A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558228 | ||||||
| chr2:209558320
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-21716T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558320 | ||||||
| chr2:209558326
|
T | C | 1 | a0002c0002t0016g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-171-21710T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558326 | ||||||
| chr2:209558338
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21698A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558338 | ||||||
| chr2:209558363
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-21673A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558363 | ||||||
| chr2:209558394
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-21642G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558394 | ||||||
| chr2:209558480
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21556C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558480 | ||||||
| chr2:209558580
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21456T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558580 | ||||||
| chr2:209558653
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-21383A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558653 | ||||||
| chr2:209558686
|
C | CTAA | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-171-21333_-171-21 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209558686 | |||||
| chr2:209558686
|
C | CTAG | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-21348_-171-21 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209558686 | |||||
| chr2:209558710
|
G | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-21326G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558710 | ||||||
| chr2:209558865
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21171C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558865 | ||||||
| chr2:209558890
|
T | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21146T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558890 | ||||||
| chr2:209558940
|
G | GT | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21095dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209558940 | |||||
| chr2:209558967
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-21069G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209558967 | ||||||
| chr2:209559043
|
C | A | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-171-20993C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559043 | ||||||
| chr2:209559064
|
A | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20972A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559064 | ||||||
| chr2:209559108
|
GT | G | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-20923delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209559108 | |||||
| chr2:209559223
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-171-20813G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559223 | ||||||
| chr2:209559236
|
C | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-20800C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559236 | ||||||
| chr2:209559479
|
C | CA | 7 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0017t0007g0036others(4): Show | 7 | HG00597.hp2 HG02055.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.-171-20532dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209559479 | |||||
| chr2:209559479
|
CA | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0125a0001c0001t0001g0126others(52): Show | 55 | HG00408.hp1 HG00733.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.-171-20532delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209559479 | |||||
| chr2:209559479
|
CAA | C | 29 | a0001c0001t0001g0128a0001c0001t0002g0015a0001c0001t0002g0017others(26): Show | 29 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-171-20533_-171-20 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209559479 | |||||
| chr2:209559518
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20518A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559518 | ||||||
| chr2:209559559
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20477A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559559 | ||||||
| chr2:209559565
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-171-20471C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559565 | ||||||
| chr2:209559574
|
G | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20462G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559574 | ||||||
| chr2:209559707
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20329T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559707 | ||||||
| chr2:209559773
|
A | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-20263A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559773 | ||||||
| chr2:209559783
|
ACT | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-20250_-171-20 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209559783 | |||||
| chr2:209559824
|
AT | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20203delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209559824 | |||||
| chr2:209559954
|
A | G | 3 | a0001c0001t0003g0074a0001c0014t0001g0101a0008c0015t0002g0075 | 3 | HG02280.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-171-20082A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559954 | ||||||
| chr2:209559980
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-20056A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209559980 | ||||||
| chr2:209560171
|
T | C | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-171-19865T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560171 | ||||||
| chr2:209560227
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0010 | 2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-171-19809G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560227 | ||||||
| chr2:209560268
|
AT | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-171-19767delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560268 | ||||||
| chr2:209560301
|
C | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19735C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560301 | ||||||
| chr2:209560334
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19702C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560334 | ||||||
| chr2:209560398
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-171-19638A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560398 | ||||||
| chr2:209560481
|
CT | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(93): Show | 96 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-171-19539delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209560481 | |||||
| chr2:209560514
|
C | T | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-171-19522C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560514 | ||||||
| chr2:209560562
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG02258.hp2 HG02486.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.-171-19474C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560562 | ||||||
| chr2:209560588
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19448C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560588 | ||||||
| chr2:209560599
|
G | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19437G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560599 | ||||||
| chr2:209560730
|
G | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-19306G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560730 | ||||||
| chr2:209560780
|
C | G | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-171-19256C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560780 | ||||||
| chr2:209560811
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19225T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560811 | ||||||
| chr2:209560845
|
T | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19191T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560845 | ||||||
| chr2:209560850
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19186G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560850 | ||||||
| chr2:209560881
|
TA | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19150delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209560881 | |||||
| chr2:209560935
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-19101G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209560935 | ||||||
| chr2:209561040
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18996T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561040 | ||||||
| chr2:209561085
|
T | A | 11 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-171-18951T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561085 | ||||||
| chr2:209561190
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18846T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561190 | ||||||
| chr2:209561197
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18839G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561197 | ||||||
| chr2:209561229
|
G | A | 1 | a0001c0006t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-171-18807G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561229 | ||||||
| chr2:209561409
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18627C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561409 | ||||||
| chr2:209561435
|
AT | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18598delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209561435 | |||||
| chr2:209561460
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18576C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561460 | ||||||
| chr2:209561511
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-171-18525G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561511 | ||||||
| chr2:209561513
|
C | T | 3 | a0002c0002t0005g0046a0002c0002t0020g0048a0002c0002t0031g0080 | 3 | HG00099.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-171-18523C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561513 | ||||||
| chr2:209561770
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18266G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561770 | ||||||
| chr2:209561846
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18190C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561846 | ||||||
| chr2:209561877
|
GC | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-18158delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561877 | ||||||
| chr2:209561942
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-18094C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209561942 | ||||||
| chr2:209562206
|
A | G | 1 | a0002c0002t0015g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-171-17830A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562206 | ||||||
| chr2:209562396
|
G | GA | 30 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(27): Show | 30 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-171-17631dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209562396 | |||||
| chr2:209562424
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-17612C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562424 | ||||||
| chr2:209562463
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-171-17573G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562463 | ||||||
| chr2:209562654
|
G | A | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-171-17382G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562654 | ||||||
| chr2:209562664
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-17372C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562664 | ||||||
| chr2:209562713
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-171-17323G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562713 | ||||||
| chr2:209562770
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-17266C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562770 | ||||||
| chr2:209562783
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-17253G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562783 | ||||||
| chr2:209562874
|
G | T | 1 | a0001c0001t0002g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-171-17162G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562874 | ||||||
| chr2:209562897
|
T | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-17139T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209562897 | ||||||
| chr2:209563063
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16973A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563063 | ||||||
| chr2:209563217
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-16819C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563217 | ||||||
| chr2:209563264
|
G | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16772G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563264 | ||||||
| chr2:209563363
|
C | CA | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16667dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209563363 | |||||
| chr2:209563401
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16635T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563401 | ||||||
| chr2:209563412
|
A | AAATGCCC others(19): Show |
8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16622_-171-16 others(32): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209563412 | |||||
| chr2:209563473
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16563C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563473 | ||||||
| chr2:209563534
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(19): Show | 22 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-171-16502G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563534 | ||||||
| chr2:209563544
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(97): Show | 100 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-171-16492T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563544 | ||||||
| chr2:209563677
|
A | G | 2 | a0001c0001t0003g0064a0002c0010t0015g0065 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-171-16359A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563677 | ||||||
| chr2:209563686
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16350C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563686 | ||||||
| chr2:209563695
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(18): Show | 21 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.-171-16341C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563695 | ||||||
| chr2:209563797
|
G | T | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-16239G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563797 | ||||||
| chr2:209563826
|
C | CA | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16210_-171-16 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563826 | ||||||
| chr2:209563873
|
A | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-16163A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563873 | ||||||
| chr2:209563892
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16144C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563892 | ||||||
| chr2:209563920
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16116A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563920 | ||||||
| chr2:209563971
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-16065A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209563971 | ||||||
| chr2:209564023
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-16013C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564023 | ||||||
| chr2:209564124
|
GA | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(19): Show | 22 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-171-15907delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209564124 | |||||
| chr2:209564300
|
T | G | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-171-15736T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564300 | ||||||
| chr2:209564556
|
T | TA | 18 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0126others(15): Show | 18 | HG00597.hp2 HG01109.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.-171-15453dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209564556 | |||||
| chr2:209564556
|
T | TAA | 5 | a0001c0001t0001g0103a0001c0001t0033g0007a0001c0003t0006g0004others(2): Show | 5 | HG00408.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-15454_-171-15 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209564556 | |||||
| chr2:209564556
|
TA | T | 52 | a0001c0001t0001g0128a0001c0001t0002g0015a0001c0001t0002g0017others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-171-15453delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209564556 | |||||
| chr2:209564642
|
A | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-15394A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564642 | ||||||
| chr2:209564644
|
GGTGCTGG others(11): Show |
G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-15390_-171-15 others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209564644 | |||||
| chr2:209564718
|
G | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-15318G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564718 | ||||||
| chr2:209564721
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-171-15315T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564721 | ||||||
| chr2:209564731
|
C | T | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-171-15305C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564731 | ||||||
| chr2:209564756
|
T | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-15280T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564756 | ||||||
| chr2:209564786
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-15250G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209564786 | ||||||
| chr2:209565031
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-15005T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565031 | ||||||
| chr2:209565081
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-14955C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565081 | ||||||
| chr2:209565309
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-171-14727T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565309 | ||||||
| chr2:209565444
|
T | C | 1 | a0002c0002t0012g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-171-14592T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565444 | ||||||
| chr2:209565687
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-14349C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565687 | ||||||
| chr2:209565695
|
C | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-14341C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565695 | ||||||
| chr2:209565842
|
C | T | 59 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-171-14194C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565842 | ||||||
| chr2:209565942
|
G | T | 7 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0003g0088others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-171-14094G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209565942 | ||||||
| chr2:209566112
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-13924G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566112 | ||||||
| chr2:209566235
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-13801T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566235 | ||||||
| chr2:209566489
|
A | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-13547A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566489 | ||||||
| chr2:209566521
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-13515C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566521 | ||||||
| chr2:209566695
|
C | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-13341C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566695 | ||||||
| chr2:209566699
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0002g0063 | 3 | HG02922.hp2 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-171-13337G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566699 | ||||||
| chr2:209566731
|
G | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-13305G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566731 | ||||||
| chr2:209566922
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-171-13114A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566922 | ||||||
| chr2:209566945
|
G | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-13091G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566945 | ||||||
| chr2:209566976
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-13060C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566976 | ||||||
| chr2:209566995
|
T | C | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-171-13041T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209566995 | ||||||
| chr2:209567098
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-12938T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209567098 | ||||||
| chr2:209567260
|
T | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-12776T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209567260 | ||||||
| chr2:209567370
|
A | G | 1 | a0002c0002t0014g0113 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-171-12666A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209567370 | ||||||
| chr2:209567644
|
C | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-12392C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209567644 | ||||||
| chr2:209567675
|
A | G | 1 | a0010c0012t0038g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-171-12361A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209567675 | ||||||
| chr2:209568033
|
C | CTA | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-12002_-171-12 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209568033 | |||||
| chr2:209568204
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-11832A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209568204 | ||||||
| chr2:209568276
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-171-11760A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209568276 | ||||||
| chr2:209568338
|
T | C | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-171-11698T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209568338 | ||||||
| chr2:209568674
|
ATGTAGCA others(8): Show |
A | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-171-11346_-171-11 others(21): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209568674 | |||||
| chr2:209568965
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-11071C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209568965 | ||||||
| chr2:209569310
|
ATTTCAGT others(1): Show |
A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-10715_-171-10 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209569310 | |||||
| chr2:209569450
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-171-10586C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209569450 | ||||||
| chr2:209569680
|
A | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-10356A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209569680 | ||||||
| chr2:209569692
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-171-10344A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209569692 | ||||||
| chr2:209569832
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-10204C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209569832 | ||||||
| chr2:209569862
|
A | G | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-171-10174A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209569862 | ||||||
| chr2:209569943
|
C | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(33): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.-171-10093C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209569943 | ||||||
| chr2:209570018
|
A | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-10018A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570018 | ||||||
| chr2:209570021
|
T | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-10015T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570021 | ||||||
| chr2:209570476
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-9560T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570476 | ||||||
| chr2:209570600
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-9436C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570600 | ||||||
| chr2:209570752
|
T | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-171-9284T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570752 | ||||||
| chr2:209570830
|
C | G | 1 | a0006c0018t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-171-9206C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570830 | ||||||
| chr2:209570866
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-9170G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570866 | ||||||
| chr2:209570904
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-9132G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570904 | ||||||
| chr2:209570966
|
A | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(33): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.-171-9070A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209570966 | ||||||
| chr2:209571114
|
A | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-8922A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209571114 | ||||||
| chr2:209571170
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-171-8866C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209571170 | ||||||
| chr2:209571292
|
C | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-8744C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209571292 | ||||||
| chr2:209571816
|
G | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(33): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.-171-8220G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209571816 | ||||||
| chr2:209571937
|
A | G | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-8099A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209571937 | ||||||
| chr2:209572094
|
A | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-171-7942A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209572094 | ||||||
| chr2:209572145
|
T | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-7891T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209572145 | ||||||
| chr2:209572148
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-171-7888A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209572148 | ||||||
| chr2:209572390
|
G | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-7646G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209572390 | ||||||
| chr2:209572397
|
TA | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-171-7636delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209572397 | |||||
| chr2:209572754
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-171-7282A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209572754 | ||||||
| chr2:209572929
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-171-7107G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209572929 | ||||||
| chr2:209573298
|
G | GGTTTTTT others(8): Show |
3 | a0001c0003t0006g0004a0001c0003t0006g0023a0001c0013t0006g0073 | 3 | HG02647.hp1 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-171-6738_-171-673 others(19): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573298 | ||||||
| chr2:209573298
|
G | GGTTTTTT others(9): Show |
1 | a0001c0003t0006g0003 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-171-6738_-171-673 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573298 | ||||||
| chr2:209573298
|
G | GGTTTTTT others(10): Show |
1 | a0002c0005t0011g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-171-6738_-171-673 others(21): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573298 | ||||||
| chr2:209573298
|
G | GGTTTTTT others(11): Show |
3 | a0001c0001t0033g0007a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-171-6738_-171-673 others(22): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573298 | ||||||
| chr2:209573298
|
G | GT | 5 | a0001c0001t0002g0052a0001c0001t0010g0116a0002c0002t0009g0098others(2): Show | 5 | HG00733.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-6722dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209573298 | |||||
| chr2:209573298
|
GT | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(28): Show | 31 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.-171-6722delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209573298 | |||||
| chr2:209573380
|
G | A | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-171-6656G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573380 | ||||||
| chr2:209573511
|
T | C | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-6525T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573511 | ||||||
| chr2:209573537
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(36): Show | 39 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-171-6499A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573537 | ||||||
| chr2:209573857
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-171-6179T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573857 | ||||||
| chr2:209573923
|
C | T | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-6113C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209573923 | ||||||
| chr2:209574218
|
C | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-171-5818C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209574218 | ||||||
| chr2:209574432
|
T | TAC | 6 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0029others(3): Show | 6 | HG02630.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-171-5576_-171-557 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574432
|
T | TACAC | 5 | a0001c0001t0003g0028a0001c0001t0010g0116a0001c0003t0018g0005others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-5578_-171-557 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574432
|
T | TACACACA others(9): Show |
2 | a0001c0001t0033g0007a0001c0013t0006g0073 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-171-5590_-171-557 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574432
|
T | TACACACA others(11): Show |
2 | a0001c0003t0006g0023a0002c0005t0027g0070 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-171-5592_-171-557 others(22): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574432
|
T | TACACACA others(13): Show |
3 | a0001c0003t0006g0003a0001c0003t0006g0004a0002c0005t0011g0072 | 3 | HG02622.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-171-5594_-171-557 others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574432
|
T | TACACACA others(17): Show |
1 | a0002c0005t0011g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-171-5598_-171-557 others(28): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574432
|
TAC | T | 78 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0137others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.-171-5576_-171-557 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209574432 | |||||
| chr2:209574483
|
TTATC | T | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-171-5552_-171-554 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209574483 | ||||||
| chr2:209574497
|
A | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-171-5539A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209574497 | ||||||
| chr2:209574529
|
A | G | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-171-5507A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209574529 | ||||||
| chr2:209574545
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-5491G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209574545 | ||||||
| chr2:209574595
|
G | A | 8 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-171-5441G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209574595 | ||||||
| chr2:209575247
|
T | C | 88 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0002g0015others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.-171-4789T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575247 | ||||||
| chr2:209575251
|
C | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-171-4785C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575251 | ||||||
| chr2:209575256
|
T | A | 2 | a0001c0001t0001g0130a0001c0001t0002g0052 | 2 | HG00140.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.-171-4780T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575256 | ||||||
| chr2:209575262
|
A | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-4774A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575262 | ||||||
| chr2:209575272
|
A | G | 6 | a0001c0001t0003g0028a0001c0001t0033g0007a0001c0003t0006g0003others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-171-4764A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575272 | ||||||
| chr2:209575296
|
C | T | 1 | a0001c0003t0036g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-171-4740C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575296 | ||||||
| chr2:209575311
|
G | A | 1 | a0002c0010t0015g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-171-4725G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575311 | ||||||
| chr2:209575335
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4701C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575335 | ||||||
| chr2:209575385
|
A | G | 8 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(5): Show | 8 | HG02055.hp1 HG02572.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-171-4651A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575385 | ||||||
| chr2:209575393
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-171-4643T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575393 | ||||||
| chr2:209575478
|
G | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(17): Show | 20 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-171-4558G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575478 | ||||||
| chr2:209575518
|
C | CA | 49 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0129others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-171-4492dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209575518 | |||||
| chr2:209575518
|
C | CAA | 20 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0030others(17): Show | 20 | HG00597.hp1 HG01109.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.-171-4493_-171-449 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209575518 | |||||
| chr2:209575518
|
CA | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(21): Show | 24 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.-171-4492delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209575518 | |||||
| chr2:209575537
|
A | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4499A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575537 | ||||||
| chr2:209575541
|
A | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4495A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575541 | ||||||
| chr2:209575649
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4387C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575649 | ||||||
| chr2:209575663
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4373T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575663 | ||||||
| chr2:209575784
|
A | G | 1 | a0001c0001t0007g0049 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-171-4252A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575784 | ||||||
| chr2:209575807
|
G | A | 49 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-171-4229G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575807 | ||||||
| chr2:209575866
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4170G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575866 | ||||||
| chr2:209575993
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-4043T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209575993 | ||||||
| chr2:209576268
|
A | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(30): Show | 33 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.-171-3768A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209576268 | ||||||
| chr2:209576283
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-171-3753G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209576283 | ||||||
| chr2:209576330
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-3706A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209576330 | ||||||
| chr2:209576506
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-171-3530C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209576506 | ||||||
| chr2:209576573
|
G | A | 1 | a0001c0003t0002g0054 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-171-3463G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209576573 | ||||||
| chr2:209576964
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-3072C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209576964 | ||||||
| chr2:209577154
|
A | G | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-2882A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209577154 | ||||||
| chr2:209577182
|
T | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-171-2854T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209577182 | ||||||
| chr2:209577211
|
A | ATT | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-2815_-171-281 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209577211 | |||||
| chr2:209577527
|
T | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-2509T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209577527 | ||||||
| chr2:209577748
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-2288T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209577748 | ||||||
| chr2:209578043
|
G | C | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-171-1993G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578043 | ||||||
| chr2:209578419
|
GA | G | 64 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-171-1604delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209578419 | |||||
| chr2:209578447
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-1589G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578447 | ||||||
| chr2:209578497
|
AT | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-1529delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209578497 | |||||
| chr2:209578607
|
G | T | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-171-1429G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578607 | ||||||
| chr2:209578633
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-1403A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578633 | ||||||
| chr2:209578689
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-171-1347A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578689 | ||||||
| chr2:209578692
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-1344A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578692 | ||||||
| chr2:209578736
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-1300T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209578736 | ||||||
| chr2:209578902
|
ATATCGGC others(6): Show |
A | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.-171-1132_-171-112 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209578902 | |||||
| chr2:209578927
|
C | CTT | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-1108_-171-110 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209578927 | |||||
| chr2:209579022
|
T | C | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-171-1014T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209579022 | ||||||
| chr2:209579266
|
T | TGTGC | 5 | a0001c0001t0001g0139a0001c0001t0002g0017a0001c0001t0002g0018others(2): Show | 5 | HG02630.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-754_-171-751d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579266 | |||||
| chr2:209579282
|
C | CGT | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0125others(10): Show | 13 | HG01975.hp1 HG01993.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-171-739_-171-738d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579282 | |||||
| chr2:209579282
|
C | CGTGT | 105 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.-171-741_-171-738d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579282 | |||||
| chr2:209579282
|
CGT | C | 4 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-171-739_-171-738d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579282 | |||||
| chr2:209579309
|
C | T | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-171-727C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209579309 | ||||||
| chr2:209579321
|
C | A | 10 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0002g0062others(7): Show | 10 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-171-715C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209579321 | ||||||
| chr2:209579798
|
A | G | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-171-238A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209579798 | ||||||
| chr2:209579825
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-171-211G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | chr2 | 209579825 | ||||||
| chr2:209579993
|
C | CAT | 55 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.-171-26_-171-25dup others(2): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579993 | |||||
| chr2:209579993
|
C | CATAT | 17 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0006t0002g0056others(14): Show | 17 | HG01358.hp1 HG01358.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-171-28_-171-25dup others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579993 | |||||
| chr2:209579993
|
C | CATATAT | 43 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(40): Show | 43 | HG00099.hp2 HG00733.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-171-30_-171-25dup others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579993 | |||||
| chr2:209579993
|
C | CATATATA others(1): Show |
9 | a0002c0002t0009g0112a0002c0002t0013g0102a0002c0002t0020g0048others(6): Show | 9 | HG00408.hp1 HG00597.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-171-32_-171-25dup others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579993 | |||||
| chr2:209579993
|
C | CATATATA others(5): Show |
1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-171-36_-171-25dup others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 209579993 | |||||
| chr2:209580612
|
G | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-107+512G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209580612 | ||||||
| chr2:209580660
|
G | T | 1 | a0001c0001t0007g0050 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-107+560G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209580660 | ||||||
| chr2:209580825
|
A | G | 1 | a0001c0001t0002g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-107+725A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209580825 | ||||||
| chr2:209580854
|
G | A | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-107+754G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209580854 | ||||||
| chr2:209580892
|
A | G | 4 | a0001c0001t0002g0020a0001c0003t0018g0005a0001c0003t0018g0016others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+792A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209580892 | ||||||
| chr2:209581017
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+917G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581017 | ||||||
| chr2:209581362
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-107+1262T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581362 | ||||||
| chr2:209581512
|
C | T | 16 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(13): Show | 16 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-107+1412C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581512 | ||||||
| chr2:209581607
|
G | T | 1 | a0002c0002t0005g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-107+1507G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581607 | ||||||
| chr2:209581908
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-107+1808A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581908 | ||||||
| chr2:209581920
|
T | C | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-107+1820T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581920 | ||||||
| chr2:209581933
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+1833G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581933 | ||||||
| chr2:209581955
|
G | A | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-107+1855G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581955 | ||||||
| chr2:209581960
|
T | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0010 | 2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-107+1860T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209581960 | ||||||
| chr2:209582026
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-107+1926A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582026 | ||||||
| chr2:209582135
|
T | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+2035T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582135 | ||||||
| chr2:209582165
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-107+2065G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582165 | ||||||
| chr2:209582402
|
C | G | 16 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(13): Show | 16 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-107+2302C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582402 | ||||||
| chr2:209582424
|
G | A | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-107+2324G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582424 | ||||||
| chr2:209582582
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-107+2482T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582582 | ||||||
| chr2:209582657
|
T | TGATA | 33 | a0001c0001t0001g0002a0001c0001t0002g0015a0001c0001t0002g0081others(30): Show | 33 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.-107+2600_-107+260 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209582657 | |||||
| chr2:209582657
|
T | TGATAGAT others(1): Show |
4 | a0002c0002t0004g0120a0002c0002t0005g0039a0002c0002t0005g0041others(1): Show | 4 | HG01192.hp1 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+2596_-107+260 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209582657 | |||||
| chr2:209582657
|
TGATA | T | 15 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0002g0017others(12): Show | 15 | HG02055.hp2 HG02280.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-107+2600_-107+260 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209582657 | |||||
| chr2:209582657
|
TGATAGAT others(1): Show |
T | 11 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0107others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.-107+2596_-107+260 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209582657 | |||||
| chr2:209582657
|
TGATAGAT others(5): Show |
T | 21 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0110others(18): Show | 21 | HG00140.hp2 HG01261.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.-107+2592_-107+260 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209582657 | |||||
| chr2:209582657
|
TGATAGAT others(9): Show |
T | 20 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0103others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.-107+2588_-107+260 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209582657 | |||||
| chr2:209582908
|
C | T | 1 | a0006c0018t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-107+2808C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209582908 | ||||||
| chr2:209583130
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+3030T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583130 | ||||||
| chr2:209583134
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+3034C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583134 | ||||||
| chr2:209583143
|
G | GTCTA | 6 | a0001c0001t0002g0018a0001c0001t0002g0019a0002c0002t0009g0112others(3): Show | 6 | HG00597.hp1 HG02572.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+3046_-107+304 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583143 | |||||
| chr2:209583143
|
G | GTCTATCT others(1): Show |
20 | a0001c0001t0001g0105a0001c0001t0002g0013a0001c0001t0002g0015others(17): Show | 20 | HG00408.hp1 HG01192.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-107+3046_-107+304 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583143 | |||||
| chr2:209583143
|
G | GTCTATCT others(5): Show |
17 | a0001c0001t0001g0115a0001c0001t0034g0096a0002c0002t0004g0001others(14): Show | 17 | HG00099.hp2 HG01261.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-107+3046_-107+304 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583143 | |||||
| chr2:209583143
|
G | GTCTATCT others(9): Show |
2 | a0002c0002t0020g0047a0005c0008t0013g0131 | 2 | HG03710.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-107+3046_-107+304 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583143 | |||||
| chr2:209583143
|
G | GTCTATCT others(13): Show |
1 | a0002c0002t0004g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-107+3046_-107+304 others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583143 | |||||
| chr2:209583143
|
G | GTCTATCT others(17): Show |
1 | a0002c0002t0012g0038 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-107+3046_-107+304 others(28): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583143 | |||||
| chr2:209583147
|
G | A | 49 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-107+3047G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583147 | ||||||
| chr2:209583147
|
G | GTCTA | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0103others(13): Show | 16 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.-107+3083_-107+308 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTATCT others(1): Show |
30 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00099.hp1 HG00140.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-107+3079_-107+308 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTATCT others(5): Show |
20 | a0001c0001t0001g0014a0001c0001t0001g0107a0001c0001t0001g0110others(17): Show | 20 | HG00140.hp2 HG01109.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-107+3075_-107+308 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTATCT others(9): Show |
7 | a0001c0001t0001g0125a0001c0001t0002g0020a0001c0001t0002g0085others(4): Show | 7 | HG01884.hp1 HG01975.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-107+3071_-107+308 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTATCT others(13): Show |
1 | a0001c0001t0001g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-107+3067_-107+308 others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTATCT others(17): Show |
1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-107+3063_-107+308 others(28): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTGTCT others(5): Show |
4 | a0001c0001t0001g0122a0001c0014t0001g0101a0003c0004t0001g0099others(1): Show | 4 | HG01358.hp1 HG01358.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+3050_-107+305 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTGTCT others(9): Show |
5 | a0001c0003t0002g0059a0003c0004t0002g0062a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+3050_-107+305 others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTGTCT others(13): Show |
5 | a0001c0003t0002g0054a0001c0003t0002g0055a0002c0005t0011g0094others(2): Show | 5 | HG02451.hp2 HG02683.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+3050_-107+305 others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTGTCT others(17): Show |
4 | a0003c0004t0003g0091a0004c0007t0010g0148a0004c0007t0017g0147others(1): Show | 4 | HG01243.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+3050_-107+305 others(28): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583147
|
G | GTCTGTCT others(21): Show |
1 | a0003c0004t0003g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-107+3050_-107+305 others(32): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583147 | |||||
| chr2:209583476
|
T | G | 2 | a0002c0005t0008g0135a0002c0005t0008g0136 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-107+3376T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583476 | ||||||
| chr2:209583690
|
C | T | 1 | a0002c0002t0020g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-107+3590C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583690 | ||||||
| chr2:209583769
|
A | AT | 32 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0128others(29): Show | 32 | HG00408.hp1 HG00597.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-107+3681dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583769 | |||||
| chr2:209583769
|
A | ATT | 98 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-107+3680_-107+368 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583769 | |||||
| chr2:209583769
|
A | ATTT | 8 | a0001c0001t0001g0110a0001c0001t0002g0079a0001c0006t0002g0056others(5): Show | 8 | HG01243.hp1 HG01261.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-107+3679_-107+368 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209583769 | |||||
| chr2:209583830
|
T | C | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.-107+3730T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583830 | ||||||
| chr2:209583923
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+3823C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209583923 | ||||||
| chr2:209584199
|
C | A | 1 | a0001c0003t0002g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-107+4099C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584199 | ||||||
| chr2:209584238
|
T | A | 4 | a0002c0002t0004g0001a0002c0002t0012g0038a0002c0002t0019g0044others(1): Show | 4 | NA18954.hp1 NA18983.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+4138T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584238 | ||||||
| chr2:209584395
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-107+4295A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584395 | ||||||
| chr2:209584431
|
A | G | 1 | a0002c0002t0009g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-107+4331A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584431 | ||||||
| chr2:209584458
|
T | A | 6 | a0002c0005t0011g0094a0003c0004t0003g0088a0003c0004t0003g0089others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-107+4358T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584458 | ||||||
| chr2:209584578
|
G | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-107+4478G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584578 | ||||||
| chr2:209584625
|
T | C | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.-107+4525T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584625 | ||||||
| chr2:209584866
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+4766G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209584866 | ||||||
| chr2:209585152
|
T | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-107+5052T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209585152 | ||||||
| chr2:209585171
|
G | A | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-107+5071G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209585171 | ||||||
| chr2:209585254
|
TA | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+5166delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209585254 | |||||
| chr2:209585445
|
T | C | 1 | a0002c0005t0008g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-107+5345T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209585445 | ||||||
| chr2:209585912
|
T | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-107+5812T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209585912 | ||||||
| chr2:209585963
|
C | A | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-107+5863C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209585963 | ||||||
| chr2:209585970
|
T | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+5870T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209585970 | ||||||
| chr2:209586057
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0103others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(13): Show |
intron_variant | MODIFIER | c.-107+5957G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586057 | ||||||
| chr2:209586066
|
C | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+5966C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586066 | ||||||
| chr2:209586142
|
C | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+6042C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586142 | ||||||
| chr2:209586195
|
C | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-107+6095C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586195 | ||||||
| chr2:209586209
|
A | G | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-107+6109A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586209 | ||||||
| chr2:209586324
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-107+6224C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586324 | ||||||
| chr2:209586514
|
G | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+6414G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586514 | ||||||
| chr2:209586830
|
A | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+6730A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209586830 | ||||||
| chr2:209587005
|
A | G | 1 | a0002c0002t0005g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-107+6905A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587005 | ||||||
| chr2:209587010
|
G | A | 1 | a0002c0002t0029g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-107+6910G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587010 | ||||||
| chr2:209587115
|
C | T | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-107+7015C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587115 | ||||||
| chr2:209587160
|
A | G | 1 | a0002c0002t0014g0113 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-107+7060A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587160 | ||||||
| chr2:209587269
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-107+7169C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587269 | ||||||
| chr2:209587313
|
G | A | 2 | a0002c0005t0008g0135a0002c0005t0008g0136 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-107+7213G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587313 | ||||||
| chr2:209587314
|
G | T | 1 | a0001c0001t0003g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-107+7214G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587314 | ||||||
| chr2:209587371
|
A | AT | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+7280dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209587371 | |||||
| chr2:209587614
|
G | A | 114 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-107+7514G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587614 | ||||||
| chr2:209587706
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+7606C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587706 | ||||||
| chr2:209587738
|
A | G | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+7638A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209587738 | ||||||
| chr2:209588036
|
G | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-107+7936G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588036 | ||||||
| chr2:209588108
|
A | G | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-107+8008A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588108 | ||||||
| chr2:209588189
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-107+8089A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588189 | ||||||
| chr2:209588216
|
T | C | 4 | a0001c0001t0002g0020a0002c0005t0008g0134a0002c0005t0008g0135others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+8116T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588216 | ||||||
| chr2:209588459
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0003g0028a0001c0001t0003g0076others(1): Show | 4 | HG02683.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+8359A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588459 | ||||||
| chr2:209588927
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+8827T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588927 | ||||||
| chr2:209588959
|
A | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+8859A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209588959 | ||||||
| chr2:209589091
|
C | A | 1 | a0001c0003t0006g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-107+8991C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209589091 | ||||||
| chr2:209589111
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(8): Show | 11 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-107+9011A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209589111 | ||||||
| chr2:209589175
|
A | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+9075A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209589175 | ||||||
| chr2:209589737
|
T | C | 2 | a0001c0001t0003g0076a0001c0001t0003g0078 | 2 | HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-107+9637T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209589737 | ||||||
| chr2:209590027
|
G | A | 24 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0105others(21): Show | 24 | HG00140.hp2 HG01109.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-107+9927G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209590027 | ||||||
| chr2:209590051
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-107+9951C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209590051 | ||||||
| chr2:209590238
|
AT | A | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-107+10145delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209590238 | |||||
| chr2:209590377
|
C | G | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-107+10277C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209590377 | ||||||
| chr2:209590404
|
C | T | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+10304C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209590404 | ||||||
| chr2:209590686
|
A | G | 3 | a0002c0002t0009g0112a0002c0002t0013g0102a0002c0002t0023g0124 | 3 | HG00408.hp1 HG00597.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-107+10586A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209590686 | ||||||
| chr2:209590935
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-107+10835C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209590935 | ||||||
| chr2:209591083
|
A | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+10983A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209591083 | ||||||
| chr2:209591132
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-107+11032G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209591132 | ||||||
| chr2:209591508
|
TATC | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-107+11411_-107+11 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209591508 | |||||
| chr2:209591944
|
T | A | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-107+11844T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209591944 | ||||||
| chr2:209591970
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-107+11870C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209591970 | ||||||
| chr2:209592097
|
C | A | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-107+11997C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592097 | ||||||
| chr2:209592104
|
T | C | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-107+12004T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592104 | ||||||
| chr2:209592146
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-107+12046G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592146 | ||||||
| chr2:209592153
|
A | T | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-107+12053A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592153 | ||||||
| chr2:209592246
|
T | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+12146T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592246 | ||||||
| chr2:209592426
|
T | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.-107+12326T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592426 | ||||||
| chr2:209592478
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-107+12378G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592478 | ||||||
| chr2:209592970
|
G | T | 10 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0002g0062others(7): Show | 10 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-107+12870G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209592970 | ||||||
| chr2:209593273
|
GTATTGT | G | 2 | a0001c0003t0006g0023a0001c0013t0006g0073 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-107+13181_-107+13 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593273 | |||||
| chr2:209593495
|
G | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+13395G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593495 | ||||||
| chr2:209593614
|
C | T | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-107+13514C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593614 | ||||||
| chr2:209593619
|
C | CA | 8 | a0001c0001t0001g0139a0001c0001t0003g0028a0001c0001t0003g0064others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-107+13535dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593619 | |||||
| chr2:209593619
|
C | CAA | 6 | a0001c0001t0001g0122a0001c0001t0001g0138a0001c0001t0003g0022others(3): Show | 6 | HG01358.hp2 HG01975.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+13534_-107+13 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593619 | |||||
| chr2:209593619
|
C | CAAA | 12 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0001g0146others(9): Show | 12 | HG00099.hp1 HG00597.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-107+13533_-107+13 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593619 | |||||
| chr2:209593619
|
C | CAAAAA | 11 | a0001c0001t0001g0008a0001c0001t0001g0111a0001c0001t0001g0128others(8): Show | 11 | HG00733.hp1 HG01993.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-107+13531_-107+13 others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593619 | |||||
| chr2:209593619
|
C | CAAAAAA | 6 | a0001c0001t0001g0014a0001c0001t0001g0137a0001c0003t0006g0003others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-107+13530_-107+13 others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593619 | |||||
| chr2:209593619
|
C | CAAAAAAA | 7 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(4): Show | 7 | HG00408.hp2 HG01261.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-107+13529_-107+13 others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593619 | |||||
| chr2:209593632
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-107+13532_-107+13 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593632 | ||||||
| chr2:209593632
|
A | T | 4 | a0001c0001t0002g0015a0002c0002t0004g0118a0002c0002t0004g0119others(1): Show | 4 | HG02622.hp1 NA18959.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+13532A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593632 | ||||||
| chr2:209593634
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-107+13535_-107+13 others(19): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593634
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0144a0001c0001t0002g0083 | 2 | HG01433.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-107+13535_-107+13 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593634
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-107+13535_-107+13 others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593634
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0132 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-107+13535_-107+13 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593634
|
A | AATATATA others(3): Show |
1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-107+13565_-107+13 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593634
|
A | ATAT | 4 | a0001c0001t0001g0002a0001c0001t0002g0063a0001c0001t0002g0087others(1): Show | 4 | HG02630.hp2 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+13534_-107+13 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593634 | ||||||
| chr2:209593634
|
A | T | 8 | a0001c0001t0002g0015a0002c0002t0004g0118a0002c0002t0004g0119others(5): Show | 8 | HG00408.hp1 HG00597.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-107+13534A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593634 | ||||||
| chr2:209593634
|
AAT | A | 7 | a0001c0001t0002g0018a0002c0002t0005g0041a0002c0002t0012g0043others(4): Show | 7 | HG01192.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-107+13573_-107+13 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593634
|
AATAT | A | 8 | a0001c0006t0002g0093a0002c0002t0005g0033a0002c0002t0005g0039others(5): Show | 8 | HG00099.hp2 HG01433.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-107+13571_-107+13 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593634 | |||||
| chr2:209593635
|
AT | A | 2 | a0001c0006t0002g0056a0002c0002t0004g0001 | 2 | NA19043.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-107+13536delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593635 | ||||||
| chr2:209593635
|
ATAT | A | 5 | a0001c0006t0002g0057a0001c0006t0002g0092a0003c0004t0002g0062others(2): Show | 5 | HG01358.hp1 HG02559.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+13536_-107+13 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593635 | ||||||
| chr2:209593635
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-107+13536_-107+13 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593635 | ||||||
| chr2:209593636
|
T | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-107+13536T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593636 | ||||||
| chr2:209593638
|
T | A | 41 | a0001c0001t0001g0103a0001c0001t0001g0111a0001c0001t0001g0122others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.-107+13538T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593638 | ||||||
| chr2:209593640
|
T | A | 33 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0130others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.-107+13540T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593640 | ||||||
| chr2:209593642
|
T | A | 27 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0002g0052others(24): Show | 27 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.-107+13542T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593642 | ||||||
| chr2:209593644
|
T | A | 25 | a0001c0001t0001g0130a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 25 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-107+13544T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593644 | ||||||
| chr2:209593646
|
T | A | 19 | a0001c0001t0001g0130a0001c0001t0002g0052a0001c0003t0002g0054others(16): Show | 19 | HG00140.hp1 HG00733.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-107+13546T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593646 | ||||||
| chr2:209593648
|
T | A | 15 | a0001c0001t0003g0074a0001c0003t0002g0054a0002c0005t0011g0094others(12): Show | 15 | HG01243.hp2 HG01358.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-107+13548T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593648 | ||||||
| chr2:209593650
|
T | A | 11 | a0001c0001t0003g0074a0001c0003t0002g0054a0002c0005t0011g0094others(8): Show | 11 | HG01358.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-107+13550T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593650 | ||||||
| chr2:209593652
|
T | A | 6 | a0001c0001t0003g0074a0001c0003t0002g0054a0002c0005t0011g0094others(3): Show | 6 | HG01358.hp1 HG02683.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+13552T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593652 | ||||||
| chr2:209593654
|
T | A | 3 | a0001c0003t0002g0054a0003c0004t0026g0109a0003c0004t0035g0021 | 3 | HG01358.hp1 HG02683.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-107+13554T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593654 | ||||||
| chr2:209593725
|
TATATAAT others(34): Show |
T | 2 | a0001c0001t0001g0114a0001c0001t0021g0104 | 2 | HG03710.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.-107+13689_-107+13 others(47): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593725 | |||||
| chr2:209593748
|
ATATTATA others(37): Show |
A | 2 | a0001c0001t0002g0025a0001c0001t0003g0022 | 2 | HG01975.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-107+13652_-107+13 others(50): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593748 | |||||
| chr2:209593759
|
AATATATA others(33): Show |
A | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-107+13661_-107+13 others(46): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593759 | |||||
| chr2:209593760
|
ATAT | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-107+13661_-107+13 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593760 | ||||||
| chr2:209593765
|
TA | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-107+13667delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593765 | |||||
| chr2:209593798
|
AT | A | 2 | a0001c0001t0002g0025a0001c0001t0003g0022 | 2 | HG01975.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-107+13699delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593798 | ||||||
| chr2:209593799
|
T | TA | 4 | a0001c0001t0001g0114a0001c0001t0002g0029a0001c0001t0002g0032others(1): Show | 4 | HG02486.hp1 HG03710.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+13701dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593799 | |||||
| chr2:209593815
|
A | G | 4 | a0001c0001t0002g0020a0002c0005t0008g0134a0002c0005t0008g0135others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+13715A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593815 | ||||||
| chr2:209593843
|
A | T | 120 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.-107+13743A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593843 | ||||||
| chr2:209593874
|
TA | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-107+13779delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593874 | |||||
| chr2:209593898
|
A | T | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-107+13798A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593898 | ||||||
| chr2:209593906
|
G | GTATATAT others(1): Show |
120 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.-107+13812_-107+13 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209593906 | |||||
| chr2:209593921
|
A | G | 4 | a0001c0001t0002g0020a0002c0005t0008g0134a0002c0005t0008g0135others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+13821A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209593921 | ||||||
| chr2:209594020
|
C | T | 4 | a0002c0002t0004g0145a0002c0002t0005g0033a0002c0002t0005g0039others(1): Show | 4 | HG02080.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+13920C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209594020 | ||||||
| chr2:209594025
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-107+13925G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209594025 | ||||||
| chr2:209594134
|
GA | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.-107+14054delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209594134 | |||||
| chr2:209594134
|
GAA | G | 10 | a0001c0001t0001g0140a0001c0001t0007g0049a0001c0003t0002g0054others(7): Show | 10 | HG01243.hp2 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-107+14053_-107+14 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209594134 | |||||
| chr2:209594267
|
G | C | 49 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-107+14167G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209594267 | ||||||
| chr2:209594464
|
G | A | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-107+14364G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209594464 | ||||||
| chr2:209594722
|
A | G | 1 | a0001c0001t0025g0141 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-107+14622A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209594722 | ||||||
| chr2:209594727
|
C | A | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-107+14627C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209594727 | ||||||
| chr2:209595196
|
AGGTTTGG others(1): Show |
A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-107+15106_-107+15 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209595196 | |||||
| chr2:209595213
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-107+15113G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595213 | ||||||
| chr2:209595359
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-107+15259T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595359 | ||||||
| chr2:209595424
|
G | C | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-107+15324G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595424 | ||||||
| chr2:209595462
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-107+15362A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595462 | ||||||
| chr2:209595656
|
C | T | 10 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0002g0062others(7): Show | 10 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-107+15556C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595656 | ||||||
| chr2:209595708
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-107+15608A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595708 | ||||||
| chr2:209595729
|
G | A | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-107+15629G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209595729 | ||||||
| chr2:209596066
|
A | G | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-107+15966A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209596066 | ||||||
| chr2:209596447
|
G | C | 54 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(51): Show | 54 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-107+16347G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209596447 | ||||||
| chr2:209596578
|
C | A | 1 | a0001c0006t0002g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-107+16478C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209596578 | ||||||
| chr2:209596866
|
A | G | 1 | a0001c0003t0036g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-107+16766A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209596866 | ||||||
| chr2:209597526
|
C | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-107+17426C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209597526 | ||||||
| chr2:209597819
|
T | G | 1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-107+17719T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209597819 | ||||||
| chr2:209598049
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-107+17949A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598049 | ||||||
| chr2:209598335
|
C | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+18235C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598335 | ||||||
| chr2:209598337
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-107+18237G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598337 | ||||||
| chr2:209598457
|
T | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+18357T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598457 | ||||||
| chr2:209598494
|
A | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-107+18394A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598494 | ||||||
| chr2:209598555
|
G | A | 1 | a0001c0003t0002g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-107+18455G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598555 | ||||||
| chr2:209598578
|
C | T | 4 | a0002c0002t0014g0113a0002c0002t0014g0143a0002c0002t0039g0051others(1): Show | 4 | HG02080.hp1 NA18942.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-107+18478C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598578 | ||||||
| chr2:209598581
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-107+18481A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598581 | ||||||
| chr2:209598668
|
A | G | 1 | a0003c0004t0003g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-107+18568A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598668 | ||||||
| chr2:209598754
|
A | G | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-107+18654A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598754 | ||||||
| chr2:209598892
|
A | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-107+18792A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598892 | ||||||
| chr2:209598909
|
C | T | 2 | a0003c0004t0026g0109a0003c0004t0035g0021 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-107+18809C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598909 | ||||||
| chr2:209598944
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-107+18844G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598944 | ||||||
| chr2:209598988
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-107+18888A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209598988 | ||||||
| chr2:209599083
|
A | C | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-107+18983A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209599083 | ||||||
| chr2:209599233
|
G | A | 1 | a0002c0002t0020g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-107+19133G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209599233 | ||||||
| chr2:209599348
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-107+19248G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209599348 | ||||||
| chr2:209599658
|
A | G | 1 | a0003c0004t0003g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-107+19558A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209599658 | ||||||
| chr2:209599846
|
G | A | 123 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-107+19746G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209599846 | ||||||
| chr2:209600043
|
G | A | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-107+19943G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209600043 | ||||||
| chr2:209600331
|
A | C | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-107+20231A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209600331 | ||||||
| chr2:209600834
|
G | A | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.-107+20734G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209600834 | ||||||
| chr2:209601647
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-107+21547A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209601647 | ||||||
| chr2:209601829
|
T | C | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-107+21729T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209601829 | ||||||
| chr2:209602132
|
C | A | 1 | a0001c0001t0002g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-107+22032C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209602132 | ||||||
| chr2:209602490
|
T | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(16): Show | 19 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-107+22390T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209602490 | ||||||
| chr2:209602746
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-106-22307G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209602746 | ||||||
| chr2:209603026
|
A | T | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-106-22027A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603026 | ||||||
| chr2:209603047
|
A | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.-106-22006A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603047 | ||||||
| chr2:209603109
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-106-21944G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603109 | ||||||
| chr2:209603722
|
A | C | 1 | a0002c0002t0015g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-106-21331A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603722 | ||||||
| chr2:209603871
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-106-21182G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603871 | ||||||
| chr2:209603887
|
T | C | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-21166T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603887 | ||||||
| chr2:209603916
|
G | A | 103 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.-106-21137G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603916 | ||||||
| chr2:209603933
|
C | T | 1 | a0002c0002t0020g0047 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-106-21120C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209603933 | ||||||
| chr2:209604158
|
A | T | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-106-20895A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209604158 | ||||||
| chr2:209604461
|
T | C | 1 | a0006c0018t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-106-20592T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209604461 | ||||||
| chr2:209604483
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-106-20570A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209604483 | ||||||
| chr2:209604635
|
G | C | 10 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0002g0062others(7): Show | 10 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106-20418G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209604635 | ||||||
| chr2:209604655
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-106-20398A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209604655 | ||||||
| chr2:209604838
|
T | A | 2 | a0001c0001t0003g0074a0012c0020t0040g0084 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-106-20215T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209604838 | ||||||
| chr2:209605149
|
G | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-106-19904G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209605149 | ||||||
| chr2:209605994
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-106-19059G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209605994 | ||||||
| chr2:209606039
|
T | C | 1 | a0002c0010t0015g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-106-19014T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606039 | ||||||
| chr2:209606075
|
T | TG | 17 | a0001c0001t0002g0083a0001c0003t0002g0054a0001c0003t0002g0055others(14): Show | 17 | HG01358.hp1 HG01433.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-106-18970dupG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209606075 | |||||
| chr2:209606096
|
T | C | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-106-18957T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606096 | ||||||
| chr2:209606283
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-106-18770A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606283 | ||||||
| chr2:209606548
|
TG | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-18501delG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209606548 | |||||
| chr2:209606552
|
G | A | 1 | a0003c0004t0003g0088 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-106-18501G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606552 | ||||||
| chr2:209606769
|
C | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(1): Show | 4 | HG01261.hp1 HG01433.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-18284C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606769 | ||||||
| chr2:209606770
|
T | G | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-106-18283T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606770 | ||||||
| chr2:209606999
|
T | C | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-106-18054T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209606999 | ||||||
| chr2:209607413
|
A | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-17640A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209607413 | ||||||
| chr2:209607598
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-106-17455C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209607598 | ||||||
| chr2:209608098
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-106-16955A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209608098 | ||||||
| chr2:209608291
|
CT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(14): Show | 17 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-106-16751delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209608291 | |||||
| chr2:209608779
|
C | A | 2 | a0001c0003t0002g0054a0001c0003t0002g0055 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-106-16274C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209608779 | ||||||
| chr2:209609144
|
T | A | 1 | a0001c0001t0007g0049 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-106-15909T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609144 | ||||||
| chr2:209609178
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-106-15875A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609178 | ||||||
| chr2:209609297
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106-15756A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609297 | ||||||
| chr2:209609324
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-106-15729T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609324 | ||||||
| chr2:209609454
|
G | A | 2 | a0002c0002t0016g0031a0010c0012t0038g0045 | 2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-106-15599G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609454 | ||||||
| chr2:209609708
|
A | C | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-15345A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609708 | ||||||
| chr2:209609766
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-106-15287G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609766 | ||||||
| chr2:209609939
|
C | G | 1 | a0002c0002t0022g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-106-15114C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209609939 | ||||||
| chr2:209610319
|
G | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-106-14734G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209610319 | ||||||
| chr2:209610438
|
T | G | 1 | a0001c0001t0002g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-106-14615T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209610438 | ||||||
| chr2:209610627
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-106-14426C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209610627 | ||||||
| chr2:209610701
|
A | G | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-106-14352A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209610701 | ||||||
| chr2:209610875
|
A | G | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-106-14178A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209610875 | ||||||
| chr2:209611005
|
A | G | 1 | a0001c0001t0007g0049 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-106-14048A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209611005 | ||||||
| chr2:209611047
|
A | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106-14006A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209611047 | ||||||
| chr2:209611128
|
C | T | 10 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0002g0062others(7): Show | 10 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106-13925C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209611128 | ||||||
| chr2:209611211
|
A | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106-13842A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209611211 | ||||||
| chr2:209611461
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(94): Show | 97 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-106-13592A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209611461 | ||||||
| chr2:209611687
|
T | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(16): Show | 19 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-106-13366T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209611687 | ||||||
| chr2:209612172
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-106-12881A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209612172 | ||||||
| chr2:209612259
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(41): Show | 44 | HG01243.hp2 HG01358.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.-106-12794C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209612259 | ||||||
| chr2:209612448
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-106-12605T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209612448 | ||||||
| chr2:209613070
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-106-11983G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209613070 | ||||||
| chr2:209613139
|
G | A | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-106-11914G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209613139 | ||||||
| chr2:209613141
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-106-11912A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209613141 | ||||||
| chr2:209613251
|
TTTTA | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(95): Show | 98 | HG00408.hp1 HG00597.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.-106-11774_-106-11 others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209613251 | |||||
| chr2:209613251
|
TTTTATTT others(5): Show |
T | 3 | a0002c0002t0005g0046a0002c0002t0020g0048a0002c0002t0031g0080 | 3 | HG00099.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-106-11782_-106-11 others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209613251 | |||||
| chr2:209613302
|
G | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-106-11751G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209613302 | ||||||
| chr2:209613438
|
G | A | 10 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0002g0062others(7): Show | 10 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106-11615G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209613438 | ||||||
| chr2:209613472
|
C | A | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-106-11581C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209613472 | ||||||
| chr2:209614332
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-106-10721A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209614332 | ||||||
| chr2:209614444
|
A | C | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-106-10609A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209614444 | ||||||
| chr2:209614581
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-106-10472G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209614581 | ||||||
| chr2:209614628
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0003g0022 | 2 | HG01975.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-106-10425C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209614628 | ||||||
| chr2:209614661
|
C | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(101): Show | 104 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.-106-10392C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209614661 | ||||||
| chr2:209615301
|
T | A | 1 | a0001c0001t0003g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-106-9752T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209615301 | ||||||
| chr2:209615304
|
G | A | 2 | a0001c0001t0003g0074a0012c0020t0040g0084 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-106-9749G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209615304 | ||||||
| chr2:209615712
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-106-9341G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209615712 | ||||||
| chr2:209616088
|
A | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-8965A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616088 | ||||||
| chr2:209616182
|
CT | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-106-8869delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209616182 | |||||
| chr2:209616188
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-8865G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616188 | ||||||
| chr2:209616190
|
CT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-8861delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209616190 | |||||
| chr2:209616212
|
T | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-8841T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616212 | ||||||
| chr2:209616242
|
C | T | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-106-8811C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616242 | ||||||
| chr2:209616259
|
A | C | 1 | a0001c0001t0002g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-106-8794A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616259 | ||||||
| chr2:209616283
|
A | G | 2 | a0002c0002t0029g0061a0002c0002t0030g0068 | 2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-106-8770A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616283 | ||||||
| chr2:209616302
|
C | A | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-106-8751C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616302 | ||||||
| chr2:209616414
|
TG | T | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-8638delG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616414 | ||||||
| chr2:209616416
|
A | T | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-8637A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616416 | ||||||
| chr2:209616636
|
G | GAATAGTT others(25): Show |
1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-106-8414_-106-838 others(36): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209616636 | |||||
| chr2:209616676
|
G | A | 2 | a0001c0001t0002g0085a0001c0001t0034g0096 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-106-8377G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616676 | ||||||
| chr2:209616692
|
ACAGT | A | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-8355_-106-835 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209616692 | |||||
| chr2:209616816
|
T | G | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-106-8237T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616816 | ||||||
| chr2:209616938
|
G | A | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106-8115G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209616938 | ||||||
| chr2:209617023
|
GC | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-8029delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209617023 | ||||||
| chr2:209617247
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-106-7806T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209617247 | ||||||
| chr2:209617452
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-7601G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209617452 | ||||||
| chr2:209617459
|
A | G | 9 | a0002c0002t0004g0001a0002c0002t0005g0035a0002c0002t0012g0034others(6): Show | 9 | HG01975.hp2 NA18954.hp1 NA18983.hp2 others(6): Show |
intron_variant | MODIFIER | c.-106-7594A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209617459 | ||||||
| chr2:209617580
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-106-7473G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209617580 | ||||||
| chr2:209618291
|
C | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-106-6762C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209618291 | ||||||
| chr2:209618482
|
C | T | 1 | a0002c0002t0009g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-106-6571C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209618482 | ||||||
| chr2:209618500
|
C | T | 1 | a0011c0016t0001g0009 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-106-6553C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209618500 | ||||||
| chr2:209618803
|
A | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-6250A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209618803 | ||||||
| chr2:209619005
|
T | C | 7 | a0001c0001t0002g0020a0001c0003t0018g0005a0001c0003t0018g0016others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-106-6048T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619005 | ||||||
| chr2:209619039
|
A | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-106-6014A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619039 | ||||||
| chr2:209619137
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-106-5916T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619137 | ||||||
| chr2:209619188
|
G | C | 1 | a0001c0001t0002g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-106-5865G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619188 | ||||||
| chr2:209619205
|
A | G | 1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-106-5848A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619205 | ||||||
| chr2:209619244
|
G | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-106-5809G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619244 | ||||||
| chr2:209619259
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-106-5794G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619259 | ||||||
| chr2:209619721
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(27): Show | 30 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-106-5332G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209619721 | ||||||
| chr2:209620053
|
C | A | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106-5000C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209620053 | ||||||
| chr2:209620252
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-106-4801A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209620252 | ||||||
| chr2:209620681
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-106-4372A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209620681 | ||||||
| chr2:209620834
|
G | T | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-106-4219G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209620834 | ||||||
| chr2:209621067
|
T | C | 49 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-106-3986T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621067 | ||||||
| chr2:209621123
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-106-3930A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621123 | ||||||
| chr2:209621181
|
C | A | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-106-3872C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621181 | ||||||
| chr2:209621257
|
A | AT | 10 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0125others(7): Show | 10 | HG00597.hp2 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.-106-3777dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209621257 | |||||
| chr2:209621257
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0002g0029a0001c0001t0002g0085a0001c0001t0002g0086others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-106-3785_-106-377 others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209621257 | |||||
| chr2:209621257
|
A | ATTTTTTT others(3): Show |
14 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0002g0032others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-106-3786_-106-377 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209621257 | |||||
| chr2:209621257
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0003g0028a0001c0014t0001g0101 | 2 | HG02280.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-106-3787_-106-377 others(15): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209621257 | |||||
| chr2:209621257
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0002a0008c0015t0002g0075 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-106-3788_-106-377 others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209621257 | |||||
| chr2:209621257
|
AT | A | 8 | a0001c0001t0002g0026a0001c0001t0002g0077a0001c0001t0033g0007others(5): Show | 8 | HG00140.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-106-3777delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209621257 | |||||
| chr2:209621354
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-106-3699G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621354 | ||||||
| chr2:209621451
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-106-3602G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621451 | ||||||
| chr2:209621556
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-106-3497A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621556 | ||||||
| chr2:209621613
|
A | G | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-106-3440A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621613 | ||||||
| chr2:209621672
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-106-3381A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209621672 | ||||||
| chr2:209622106
|
C | G | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-106-2947C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209622106 | ||||||
| chr2:209622393
|
T | C | 2 | a0001c0001t0002g0025a0001c0001t0003g0022 | 2 | HG01975.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-106-2660T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209622393 | ||||||
| chr2:209622664
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-106-2389T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209622664 | ||||||
| chr2:209622690
|
G | GGATC | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-2362_-106-235 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 209622690 | |||||
| chr2:209622753
|
G | T | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-106-2300G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209622753 | ||||||
| chr2:209622757
|
C | T | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-106-2296C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209622757 | ||||||
| chr2:209623252
|
G | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-106-1801G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209623252 | ||||||
| chr2:209623827
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-106-1226C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209623827 | ||||||
| chr2:209624018
|
C | T | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-106-1035C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624018 | ||||||
| chr2:209624227
|
G | A | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-106-826G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624227 | ||||||
| chr2:209624350
|
T | C | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-106-703T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624350 | ||||||
| chr2:209624724
|
A | G | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-106-329A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624724 | ||||||
| chr2:209624831
|
A | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-106-222A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624831 | ||||||
| chr2:209624839
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-106-214G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624839 | ||||||
| chr2:209624896
|
T | A | 1 | a0001c0001t0003g0022 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-106-157T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | chr2 | 209624896 | ||||||
| chr2:209625511
|
A | G | 2 | a0001c0001t0002g0025a0001c0001t0003g0022 | 2 | HG01975.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-30+382A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625511 | ||||||
| chr2:209625536
|
C | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+407C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625536 | ||||||
| chr2:209625555
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0002g0063others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+426A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625555 | ||||||
| chr2:209625563
|
G | A | 1 | a0001c0003t0006g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-30+434G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625563 | ||||||
| chr2:209625620
|
G | T | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30+491G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625620 | ||||||
| chr2:209625769
|
C | T | 3 | a0002c0002t0009g0112a0002c0002t0013g0102a0002c0002t0023g0124 | 3 | HG00408.hp1 HG00597.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-30+640C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625769 | ||||||
| chr2:209625965
|
A | G | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+836A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209625965 | ||||||
| chr2:209626208
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30+1079G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626208 | ||||||
| chr2:209626243
|
A | G | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+1114A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626243 | ||||||
| chr2:209626376
|
T | C | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+1247T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626376 | ||||||
| chr2:209626390
|
G | A | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+1261G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626390 | ||||||
| chr2:209626416
|
A | T | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+1287A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626416 | ||||||
| chr2:209626625
|
A | G | 6 | a0002c0002t0004g0001a0002c0002t0012g0034a0002c0002t0012g0038others(3): Show | 6 | HG01975.hp2 NA18954.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1496A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626625 | ||||||
| chr2:209626733
|
A | G | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-30+1604A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209626733 | ||||||
| chr2:209627115
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(93): Show | 96 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-30+1986C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627115 | ||||||
| chr2:209627385
|
G | A | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-30+2256G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627385 | ||||||
| chr2:209627394
|
G | A | 2 | a0001c0006t0002g0092a0001c0006t0002g0093 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-30+2265G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627394 | ||||||
| chr2:209627462
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-30+2333A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627462 | ||||||
| chr2:209627500
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0002g0063a0001c0001t0003g0064 | 3 | HG02055.hp2 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-30+2371T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627500 | ||||||
| chr2:209627687
|
G | A | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-30+2558G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627687 | ||||||
| chr2:209627846
|
C | T | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+2717C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209627846 | ||||||
| chr2:209628084
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+2955C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209628084 | ||||||
| chr2:209628156
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30+3027G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209628156 | ||||||
| chr2:209628237
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+3108T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209628237 | ||||||
| chr2:209628280
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-30+3151G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209628280 | ||||||
| chr2:209628372
|
AGTTT | A | 7 | a0002c0005t0011g0094a0003c0004t0001g0099a0003c0004t0003g0088others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+3252_-30+3255d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209628372 | |||||
| chr2:209628615
|
A | G | 1 | a0002c0002t0028g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-30+3486A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209628615 | ||||||
| chr2:209628867
|
T | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+3738T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209628867 | ||||||
| chr2:209629043
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-30+3914T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209629043 | ||||||
| chr2:209629420
|
G | A | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-30+4291G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209629420 | ||||||
| chr2:209629732
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-30+4603A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209629732 | ||||||
| chr2:209629925
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+4796G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209629925 | ||||||
| chr2:209630215
|
G | A | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-30+5086G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209630215 | ||||||
| chr2:209630277
|
C | T | 1 | a0002c0002t0009g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30+5148C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209630277 | ||||||
| chr2:209630303
|
G | A | 2 | a0003c0004t0026g0109a0003c0004t0035g0021 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-30+5174G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209630303 | ||||||
| chr2:209630696
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+5567A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209630696 | ||||||
| chr2:209631005
|
C | CAAAAAAA | 10 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0103others(7): Show | 10 | HG00408.hp2 HG00597.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+5900_-30+5906d others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+5899_-30+5906d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0115others(9): Show | 12 | HG00140.hp2 HG01109.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30+5898_-30+5906d others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0142 | 2 | NA18943.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-30+5897_-30+5906d others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0012 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-30+5896_-30+5906d others(13): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0025g0141a0002c0005t0011g0072 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-30+5894_-30+5906d others(15): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0003g0074a0002c0005t0011g0071 | 2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-30+5891_-30+5906d others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631005
|
C | CAAAAAAA others(14): Show |
1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+5886_-30+5906d others(23): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631005 | |||||
| chr2:209631018
|
A | G | 1 | a0001c0003t0002g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-30+5889A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209631018 | ||||||
| chr2:209631027
|
AAAAAAAA others(2): Show |
A | 6 | a0002c0002t0015g0066a0002c0002t0029g0061a0002c0002t0030g0068others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+5900_-30+5908d others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631027 | |||||
| chr2:209631028
|
AAAAAAAA others(1): Show |
A | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-30+5901_-30+5908d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631028 | |||||
| chr2:209631029
|
AAAAAAAG | A | 5 | a0002c0002t0005g0035a0002c0002t0009g0112a0002c0002t0019g0040others(2): Show | 5 | HG00597.hp1 HG02451.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+5902_-30+5908d others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631029 | |||||
| chr2:209631031
|
AAAAAG | A | 14 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0002g0085others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+5904_-30+5908d others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631031 | |||||
| chr2:209631032
|
AAAAG | A | 9 | a0001c0001t0001g0002a0001c0001t0002g0020a0001c0001t0002g0081others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+5905_-30+5908d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631032 | |||||
| chr2:209631034
|
A | AAAAAAAA others(17): Show |
1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-30+5906_-30+5907i others(26): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631034 | |||||
| chr2:209631034
|
A | AAAAAAAA others(15): Show |
1 | a0001c0003t0006g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-30+5906_-30+5907i others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631034 | |||||
| chr2:209631034
|
A | AAAAAAAA others(14): Show |
1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+5906_-30+5907i others(23): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631034 | |||||
| chr2:209631034
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30+5906_-30+5907i others(21): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631034 | |||||
| chr2:209631034
|
A | AAAAAAAA others(10): Show |
1 | a0001c0003t0006g0003 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30+5906_-30+5907i others(19): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209631034 | |||||
| chr2:209631035
|
AG | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-30+5907delG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209631035 | ||||||
| chr2:209631036
|
G | A | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-30+5907G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209631036 | ||||||
| chr2:209631408
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30+6279C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209631408 | ||||||
| chr2:209632075
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0003g0028a0001c0001t0003g0076others(1): Show | 4 | HG02683.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+6946G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209632075 | ||||||
| chr2:209632465
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+7336C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209632465 | ||||||
| chr2:209632633
|
T | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-30+7504T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209632633 | ||||||
| chr2:209632703
|
C | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-30+7574C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209632703 | ||||||
| chr2:209632888
|
C | A | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+7759C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209632888 | ||||||
| chr2:209633080
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-30+7951G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633080 | ||||||
| chr2:209633242
|
A | G | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+8113A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633242 | ||||||
| chr2:209633333
|
G | A | 70 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(67): Show | 70 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.-30+8204G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633333 | ||||||
| chr2:209633400
|
C | T | 53 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-30+8271C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633400 | ||||||
| chr2:209633418
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+8289A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633418 | ||||||
| chr2:209633537
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(91): Show | 94 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-30+8408G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633537 | ||||||
| chr2:209633650
|
G | T | 1 | a0001c0003t0018g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+8521G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633650 | ||||||
| chr2:209633745
|
A | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-30+8616A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633745 | ||||||
| chr2:209633838
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-30+8709G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209633838 | ||||||
| chr2:209634208
|
G | C | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+9079G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634208 | ||||||
| chr2:209634258
|
A | G | 2 | a0002c0002t0016g0031a0010c0012t0038g0045 | 2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-30+9129A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634258 | ||||||
| chr2:209634368
|
A | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+9239A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634368 | ||||||
| chr2:209634478
|
C | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-30+9349C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634478 | ||||||
| chr2:209634519
|
GTACCTGA others(7): Show |
G | 51 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(48): Show | 51 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-30+9392_-30+9405d others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209634519 | |||||
| chr2:209634844
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-30+9715T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634844 | ||||||
| chr2:209634907
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30+9778C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634907 | ||||||
| chr2:209634978
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+9849C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209634978 | ||||||
| chr2:209635346
|
T | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+10217T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635346 | ||||||
| chr2:209635429
|
T | C | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+10300T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635429 | ||||||
| chr2:209635610
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-30+10481T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635610 | ||||||
| chr2:209635616
|
G | A | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-30+10487G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635616 | ||||||
| chr2:209635670
|
AT | A | 5 | a0001c0001t0033g0007a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+10544delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209635670 | |||||
| chr2:209635680
|
TA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(79): Show | 82 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-30+10558delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209635680 | |||||
| chr2:209635692
|
A | T | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+10563A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635692 | ||||||
| chr2:209635820
|
G | A | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30+10691G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635820 | ||||||
| chr2:209635957
|
G | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-30+10828G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635957 | ||||||
| chr2:209635965
|
T | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+10836T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209635965 | ||||||
| chr2:209636137
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30+11008T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636137 | ||||||
| chr2:209636154
|
T | G | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-30+11025T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636154 | ||||||
| chr2:209636318
|
C | A | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+11189C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636318 | ||||||
| chr2:209636408
|
G | A | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-30+11279G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636408 | ||||||
| chr2:209636538
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(79): Show | 82 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-30+11409C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636538 | ||||||
| chr2:209636556
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+11427G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636556 | ||||||
| chr2:209636561
|
T | C | 1 | a0006c0018t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+11432T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636561 | ||||||
| chr2:209636563
|
T | TTA | 15 | a0001c0001t0003g0074a0001c0003t0002g0054a0001c0003t0002g0055others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-30+11449_-30+1145 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209636563 | |||||
| chr2:209636563
|
TTA | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+11449_-30+1145 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209636563 | |||||
| chr2:209636563
|
TTATA | T | 56 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-30+11447_-30+1145 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209636563 | |||||
| chr2:209636578
|
TAC | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0010 | 2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-30+11462_-30+1146 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209636578 | |||||
| chr2:209636684
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+11555T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636684 | ||||||
| chr2:209636691
|
T | C | 1 | a0012c0020t0040g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30+11562T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209636691 | ||||||
| chr2:209637164
|
C | G | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30+12035C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209637164 | ||||||
| chr2:209637225
|
T | C | 1 | a0002c0002t0009g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30+12096T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209637225 | ||||||
| chr2:209637357
|
C | G | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-30+12228C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209637357 | ||||||
| chr2:209637708
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-30+12579G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209637708 | ||||||
| chr2:209637740
|
ATATGT | A | 2 | a0003c0004t0026g0109a0003c0004t0035g0021 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-30+12614_-30+1261 others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209637740 | |||||
| chr2:209637799
|
C | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-30+12670C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209637799 | ||||||
| chr2:209637808
|
C | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-30+12679C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209637808 | ||||||
| chr2:209638062
|
T | C | 47 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-30+12933T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638062 | ||||||
| chr2:209638093
|
G | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-30+12964G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638093 | ||||||
| chr2:209638378
|
C | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0129 | 2 | HG01358.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-30+13249C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638378 | ||||||
| chr2:209638504
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-30+13375C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638504 | ||||||
| chr2:209638524
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30+13395G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638524 | ||||||
| chr2:209638662
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+13533A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638662 | ||||||
| chr2:209638826
|
A | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-30+13697A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638826 | ||||||
| chr2:209638835
|
C | A | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-30+13706C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638835 | ||||||
| chr2:209638917
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+13788A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209638917 | ||||||
| chr2:209639462
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-29-13680A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209639462 | ||||||
| chr2:209639624
|
A | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29-13518A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209639624 | ||||||
| chr2:209639699
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-29-13443C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209639699 | ||||||
| chr2:209639800
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-29-13342G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209639800 | ||||||
| chr2:209640034
|
C | T | 6 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(3): Show | 6 | HG01109.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-13108C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640034 | ||||||
| chr2:209640239
|
T | C | 1 | a0001c0001t0025g0141 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-29-12903T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640239 | ||||||
| chr2:209640328
|
G | T | 14 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(11): Show | 14 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-12814G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640328 | ||||||
| chr2:209640358
|
A | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29-12784A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640358 | ||||||
| chr2:209640466
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(38): Show | 41 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-29-12676A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640466 | ||||||
| chr2:209640552
|
C | CA | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-29-12577dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209640552 | |||||
| chr2:209640552
|
C | CAA | 35 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(32): Show | 35 | HG01358.hp1 HG01884.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.-29-12578_-29-1257 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209640552 | |||||
| chr2:209640552
|
C | CAAA | 6 | a0001c0001t0002g0020a0001c0001t0010g0116a0002c0005t0008g0134others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-12579_-29-1257 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209640552 | |||||
| chr2:209640770
|
T | C | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-29-12372T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640770 | ||||||
| chr2:209640880
|
C | CT | 110 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-29-12248dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209640880 | |||||
| chr2:209640880
|
C | CTT | 7 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG00408.hp2 HG01975.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-12249_-29-1224 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209640880 | |||||
| chr2:209640969
|
T | G | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-29-12173T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209640969 | ||||||
| chr2:209641022
|
A | G | 47 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-12120A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641022 | ||||||
| chr2:209641112
|
T | C | 1 | a0001c0006t0002g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-29-12030T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641112 | ||||||
| chr2:209641325
|
C | T | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-11817C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641325 | ||||||
| chr2:209641447
|
C | G | 1 | a0002c0002t0023g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-29-11695C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641447 | ||||||
| chr2:209641625
|
C | T | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-29-11517C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641625 | ||||||
| chr2:209641842
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29-11300A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641842 | ||||||
| chr2:209641960
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29-11182T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641960 | ||||||
| chr2:209641961
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29-11181C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209641961 | ||||||
| chr2:209642209
|
G | A | 52 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0007g0049others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-29-10933G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209642209 | ||||||
| chr2:209642252
|
C | G | 52 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0007g0049others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-29-10890C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209642252 | ||||||
| chr2:209642480
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-29-10662G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209642480 | ||||||
| chr2:209642734
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29-10408C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209642734 | ||||||
| chr2:209642848
|
C | G | 1 | a0001c0001t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-29-10294C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209642848 | ||||||
| chr2:209642975
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-10167T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209642975 | ||||||
| chr2:209643003
|
TA | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29-10137delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209643003 | |||||
| chr2:209643249
|
T | G | 47 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-9893T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643249 | ||||||
| chr2:209643392
|
T | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-29-9750T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643392 | ||||||
| chr2:209643477
|
A | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29-9665A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643477 | ||||||
| chr2:209643526
|
C | T | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-29-9616C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643526 | ||||||
| chr2:209643535
|
C | G | 2 | a0001c0003t0006g0023a0001c0013t0006g0073 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-29-9607C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643535 | ||||||
| chr2:209643596
|
A | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-9546A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643596 | ||||||
| chr2:209643644
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(14): Show | 17 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-9498C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643644 | ||||||
| chr2:209643693
|
A | AT | 77 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-29-9441dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209643693 | |||||
| chr2:209643724
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-29-9418T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643724 | ||||||
| chr2:209643800
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-29-9342G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643800 | ||||||
| chr2:209643878
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0002g0013 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-29-9264A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643878 | ||||||
| chr2:209643879
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-9263T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209643879 | ||||||
| chr2:209644206
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-29-8936A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644206 | ||||||
| chr2:209644254
|
C | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-8888C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644254 | ||||||
| chr2:209644256
|
T | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-29-8886T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644256 | ||||||
| chr2:209644404
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-8738G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644404 | ||||||
| chr2:209644623
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-29-8519A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644623 | ||||||
| chr2:209644662
|
C | A | 47 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-8480C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644662 | ||||||
| chr2:209644670
|
CA | C | 13 | a0001c0001t0001g0126a0001c0001t0010g0116a0001c0003t0002g0054others(10): Show | 13 | HG01884.hp2 HG01993.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-8451delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209644670 | |||||
| chr2:209644670
|
CAA | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(25): Show | 28 | HG01358.hp1 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-29-8452_-29-8451d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209644670 | |||||
| chr2:209644671
|
A | AG | 40 | a0001c0001t0007g0049a0002c0002t0004g0118a0002c0002t0004g0119others(37): Show | 40 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29-8471_-29-8470i others(3): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644671 | ||||||
| chr2:209644672
|
A | G | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-8470A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644672 | ||||||
| chr2:209644841
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-29-8301A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644841 | ||||||
| chr2:209644859
|
G | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29-8283G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644859 | ||||||
| chr2:209644891
|
G | GC | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-8250dupC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209644891 | |||||
| chr2:209644893
|
A | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-8249A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209644893 | ||||||
| chr2:209645198
|
A | G | 47 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-7944A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209645198 | ||||||
| chr2:209645456
|
T | A | 1 | a0003c0004t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-29-7686T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209645456 | ||||||
| chr2:209645456
|
T | TA | 47 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-7676dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209645456 | |||||
| chr2:209645475
|
T | C | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-29-7667T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209645475 | ||||||
| chr2:209645782
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-29-7360A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209645782 | ||||||
| chr2:209645810
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-29-7332A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209645810 | ||||||
| chr2:209646059
|
G | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-29-7083G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646059 | ||||||
| chr2:209646163
|
T | C | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-6979T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646163 | ||||||
| chr2:209646354
|
G | T | 1 | a0002c0002t0012g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-29-6788G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646354 | ||||||
| chr2:209646414
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-6728C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646414 | ||||||
| chr2:209646477
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(7): Show | 10 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-6665C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646477 | ||||||
| chr2:209646782
|
T | TTTGTTGT others(5): Show |
3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29-6348_-29-6337d others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209646782 | |||||
| chr2:209646848
|
C | T | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29-6294C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646848 | ||||||
| chr2:209646850
|
G | A | 50 | a0001c0001t0007g0049a0001c0006t0002g0056a0001c0006t0002g0057others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-29-6292G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646850 | ||||||
| chr2:209646883
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(75): Show | 78 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-29-6259G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209646883 | ||||||
| chr2:209647048
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-6094A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209647048 | ||||||
| chr2:209647250
|
A | C | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-5892A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209647250 | ||||||
| chr2:209647408
|
C | G | 4 | a0002c0002t0004g0145a0002c0002t0005g0033a0002c0002t0005g0039others(1): Show | 4 | HG02080.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-5734C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209647408 | ||||||
| chr2:209647452
|
C | T | 40 | a0001c0001t0007g0049a0002c0002t0004g0001a0002c0002t0004g0118others(37): Show | 40 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29-5690C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209647452 | ||||||
| chr2:209647664
|
T | C | 13 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(10): Show | 13 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-5478T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209647664 | ||||||
| chr2:209647916
|
A | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-5226A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209647916 | ||||||
| chr2:209648104
|
AT | A | 7 | a0001c0001t0010g0116a0001c0001t0021g0104a0001c0003t0018g0005others(4): Show | 7 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-5021delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648104 | |||||
| chr2:209648104
|
ATTT | A | 59 | a0001c0001t0007g0049a0001c0003t0002g0054a0001c0003t0002g0055others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-5023_-29-5021d others(5): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648104 | |||||
| chr2:209648158
|
A | G | 74 | a0001c0001t0007g0049a0001c0003t0002g0054a0001c0003t0002g0055others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-29-4984A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648158 | ||||||
| chr2:209648169
|
G | A | 13 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(10): Show | 13 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-4973G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648169 | ||||||
| chr2:209648188
|
G | A | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-4954G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648188 | ||||||
| chr2:209648244
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0107 | 2 | HG00408.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-29-4898G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648244 | ||||||
| chr2:209648478
|
A | G | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-4664A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648478 | ||||||
| chr2:209648499
|
T | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-4643T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648499 | ||||||
| chr2:209648593
|
C | T | 5 | a0003c0004t0003g0088a0003c0004t0003g0089a0003c0004t0003g0090others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-4549C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648593 | ||||||
| chr2:209648621
|
C | CA | 52 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0122others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-29-4500dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648621 | |||||
| chr2:209648621
|
C | CAA | 16 | a0001c0001t0002g0015a0001c0003t0002g0054a0001c0003t0002g0055others(13): Show | 16 | HG01261.hp2 HG01358.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-4501_-29-4500d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648621 | |||||
| chr2:209648621
|
CAA | C | 10 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29-4501_-29-4500d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648621 | |||||
| chr2:209648657
|
C | T | 60 | a0001c0001t0007g0049a0001c0003t0002g0054a0001c0003t0002g0055others(57): Show | 60 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-29-4485C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648657 | ||||||
| chr2:209648734
|
A | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-4408A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648734 | ||||||
| chr2:209648784
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-29-4358G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648784 | ||||||
| chr2:209648788
|
C | CA | 50 | a0001c0001t0010g0116a0001c0003t0006g0003a0001c0003t0006g0004others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-29-4339dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648788 | |||||
| chr2:209648788
|
C | CAA | 10 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006others(7): Show | 10 | HG00597.hp1 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29-4340_-29-4339d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648788 | |||||
| chr2:209648804
|
G | A | 66 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(63): Show | 66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-29-4338G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648804 | ||||||
| chr2:209648825
|
G | GTAGCATC | 66 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(63): Show | 66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-29-4315_-29-4309d others(9): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209648825 | |||||
| chr2:209648915
|
T | C | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-29-4227T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209648915 | ||||||
| chr2:209649103
|
G | A | 2 | a0002c0002t0005g0035a0002c0002t0024g0121 | 2 | NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-29-4039G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649103 | ||||||
| chr2:209649116
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-4026C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649116 | ||||||
| chr2:209649138
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-4004A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649138 | ||||||
| chr2:209649185
|
A | C | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-3957A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649185 | ||||||
| chr2:209649189
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-29-3953A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649189 | ||||||
| chr2:209649204
|
T | TG | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-3933dupG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209649204 | |||||
| chr2:209649348
|
T | C | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-3794T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649348 | ||||||
| chr2:209649485
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-3657A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649485 | ||||||
| chr2:209649560
|
G | A | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-3582G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649560 | ||||||
| chr2:209649595
|
C | T | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-29-3547C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649595 | ||||||
| chr2:209649637
|
T | C | 1 | a0001c0001t0002g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-29-3505T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649637 | ||||||
| chr2:209649645
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-3497G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649645 | ||||||
| chr2:209649873
|
C | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-3269C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649873 | ||||||
| chr2:209649993
|
A | G | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-3149A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209649993 | ||||||
| chr2:209650362
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29-2780C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650362 | ||||||
| chr2:209650392
|
C | T | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-2750C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650392 | ||||||
| chr2:209650545
|
G | A | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-2597G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650545 | ||||||
| chr2:209650596
|
G | A | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-2546G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650596 | ||||||
| chr2:209650668
|
A | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-2474A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650668 | ||||||
| chr2:209650693
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-2449T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650693 | ||||||
| chr2:209650886
|
G | A | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-29-2256G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209650886 | ||||||
| chr2:209651133
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-2009A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651133 | ||||||
| chr2:209651281
|
C | T | 1 | a0002c0005t0008g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-29-1861C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651281 | ||||||
| chr2:209651347
|
G | A | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-1795G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651347 | ||||||
| chr2:209651604
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-1538A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651604 | ||||||
| chr2:209651726
|
A | G | 66 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(63): Show | 66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-29-1416A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651726 | ||||||
| chr2:209651742
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-29-1400G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651742 | ||||||
| chr2:209651950
|
A | G | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-1192A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209651950 | ||||||
| chr2:209652040
|
G | A | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-1102G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209652040 | ||||||
| chr2:209652092
|
G | A | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-1050G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209652092 | ||||||
| chr2:209652761
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-29-381G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209652761 | ||||||
| chr2:209652825
|
A | G | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-29-317A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209652825 | ||||||
| chr2:209652848
|
TC | T | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-293delC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209652848 | ||||||
| chr2:209652863
|
TTTTTG | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-29-259_-29-255del others(5): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 209652863 | |||||
| chr2:209653037
|
C | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-105C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209653037 | ||||||
| chr2:209653061
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-29-81C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | chr2 | 209653061 | ||||||
| chr2:209653448
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+16A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653448 | ||||||
| chr2:209653507
|
A | G | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+75A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653507 | ||||||
| chr2:209653668
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+236C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653668 | ||||||
| chr2:209653749
|
T | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.262+317T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653749 | ||||||
| chr2:209653761
|
A | G | 4 | a0002c0002t0004g0145a0002c0002t0005g0033a0002c0002t0005g0039others(1): Show | 4 | HG02080.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+329A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653761 | ||||||
| chr2:209653770
|
G | A | 59 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.262+338G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653770 | ||||||
| chr2:209653820
|
A | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+388A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653820 | ||||||
| chr2:209653853
|
T | A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+421T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653853 | ||||||
| chr2:209653858
|
C | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+426C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653858 | ||||||
| chr2:209653889
|
T | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.262+457T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653889 | ||||||
| chr2:209653895
|
C | T | 7 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.262+463C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653895 | ||||||
| chr2:209653972
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.262+540A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209653972 | ||||||
| chr2:209654019
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+587C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654019 | ||||||
| chr2:209654091
|
C | T | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.262+659C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654091 | ||||||
| chr2:209654190
|
A | G | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262+758A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654190 | ||||||
| chr2:209654197
|
T | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+765T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654197 | ||||||
| chr2:209654207
|
C | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+775C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654207 | ||||||
| chr2:209654288
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+856A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654288 | ||||||
| chr2:209654292
|
G | C | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.262+860G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654292 | ||||||
| chr2:209654546
|
GTTAA | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.262+1121_262+1124d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209654546 | |||||
| chr2:209654585
|
C | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.262+1153C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654585 | ||||||
| chr2:209654609
|
G | A | 1 | a0001c0003t0018g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.262+1177G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654609 | ||||||
| chr2:209654667
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.262+1235G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654667 | ||||||
| chr2:209654677
|
C | CACTA | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+1247_262+1250d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209654677 | |||||
| chr2:209654688
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+1256T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654688 | ||||||
| chr2:209654704
|
G | T | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.262+1272G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654704 | ||||||
| chr2:209654738
|
A | G | 76 | a0001c0001t0010g0116a0001c0003t0002g0054a0001c0003t0002g0055others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.262+1306A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654738 | ||||||
| chr2:209654776
|
T | C | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.262+1344T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654776 | ||||||
| chr2:209654828
|
T | C | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.262+1396T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654828 | ||||||
| chr2:209654944
|
G | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+1512G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209654944 | ||||||
| chr2:209655109
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+1677A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655109 | ||||||
| chr2:209655147
|
A | G | 33 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(30): Show | 33 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.262+1715A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655147 | ||||||
| chr2:209655229
|
A | G | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.262+1797A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655229 | ||||||
| chr2:209655256
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+1824T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655256 | ||||||
| chr2:209655299
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.262+1867T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655299 | ||||||
| chr2:209655362
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+1930T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655362 | ||||||
| chr2:209655479
|
G | A | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.262+2047G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655479 | ||||||
| chr2:209655483
|
T | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+2051T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655483 | ||||||
| chr2:209655625
|
A | T | 1 | a0002c0002t0019g0044 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.262+2193A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655625 | ||||||
| chr2:209655689
|
C | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+2257C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655689 | ||||||
| chr2:209655784
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+2352A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655784 | ||||||
| chr2:209655908
|
G | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+2476G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655908 | ||||||
| chr2:209655985
|
A | G | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.262+2553A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209655985 | ||||||
| chr2:209656028
|
C | T | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+2596C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656028 | ||||||
| chr2:209656113
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+2681T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656113 | ||||||
| chr2:209656168
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.262+2736A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656168 | ||||||
| chr2:209656189
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262+2757G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656189 | ||||||
| chr2:209656200
|
TG | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.262+2770delG | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209656200 | |||||
| chr2:209656407
|
G | A | 1 | a0001c0001t0002g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.262+2975G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656407 | ||||||
| chr2:209656496
|
C | A | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+3064C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656496 | ||||||
| chr2:209656520
|
T | A | 1 | a0011c0016t0001g0009 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.262+3088T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656520 | ||||||
| chr2:209656547
|
C | CT | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+3121dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209656547 | |||||
| chr2:209656725
|
T | TTA | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.262+3296_262+3297d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209656725 | |||||
| chr2:209656869
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.262+3437G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656869 | ||||||
| chr2:209656981
|
T | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(91): Show | 94 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.262+3549T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209656981 | ||||||
| chr2:209657141
|
G | A | 1 | a0002c0010t0015g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.262+3709G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209657141 | ||||||
| chr2:209657278
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+3846T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209657278 | ||||||
| chr2:209657368
|
A | G | 1 | a0002c0002t0014g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.262+3936A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209657368 | ||||||
| chr2:209657421
|
A | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+3989A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209657421 | ||||||
| chr2:209657817
|
T | G | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+4385T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209657817 | ||||||
| chr2:209658142
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+4710A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658142 | ||||||
| chr2:209658320
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+4888T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658320 | ||||||
| chr2:209658340
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.262+4908T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658340 | ||||||
| chr2:209658489
|
GA | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+5066delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209658489 | |||||
| chr2:209658490
|
A | G | 11 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(8): Show | 11 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.262+5058A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658490 | ||||||
| chr2:209658502
|
T | C | 4 | a0002c0002t0004g0001a0002c0002t0012g0038a0002c0002t0019g0044others(1): Show | 4 | NA18954.hp1 NA18983.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+5070T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658502 | ||||||
| chr2:209658511
|
C | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+5079C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658511 | ||||||
| chr2:209658513
|
A | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+5081A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658513 | ||||||
| chr2:209658536
|
C | T | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+5104C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658536 | ||||||
| chr2:209658568
|
A | G | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+5136A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658568 | ||||||
| chr2:209658600
|
G | A | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+5168G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658600 | ||||||
| chr2:209658680
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.262+5248T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658680 | ||||||
| chr2:209658947
|
G | A | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.262+5515G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658947 | ||||||
| chr2:209658971
|
C | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+5539C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209658971 | ||||||
| chr2:209659109
|
T | G | 1 | a0002c0005t0011g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262+5677T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659109 | ||||||
| chr2:209659151
|
CA | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.262+5721delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209659151 | |||||
| chr2:209659187
|
A | C | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+5755A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659187 | ||||||
| chr2:209659357
|
A | T | 2 | a0001c0001t0001g0125a0001c0001t0007g0049 | 2 | NA19004.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.262+5925A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659357 | ||||||
| chr2:209659732
|
T | TA | 34 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.262+6313dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209659732 | |||||
| chr2:209659764
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.262+6332C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659764 | ||||||
| chr2:209659796
|
T | A | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+6364T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659796 | ||||||
| chr2:209659896
|
G | A | 2 | a0001c0003t0006g0023a0001c0013t0006g0073 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.262+6464G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659896 | ||||||
| chr2:209659944
|
A | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+6512A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209659944 | ||||||
| chr2:209660113
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.262+6681A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209660113 | ||||||
| chr2:209660385
|
A | AT | 8 | a0001c0001t0002g0020a0001c0001t0002g0081a0001c0001t0003g0064others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+6979dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660385 | |||||
| chr2:209660385
|
AT | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.262+6979delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660385 | |||||
| chr2:209660385
|
ATT | A | 19 | a0001c0001t0002g0015a0001c0001t0010g0116a0001c0003t0002g0054others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.262+6978_262+6979d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660385 | |||||
| chr2:209660385
|
ATTTTT | A | 5 | a0001c0003t0006g0003a0001c0006t0002g0056a0001c0006t0002g0057others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+6975_262+6979d others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660385 | |||||
| chr2:209660416
|
T | C | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+6984T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209660416 | ||||||
| chr2:209660549
|
A | C | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+7117A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209660549 | ||||||
| chr2:209660559
|
A | AT | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.262+7135dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660559 | |||||
| chr2:209660701
|
A | AATT | 35 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0106others(32): Show | 35 | HG00140.hp2 HG00408.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.262+7315_262+7317d others(5): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660701
|
A | AATTATT | 5 | a0001c0001t0001g0014a0001c0003t0018g0005a0002c0002t0009g0112others(2): Show | 5 | HG00408.hp1 HG00597.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+7312_262+7317d others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660701
|
AATT | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.262+7315_262+7317d others(5): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660701
|
AATTATT | A | 11 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0002g0017others(8): Show | 11 | HG02055.hp2 HG02486.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.262+7312_262+7317d others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660701
|
AATTATTA others(2): Show |
A | 5 | a0001c0001t0002g0086a0001c0001t0010g0116a0002c0005t0008g0134others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+7309_262+7317d others(11): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660701
|
AATTATTA others(8): Show |
A | 1 | a0004c0007t0017g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.262+7303_262+7317d others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660701
|
AATTATTA others(11): Show |
A | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262+7300_262+7317d others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660701 | |||||
| chr2:209660772
|
C | T | 3 | a0001c0001t0002g0063a0001c0001t0002g0081a0001c0001t0002g0082 | 3 | HG02615.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.262+7340C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209660772 | ||||||
| chr2:209660782
|
G | A | 3 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094 | 3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.262+7350G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209660782 | ||||||
| chr2:209660910
|
A | AT | 6 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006others(3): Show | 6 | HG01243.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.262+7493dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209660910 | |||||
| chr2:209661060
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.262+7628A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209661060 | ||||||
| chr2:209661098
|
C | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+7666C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209661098 | ||||||
| chr2:209661283
|
T | A | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.262+7851T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209661283 | ||||||
| chr2:209661385
|
T | A | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.262+7953T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209661385 | ||||||
| chr2:209661523
|
T | C | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.262+8091T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209661523 | ||||||
| chr2:209662044
|
A | G | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+8612A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209662044 | ||||||
| chr2:209662138
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.262+8706T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209662138 | ||||||
| chr2:209662298
|
C | T | 1 | a0002c0002t0012g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.262+8866C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209662298 | ||||||
| chr2:209662817
|
C | T | 5 | a0001c0001t0002g0030a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+9385C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209662817 | ||||||
| chr2:209662953
|
G | GAT | 62 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.262+9535_262+9536d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209662953 | |||||
| chr2:209662953
|
G | GATAT | 3 | a0001c0006t0002g0056a0001c0006t0002g0092a0001c0006t0002g0093 | 3 | HG02559.hp2 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.262+9533_262+9536d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209662953 | |||||
| chr2:209663030
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.262+9598T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209663030 | ||||||
| chr2:209663565
|
G | A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+10133G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209663565 | ||||||
| chr2:209663722
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0002g0013 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.262+10290T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209663722 | ||||||
| chr2:209663755
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.262+10323G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209663755 | ||||||
| chr2:209663891
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.262+10459T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209663891 | ||||||
| chr2:209663926
|
A | G | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+10494A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209663926 | ||||||
| chr2:209664029
|
C | A | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262+10597C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664029 | ||||||
| chr2:209664060
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.262+10628A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664060 | ||||||
| chr2:209664077
|
T | C | 2 | a0002c0002t0005g0033a0002c0002t0005g0039 | 2 | NA18984.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.262+10645T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664077 | ||||||
| chr2:209664086
|
G | A | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+10654G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664086 | ||||||
| chr2:209664116
|
T | C | 1 | a0002c0002t0009g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.262+10684T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664116 | ||||||
| chr2:209664156
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+10724A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664156 | ||||||
| chr2:209664289
|
C | T | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+10857C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664289 | ||||||
| chr2:209664324
|
C | T | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262+10892C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664324 | ||||||
| chr2:209664325
|
A | G | 76 | a0001c0001t0010g0116a0001c0003t0002g0054a0001c0003t0002g0055others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.262+10893A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664325 | ||||||
| chr2:209664379
|
G | A | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+10947G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664379 | ||||||
| chr2:209664506
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.262+11074G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664506 | ||||||
| chr2:209664724
|
A | G | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.262+11292A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664724 | ||||||
| chr2:209664962
|
C | CA | 8 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0144others(5): Show | 8 | HG00597.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+11555dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209664962 | |||||
| chr2:209664962
|
CA | C | 8 | a0001c0001t0010g0116a0002c0002t0028g0067a0002c0005t0008g0134others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+11555delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209664962 | |||||
| chr2:209664962
|
CAA | C | 45 | a0001c0001t0001g0128a0001c0001t0002g0032a0001c0006t0002g0056others(42): Show | 45 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.262+11554_262+1155 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209664962 | |||||
| chr2:209664962
|
CAAA | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0002g0020others(27): Show | 30 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.262+11553_262+1155 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209664962 | |||||
| chr2:209664962
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.262+11546_262+1155 others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209664962 | |||||
| chr2:209664962
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.262+11543_262+1155 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209664962 | |||||
| chr2:209664985
|
A | G | 2 | a0001c0001t0002g0063a0012c0020t0040g0084 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.262+11553A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209664985 | ||||||
| chr2:209665040
|
G | A | 1 | a0002c0002t0031g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.262+11608G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665040 | ||||||
| chr2:209665080
|
G | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.262+11648G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665080 | ||||||
| chr2:209665218
|
G | T | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+11786G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665218 | ||||||
| chr2:209665316
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+11884G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665316 | ||||||
| chr2:209665429
|
A | G | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262+11997A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665429 | ||||||
| chr2:209665586
|
G | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.262+12154G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665586 | ||||||
| chr2:209665593
|
C | G | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262+12161C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665593 | ||||||
| chr2:209665623
|
C | A | 1 | a0005c0008t0013g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.262+12191C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209665623 | ||||||
| chr2:209666352
|
G | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-12220G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209666352 | ||||||
| chr2:209666413
|
GGGATAAC others(6): Show |
G | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.263-12142_263-1213 others(17): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209666413 | |||||
| chr2:209666772
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-11800C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209666772 | ||||||
| chr2:209666994
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-11578A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209666994 | ||||||
| chr2:209667061
|
T | TATTTTGG others(21): Show |
4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-11508_263-1148 others(32): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209667061 | |||||
| chr2:209667145
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.263-11427T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209667145 | ||||||
| chr2:209667613
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.263-10959A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209667613 | ||||||
| chr2:209667712
|
A | T | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.263-10860A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209667712 | ||||||
| chr2:209667746
|
T | A | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.263-10826T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209667746 | ||||||
| chr2:209667819
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.263-10753G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209667819 | ||||||
| chr2:209667983
|
A | G | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-10589A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209667983 | ||||||
| chr2:209668264
|
A | G | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-10308A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668264 | ||||||
| chr2:209668327
|
C | T | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.263-10245C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668327 | ||||||
| chr2:209668361
|
C | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-10211C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668361 | ||||||
| chr2:209668363
|
C | A | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.263-10209C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668363 | ||||||
| chr2:209668380
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-10192A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668380 | ||||||
| chr2:209668535
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0019 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.263-10037G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668535 | ||||||
| chr2:209668692
|
G | T | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.263-9880G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668692 | ||||||
| chr2:209668741
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.263-9831A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668741 | ||||||
| chr2:209668950
|
T | C | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.263-9622T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209668950 | ||||||
| chr2:209669032
|
A | G | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.263-9540A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669032 | ||||||
| chr2:209669193
|
C | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-9379C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669193 | ||||||
| chr2:209669200
|
C | T | 4 | a0002c0002t0004g0145a0002c0002t0005g0033a0002c0002t0005g0039others(1): Show | 4 | HG02080.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-9372C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669200 | ||||||
| chr2:209669215
|
G | A | 1 | a0002c0002t0012g0043 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.263-9357G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669215 | ||||||
| chr2:209669231
|
G | A | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.263-9341G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669231 | ||||||
| chr2:209669291
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.263-9281G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669291 | ||||||
| chr2:209669327
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.263-9245T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669327 | ||||||
| chr2:209669530
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.263-9042A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669530 | ||||||
| chr2:209669599
|
A | G | 2 | a0002c0002t0016g0031a0010c0012t0038g0045 | 2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.263-8973A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669599 | ||||||
| chr2:209669622
|
G | C | 1 | a0001c0003t0002g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263-8950G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669622 | ||||||
| chr2:209669993
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.263-8579A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209669993 | ||||||
| chr2:209670177
|
C | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.263-8395C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209670177 | ||||||
| chr2:209670579
|
G | A | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.263-7993G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209670579 | ||||||
| chr2:209670659
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-7913C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209670659 | ||||||
| chr2:209670695
|
G | A | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.263-7877G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209670695 | ||||||
| chr2:209670842
|
CAT | C | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-7729_263-7728d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209670842 | ||||||
| chr2:209670960
|
T | G | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.263-7612T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209670960 | ||||||
| chr2:209671093
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0033g0007 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263-7479T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671093 | ||||||
| chr2:209671136
|
A | G | 1 | a0002c0002t0005g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.263-7436A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671136 | ||||||
| chr2:209671224
|
A | G | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-7348A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671224 | ||||||
| chr2:209671292
|
G | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-7280G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671292 | ||||||
| chr2:209671604
|
C | T | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.263-6968C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671604 | ||||||
| chr2:209671791
|
T | A | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-6781T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671791 | ||||||
| chr2:209671974
|
G | GCT | 68 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.263-6598_263-6597i others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671974 | ||||||
| chr2:209671975
|
G | C | 68 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.263-6597G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209671975 | ||||||
| chr2:209672102
|
T | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-6470T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209672102 | ||||||
| chr2:209672160
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.263-6412C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209672160 | ||||||
| chr2:209672261
|
G | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-6311G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209672261 | ||||||
| chr2:209672278
|
A | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.263-6294A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209672278 | ||||||
| chr2:209673119
|
A | G | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.263-5453A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209673119 | ||||||
| chr2:209673184
|
A | G | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.263-5388A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209673184 | ||||||
| chr2:209673282
|
G | A | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.263-5290G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209673282 | ||||||
| chr2:209673283
|
C | T | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.263-5289C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209673283 | ||||||
| chr2:209673886
|
G | T | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.263-4686G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209673886 | ||||||
| chr2:209674273
|
A | G | 7 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.263-4299A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209674273 | ||||||
| chr2:209674526
|
T | C | 1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.263-4046T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209674526 | ||||||
| chr2:209674533
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.263-4039C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209674533 | ||||||
| chr2:209674621
|
A | AGATG | 34 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(31): Show | 34 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.263-3914_263-3911d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209674621 | |||||
| chr2:209674621
|
A | AGATGGAT others(1): Show |
2 | a0002c0005t0008g0134a0002c0005t0008g0136 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.263-3918_263-3911d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209674621 | |||||
| chr2:209674621
|
AGATGGAT others(1): Show |
A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-3918_263-3911d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209674621 | |||||
| chr2:209674621
|
AGATGGAT others(5): Show |
A | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-3922_263-3911d others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209674621 | |||||
| chr2:209674829
|
C | A | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.263-3743C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209674829 | ||||||
| chr2:209674905
|
G | C | 61 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.263-3667G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209674905 | ||||||
| chr2:209675082
|
G | A | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-3490G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209675082 | ||||||
| chr2:209675702
|
A | C | 4 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0007g0050others(1): Show | 4 | NA18943.hp2 NA18959.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-2870A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209675702 | ||||||
| chr2:209675916
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-2656G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209675916 | ||||||
| chr2:209676044
|
G | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-2528G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676044 | ||||||
| chr2:209676316
|
T | C | 1 | a0006c0018t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.263-2256T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676316 | ||||||
| chr2:209676324
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.263-2248A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676324 | ||||||
| chr2:209676397
|
A | G | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.263-2175A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676397 | ||||||
| chr2:209676429
|
T | C | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.263-2143T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676429 | ||||||
| chr2:209676621
|
A | C | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.263-1951A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676621 | ||||||
| chr2:209676676
|
G | A | 2 | a0001c0001t0002g0085a0001c0001t0033g0007 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263-1896G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676676 | ||||||
| chr2:209676697
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0002g0083 | 2 | HG01433.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.263-1875A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676697 | ||||||
| chr2:209676720
|
C | CAT | 13 | a0001c0001t0001g0110a0001c0001t0034g0096a0001c0003t0006g0004others(10): Show | 13 | HG00733.hp2 HG01358.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.263-1801_263-1800d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
C | CATAT | 6 | a0001c0001t0003g0028a0002c0002t0004g0118a0002c0002t0004g0119others(3): Show | 6 | HG01884.hp2 HG02080.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-1803_263-1800d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CAT | C | 6 | a0001c0001t0002g0081a0001c0001t0003g0074a0001c0003t0006g0023others(3): Show | 6 | HG00099.hp2 HG03098.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-1801_263-1800d others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATAT | C | 11 | a0001c0001t0002g0027a0001c0001t0002g0082a0001c0001t0003g0064others(8): Show | 11 | HG00099.hp1 HG00408.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.263-1803_263-1800d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATAT | C | 18 | a0001c0001t0001g0128a0001c0001t0002g0020a0001c0001t0002g0052others(15): Show | 18 | HG00733.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.263-1805_263-1800d others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(1): Show |
C | 17 | a0001c0001t0002g0032a0001c0001t0002g0087a0001c0001t0002g0095others(14): Show | 17 | HG01261.hp2 HG01975.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.263-1807_263-1800d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(3): Show |
C | 16 | a0001c0001t0001g0002a0001c0001t0001g0142a0001c0001t0002g0025others(13): Show | 16 | HG00597.hp1 HG01243.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.263-1809_263-1800d others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(5): Show |
C | 4 | a0001c0001t0001g0138a0001c0001t0002g0015a0001c0003t0002g0059others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1811_263-1800d others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0130a0001c0001t0002g0030 | 2 | HG00140.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.263-1813_263-1800d others(16): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(9): Show |
C | 3 | a0001c0001t0010g0116a0001c0003t0002g0054a0001c0003t0002g0055 | 3 | HG02257.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.263-1815_263-1800d others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(11): Show |
C | 5 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1817_263-1800d others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0001g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.263-1821_263-1800d others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(19): Show |
C | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | HG00140.hp2 HG00408.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.263-1825_263-1800d others(28): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676720
|
CATATATA others(21): Show |
C | 2 | a0001c0001t0001g0014a0001c0001t0007g0049 | 2 | NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.263-1827_263-1800d others(30): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209676720 | |||||
| chr2:209676769
|
A | C | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.263-1803A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676769 | ||||||
| chr2:209676966
|
C | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1606C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676966 | ||||||
| chr2:209676967
|
G | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1605G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676967 | ||||||
| chr2:209676977
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.263-1595G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209676977 | ||||||
| chr2:209677199
|
A | T | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-1373A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677199 | ||||||
| chr2:209677323
|
A | G | 1 | a0001c0001t0007g0050 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.263-1249A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677323 | ||||||
| chr2:209677386
|
T | TTAGA | 2 | a0002c0002t0009g0098a0002c0002t0014g0143 | 2 | HG06807.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.263-1169_263-1166d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677386 | |||||
| chr2:209677386
|
TTAGA | T | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.263-1169_263-1166d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677386 | |||||
| chr2:209677399
|
TAGATAGA others(5): Show |
T | 3 | a0001c0001t0001g0012a0002c0005t0011g0094a0002c0005t0027g0070 | 3 | HG01891.hp1 HG03130.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.263-1169_263-1158d others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677399 | |||||
| chr2:209677399
|
TAGATAGA others(9): Show |
T | 2 | a0002c0005t0011g0071a0002c0005t0011g0072 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.263-1169_263-1154d others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677399 | |||||
| chr2:209677403
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.263-1169T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677403 | ||||||
| chr2:209677403
|
T | TAGAC | 9 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0122others(6): Show | 9 | HG01358.hp2 HG01975.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-1133_263-1130d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677403
|
T | TAGATAGA others(1): Show |
24 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0120others(21): Show | 24 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.263-1166_263-1165i others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677403
|
T | TAGATAGA others(5): Show |
4 | a0002c0002t0029g0061a0002c0002t0030g0068a0002c0010t0015g0065others(1): Show | 4 | HG02886.hp2 HG03139.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1166_263-1165i others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677403
|
T | TAGATAGA others(9): Show |
2 | a0002c0002t0015g0066a0005c0008t0013g0131 | 2 | HG02280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.263-1166_263-1165i others(18): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677403
|
TAGAC | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0125others(16): Show | 19 | HG00099.hp1 HG01993.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.263-1133_263-1130d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677403
|
TAGACAGA others(1): Show |
T | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.263-1137_263-1130d others(10): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677403
|
TAGACAGA others(5): Show |
T | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263-1141_263-1130d others(14): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677403 | |||||
| chr2:209677411
|
C | T | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.263-1161C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677411 | ||||||
| chr2:209677439
|
CAGAT | C | 5 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1128_263-1125d others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 209677439 | |||||
| chr2:209677443
|
T | C | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1129T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677443 | ||||||
| chr2:209677456
|
A | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1116A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677456 | ||||||
| chr2:209677994
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-578A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209677994 | ||||||
| chr2:209678095
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-477C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209678095 | ||||||
| chr2:209678206
|
G | C | 76 | a0001c0001t0010g0116a0001c0003t0002g0054a0001c0003t0002g0055others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.263-366G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | chr2 | 209678206 | ||||||
| chr2:209678922
|
GT | G | 2 | a0005c0008t0013g0131a0005c0008t0016g0024 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.376+238delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209678922 | ||||||
| chr2:209678987
|
C | A | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.376+302C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209678987 | ||||||
| chr2:209679012
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.376+327G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679012 | ||||||
| chr2:209679251
|
A | G | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.376+566A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679251 | ||||||
| chr2:209679322
|
C | CATAG | 4 | a0001c0001t0001g0105a0001c0001t0002g0026a0001c0001t0002g0063others(1): Show | 4 | HG00140.hp2 HG03225.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+678_376+681dup others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679322 | |||||
| chr2:209679322
|
CATAG | C | 35 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(32): Show | 35 | HG00597.hp2 HG00733.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.376+678_376+681del others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679322 | |||||
| chr2:209679322
|
CATAGATA others(1): Show |
C | 9 | a0001c0001t0001g0144a0001c0001t0002g0018a0001c0001t0002g0086others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+674_376+681del others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679322 | |||||
| chr2:209679322
|
CATAGATA others(5): Show |
C | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.376+670_376+681del others(12): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679322 | |||||
| chr2:209679322
|
CATAGATA others(13): Show |
C | 64 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.376+662_376+681del others(20): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679322 | |||||
| chr2:209679322
|
CATAGATA others(17): Show |
C | 1 | a0002c0002t0004g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.376+658_376+681del others(24): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679322 | |||||
| chr2:209679402
|
C | CAGAT | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.376+729_376+732dup others(4): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 209679402 | |||||
| chr2:209679523
|
T | G | 76 | a0001c0001t0010g0116a0001c0003t0002g0054a0001c0003t0002g0055others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.376+838T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679523 | ||||||
| chr2:209679540
|
A | AT | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.376+855_376+856ins others(1): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679540 | ||||||
| chr2:209679696
|
G | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.376+1011G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679696 | ||||||
| chr2:209679701
|
T | G | 1 | a0002c0002t0031g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.376+1016T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679701 | ||||||
| chr2:209679803
|
G | A | 1 | a0001c0003t0036g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-947G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679803 | ||||||
| chr2:209679910
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(9): Show | 12 | HG00408.hp2 HG01192.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.377-840A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209679910 | ||||||
| chr2:209680328
|
G | A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-422G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209680328 | ||||||
| chr2:209680361
|
A | G | 63 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.377-389A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209680361 | ||||||
| chr2:209680540
|
G | T | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.377-210G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209680540 | ||||||
| chr2:209680541
|
A | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.377-209A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209680541 | ||||||
| chr2:209680585
|
A | G | 3 | a0002c0002t0005g0046a0002c0002t0020g0048a0002c0002t0031g0080 | 3 | HG00099.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.377-165A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209680585 | ||||||
| chr2:209680622
|
G | A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-128G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 6/15 | chr2 | 209680622 | ||||||
| chr2:209681143
|
T | G | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.454+316T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209681143 | ||||||
| chr2:209681322
|
A | AT | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.454+497dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209681322 | |||||
| chr2:209681824
|
G | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.454+997G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209681824 | ||||||
| chr2:209681921
|
G | C | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+1094G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209681921 | ||||||
| chr2:209681958
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.454+1131T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209681958 | ||||||
| chr2:209682396
|
C | A | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+1569C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682396 | ||||||
| chr2:209682422
|
C | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+1595C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682422 | ||||||
| chr2:209682505
|
A | G | 1 | a0002c0011t0037g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.454+1678A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682505 | ||||||
| chr2:209682622
|
C | T | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+1795C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682622 | ||||||
| chr2:209682720
|
G | A | 4 | a0001c0006t0002g0056a0001c0006t0002g0057a0001c0006t0002g0092others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+1893G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682720 | ||||||
| chr2:209682767
|
C | A | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+1940C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682767 | ||||||
| chr2:209682791
|
G | A | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.454+1964G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209682791 | ||||||
| chr2:209683124
|
A | G | 1 | a0001c0014t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454+2297A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683124 | ||||||
| chr2:209683132
|
G | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+2305G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683132 | ||||||
| chr2:209683542
|
A | AT | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+2721dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209683542 | |||||
| chr2:209683589
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.454+2762A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683589 | ||||||
| chr2:209683742
|
C | A | 1 | a0002c0002t0005g0041 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.454+2915C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683742 | ||||||
| chr2:209683766
|
G | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454+2939G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683766 | ||||||
| chr2:209683836
|
G | A | 1 | a0002c0002t0016g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.454+3009G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683836 | ||||||
| chr2:209683934
|
T | C | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+3107T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209683934 | ||||||
| chr2:209684049
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+3222A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684049 | ||||||
| chr2:209684195
|
G | A | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.454+3368G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684195 | ||||||
| chr2:209684240
|
C | T | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.454+3413C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684240 | ||||||
| chr2:209684437
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.454+3610C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684437 | ||||||
| chr2:209684454
|
C | A | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+3627C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684454 | ||||||
| chr2:209684728
|
T | G | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+3901T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684728 | ||||||
| chr2:209684750
|
G | A | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.454+3923G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684750 | ||||||
| chr2:209684758
|
A | G | 1 | a0002c0002t0030g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.454+3931A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209684758 | ||||||
| chr2:209684974
|
G | GATGCTAA others(17): Show |
2 | a0001c0001t0001g0115a0001c0001t0002g0013 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.454+4150_454+4173d others(26): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209684974 | |||||
| chr2:209685001
|
T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0107 | 2 | HG00408.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.454+4174T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685001 | ||||||
| chr2:209685106
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454+4279G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685106 | ||||||
| chr2:209685262
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.454+4435T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685262 | ||||||
| chr2:209685501
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.454+4674C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685501 | ||||||
| chr2:209685508
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.454+4681C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685508 | ||||||
| chr2:209685681
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+4854G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685681 | ||||||
| chr2:209685697
|
T | C | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+4870T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685697 | ||||||
| chr2:209685702
|
T | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.454+4875T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685702 | ||||||
| chr2:209685737
|
A | G | 1 | a0002c0002t0030g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.454+4910A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209685737 | ||||||
| chr2:209686337
|
T | C | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.454+5510T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209686337 | ||||||
| chr2:209686511
|
CTTA | C | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+5690_454+5692d others(5): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209686511 | |||||
| chr2:209686612
|
C | T | 69 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.454+5785C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209686612 | ||||||
| chr2:209686656
|
G | A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+5829G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209686656 | ||||||
| chr2:209686958
|
T | A | 1 | a0002c0002t0009g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.455-5667T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209686958 | ||||||
| chr2:209686992
|
T | C | 65 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.455-5633T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209686992 | ||||||
| chr2:209687081
|
C | T | 2 | a0001c0003t0002g0054a0001c0003t0002g0055 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.455-5544C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209687081 | ||||||
| chr2:209687438
|
C | T | 71 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.455-5187C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209687438 | ||||||
| chr2:209687625
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(37): Show | 40 | HG00140.hp2 HG00408.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.455-5000C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209687625 | ||||||
| chr2:209687651
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.455-4974G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209687651 | ||||||
| chr2:209687926
|
C | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.455-4699C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209687926 | ||||||
| chr2:209687994
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18954.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.455-4631G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209687994 | ||||||
| chr2:209688245
|
A | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-4380A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209688245 | ||||||
| chr2:209688834
|
A | G | 1 | a0002c0002t0019g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.455-3791A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209688834 | ||||||
| chr2:209688943
|
C | T | 1 | a0001c0001t0021g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.455-3682C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209688943 | ||||||
| chr2:209689055
|
A | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-3570A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209689055 | ||||||
| chr2:209689263
|
A | G | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.455-3362A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209689263 | ||||||
| chr2:209689295
|
T | C | 56 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.455-3330T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209689295 | ||||||
| chr2:209689300
|
AT | A | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.455-3316delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209689300 | |||||
| chr2:209689385
|
G | A | 1 | a0003c0004t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.455-3240G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209689385 | ||||||
| chr2:209689522
|
A | AT | 7 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-3098dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209689522 | |||||
| chr2:209689860
|
C | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.455-2765C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209689860 | ||||||
| chr2:209690019
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.455-2606T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209690019 | ||||||
| chr2:209690515
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.455-2110T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209690515 | ||||||
| chr2:209690540
|
A | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-2085A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209690540 | ||||||
| chr2:209691052
|
C | T | 31 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0110others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.455-1573C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209691052 | ||||||
| chr2:209691141
|
G | GC | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-1477dupC | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209691141 | |||||
| chr2:209691147
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.455-1478C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209691147 | ||||||
| chr2:209691465
|
AT | A | 49 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.455-1151delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209691465 | |||||
| chr2:209691543
|
G | T | 1 | a0007c0009t0002g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.455-1082G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209691543 | ||||||
| chr2:209691613
|
C | A | 49 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.455-1012C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209691613 | ||||||
| chr2:209691653
|
T | C | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-972T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209691653 | ||||||
| chr2:209691870
|
T | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.455-755T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209691870 | ||||||
| chr2:209692060
|
C | A | 1 | a0001c0001t0003g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.455-565C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209692060 | ||||||
| chr2:209692178
|
T | G | 49 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.455-447T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209692178 | ||||||
| chr2:209692222
|
T | G | 49 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.455-403T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209692222 | ||||||
| chr2:209692337
|
C | CA | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.455-274dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209692337 | |||||
| chr2:209692337
|
CA | C | 10 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.455-274delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 209692337 | |||||
| chr2:209692395
|
T | C | 1 | a0002c0002t0012g0038 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.455-230T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209692395 | ||||||
| chr2:209692491
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.455-134G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 7/15 | chr2 | 209692491 | ||||||
| chr2:209696809
|
C | CAGA | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4387+63_4387+65dup others(3): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 209696809 | |||||
| chr2:209697107
|
A | T | 1 | a0001c0001t0001g0014 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4522+56A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697107 | ||||||
| chr2:209697204
|
C | CT | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.4522+159dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 209697204 | |||||
| chr2:209697238
|
C | T | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.4522+187C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697238 | ||||||
| chr2:209697543
|
G | C | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4522+492G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697543 | ||||||
| chr2:209697606
|
A | C | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4522+555A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697606 | ||||||
| chr2:209697691
|
T | C | 1 | a0005c0008t0013g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4522+640T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697691 | ||||||
| chr2:209697825
|
C | T | 1 | a0002c0002t0009g0112 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4522+774C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697825 | ||||||
| chr2:209697973
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0003g0028a0001c0001t0003g0076others(1): Show | 4 | HG02683.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4522+922G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209697973 | ||||||
| chr2:209698007
|
A | AT | 12 | a0002c0002t0004g0145a0002c0002t0005g0033a0002c0002t0005g0039others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.4522+970dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 209698007 | |||||
| chr2:209698007
|
AT | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.4522+970delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 209698007 | |||||
| chr2:209698095
|
G | T | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4522+1044G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698095 | ||||||
| chr2:209698346
|
A | G | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4522+1295A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698346 | ||||||
| chr2:209698466
|
C | G | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4522+1415C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698466 | ||||||
| chr2:209698511
|
G | C | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4522+1460G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698511 | ||||||
| chr2:209698542
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0122others(1): Show | 4 | HG01192.hp2 HG01358.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.4522+1491T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698542 | ||||||
| chr2:209698662
|
G | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4522+1611G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698662 | ||||||
| chr2:209698803
|
G | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4523-1474G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698803 | ||||||
| chr2:209698844
|
A | C | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4523-1433A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698844 | ||||||
| chr2:209698885
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4523-1392G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209698885 | ||||||
| chr2:209699168
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4523-1109G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699168 | ||||||
| chr2:209699315
|
A | G | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.4523-962A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699315 | ||||||
| chr2:209699344
|
C | T | 19 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.4523-933C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699344 | ||||||
| chr2:209699345
|
A | AT | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4523-924dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 209699345 | |||||
| chr2:209699366
|
A | C | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4523-911A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699366 | ||||||
| chr2:209699402
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4523-875A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699402 | ||||||
| chr2:209699464
|
G | A | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4523-813G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699464 | ||||||
| chr2:209699514
|
C | A | 1 | a0002c0002t0029g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4523-763C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209699514 | ||||||
| chr2:209700075
|
T | A | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4523-202T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209700075 | ||||||
| chr2:209700081
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.4523-196A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209700081 | ||||||
| chr2:209700091
|
T | A | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4523-186T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 10/15 | chr2 | 209700091 | ||||||
| chr2:209700478
|
C | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4584+140C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209700478 | ||||||
| chr2:209700561
|
T | A | 19 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.4584+223T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209700561 | ||||||
| chr2:209700709
|
A | T | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4584+371A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209700709 | ||||||
| chr2:209700936
|
A | T | 19 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.4584+598A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209700936 | ||||||
| chr2:209701155
|
G | A | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4584+817G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209701155 | ||||||
| chr2:209701263
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4584+925A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209701263 | ||||||
| chr2:209701446
|
A | T | 19 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.4584+1108A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209701446 | ||||||
| chr2:209701589
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4584+1251A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209701589 | ||||||
| chr2:209701831
|
A | G | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4584+1493A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209701831 | ||||||
| chr2:209702118
|
T | C | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4584+1780T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702118 | ||||||
| chr2:209702136
|
T | G | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4584+1798T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702136 | ||||||
| chr2:209702293
|
T | C | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4584+1955T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702293 | ||||||
| chr2:209702415
|
A | G | 1 | a0002c0010t0015g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4584+2077A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702415 | ||||||
| chr2:209702455
|
T | C | 1 | a0009c0019t0007g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4584+2117T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702455 | ||||||
| chr2:209702507
|
T | A | 1 | a0001c0006t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4584+2169T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702507 | ||||||
| chr2:209702597
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4584+2259C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702597 | ||||||
| chr2:209702635
|
T | C | 1 | a0002c0005t0008g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4584+2297T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702635 | ||||||
| chr2:209702657
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4584+2319G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702657 | ||||||
| chr2:209702705
|
C | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4584+2367C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702705 | ||||||
| chr2:209702766
|
C | G | 1 | a0002c0002t0029g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4584+2428C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702766 | ||||||
| chr2:209702781
|
A | G | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4584+2443A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702781 | ||||||
| chr2:209702930
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4584+2592A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209702930 | ||||||
| chr2:209703171
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(1): Show | 4 | HG01261.hp1 HG01433.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.4585-2409G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209703171 | ||||||
| chr2:209703287
|
C | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4585-2293C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209703287 | ||||||
| chr2:209703677
|
A | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4585-1903A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209703677 | ||||||
| chr2:209703749
|
TA | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4585-1830delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209703749 | ||||||
| chr2:209703810
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4585-1770C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209703810 | ||||||
| chr2:209704024
|
G | A | 1 | a0002c0002t0009g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4585-1556G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704024 | ||||||
| chr2:209704058
|
C | T | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4585-1522C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704058 | ||||||
| chr2:209704080
|
C | T | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4585-1500C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704080 | ||||||
| chr2:209704166
|
C | T | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4585-1414C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704166 | ||||||
| chr2:209704333
|
A | C | 1 | a0003c0004t0002g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4585-1247A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704333 | ||||||
| chr2:209704417
|
T | G | 19 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.4585-1163T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704417 | ||||||
| chr2:209704575
|
A | G | 1 | a0001c0013t0006g0073 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4585-1005A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704575 | ||||||
| chr2:209704735
|
G | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4585-845G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704735 | ||||||
| chr2:209704907
|
A | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4585-673A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209704907 | ||||||
| chr2:209705176
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4585-404C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209705176 | ||||||
| chr2:209705177
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0002g0013 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4585-403G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209705177 | ||||||
| chr2:209705295
|
T | A | 1 | a0001c0001t0033g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4585-285T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 11/15 | chr2 | 209705295 | ||||||
| chr2:209705911
|
A | G | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4732+184A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209705911 | ||||||
| chr2:209706193
|
A | T | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4732+466A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706193 | ||||||
| chr2:209706288
|
T | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.4732+561T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706288 | ||||||
| chr2:209706354
|
G | A | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4732+627G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706354 | ||||||
| chr2:209706493
|
C | A | 3 | a0004c0007t0010g0148a0004c0007t0017g0058a0004c0007t0017g0147 | 3 | HG01243.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4732+766C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706493 | ||||||
| chr2:209706510
|
GACCCTCT others(22): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4732+804_4732+832d others(31): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 209706510 | |||||
| chr2:209706547
|
A | G | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4732+820A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706547 | ||||||
| chr2:209706615
|
A | G | 1 | a0002c0002t0009g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4732+888A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706615 | ||||||
| chr2:209706626
|
T | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4732+899T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706626 | ||||||
| chr2:209706646
|
T | C | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4732+919T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706646 | ||||||
| chr2:209706714
|
G | A | 75 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.4732+987G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706714 | ||||||
| chr2:209706715
|
A | T | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4732+988A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706715 | ||||||
| chr2:209706862
|
A | G | 1 | a0002c0002t0019g0044 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.4732+1135A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209706862 | ||||||
| chr2:209706881
|
AT | A | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4732+1157delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 209706881 | |||||
| chr2:209707087
|
G | A | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4732+1360G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707087 | ||||||
| chr2:209707224
|
A | G | 2 | a0002c0002t0016g0031a0010c0012t0038g0045 | 2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.4732+1497A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707224 | ||||||
| chr2:209707291
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.4732+1564G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707291 | ||||||
| chr2:209707419
|
C | T | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4732+1692C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707419 | ||||||
| chr2:209707443
|
T | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4732+1716T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707443 | ||||||
| chr2:209707536
|
A | G | 1 | a0002c0002t0032g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4732+1809A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707536 | ||||||
| chr2:209707560
|
T | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4732+1833T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707560 | ||||||
| chr2:209707585
|
GCA | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4732+1861_4732+186 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 209707585 | |||||
| chr2:209707598
|
A | G | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4732+1871A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209707598 | ||||||
| chr2:209708199
|
T | C | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4733-1715T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209708199 | ||||||
| chr2:209708442
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4733-1472G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209708442 | ||||||
| chr2:209708450
|
C | G | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4733-1464C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209708450 | ||||||
| chr2:209708858
|
A | T | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4733-1056A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209708858 | ||||||
| chr2:209709000
|
G | A | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4733-914G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209709000 | ||||||
| chr2:209709233
|
G | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4733-681G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209709233 | ||||||
| chr2:209709265
|
C | G | 10 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.4733-649C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209709265 | ||||||
| chr2:209709269
|
CT | C | 10 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(7): Show | 10 | HG01109.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4733-636delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 209709269 | |||||
| chr2:209709432
|
C | T | 16 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(13): Show | 16 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4733-482C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209709432 | ||||||
| chr2:209709549
|
G | A | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4733-365G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 12/15 | chr2 | 209709549 | ||||||
| chr2:209710949
|
G | A | 13 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(10): Show | 13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.5073+695G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209710949 | ||||||
| chr2:209711130
|
A | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5073+876A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209711130 | ||||||
| chr2:209711370
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5073+1116C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209711370 | ||||||
| chr2:209711539
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5073+1285A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209711539 | ||||||
| chr2:209711706
|
A | T | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5073+1452A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209711706 | ||||||
| chr2:209711876
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5073+1622C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209711876 | ||||||
| chr2:209712211
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5073+1957A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209712211 | ||||||
| chr2:209712688
|
C | T | 1 | a0008c0015t0002g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5073+2434C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209712688 | ||||||
| chr2:209712946
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.5073+2692G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209712946 | ||||||
| chr2:209713042
|
C | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.5073+2788C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713042 | ||||||
| chr2:209713326
|
GT | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5073+3076delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209713326 | |||||
| chr2:209713329
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.5073+3075T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713329 | ||||||
| chr2:209713442
|
C | A | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5073+3188C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713442 | ||||||
| chr2:209713568
|
T | C | 16 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(13): Show | 16 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.5073+3314T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713568 | ||||||
| chr2:209713852
|
G | A | 1 | a0003c0004t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5073+3598G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713852 | ||||||
| chr2:209713856
|
T | C | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.5073+3602T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713856 | ||||||
| chr2:209713928
|
C | G | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5073+3674C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713928 | ||||||
| chr2:209713961
|
G | C | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5073+3707G>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209713961 | ||||||
| chr2:209714037
|
C | CA | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5073+3793dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209714037 | |||||
| chr2:209714063
|
T | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0125others(5): Show | 8 | HG01993.hp1 NA18963.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.5073+3809T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209714063 | ||||||
| chr2:209714493
|
C | T | 3 | a0001c0006t0002g0057a0001c0006t0002g0092a0001c0006t0002g0093 | 3 | HG02559.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5073+4239C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209714493 | ||||||
| chr2:209714541
|
T | C | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5073+4287T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209714541 | ||||||
| chr2:209714702
|
C | A | 1 | a0001c0001t0002g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5073+4448C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209714702 | ||||||
| chr2:209715081
|
A | G | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5073+4827A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715081 | ||||||
| chr2:209715560
|
G | A | 3 | a0001c0003t0018g0005a0001c0003t0018g0016a0001c0003t0036g0006 | 3 | HG02559.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5073+5306G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715560 | ||||||
| chr2:209715598
|
G | A | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5073+5344G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715598 | ||||||
| chr2:209715675
|
A | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.5073+5421A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715675 | ||||||
| chr2:209715709
|
C | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5073+5455C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715709 | ||||||
| chr2:209715766
|
A | G | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5073+5512A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715766 | ||||||
| chr2:209715841
|
A | G | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5073+5587A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209715841 | ||||||
| chr2:209716270
|
T | C | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5073+6016T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209716270 | ||||||
| chr2:209716323
|
A | G | 9 | a0002c0002t0005g0033a0002c0002t0005g0039a0002c0005t0008g0134others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.5073+6069A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209716323 | ||||||
| chr2:209716348
|
G | A | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5073+6094G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209716348 | ||||||
| chr2:209716611
|
A | G | 3 | a0002c0002t0004g0118a0002c0002t0004g0119a0002c0002t0004g0120 | 3 | NA18959.hp2 NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.5073+6357A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209716611 | ||||||
| chr2:209716732
|
AT | A | 5 | a0001c0001t0002g0032a0001c0003t0006g0003a0001c0003t0006g0004others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5073+6488delT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209716732 | |||||
| chr2:209716813
|
G | A | 17 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5073+6559G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209716813 | ||||||
| chr2:209716870
|
G | A | 17 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5073+6616G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209716870 | ||||||
| chr2:209716991
|
GGT | G | 17 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5073+6740_5073+674 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209716991 | |||||
| chr2:209717048
|
G | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5073+6794G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717048 | ||||||
| chr2:209717083
|
A | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5073+6829A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717083 | ||||||
| chr2:209717474
|
C | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5073+7220C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717474 | ||||||
| chr2:209717657
|
A | G | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5073+7403A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717657 | ||||||
| chr2:209717772
|
C | G | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5073+7518C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717772 | ||||||
| chr2:209717785
|
T | C | 5 | a0002c0002t0015g0066a0002c0002t0029g0061a0002c0002t0030g0068others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5073+7531T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717785 | ||||||
| chr2:209717961
|
G | A | 6 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(3): Show | 6 | HG00140.hp2 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.5073+7707G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209717961 | ||||||
| chr2:209718840
|
T | A | 1 | a0001c0006t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5074-6869T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209718840 | ||||||
| chr2:209719035
|
G | A | 1 | a0004c0007t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5074-6674G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719035 | ||||||
| chr2:209719124
|
A | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5074-6585A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719124 | ||||||
| chr2:209719164
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0125others(5): Show | 8 | HG01993.hp1 NA18963.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.5074-6545G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719164 | ||||||
| chr2:209719173
|
C | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5074-6536C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719173 | ||||||
| chr2:209719519
|
G | GT | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5074-6183dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209719519 | |||||
| chr2:209719595
|
C | T | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5074-6114C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719595 | ||||||
| chr2:209719606
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5074-6103A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719606 | ||||||
| chr2:209719648
|
G | A | 1 | a0002c0005t0027g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5074-6061G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719648 | ||||||
| chr2:209719700
|
C | T | 1 | a0001c0003t0002g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5074-6009C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719700 | ||||||
| chr2:209719712
|
A | G | 1 | a0002c0002t0005g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.5074-5997A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719712 | ||||||
| chr2:209719731
|
C | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5074-5978C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719731 | ||||||
| chr2:209719783
|
A | C | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5074-5926A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719783 | ||||||
| chr2:209719813
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0002g0063others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.5074-5896C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209719813 | ||||||
| chr2:209720210
|
T | C | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.5074-5499T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720210 | ||||||
| chr2:209720235
|
C | A | 1 | a0001c0006t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5074-5474C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720235 | ||||||
| chr2:209720251
|
A | G | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5074-5458A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720251 | ||||||
| chr2:209720301
|
C | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5074-5408C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720301 | ||||||
| chr2:209720392
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0002g0013others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.5074-5317G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720392 | ||||||
| chr2:209720416
|
A | G | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5074-5293A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720416 | ||||||
| chr2:209720528
|
A | G | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.5074-5181A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209720528 | ||||||
| chr2:209720638
|
CA | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.5074-5048delA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209720638 | |||||
| chr2:209720638
|
CAA | C | 9 | a0001c0001t0001g0138a0001c0001t0002g0053a0001c0001t0003g0022others(6): Show | 9 | HG01975.hp1 HG02280.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.5074-5049_5074-504 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209720638 | |||||
| chr2:209720739
|
TATC | T | 17 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5074-4967_5074-496 others(7): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209720739 | |||||
| chr2:209721144
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5074-4565G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721144 | ||||||
| chr2:209721170
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5074-4539T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721170 | ||||||
| chr2:209721257
|
C | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5074-4452C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721257 | ||||||
| chr2:209721310
|
A | G | 1 | a0002c0002t0014g0113 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5074-4399A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721310 | ||||||
| chr2:209721340
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0032 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5074-4369A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721340 | ||||||
| chr2:209721834
|
C | T | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5074-3875C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721834 | ||||||
| chr2:209721944
|
G | A | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5074-3765G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721944 | ||||||
| chr2:209721961
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.5074-3748T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209721961 | ||||||
| chr2:209722423
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.5074-3286T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209722423 | ||||||
| chr2:209722766
|
A | G | 17 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5074-2943A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209722766 | ||||||
| chr2:209723188
|
G | A | 1 | a0001c0003t0006g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5074-2521G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723188 | ||||||
| chr2:209723200
|
C | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.5074-2509C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723200 | ||||||
| chr2:209723358
|
C | G | 2 | a0001c0003t0002g0054a0001c0003t0002g0055 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5074-2351C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723358 | ||||||
| chr2:209723419
|
A | G | 1 | a0002c0002t0019g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5074-2290A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723419 | ||||||
| chr2:209723458
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5074-2251C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723458 | ||||||
| chr2:209723776
|
A | C | 38 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5074-1933A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723776 | ||||||
| chr2:209723889
|
T | C | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.5074-1820T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209723889 | ||||||
| chr2:209724114
|
G | T | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5074-1595G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209724114 | ||||||
| chr2:209724462
|
C | G | 2 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.5074-1247C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209724462 | ||||||
| chr2:209724583
|
A | AAG | 5 | a0001c0001t0002g0018a0001c0001t0003g0028a0001c0003t0018g0005others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.5074-1102_5074-110 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209724583 | |||||
| chr2:209724583
|
AAG | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5074-1102_5074-110 others(6): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209724583 | |||||
| chr2:209724583
|
AAGAG | A | 5 | a0001c0001t0002g0020a0002c0005t0011g0071a0002c0005t0011g0072others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5074-1104_5074-110 others(8): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 209724583 | |||||
| chr2:209724671
|
C | A | 1 | a0001c0001t0010g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5074-1038C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209724671 | ||||||
| chr2:209724904
|
C | A | 4 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.5074-805C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209724904 | ||||||
| chr2:209725153
|
C | A | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5074-556C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209725153 | ||||||
| chr2:209725282
|
A | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5074-427A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209725282 | ||||||
| chr2:209725466
|
T | G | 2 | a0001c0003t0018g0005a0001c0003t0036g0006 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5074-243T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 13/15 | chr2 | 209725466 | ||||||
| chr2:209725963
|
G | T | 3 | a0002c0002t0014g0113a0002c0002t0014g0143a0002c0002t0039g0051 | 3 | NA18942.hp1 NA18943.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.5155+173G>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209725963 | ||||||
| chr2:209726350
|
C | A | 1 | a0005c0008t0016g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5155+560C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726350 | ||||||
| chr2:209726580
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5155+790A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726580 | ||||||
| chr2:209726581
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5155+791A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726581 | ||||||
| chr2:209726582
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5155+792A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726582 | ||||||
| chr2:209726603
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.5155+813A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726603 | ||||||
| chr2:209726679
|
A | G | 2 | a0001c0003t0006g0003a0001c0003t0006g0004 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.5155+889A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726679 | ||||||
| chr2:209726903
|
G | A | 2 | a0001c0014t0001g0101a0008c0015t0002g0075 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5155+1113G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209726903 | ||||||
| chr2:209727014
|
A | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0095 | 3 | HG02630.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.5155+1224A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209727014 | ||||||
| chr2:209727129
|
C | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5155+1339C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209727129 | ||||||
| chr2:209727214
|
C | T | 7 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.5155+1424C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209727214 | ||||||
| chr2:209727256
|
T | C | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5155+1466T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209727256 | ||||||
| chr2:209727641
|
A | T | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5155+1851A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209727641 | ||||||
| chr2:209727875
|
A | T | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5156-1975A>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209727875 | ||||||
| chr2:209728043
|
A | G | 15 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(12): Show | 15 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.5156-1807A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728043 | ||||||
| chr2:209728345
|
C | T | 1 | a0001c0001t0034g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5156-1505C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728345 | ||||||
| chr2:209728362
|
G | A | 1 | a0002c0002t0009g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5156-1488G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728362 | ||||||
| chr2:209728517
|
T | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.5156-1333T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728517 | ||||||
| chr2:209728852
|
C | T | 42 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.5156-998C>T | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728852 | ||||||
| chr2:209728855
|
T | TG | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5156-995_5156-994i others(3): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728855 | ||||||
| chr2:209728856
|
T | G | 46 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.5156-994T>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728856 | ||||||
| chr2:209728980
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5156-870G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209728980 | ||||||
| chr2:209729134
|
A | C | 38 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5156-716A>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729134 | ||||||
| chr2:209729210
|
C | G | 3 | a0002c0005t0008g0134a0002c0005t0008g0135a0002c0005t0008g0136 | 3 | HG02055.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5156-640C>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729210 | ||||||
| chr2:209729374
|
C | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5156-476C>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729374 | ||||||
| chr2:209729605
|
G | A | 17 | a0001c0003t0002g0054a0001c0003t0002g0055a0001c0003t0002g0059others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5156-245G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729605 | ||||||
| chr2:209729673
|
T | C | 9 | a0003c0004t0001g0099a0003c0004t0002g0062a0003c0004t0003g0088others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.5156-177T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729673 | ||||||
| chr2:209729765
|
G | A | 4 | a0001c0003t0006g0003a0001c0003t0006g0004a0001c0003t0006g0023others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5156-85G>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729765 | ||||||
| chr2:209729816
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.5156-34A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 14/15 | chr2 | 209729816 | ||||||
| chr2:209729993
|
C | CT | 72 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.5268+36dupT | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 209729993 | |||||
| chr2:209729997
|
T | TA | 3 | a0002c0002t0005g0046a0002c0002t0020g0048a0002c0002t0031g0080 | 3 | HG00099.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.5268+35_5268+36ins others(1): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | chr2 | 209729997 | ||||||
| chr2:209729997
|
T | TAA | 36 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(33): Show | 36 | HG00408.hp1 HG00597.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.5268+35_5268+36ins others(2): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | chr2 | 209729997 | ||||||
| chr2:209729998
|
T | A | 39 | a0002c0002t0004g0001a0002c0002t0004g0118a0002c0002t0004g0119others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.5268+36T>A | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | chr2 | 209729998 | ||||||
| chr2:209729998
|
T | TA | 25 | a0001c0001t0002g0020a0001c0003t0002g0054a0001c0003t0002g0055others(22): Show | 25 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.5268+44dupA | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 209729998 | |||||
| chr2:209730030
|
A | G | 4 | a0002c0005t0011g0071a0002c0005t0011g0072a0002c0005t0011g0094others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5268+68A>G | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | chr2 | 209730030 | ||||||
| chr2:209730044
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.5268+82T>C | MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 15/15 | chr2 | 209730044 |