Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 93986 |
|---|---|
| ensemblid | ENSG00000128573.28 |
| hgncid | 13875 |
| symbol | FOXP2 |
| name | forkhead box P2 |
| refseq_nuc | NM_014491.4 |
| refseq_prot | NP_055306.1 |
| ensembl_nuc | ENST00000350908.9 |
| ensembl_prot | ENSP00000265436.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 114414815 |
| end | 114693765 |
| strand | + |
| ver | v1.2 |
| region | chr7:114414815-114693765 |
| region5000 | chr7:114409815-114698765 |
| regionname0 | FOXP2_chr7_114414815_114693765 |
| regionname5000 | FOXP2_chr7_114409815_114698765 |
| 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 | 715 | 172 | 62 | 33 | 42 | 8 | 25 | 24 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0002 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0003 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| 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 | 2148 | 165 | 55 | 33 | 42 | 8 | 25 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| c0002 | 0/0 | 2148 | 5 | 5 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| c0003 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| c0004 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| c0005 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4396 | 44 | 20 | 10 | 4 | 2 | 7 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0002 | 0/0 | 4395 | 30 | 8 | 3 | 16 | 0 | 3 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0003 | 0/0 | 4396 | 28 | 1 | 9 | 13 | 2 | 3 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0004 | 0/1 | 4393 | 24 | 3 | 8 | 3 | 3 | 6 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0005 | 0/0 | 4396 | 10 | 9 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0006 | 0/0 | 4397 | 10 | 9 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0007 | 0/0 | 4393 | 2 | 0 | 0 | 0 | 0 | 2 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0008 | 0/0 | 4394 | 2 | 0 | 1 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0009 | 0/0 | 4397 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0010 | 0/0 | 4391 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0011 | 0/0 | 4394 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0012 | 0/0 | 4393 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0013 | 0/0 | 4396 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0014 | 0/0 | 4396 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0015 | 0/0 | 4397 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0016 | 0/0 | 4396 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0017 | 0/0 | 4393 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0018 | 0/0 | 4394 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0019 | 0/0 | 4394 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0020 | 0/0 | 4393 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0021 | 0/0 | 4393 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0022 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0023 | 0/0 | 4395 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0024 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0025 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0026 | 0/0 | 4395 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0027 | 0/0 | 4396 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0028 | 0/0 | 4396 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0029 | 0/0 | 4397 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0030 | 0/0 | 4397 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| t0031 | 0/0 | 4397 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| 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 | 2148 | 165 | 55 | 33 | 42 | 8 | 25 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0002 | 0/0 | 2148 | 5 | 5 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0003 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0002c0004 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0003c0005 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6543 | 41 | 17 | 10 | 4 | 2 | 7 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0002 | 0/0 | 6542 | 29 | 7 | 3 | 16 | 0 | 3 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0003 | 0/0 | 6543 | 27 | 1 | 8 | 13 | 2 | 3 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0004 | 0/1 | 6540 | 24 | 3 | 8 | 3 | 3 | 6 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0005 | 0/0 | 6543 | 9 | 8 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0006 | 0/0 | 6544 | 8 | 7 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0007 | 0/0 | 6540 | 2 | 0 | 0 | 0 | 0 | 2 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0008 | 0/0 | 6541 | 2 | 0 | 1 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0009 | 0/0 | 6544 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0010 | 0/0 | 6538 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0011 | 0/0 | 6541 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0013 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0014 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0015 | 0/0 | 6544 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0016 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0017 | 0/0 | 6540 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0018 | 0/0 | 6541 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0019 | 0/0 | 6541 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0020 | 0/0 | 6540 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0021 | 0/0 | 6540 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0022 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0023 | 0/0 | 6542 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0024 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0025 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0026 | 0/0 | 6542 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0027 | 0/0 | 6543 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0028 | 0/0 | 6543 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0029 | 0/0 | 6544 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0030 | 0/0 | 6544 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0001t0031 | 0/0 | 6544 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0002t0001 | 0/0 | 6543 | 3 | 3 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0002t0002 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0002t0005 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0001c0003t0006 | 0/0 | 6544 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0002c0004t0012 | 0/0 | 6540 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| a0003c0005t0003 | 0/0 | 6543 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | copy fasta | chr7 | 114409815 | 114698765 |
| 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 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0014g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0017g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0018g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0021g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0023g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0024g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0025g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0026g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0027g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0028g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0029g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0030g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0001t0031g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0002t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0003t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0001c0003t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0002c0004t0012g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0003c0005t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0005 | EUR | GBR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0131 | EUR | GBR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00423 | hp1 | a0001 | c0001 | t0017 | g0031 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00639 | hp1 | a0001 | c0001 | t0028 | g0040 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG00673 | hp2 | a0001 | c0001 | t0020 | g0047 | EAS | CHS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0119 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01243 | hp2 | a0003 | c0005 | t0003 | g0158 | AMR | PUR | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | CLM | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0129 | AMR | CLM | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0117 | AMR | CLM | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | IBS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01515 | hp2 | a0001 | c0001 | t0010 | g0142 | EUR | IBS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | IBS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0156 | EUR | IBS | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0173 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0169 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02280 | hp2 | a0001 | c0003 | t0006 | g0150 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0126 | AMR | PEL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PEL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02602 | hp2 | a0001 | c0001 | t0021 | g0128 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02622 | hp1 | a0001 | c0001 | t0024 | g0132 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0085 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0146 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0093 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02818 | hp1 | a0001 | c0001 | t0022 | g0043 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0092 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0073 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02970 | hp1 | a0001 | c0003 | t0006 | g0149 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03041 | hp1 | a0001 | c0001 | t0025 | g0012 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0064 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03225 | hp1 | a0001 | c0001 | t0031 | g0114 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0060 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0095 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0140 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0141 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | MSL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03669 | hp1 | a0002 | c0004 | t0012 | g0063 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0143 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | STU | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | STU | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03704 | hp2 | a0001 | c0001 | t0026 | g0011 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03710 | hp2 | a0001 | c0001 | t0023 | g0018 | SAS | PJL | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | STU | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | YRI | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18952 | hp1 | a0001 | c0001 | t0029 | g0079 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18957 | hp2 | a0001 | c0001 | t0030 | g0068 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18970 | hp2 | a0001 | c0001 | t0027 | g0030 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | LWK | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19086 | hp1 | a0001 | c0001 | t0018 | g0080 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0103 | AFR | YRI | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | USA | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | USA | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | USA | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | USA | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0137 | REF | REF | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114629925
|
C | A | 1 | a0002 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.517C>A | p.Gln173Lys | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/17 | 1073/6543 | 517/2148 | 173/715 | chr7 | 114629925 | ||
| chr7:114631524
|
C | CCAG | 1 | a0001 | 2 | HG02280.hp2 HG02970.hp1 |
disruptive_inframe_insertion | MODERATE | c.618_620dupGCA | p.Gln207dup | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/17 | 1177/6543 | 621/2148 | 207/715 | INFO_REALIGN_3_PRIME | chr7 | 114631524 | |
| chr7:114658151
|
C | T | 1 | a0003 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1352C>T | p.Thr451Met | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 11/17 | 1908/6543 | 1352/2148 | 451/715 | chr7 | 114658151 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114629939
|
A | G | 1 | a0001c0003 | 2 | HG02280.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.531A>G | p.Gln177Gln | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/17 | 1087/6543 | 531/2148 | 177/715 | chr7 | 114629939 | ||
| chr7:114631671
|
C | T | 1 | a0001c0002 | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
synonymous_variant | LOW | c.741C>T | p.Gly247Gly | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/17 | 1297/6543 | 741/2148 | 247/715 | chr7 | 114631671 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114414902
|
ACT | A | 3 | a0001c0001t0007a0001c0001t0008a0001c0001t0010 | 5 | HG01515.hp2 HG02293.hp1 HG03490.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-467_-466delTC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/17 | 11607 | INFO_REALIGN_3_PRIME | chr7 | 114414902 | ||||
| chr7:114414921
|
T | C | 6 | a0001c0001t0011a0001c0001t0013a0001c0001t0014others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-450T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/17 | 11591 | chr7 | 114414921 | |||||
| chr7:114414924
|
A | G | 1 | a0001c0001t0016 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-447A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/17 | 11588 | chr7 | 114414924 | |||||
| chr7:114415272
|
G | A | 1 | a0001c0001t0016 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/17 | 11240 | chr7 | 114415272 | |||||
| chr7:114690129
|
C | CT | 6 | a0001c0001t0006a0001c0001t0015a0001c0001t0029others(3): Show | 14 | HG01496.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*220dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 221 | INFO_REALIGN_3_PRIME | chr7 | 114690129 | ||||
| chr7:114690129
|
CT | C | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0022others(5): Show | 37 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*220delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 220 | INFO_REALIGN_3_PRIME | chr7 | 114690129 | ||||
| chr7:114690129
|
CTT | C | 9 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(6): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*219_*220delTT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 219 | INFO_REALIGN_3_PRIME | chr7 | 114690129 | ||||
| chr7:114690131
|
T | TC | 1 | a0001c0001t0009 | 2 | HG02055.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*205_*206insC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 206 | chr7 | 114690131 | |||||
| chr7:114691672
|
G | A | 1 | a0001c0001t0017 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1746G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 1746 | chr7 | 114691672 | |||||
| chr7:114691870
|
C | T | 2 | a0001c0001t0026a0001c0001t0028 | 2 | HG00639.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1944C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 1944 | chr7 | 114691870 | |||||
| chr7:114691943
|
GA | G | 6 | a0001c0001t0004a0001c0001t0010a0001c0001t0017others(3): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2030delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2030 | INFO_REALIGN_3_PRIME | chr7 | 114691943 | ||||
| chr7:114692008
|
A | G | 1 | a0001c0001t0021 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2082A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2082 | chr7 | 114692008 | |||||
| chr7:114692041
|
G | A | 1 | a0001c0001t0027 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2115G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2115 | chr7 | 114692041 | |||||
| chr7:114692179
|
A | T | 2 | a0001c0001t0026a0001c0001t0028 | 2 | HG00639.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2253A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2253 | chr7 | 114692179 | |||||
| chr7:114692191
|
G | T | 9 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(6): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2265G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2265 | chr7 | 114692191 | |||||
| chr7:114692199
|
A | C | 1 | a0001c0001t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2273A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2273 | chr7 | 114692199 | |||||
| chr7:114692200
|
A | T | 1 | a0001c0001t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2274A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 2274 | chr7 | 114692200 | |||||
| chr7:114693125
|
G | A | 1 | a0001c0001t0022 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3199G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 3199 | chr7 | 114693125 | |||||
| chr7:114693383
|
G | A | 1 | a0001c0001t0020 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3457G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 3457 | chr7 | 114693383 | |||||
| chr7:114693609
|
C | T | 5 | a0001c0001t0003a0001c0001t0008a0001c0001t0027others(2): Show | 32 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3683C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 3683 | chr7 | 114693609 | |||||
| chr7:114693633
|
T | C | 1 | a0001c0001t0023 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3707T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 3707 | chr7 | 114693633 | |||||
| chr7:114693703
|
C | A | 1 | a0001c0001t0024 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3777C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 3777 | chr7 | 114693703 | |||||
| chr7:114693748
|
C | T | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(6): Show | 26 | HG01243.hp1 HG01496.hp2 HG02055.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3822C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 17/17 | 3822 | chr7 | 114693748 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114415741
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-11+381G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114415741 | ||||||
| chr7:114416000
|
G | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+640G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416000 | ||||||
| chr7:114416405
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0003g0058 | 2 | HG01099.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-11+1045A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416405 | ||||||
| chr7:114416440
|
A | AAATTTCA others(1): Show |
57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+1081_-11+1088d others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114416440 | |||||
| chr7:114416510
|
C | CA | 7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0003g0059others(4): Show | 7 | HG01099.hp2 HG03209.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+1169dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114416510 | |||||
| chr7:114416510
|
CA | C | 9 | a0001c0001t0001g0056a0001c0001t0002g0053a0001c0001t0002g0054others(6): Show | 9 | HG00597.hp2 HG01169.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+1169delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114416510 | |||||
| chr7:114416514
|
A | G | 2 | a0001c0001t0002g0172a0001c0001t0009g0173 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+1154A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416514 | ||||||
| chr7:114416564
|
G | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0089a0001c0001t0001g0090others(26): Show | 29 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11+1204G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416564 | ||||||
| chr7:114416566
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+1206A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416566 | ||||||
| chr7:114416694
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+1334G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416694 | ||||||
| chr7:114416732
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-11+1372A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416732 | ||||||
| chr7:114416894
|
T | A | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0015g0092 | 3 | HG02717.hp2 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-11+1534T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416894 | ||||||
| chr7:114416895
|
T | C | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0015g0092 | 3 | HG02717.hp2 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-11+1535T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416895 | ||||||
| chr7:114416896
|
TGAC | T | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0015g0092 | 3 | HG02717.hp2 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-11+1537_-11+1539d others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114416896 | ||||||
| chr7:114417054
|
G | T | 19 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(16): Show | 19 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11+1694G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114417054 | ||||||
| chr7:114417871
|
T | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-11+2511T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114417871 | ||||||
| chr7:114418017
|
T | C | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-11+2657T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114418017 | ||||||
| chr7:114418286
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11+2926C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114418286 | ||||||
| chr7:114418676
|
CA | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0046others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+3326delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114418676 | |||||
| chr7:114418683
|
A | G | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-11+3323A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114418683 | ||||||
| chr7:114418726
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0005g0094 | 2 | HG02523.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11+3366G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114418726 | ||||||
| chr7:114419101
|
C | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-11+3741C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419101 | ||||||
| chr7:114419144
|
C | G | 20 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+3784C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419144 | ||||||
| chr7:114419343
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0009g0173 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+3983G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419343 | ||||||
| chr7:114419443
|
A | C | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11+4083A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419443 | ||||||
| chr7:114419591
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0015g0092 | 3 | HG02717.hp2 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-11+4231G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419591 | ||||||
| chr7:114419673
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+4313C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419673 | ||||||
| chr7:114419713
|
G | GAC | 33 | a0001c0001t0001g0061a0001c0001t0001g0100a0001c0001t0001g0101others(30): Show | 33 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11+4386_-11+4387d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114419713 | |||||
| chr7:114419713
|
G | GACAC | 14 | a0001c0001t0001g0007a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11+4384_-11+4387d others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114419713 | |||||
| chr7:114419713
|
G | GACACACA others(19): Show |
1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11+4362_-11+4387d others(28): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114419713 | |||||
| chr7:114419713
|
GAC | G | 2 | a0001c0001t0001g0033a0001c0001t0014g0146 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-11+4386_-11+4387d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114419713 | |||||
| chr7:114419744
|
A | C | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11+4384A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419744 | ||||||
| chr7:114419747
|
C | CA | 2 | a0001c0001t0002g0036a0001c0001t0003g0052 | 2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-11+4387_-11+4388i others(3): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419747 | ||||||
| chr7:114419748
|
C | A | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11+4388C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114419748 | ||||||
| chr7:114420386
|
T | A | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-11+5026T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420386 | ||||||
| chr7:114420400
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+5040T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420400 | ||||||
| chr7:114420421
|
A | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0056others(13): Show | 16 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+5061A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420421 | ||||||
| chr7:114420608
|
A | T | 23 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0144others(20): Show | 23 | HG00140.hp2 HG00642.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-11+5248A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420608 | ||||||
| chr7:114420668
|
TA | T | 2 | a0001c0001t0014g0146a0002c0004t0012g0063 | 2 | HG02647.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-11+5311delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 114420668 | |||||
| chr7:114420671
|
A | T | 2 | a0001c0001t0014g0146a0002c0004t0012g0063 | 2 | HG02647.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-11+5311A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420671 | ||||||
| chr7:114420812
|
G | A | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11+5452G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420812 | ||||||
| chr7:114420866
|
A | C | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-11+5506A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420866 | ||||||
| chr7:114420919
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+5559A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114420919 | ||||||
| chr7:114421314
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-10-5188A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114421314 | ||||||
| chr7:114421930
|
C | A | 9 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-4572C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114421930 | ||||||
| chr7:114422029
|
T | C | 1 | a0001c0001t0002g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-10-4473T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422029 | ||||||
| chr7:114422033
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-10-4469G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422033 | ||||||
| chr7:114422048
|
G | T | 2 | a0001c0001t0002g0172a0001c0001t0009g0173 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-10-4454G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422048 | ||||||
| chr7:114422090
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-10-4412G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422090 | ||||||
| chr7:114422599
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-10-3903G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422599 | ||||||
| chr7:114422612
|
G | A | 2 | a0001c0002t0001g0097a0001c0002t0001g0098 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-10-3890G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422612 | ||||||
| chr7:114422804
|
A | G | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3698A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114422804 | ||||||
| chr7:114423426
|
A | C | 4 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0049others(1): Show | 4 | HG00099.hp2 HG01106.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-3076A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114423426 | ||||||
| chr7:114423490
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10-3012G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114423490 | ||||||
| chr7:114424796
|
G | C | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-10-1706G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114424796 | ||||||
| chr7:114425545
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-10-957A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114425545 | ||||||
| chr7:114425841
|
T | C | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10-661T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114425841 | ||||||
| chr7:114425916
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10-586T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114425916 | ||||||
| chr7:114426205
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-10-297G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 1/16 | chr7 | 114426205 | ||||||
| chr7:114426794
|
A | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.168+115A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114426794 | ||||||
| chr7:114426853
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.168+174G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114426853 | ||||||
| chr7:114427088
|
A | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.168+409A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114427088 | ||||||
| chr7:114427188
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168+509C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114427188 | ||||||
| chr7:114427397
|
TA | T | 13 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0105others(10): Show | 13 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+733delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114427397 | |||||
| chr7:114427729
|
A | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+1050A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114427729 | ||||||
| chr7:114428147
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+1468A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114428147 | ||||||
| chr7:114428505
|
G | T | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+1826G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114428505 | ||||||
| chr7:114428957
|
G | T | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.168+2278G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114428957 | ||||||
| chr7:114429005
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0009g0173 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.168+2326G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429005 | ||||||
| chr7:114429059
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168+2380G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429059 | ||||||
| chr7:114429152
|
G | A | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+2473G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429152 | ||||||
| chr7:114429202
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168+2523G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429202 | ||||||
| chr7:114429230
|
T | A | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+2551T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429230 | ||||||
| chr7:114429297
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.168+2618A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429297 | ||||||
| chr7:114429481
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.168+2802C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429481 | ||||||
| chr7:114429656
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168+2977C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429656 | ||||||
| chr7:114429794
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+3115G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429794 | ||||||
| chr7:114429885
|
A | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+3206A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114429885 | ||||||
| chr7:114430194
|
A | C | 2 | a0001c0001t0011g0060a0001c0001t0015g0092 | 2 | HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+3515A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114430194 | ||||||
| chr7:114430479
|
G | C | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+3800G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114430479 | ||||||
| chr7:114430665
|
A | T | 4 | a0001c0001t0001g0056a0001c0001t0004g0008a0001c0001t0004g0032others(1): Show | 4 | HG00423.hp1 HG02293.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+3986A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114430665 | ||||||
| chr7:114430786
|
A | G | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+4107A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114430786 | ||||||
| chr7:114430980
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.168+4301C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114430980 | ||||||
| chr7:114431267
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+4588C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114431267 | ||||||
| chr7:114431491
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0003g0009 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.168+4812G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114431491 | ||||||
| chr7:114431562
|
A | C | 1 | a0001c0001t0003g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168+4883A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114431562 | ||||||
| chr7:114431619
|
G | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+4940G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114431619 | ||||||
| chr7:114431848
|
C | T | 2 | a0001c0001t0003g0039a0001c0001t0020g0047 | 2 | HG00423.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.168+5169C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114431848 | ||||||
| chr7:114432108
|
A | G | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+5429A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114432108 | ||||||
| chr7:114432388
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.168+5709A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114432388 | ||||||
| chr7:114432494
|
A | T | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+5815A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114432494 | ||||||
| chr7:114432638
|
G | A | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+5959G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114432638 | ||||||
| chr7:114433131
|
A | G | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.168+6452A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433131 | ||||||
| chr7:114433137
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.168+6458C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433137 | ||||||
| chr7:114433174
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0113 | 2 | HG01099.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.168+6495T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433174 | ||||||
| chr7:114433237
|
T | C | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+6558T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433237 | ||||||
| chr7:114433238
|
A | G | 11 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0002g0123others(8): Show | 11 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+6559A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433238 | ||||||
| chr7:114433582
|
T | C | 11 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0002g0123others(8): Show | 11 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+6903T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433582 | ||||||
| chr7:114433690
|
C | T | 12 | a0001c0001t0001g0101a0001c0001t0011g0060a0001c0001t0013g0093others(9): Show | 12 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+7011C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433690 | ||||||
| chr7:114433891
|
T | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+7212T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114433891 | ||||||
| chr7:114434002
|
A | T | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+7323A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114434002 | ||||||
| chr7:114434112
|
T | C | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+7433T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114434112 | ||||||
| chr7:114434202
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(77): Show | 80 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.168+7523C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114434202 | ||||||
| chr7:114434438
|
TG | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.168+7770delG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114434438 | |||||
| chr7:114434489
|
A | G | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+7810A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114434489 | ||||||
| chr7:114434604
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.168+7925C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114434604 | ||||||
| chr7:114435085
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(76): Show | 79 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.168+8406T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435085 | ||||||
| chr7:114435112
|
T | C | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+8433T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435112 | ||||||
| chr7:114435159
|
A | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+8480A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435159 | ||||||
| chr7:114435195
|
C | T | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+8516C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435195 | ||||||
| chr7:114435392
|
A | G | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+8713A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435392 | ||||||
| chr7:114435631
|
A | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(77): Show | 80 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.168+8952A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435631 | ||||||
| chr7:114435714
|
T | C | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+9035T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435714 | ||||||
| chr7:114435887
|
A | AT | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+9216dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114435887 | |||||
| chr7:114435956
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.168+9277G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114435956 | ||||||
| chr7:114436176
|
T | C | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0015g0092 | 3 | HG02717.hp2 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+9497T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436176 | ||||||
| chr7:114436198
|
T | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+9519T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436198 | ||||||
| chr7:114436222
|
T | C | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+9543T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436222 | ||||||
| chr7:114436339
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.168+9660C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436339 | ||||||
| chr7:114436500
|
A | G | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+9821A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436500 | ||||||
| chr7:114436706
|
T | C | 2 | a0001c0001t0002g0001a0001c0001t0004g0014 | 3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.168+10027T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436706 | ||||||
| chr7:114436743
|
G | A | 1 | a0001c0001t0005g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+10064G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436743 | ||||||
| chr7:114436749
|
T | A | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+10070T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436749 | ||||||
| chr7:114436770
|
G | T | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+10091G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436770 | ||||||
| chr7:114436847
|
A | G | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10168A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436847 | ||||||
| chr7:114436989
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.168+10310A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114436989 | ||||||
| chr7:114437097
|
AC | A | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+10420delC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114437097 | |||||
| chr7:114437602
|
C | A | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+10923C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114437602 | ||||||
| chr7:114437880
|
T | G | 1 | a0001c0001t0008g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.168+11201T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114437880 | ||||||
| chr7:114437892
|
C | T | 1 | a0001c0001t0005g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+11213C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114437892 | ||||||
| chr7:114437934
|
A | G | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+11255A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114437934 | ||||||
| chr7:114438303
|
G | A | 26 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.168+11624G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114438303 | ||||||
| chr7:114438605
|
A | G | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+11926A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114438605 | ||||||
| chr7:114438608
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+11929T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114438608 | ||||||
| chr7:114438814
|
A | G | 5 | a0001c0001t0007g0140a0001c0001t0007g0141a0001c0001t0008g0126others(2): Show | 5 | HG01515.hp2 HG02293.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+12135A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114438814 | ||||||
| chr7:114438865
|
T | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+12186T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114438865 | ||||||
| chr7:114438875
|
A | T | 10 | a0001c0001t0001g0101a0001c0001t0011g0060a0001c0001t0013g0093others(7): Show | 10 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+12196A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114438875 | ||||||
| chr7:114439019
|
T | C | 5 | a0001c0001t0001g0160a0001c0001t0003g0157a0001c0001t0004g0156others(2): Show | 5 | HG01070.hp1 HG01243.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+12340T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114439019 | ||||||
| chr7:114439628
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+12949C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114439628 | ||||||
| chr7:114439735
|
A | ATGTG | 2 | a0001c0001t0016g0169a0001c0001t0019g0095 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168+13070_168+1307 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114439735 | |||||
| chr7:114439735
|
A | ATGTGTG | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+13068_168+1307 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114439735 | |||||
| chr7:114439863
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.168+13184C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114439863 | ||||||
| chr7:114440281
|
T | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(70): Show | 73 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.168+13602T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114440281 | ||||||
| chr7:114440380
|
A | G | 10 | a0001c0001t0001g0135a0001c0001t0003g0134a0001c0001t0004g0136others(7): Show | 10 | HG00642.hp2 HG01069.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+13701A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114440380 | ||||||
| chr7:114440614
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.168+13935G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114440614 | ||||||
| chr7:114440751
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.168+14072A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114440751 | ||||||
| chr7:114440753
|
G | C | 3 | a0001c0001t0004g0072a0001c0001t0005g0073a0001c0001t0006g0071 | 3 | HG02145.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168+14074G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114440753 | ||||||
| chr7:114440989
|
G | A | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+14310G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114440989 | ||||||
| chr7:114441274
|
C | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+14595C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114441274 | ||||||
| chr7:114441507
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+14828A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114441507 | ||||||
| chr7:114441605
|
C | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+14926C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114441605 | ||||||
| chr7:114441648
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+14969C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114441648 | ||||||
| chr7:114441843
|
A | C | 1 | a0001c0001t0004g0032 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.168+15164A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114441843 | ||||||
| chr7:114441977
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+15298T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114441977 | ||||||
| chr7:114442086
|
T | C | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+15407T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114442086 | ||||||
| chr7:114442185
|
T | C | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+15506T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114442185 | ||||||
| chr7:114442348
|
AT | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(58): Show | 61 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.168+15684delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114442348 | |||||
| chr7:114442439
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(69): Show | 72 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.168+15760T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114442439 | ||||||
| chr7:114442544
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+15865A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114442544 | ||||||
| chr7:114442753
|
T | C | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.168+16074T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114442753 | ||||||
| chr7:114443171
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.168+16492T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114443171 | ||||||
| chr7:114443291
|
C | G | 5 | a0001c0001t0001g0144a0001c0001t0004g0129a0001c0001t0004g0131others(2): Show | 5 | HG00140.hp2 HG01361.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+16612C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114443291 | ||||||
| chr7:114443429
|
A | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+16750A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114443429 | ||||||
| chr7:114443474
|
T | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+16795T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114443474 | ||||||
| chr7:114443495
|
C | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.168+16816C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114443495 | ||||||
| chr7:114444339
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+17660T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444339 | ||||||
| chr7:114444459
|
A | T | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168+17780A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444459 | ||||||
| chr7:114444573
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+17894T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444573 | ||||||
| chr7:114444650
|
GT | G | 13 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0002g0145others(10): Show | 13 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+17972delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444650 | ||||||
| chr7:114444730
|
A | G | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168+18051A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444730 | ||||||
| chr7:114444779
|
G | T | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+18100G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444779 | ||||||
| chr7:114444843
|
A | G | 2 | a0001c0001t0002g0172a0001c0001t0009g0173 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.168+18164A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444843 | ||||||
| chr7:114444886
|
TA | T | 5 | a0001c0001t0007g0140a0001c0001t0007g0141a0001c0001t0008g0126others(2): Show | 5 | HG01515.hp2 HG02293.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+18208delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114444886 | ||||||
| chr7:114445100
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+18421G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445100 | ||||||
| chr7:114445112
|
A | G | 5 | a0001c0001t0001g0046a0001c0001t0003g0034a0001c0001t0003g0035others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+18433A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445112 | ||||||
| chr7:114445445
|
C | T | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+18766C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445445 | ||||||
| chr7:114445510
|
C | A | 1 | a0001c0001t0003g0050 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.168+18831C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445510 | ||||||
| chr7:114445545
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.168+18866A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445545 | ||||||
| chr7:114445607
|
G | C | 2 | a0001c0001t0003g0091a0001c0001t0004g0074 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.168+18928G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445607 | ||||||
| chr7:114445840
|
C | T | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+19161C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445840 | ||||||
| chr7:114445842
|
G | A | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+19163G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445842 | ||||||
| chr7:114445846
|
TA | T | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+19169delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114445846 | |||||
| chr7:114445898
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0003g0034a0001c0001t0003g0035 | 3 | HG01515.hp1 HG01517.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.168+19219C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445898 | ||||||
| chr7:114445982
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.168+19303T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114445982 | ||||||
| chr7:114446042
|
G | GA | 112 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0065others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.168+19363_168+1936 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114446042 | ||||||
| chr7:114446078
|
GTC | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0089a0001c0001t0001g0127others(47): Show | 50 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.168+19401_168+1940 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114446078 | |||||
| chr7:114446108
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.168+19429A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114446108 | ||||||
| chr7:114446139
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0046others(14): Show | 17 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+19460A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114446139 | ||||||
| chr7:114446190
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.168+19511A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114446190 | ||||||
| chr7:114446399
|
T | C | 1 | a0001c0001t0021g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.168+19720T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114446399 | ||||||
| chr7:114446626
|
C | G | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+19947C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114446626 | ||||||
| chr7:114446747
|
C | CT | 6 | a0001c0001t0001g0046a0001c0001t0002g0172a0001c0001t0003g0035others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+20083dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114446747 | |||||
| chr7:114447316
|
T | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+20637T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447316 | ||||||
| chr7:114447705
|
G | A | 2 | a0001c0002t0002g0102a0001c0002t0005g0103 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.168+21026G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447705 | ||||||
| chr7:114447730
|
G | C | 5 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0014g0146others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+21051G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447730 | ||||||
| chr7:114447832
|
T | A | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168+21153T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447832 | ||||||
| chr7:114447899
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0004g0014 | 3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.168+21220A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447899 | ||||||
| chr7:114447907
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+21228A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447907 | ||||||
| chr7:114447919
|
G | T | 3 | a0001c0001t0002g0096a0001c0001t0002g0172a0001c0001t0009g0173 | 3 | HG02055.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.168+21240G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114447919 | ||||||
| chr7:114448104
|
G | T | 1 | a0001c0001t0004g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.168+21425G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114448104 | ||||||
| chr7:114448191
|
C | T | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+21512C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114448191 | ||||||
| chr7:114448665
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+21986G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114448665 | ||||||
| chr7:114448788
|
T | C | 5 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0001t0006g0070others(2): Show | 5 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+22109T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114448788 | ||||||
| chr7:114448869
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.168+22190G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114448869 | ||||||
| chr7:114449574
|
C | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+22895C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114449574 | ||||||
| chr7:114449686
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.168+23007A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114449686 | ||||||
| chr7:114450403
|
T | C | 6 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0014g0146others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+23724T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114450403 | ||||||
| chr7:114450528
|
T | G | 1 | a0001c0001t0003g0015 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.168+23849T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114450528 | ||||||
| chr7:114450912
|
C | CATGTAAA others(22): Show |
1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+24235_168+2426 others(33): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114450912 | |||||
| chr7:114450952
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+24273G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114450952 | ||||||
| chr7:114451046
|
A | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+24367A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451046 | ||||||
| chr7:114451136
|
A | G | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.168+24457A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451136 | ||||||
| chr7:114451171
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.168+24492A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451171 | ||||||
| chr7:114451299
|
A | G | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+24620A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451299 | ||||||
| chr7:114451487
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.168+24808G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451487 | ||||||
| chr7:114451698
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0089others(58): Show | 61 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.168+25019G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451698 | ||||||
| chr7:114451705
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0003g0148 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.168+25026C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451705 | ||||||
| chr7:114451789
|
C | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.168+25110C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451789 | ||||||
| chr7:114451798
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.168+25119G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114451798 | ||||||
| chr7:114452393
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168+25714T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114452393 | ||||||
| chr7:114452526
|
G | A | 3 | a0001c0001t0015g0092a0001c0001t0016g0169a0001c0001t0019g0095 | 3 | HG02258.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.168+25847G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114452526 | ||||||
| chr7:114452592
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+25913T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114452592 | ||||||
| chr7:114452788
|
C | A | 1 | a0001c0001t0031g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.168+26109C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114452788 | ||||||
| chr7:114452864
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0024g0132 | 3 | HG02622.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+26185A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114452864 | ||||||
| chr7:114453073
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168+26394G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453073 | ||||||
| chr7:114453136
|
G | A | 3 | a0001c0001t0015g0092a0001c0001t0016g0169a0001c0001t0019g0095 | 3 | HG02258.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.168+26457G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453136 | ||||||
| chr7:114453136
|
G | C | 11 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0002g0123others(8): Show | 11 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+26457G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453136 | ||||||
| chr7:114453147
|
G | A | 7 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0014g0146others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+26468G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453147 | ||||||
| chr7:114453301
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.168+26622G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453301 | ||||||
| chr7:114453383
|
G | A | 1 | a0001c0001t0004g0075 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.168+26704G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453383 | ||||||
| chr7:114453398
|
C | A | 1 | a0001c0001t0003g0009 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.168+26719C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453398 | ||||||
| chr7:114453402
|
C | T | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0024g0132 | 3 | HG02622.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+26723C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453402 | ||||||
| chr7:114453454
|
C | T | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+26775C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453454 | ||||||
| chr7:114453568
|
A | C | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+26889A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453568 | ||||||
| chr7:114453713
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.168+27034G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114453713 | ||||||
| chr7:114454079
|
G | A | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+27400G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454079 | ||||||
| chr7:114454085
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+27406T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454085 | ||||||
| chr7:114454087
|
C | T | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+27408C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454087 | ||||||
| chr7:114454204
|
T | C | 7 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0014g0146others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+27525T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454204 | ||||||
| chr7:114454296
|
A | G | 5 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0001t0006g0070others(2): Show | 5 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+27617A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454296 | ||||||
| chr7:114454311
|
A | G | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+27632A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454311 | ||||||
| chr7:114454406
|
T | G | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+27727T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454406 | ||||||
| chr7:114454418
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+27739A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454418 | ||||||
| chr7:114454517
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+27838G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454517 | ||||||
| chr7:114454595
|
A | G | 4 | a0001c0001t0004g0129a0001c0001t0006g0130a0001c0001t0011g0060others(1): Show | 4 | HG01361.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+27916A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454595 | ||||||
| chr7:114454730
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.168+28051A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454730 | ||||||
| chr7:114454762
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+28083C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454762 | ||||||
| chr7:114454763
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0004g0129a0001c0001t0006g0130 | 3 | HG00140.hp1 HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+28084A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454763 | ||||||
| chr7:114454768
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+28089A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454768 | ||||||
| chr7:114454780
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+28101A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454780 | ||||||
| chr7:114454786
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+28107A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454786 | ||||||
| chr7:114454882
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0028g0040 | 3 | HG00140.hp1 HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.168+28203G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454882 | ||||||
| chr7:114454899
|
T | C | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+28220T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454899 | ||||||
| chr7:114454950
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0004g0136a0001c0001t0004g0137others(3): Show | 6 | HG00642.hp2 HG01257.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+28271C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114454950 | ||||||
| chr7:114455019
|
TA | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0011g0060others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+28350delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114455019 | |||||
| chr7:114455020
|
A | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+28341A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455020 | ||||||
| chr7:114455069
|
G | A | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+28390G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455069 | ||||||
| chr7:114455128
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.168+28449A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455128 | ||||||
| chr7:114455223
|
C | A | 5 | a0001c0001t0001g0101a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+28544C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455223 | ||||||
| chr7:114455257
|
C | A | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.168+28578C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455257 | ||||||
| chr7:114455501
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+28822A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455501 | ||||||
| chr7:114455572
|
C | T | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+28893C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455572 | ||||||
| chr7:114455661
|
T | G | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.168+28982T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455661 | ||||||
| chr7:114455924
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0014g0146 | 2 | HG01361.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.168+29245A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114455924 | ||||||
| chr7:114456036
|
C | G | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+29357C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114456036 | ||||||
| chr7:114456302
|
G | A | 7 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0014g0146others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+29623G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114456302 | ||||||
| chr7:114456463
|
T | C | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.168+29784T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114456463 | ||||||
| chr7:114456630
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.168+29951G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114456630 | ||||||
| chr7:114456668
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.168+29989G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114456668 | ||||||
| chr7:114456791
|
A | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0089others(58): Show | 61 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.168+30112A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114456791 | ||||||
| chr7:114456927
|
GA | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0089a0001c0001t0002g0077others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.168+30258delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114456927 | |||||
| chr7:114457695
|
G | C | 16 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+31016G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114457695 | ||||||
| chr7:114457699
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+31020C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114457699 | ||||||
| chr7:114457833
|
G | T | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.168+31154G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114457833 | ||||||
| chr7:114457894
|
C | CA | 64 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(61): Show | 64 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.168+31231dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114457894 | |||||
| chr7:114457919
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+31240A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114457919 | ||||||
| chr7:114458190
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+31511A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458190 | ||||||
| chr7:114458200
|
A | G | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.168+31521A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458200 | ||||||
| chr7:114458212
|
GTGT | G | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.168+31538_168+3154 others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114458212 | |||||
| chr7:114458281
|
C | A | 2 | a0001c0001t0004g0129a0001c0001t0006g0130 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.168+31602C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458281 | ||||||
| chr7:114458364
|
T | A | 1 | a0001c0001t0002g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.168+31685T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458364 | ||||||
| chr7:114458471
|
T | G | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.168+31792T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458471 | ||||||
| chr7:114458495
|
A | T | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.168+31816A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458495 | ||||||
| chr7:114458546
|
C | CT | 65 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0041others(62): Show | 65 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.168+31886dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114458546 | |||||
| chr7:114458546
|
CT | C | 5 | a0001c0001t0002g0145a0001c0001t0004g0016a0001c0001t0014g0146others(2): Show | 5 | HG01168.hp1 HG02647.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+31886delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114458546 | |||||
| chr7:114458843
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+32164A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458843 | ||||||
| chr7:114458957
|
G | T | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+32278G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458957 | ||||||
| chr7:114458968
|
C | A | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+32289C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458968 | ||||||
| chr7:114458969
|
T | G | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+32290T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114458969 | ||||||
| chr7:114459173
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.168+32494C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114459173 | ||||||
| chr7:114459598
|
G | T | 2 | a0001c0001t0007g0140a0001c0001t0007g0141 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.168+32919G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114459598 | ||||||
| chr7:114459639
|
G | A | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168+32960G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114459639 | ||||||
| chr7:114459738
|
T | G | 1 | a0001c0001t0004g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.168+33059T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114459738 | ||||||
| chr7:114460121
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+33442T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460121 | ||||||
| chr7:114460168
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+33489C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460168 | ||||||
| chr7:114460246
|
G | T | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+33567G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460246 | ||||||
| chr7:114460520
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+33841C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460520 | ||||||
| chr7:114460547
|
A | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00642.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.168+33868A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460547 | ||||||
| chr7:114460819
|
G | A | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+34140G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460819 | ||||||
| chr7:114460954
|
T | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+34275T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460954 | ||||||
| chr7:114460985
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+34306C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114460985 | ||||||
| chr7:114461268
|
C | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+34589C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114461268 | ||||||
| chr7:114461397
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0002g0083 | 2 | HG02523.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.168+34718C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114461397 | ||||||
| chr7:114461813
|
T | C | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+35134T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114461813 | ||||||
| chr7:114461998
|
C | A | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+35319C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114461998 | ||||||
| chr7:114462029
|
A | C | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+35350A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462029 | ||||||
| chr7:114462046
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+35367C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462046 | ||||||
| chr7:114462086
|
C | A | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.168+35407C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462086 | ||||||
| chr7:114462091
|
C | A | 1 | a0001c0001t0003g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.168+35412C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462091 | ||||||
| chr7:114462238
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+35559G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462238 | ||||||
| chr7:114462275
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+35596G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462275 | ||||||
| chr7:114462277
|
G | GA | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0026others(76): Show | 80 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.168+35623dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462277 | |||||
| chr7:114462277
|
G | GAA | 36 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0061others(33): Show | 36 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.168+35622_168+3562 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462277 | |||||
| chr7:114462277
|
G | GAAA | 5 | a0001c0001t0001g0164a0001c0001t0002g0096a0001c0001t0003g0148others(2): Show | 5 | HG00642.hp1 HG01106.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+35621_168+3562 others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462277 | |||||
| chr7:114462277
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+35613_168+3562 others(15): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462277 | |||||
| chr7:114462277
|
GAAAAAAA others(5): Show |
G | 3 | a0001c0001t0001g0118a0001c0001t0015g0092a0001c0001t0024g0132 | 3 | HG02622.hp1 HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.168+35612_168+3562 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462277 | |||||
| chr7:114462310
|
A | G | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.168+35631A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462310 | ||||||
| chr7:114462366
|
C | CT | 46 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0089others(43): Show | 46 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.168+35710dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462366 | |||||
| chr7:114462366
|
C | CTTTTTT | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0165others(4): Show | 7 | HG01070.hp1 HG01106.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+35705_168+3571 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462366 | |||||
| chr7:114462366
|
C | CTTTTTTT | 5 | a0001c0001t0001g0135a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+35704_168+3571 others(11): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462366 | |||||
| chr7:114462366
|
CT | C | 22 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0127others(19): Show | 23 | HG00140.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.168+35710delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114462366 | |||||
| chr7:114462393
|
A | C | 1 | a0001c0001t0004g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.168+35714A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462393 | ||||||
| chr7:114462520
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.168+35841T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462520 | ||||||
| chr7:114462628
|
C | T | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+35949C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462628 | ||||||
| chr7:114462958
|
A | G | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+36279A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114462958 | ||||||
| chr7:114463025
|
A | G | 1 | a0001c0001t0022g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168+36346A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463025 | ||||||
| chr7:114463096
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168+36417A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463096 | ||||||
| chr7:114463153
|
G | C | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+36474G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463153 | ||||||
| chr7:114463254
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+36575G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463254 | ||||||
| chr7:114463371
|
C | G | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+36692C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463371 | ||||||
| chr7:114463509
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+36830T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463509 | ||||||
| chr7:114463546
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.168+36867G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463546 | ||||||
| chr7:114463656
|
A | G | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+36977A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463656 | ||||||
| chr7:114463749
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0006g0070a0001c0001t0006g0117others(1): Show | 4 | HG01496.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+37070C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463749 | ||||||
| chr7:114463758
|
C | T | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+37079C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463758 | ||||||
| chr7:114463816
|
C | T | 3 | a0001c0001t0004g0081a0001c0001t0004g0088a0001c0001t0029g0079 | 3 | HG00621.hp2 NA18952.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.168+37137C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463816 | ||||||
| chr7:114463871
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.168+37192A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463871 | ||||||
| chr7:114463957
|
T | A | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+37278T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114463957 | ||||||
| chr7:114464322
|
AG | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+37646delG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114464322 | |||||
| chr7:114464334
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.168+37655T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464334 | ||||||
| chr7:114464340
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.168+37661T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464340 | ||||||
| chr7:114464353
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+37674G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464353 | ||||||
| chr7:114464458
|
T | C | 2 | a0001c0001t0002g0017a0001c0001t0023g0018 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.168+37779T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464458 | ||||||
| chr7:114464464
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.168+37785G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464464 | ||||||
| chr7:114464759
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0003g0076 | 2 | HG02071.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.168+38080G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464759 | ||||||
| chr7:114464907
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+38228C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114464907 | ||||||
| chr7:114465108
|
G | T | 1 | a0001c0001t0003g0134 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.168+38429G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114465108 | ||||||
| chr7:114465165
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+38486G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114465165 | ||||||
| chr7:114465398
|
T | A | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+38719T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114465398 | ||||||
| chr7:114466095
|
C | A | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+39416C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114466095 | ||||||
| chr7:114466181
|
A | T | 1 | a0001c0001t0003g0050 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.168+39502A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114466181 | ||||||
| chr7:114466796
|
A | G | 27 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0100others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+40117A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114466796 | ||||||
| chr7:114466947
|
G | T | 12 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0003g0039others(9): Show | 12 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+40268G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114466947 | ||||||
| chr7:114467001
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0006g0121a0001c0001t0006g0122 | 3 | HG02818.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.168+40322C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467001 | ||||||
| chr7:114467130
|
C | T | 1 | a0001c0001t0006g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+40451C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467130 | ||||||
| chr7:114467416
|
A | G | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+40737A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467416 | ||||||
| chr7:114467539
|
C | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 162 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.168+40860C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467539 | ||||||
| chr7:114467564
|
A | G | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+40885A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467564 | ||||||
| chr7:114467646
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+40967A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467646 | ||||||
| chr7:114467968
|
G | A | 2 | a0001c0001t0004g0081a0001c0001t0004g0088 | 2 | HG00621.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.168+41289G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467968 | ||||||
| chr7:114467973
|
C | G | 4 | a0001c0001t0001g0118a0001c0001t0015g0092a0001c0001t0016g0169others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+41294C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114467973 | ||||||
| chr7:114468251
|
T | G | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+41572T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468251 | ||||||
| chr7:114468318
|
G | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.168+41639G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468318 | ||||||
| chr7:114468364
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+41685G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468364 | ||||||
| chr7:114468600
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.168+41921C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468600 | ||||||
| chr7:114468768
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+42089C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468768 | ||||||
| chr7:114468774
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+42095C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468774 | ||||||
| chr7:114468805
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.168+42126A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468805 | ||||||
| chr7:114468947
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.168+42268T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468947 | ||||||
| chr7:114468983
|
A | G | 2 | a0001c0001t0004g0159a0003c0005t0003g0158 | 2 | HG01070.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.168+42304A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114468983 | ||||||
| chr7:114469294
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.168+42615A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469294 | ||||||
| chr7:114469301
|
A | G | 3 | a0001c0001t0002g0082a0001c0001t0003g0059a0001c0001t0004g0075 | 3 | HG03688.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.168+42622A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469301 | ||||||
| chr7:114469483
|
A | G | 1 | a0001c0001t0003g0050 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.168+42804A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469483 | ||||||
| chr7:114469537
|
A | G | 1 | a0001c0001t0008g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.168+42858A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469537 | ||||||
| chr7:114469538
|
T | C | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+42859T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469538 | ||||||
| chr7:114469568
|
T | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+42889T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469568 | ||||||
| chr7:114469666
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.168+42987T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469666 | ||||||
| chr7:114469949
|
C | G | 2 | a0001c0001t0003g0039a0001c0001t0020g0047 | 2 | HG00423.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.168+43270C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114469949 | ||||||
| chr7:114470138
|
G | A | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.168+43459G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470138 | ||||||
| chr7:114470203
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+43524G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470203 | ||||||
| chr7:114470393
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.168+43714C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470393 | ||||||
| chr7:114470461
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.168+43782G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470461 | ||||||
| chr7:114470511
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+43832G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470511 | ||||||
| chr7:114470513
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.168+43834C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470513 | ||||||
| chr7:114470571
|
G | A | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+43892G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114470571 | ||||||
| chr7:114471151
|
C | A | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.168+44472C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471151 | ||||||
| chr7:114471237
|
T | C | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+44558T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471237 | ||||||
| chr7:114471239
|
A | G | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+44560A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471239 | ||||||
| chr7:114471258
|
G | A | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+44579G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471258 | ||||||
| chr7:114471450
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.168+44771G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471450 | ||||||
| chr7:114471716
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0004g0032 | 2 | HG02293.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.168+45037G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471716 | ||||||
| chr7:114471725
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+45046G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471725 | ||||||
| chr7:114471766
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+45087A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471766 | ||||||
| chr7:114471831
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.168+45152G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114471831 | ||||||
| chr7:114471962
|
GA | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0111a0001c0001t0001g0135others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+45299delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114471962 | |||||
| chr7:114472195
|
C | G | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+45516C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472195 | ||||||
| chr7:114472330
|
C | T | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+45651C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472330 | ||||||
| chr7:114472345
|
C | A | 1 | a0001c0001t0003g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.168+45666C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472345 | ||||||
| chr7:114472345
|
C | CT | 7 | a0001c0001t0002g0027a0001c0001t0003g0015a0001c0001t0003g0067others(4): Show | 7 | HG00597.hp1 HG01981.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+45682dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114472345 | |||||
| chr7:114472451
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0015g0092a0001c0001t0016g0169others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+45772T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472451 | ||||||
| chr7:114472457
|
T | C | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+45778T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472457 | ||||||
| chr7:114472505
|
T | C | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+45826T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472505 | ||||||
| chr7:114472599
|
C | T | 1 | a0001c0001t0027g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.168+45920C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472599 | ||||||
| chr7:114472931
|
A | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+46252A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472931 | ||||||
| chr7:114472995
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.168+46316T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114472995 | ||||||
| chr7:114473219
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.168+46540G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114473219 | ||||||
| chr7:114473431
|
G | A | 4 | a0001c0001t0001g0118a0001c0001t0015g0092a0001c0001t0016g0169others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+46752G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114473431 | ||||||
| chr7:114473471
|
C | T | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+46792C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114473471 | ||||||
| chr7:114473629
|
G | C | 1 | a0001c0001t0005g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+46950G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114473629 | ||||||
| chr7:114473691
|
A | T | 27 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0100others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+47012A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114473691 | ||||||
| chr7:114473885
|
T | TA | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+47216dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114473885 | |||||
| chr7:114474151
|
G | C | 1 | a0001c0001t0001g0007 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.168+47472G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114474151 | ||||||
| chr7:114474169
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.168+47490A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114474169 | ||||||
| chr7:114474455
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+47776A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114474455 | ||||||
| chr7:114474812
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+48133G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114474812 | ||||||
| chr7:114474835
|
A | T | 2 | a0001c0001t0002g0084a0001c0001t0003g0086 | 2 | NA18961.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.168+48156A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114474835 | ||||||
| chr7:114474994
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.168+48315A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114474994 | ||||||
| chr7:114475177
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.168+48498A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114475177 | ||||||
| chr7:114475200
|
G | A | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.168+48521G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114475200 | ||||||
| chr7:114475213
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.168+48534T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114475213 | ||||||
| chr7:114475388
|
T | G | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.168+48709T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114475388 | ||||||
| chr7:114475696
|
C | T | 2 | a0001c0001t0006g0117a0001c0001t0031g0114 | 2 | HG01496.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.168+49017C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114475696 | ||||||
| chr7:114475835
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+49156A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114475835 | ||||||
| chr7:114476088
|
G | GT | 19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(16): Show | 19 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+49423dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114476088 | |||||
| chr7:114476088
|
G | T | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168+49409G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114476088 | ||||||
| chr7:114476826
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.168+50147G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114476826 | ||||||
| chr7:114477406
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+50727A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114477406 | ||||||
| chr7:114477714
|
C | T | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+51035C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114477714 | ||||||
| chr7:114477722
|
C | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+51043C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114477722 | ||||||
| chr7:114477742
|
T | G | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+51063T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114477742 | ||||||
| chr7:114477807
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.168+51128G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114477807 | ||||||
| chr7:114478049
|
A | C | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.168+51370A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478049 | ||||||
| chr7:114478057
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.168+51378C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478057 | ||||||
| chr7:114478165
|
G | A | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+51486G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478165 | ||||||
| chr7:114478185
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+51506A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478185 | ||||||
| chr7:114478224
|
T | A | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+51545T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478224 | ||||||
| chr7:114478244
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.168+51565A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478244 | ||||||
| chr7:114478268
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.168+51589G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478268 | ||||||
| chr7:114478290
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.168+51611G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478290 | ||||||
| chr7:114478581
|
G | A | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.168+51902G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114478581 | ||||||
| chr7:114479019
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.168+52340G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479019 | ||||||
| chr7:114479375
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.168+52696G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479375 | ||||||
| chr7:114479386
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.168+52707C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479386 | ||||||
| chr7:114479426
|
G | T | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.168+52747G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479426 | ||||||
| chr7:114479430
|
T | C | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+52751T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479430 | ||||||
| chr7:114479541
|
G | GA | 16 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.168+52876dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114479541 | |||||
| chr7:114479541
|
GA | G | 16 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0002g0054others(13): Show | 16 | HG00597.hp2 HG01496.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+52876delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114479541 | |||||
| chr7:114479542
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(1): Show | 4 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+52863A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479542 | ||||||
| chr7:114479543
|
A | G | 2 | a0001c0001t0006g0117a0001c0001t0031g0114 | 2 | HG01496.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.168+52864A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479543 | ||||||
| chr7:114479595
|
G | A | 27 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0100others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+52916G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479595 | ||||||
| chr7:114479651
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+52972G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479651 | ||||||
| chr7:114479657
|
G | C | 1 | a0001c0001t0002g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.168+52978G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479657 | ||||||
| chr7:114479746
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168+53067G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479746 | ||||||
| chr7:114479757
|
A | G | 1 | a0001c0001t0027g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.168+53078A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479757 | ||||||
| chr7:114479834
|
A | G | 12 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0003g0039others(9): Show | 12 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+53155A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479834 | ||||||
| chr7:114479880
|
T | G | 6 | a0001c0001t0003g0134a0001c0001t0004g0136a0001c0001t0004g0137others(3): Show | 6 | HG00642.hp2 HG01069.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+53201T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114479880 | ||||||
| chr7:114480084
|
T | C | 1 | a0001c0001t0005g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.168+53405T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114480084 | ||||||
| chr7:114480104
|
T | G | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+53425T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114480104 | ||||||
| chr7:114480606
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.168+53927C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114480606 | ||||||
| chr7:114480619
|
ATATACAT others(1): Show |
A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+53948_168+5395 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114480619 | |||||
| chr7:114480754
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-53863C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114480754 | ||||||
| chr7:114480755
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.169-53862G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114480755 | ||||||
| chr7:114481130
|
C | CAAT | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-53485_169-5348 others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481130 | |||||
| chr7:114481543
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-53074A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114481543 | ||||||
| chr7:114481568
|
C | A | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-53049C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114481568 | ||||||
| chr7:114481645
|
C | T | 12 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(9): Show | 12 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-52972C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114481645 | ||||||
| chr7:114481712
|
T | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-52905T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114481712 | ||||||
| chr7:114481738
|
G | A | 1 | a0001c0001t0003g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.169-52879G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114481738 | ||||||
| chr7:114481762
|
C | CTCTA | 16 | a0001c0001t0001g0033a0001c0001t0001g0127a0001c0001t0001g0166others(13): Show | 17 | HG00099.hp1 HG00597.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-52809_169-5280 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481762 | |||||
| chr7:114481762
|
C | CTCTATCT others(1): Show |
8 | a0001c0001t0001g0118a0001c0001t0001g0164a0001c0001t0002g0017others(5): Show | 8 | HG00642.hp1 HG01106.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-52813_169-5280 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481762 | |||||
| chr7:114481762
|
CTCTA | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 73 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.169-52809_169-5280 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481762 | |||||
| chr7:114481762
|
CTCTATCT others(1): Show |
C | 4 | a0001c0001t0003g0050a0001c0001t0004g0051a0001c0001t0011g0060others(1): Show | 4 | HG03041.hp2 HG03225.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-52813_169-5280 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481762 | |||||
| chr7:114481762
|
CTCTATCT others(5): Show |
C | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169-52817_169-5280 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481762 | |||||
| chr7:114481794
|
A | ATCTG | 2 | a0001c0001t0003g0091a0001c0001t0004g0074 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.169-52820_169-5281 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481794 | |||||
| chr7:114481800
|
C | CTATCTAT others(5): Show |
1 | a0001c0001t0005g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169-52805_169-5279 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481800 | |||||
| chr7:114481800
|
CTATCTAT others(5): Show |
C | 2 | a0001c0001t0016g0169a0001c0001t0019g0095 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.169-52805_169-5279 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114481800 | |||||
| chr7:114481848
|
T | C | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.169-52769T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114481848 | ||||||
| chr7:114482451
|
C | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0001g0127others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.169-52166C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114482451 | ||||||
| chr7:114482578
|
C | G | 1 | a0001c0001t0028g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.169-52039C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114482578 | ||||||
| chr7:114482708
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.169-51909T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114482708 | ||||||
| chr7:114483198
|
A | G | 2 | a0001c0002t0002g0102a0001c0002t0005g0103 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.169-51419A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114483198 | ||||||
| chr7:114483253
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.169-51364C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114483253 | ||||||
| chr7:114483325
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.169-51292C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114483325 | ||||||
| chr7:114483434
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.169-51183T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114483434 | ||||||
| chr7:114483545
|
G | T | 2 | a0001c0001t0002g0084a0001c0001t0003g0086 | 2 | NA18961.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.169-51072G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114483545 | ||||||
| chr7:114484187
|
G | T | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-50430G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114484187 | ||||||
| chr7:114484216
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-50401A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114484216 | ||||||
| chr7:114484589
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169-50028A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114484589 | ||||||
| chr7:114484605
|
C | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-50012C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114484605 | ||||||
| chr7:114484771
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-49846G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114484771 | ||||||
| chr7:114484931
|
A | G | 12 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(9): Show | 12 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-49686A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114484931 | ||||||
| chr7:114485213
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-49404T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485213 | ||||||
| chr7:114485368
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-49249A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485368 | ||||||
| chr7:114485455
|
A | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.169-49162A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485455 | ||||||
| chr7:114485465
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-49152G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485465 | ||||||
| chr7:114485525
|
AG | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.169-49089delG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114485525 | |||||
| chr7:114485655
|
G | A | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-48962G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485655 | ||||||
| chr7:114485918
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-48699C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485918 | ||||||
| chr7:114485937
|
G | A | 1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169-48680G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485937 | ||||||
| chr7:114485966
|
T | G | 2 | a0001c0001t0004g0131a0001c0001t0021g0128 | 2 | HG00140.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.169-48651T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485966 | ||||||
| chr7:114485977
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169-48640G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114485977 | ||||||
| chr7:114486083
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-48534A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486083 | ||||||
| chr7:114486178
|
A | G | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.169-48439A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486178 | ||||||
| chr7:114486267
|
C | A | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-48350C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486267 | ||||||
| chr7:114486344
|
G | A | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-48273G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486344 | ||||||
| chr7:114486351
|
A | T | 1 | a0001c0001t0005g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169-48266A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486351 | ||||||
| chr7:114486377
|
C | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 162 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.169-48240C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486377 | ||||||
| chr7:114486470
|
AC | A | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-48143delC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114486470 | |||||
| chr7:114486724
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.169-47893G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114486724 | ||||||
| chr7:114487100
|
A | G | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-47517A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487100 | ||||||
| chr7:114487152
|
G | A | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-47465G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487152 | ||||||
| chr7:114487277
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-47340G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487277 | ||||||
| chr7:114487279
|
G | A | 1 | a0001c0001t0003g0015 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.169-47338G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487279 | ||||||
| chr7:114487314
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.169-47303C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487314 | ||||||
| chr7:114487315
|
G | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-47302G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487315 | ||||||
| chr7:114487421
|
G | A | 2 | a0001c0001t0004g0131a0001c0001t0021g0128 | 2 | HG00140.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.169-47196G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487421 | ||||||
| chr7:114487839
|
G | A | 5 | a0001c0001t0004g0136a0001c0001t0004g0137a0001c0001t0004g0138others(2): Show | 5 | HG00642.hp2 HG01257.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-46778G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114487839 | ||||||
| chr7:114488099
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-46518G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114488099 | ||||||
| chr7:114488112
|
C | T | 27 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0100others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.169-46505C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114488112 | ||||||
| chr7:114488251
|
A | AC | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-46361dupC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114488251 | |||||
| chr7:114488611
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169-46006G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114488611 | ||||||
| chr7:114488937
|
G | A | 10 | a0001c0001t0002g0172a0001c0001t0003g0134a0001c0001t0004g0136others(7): Show | 10 | HG00642.hp2 HG01069.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-45680G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114488937 | ||||||
| chr7:114489005
|
A | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-45612A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114489005 | ||||||
| chr7:114489082
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-45535G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114489082 | ||||||
| chr7:114489401
|
A | G | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169-45216A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114489401 | ||||||
| chr7:114489448
|
C | T | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-45169C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114489448 | ||||||
| chr7:114489973
|
T | C | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-44644T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114489973 | ||||||
| chr7:114490047
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.169-44570A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490047 | ||||||
| chr7:114490120
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-44497A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490120 | ||||||
| chr7:114490373
|
T | C | 3 | a0001c0001t0004g0081a0001c0001t0004g0088a0001c0001t0029g0079 | 3 | HG00621.hp2 NA18952.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.169-44244T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490373 | ||||||
| chr7:114490432
|
G | A | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-44185G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490432 | ||||||
| chr7:114490955
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-43662G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490955 | ||||||
| chr7:114490956
|
T | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-43661T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490956 | ||||||
| chr7:114490968
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0106 | 2 | HG01074.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.169-43649G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490968 | ||||||
| chr7:114490974
|
A | C | 2 | a0001c0001t0005g0119a0001c0001t0005g0120 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.169-43643A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114490974 | ||||||
| chr7:114491008
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-43609T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491008 | ||||||
| chr7:114491307
|
T | C | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169-43310T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491307 | ||||||
| chr7:114491376
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169-43241G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491376 | ||||||
| chr7:114491385
|
C | A | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-43232C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491385 | ||||||
| chr7:114491400
|
A | C | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169-43217A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491400 | ||||||
| chr7:114491456
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.169-43161T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491456 | ||||||
| chr7:114491458
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.169-43159C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491458 | ||||||
| chr7:114491534
|
G | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-43083G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491534 | ||||||
| chr7:114491585
|
T | C | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-43032T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491585 | ||||||
| chr7:114491591
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-43026T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491591 | ||||||
| chr7:114491595
|
G | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-43022G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491595 | ||||||
| chr7:114491764
|
C | G | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-42853C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491764 | ||||||
| chr7:114491870
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-42747C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491870 | ||||||
| chr7:114491977
|
C | G | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-42640C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114491977 | ||||||
| chr7:114492002
|
A | G | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.169-42615A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492002 | ||||||
| chr7:114492105
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.169-42512T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492105 | ||||||
| chr7:114492280
|
C | T | 7 | a0001c0001t0001g0160a0001c0001t0003g0157a0001c0002t0001g0097others(4): Show | 7 | HG02683.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-42337C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492280 | ||||||
| chr7:114492283
|
G | C | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-42334G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492283 | ||||||
| chr7:114492304
|
C | T | 11 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-42313C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492304 | ||||||
| chr7:114492320
|
C | T | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.169-42297C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492320 | ||||||
| chr7:114492498
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-42119G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492498 | ||||||
| chr7:114492659
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-41958T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492659 | ||||||
| chr7:114492661
|
C | G | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-41956C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492661 | ||||||
| chr7:114492860
|
G | C | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-41757G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492860 | ||||||
| chr7:114492930
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169-41687G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114492930 | ||||||
| chr7:114493310
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.169-41307C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114493310 | ||||||
| chr7:114493435
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-41182A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114493435 | ||||||
| chr7:114493642
|
G | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0024others(2): Show | 5 | HG00597.hp2 NA18951.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-40975G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114493642 | ||||||
| chr7:114493658
|
ACT | A | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.169-40941_169-4094 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114493658 | |||||
| chr7:114493748
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-40869T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114493748 | ||||||
| chr7:114493925
|
G | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0164others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-40692G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114493925 | ||||||
| chr7:114494099
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-40518T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494099 | ||||||
| chr7:114494158
|
T | G | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-40459T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494158 | ||||||
| chr7:114494507
|
C | T | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.169-40110C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494507 | ||||||
| chr7:114494558
|
A | G | 1 | a0001c0001t0030g0068 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.169-40059A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494558 | ||||||
| chr7:114494596
|
G | C | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.169-40021G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494596 | ||||||
| chr7:114494663
|
T | C | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-39954T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494663 | ||||||
| chr7:114494753
|
A | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-39864A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494753 | ||||||
| chr7:114494763
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0005g0094 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.169-39854C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494763 | ||||||
| chr7:114494979
|
T | C | 1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169-39638T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114494979 | ||||||
| chr7:114495454
|
T | G | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-39163T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495454 | ||||||
| chr7:114495460
|
C | G | 1 | a0001c0001t0002g0084 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.169-39157C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495460 | ||||||
| chr7:114495481
|
C | T | 1 | a0001c0001t0016g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.169-39136C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495481 | ||||||
| chr7:114495483
|
C | CT | 9 | a0001c0001t0002g0019a0001c0001t0003g0045a0001c0001t0003g0049others(6): Show | 9 | HG00099.hp2 HG00673.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-39104dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
C | T | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-39134C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495483 | ||||||
| chr7:114495483
|
CT | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 55 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.169-39104delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTT | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0108others(3): Show | 6 | HG01074.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-39105_169-3910 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTTTT | C | 5 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(2): Show | 5 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-39107_169-3910 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTTTTTTT others(1): Show |
C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-39111_169-3910 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.169-39113_169-3910 others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-39114_169-3910 others(15): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTTTTTTT others(5): Show |
C | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.169-39115_169-3910 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495483
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-39116_169-3910 others(17): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114495483 | |||||
| chr7:114495485
|
T | C | 14 | a0001c0001t0001g0089a0001c0001t0001g0105a0001c0001t0001g0127others(11): Show | 14 | HG00423.hp2 HG00673.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-39132T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495485 | ||||||
| chr7:114495486
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(37): Show | 40 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.169-39131T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495486 | ||||||
| chr7:114495487
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0005g0107 | 3 | HG01074.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.169-39130T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495487 | ||||||
| chr7:114495493
|
T | C | 2 | a0001c0001t0004g0088a0001c0001t0004g0171 | 2 | HG01169.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.169-39124T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495493 | ||||||
| chr7:114495497
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.169-39120T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495497 | ||||||
| chr7:114495662
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.169-38955T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114495662 | ||||||
| chr7:114496327
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169-38290A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114496327 | ||||||
| chr7:114496513
|
T | C | 2 | a0001c0001t0004g0131a0001c0001t0021g0128 | 2 | HG00140.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.169-38104T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114496513 | ||||||
| chr7:114497413
|
C | T | 3 | a0001c0001t0004g0081a0001c0001t0004g0088a0001c0001t0029g0079 | 3 | HG00621.hp2 NA18952.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.169-37204C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114497413 | ||||||
| chr7:114497665
|
G | GTAAA | 4 | a0001c0001t0001g0033a0001c0001t0001g0104a0001c0001t0002g0053others(1): Show | 4 | HG02040.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-36911_169-3690 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114497665 | |||||
| chr7:114497665
|
GTAAA | G | 83 | a0001c0001t0001g0006a0001c0001t0001g0065a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.169-36911_169-3690 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114497665 | |||||
| chr7:114497665
|
GTAAATAA others(1): Show |
G | 24 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(21): Show | 24 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.169-36915_169-3690 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114497665 | |||||
| chr7:114497665
|
GTAAATAA others(5): Show |
G | 2 | a0001c0001t0001g0165a0001c0001t0004g0042 | 2 | HG01257.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.169-36919_169-3690 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114497665 | |||||
| chr7:114497665
|
GTAAATAA others(9): Show |
G | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-36923_169-3690 others(20): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114497665 | |||||
| chr7:114497665
|
GTAAATAA others(13): Show |
G | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-36927_169-3690 others(24): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114497665 | |||||
| chr7:114497885
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-36732A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114497885 | ||||||
| chr7:114498055
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.169-36562G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498055 | ||||||
| chr7:114498057
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.169-36560A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498057 | ||||||
| chr7:114498083
|
T | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0164others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-36534T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498083 | ||||||
| chr7:114498132
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-36485G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498132 | ||||||
| chr7:114498187
|
A | G | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-36430A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498187 | ||||||
| chr7:114498211
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-36406A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498211 | ||||||
| chr7:114498239
|
G | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-36378G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498239 | ||||||
| chr7:114498290
|
A | G | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-36327A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498290 | ||||||
| chr7:114498696
|
G | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-35921G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498696 | ||||||
| chr7:114498741
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-35876G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114498741 | ||||||
| chr7:114499440
|
G | A | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-35177G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114499440 | ||||||
| chr7:114499629
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.169-34988G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114499629 | ||||||
| chr7:114499733
|
C | T | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-34884C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114499733 | ||||||
| chr7:114499778
|
C | T | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-34839C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114499778 | ||||||
| chr7:114499824
|
C | T | 2 | a0001c0001t0003g0091a0001c0001t0004g0074 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.169-34793C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114499824 | ||||||
| chr7:114499984
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0006g0070a0001c0001t0006g0117others(1): Show | 4 | HG01496.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-34633G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114499984 | ||||||
| chr7:114500039
|
C | T | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-34578C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500039 | ||||||
| chr7:114500203
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.169-34414A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500203 | ||||||
| chr7:114500215
|
C | CA | 15 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0090others(12): Show | 15 | HG00099.hp1 HG01106.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.169-34382dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114500215 | |||||
| chr7:114500215
|
CA | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0152others(12): Show | 15 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.169-34382delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114500215 | |||||
| chr7:114500249
|
A | G | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-34368A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500249 | ||||||
| chr7:114500285
|
T | TA | 2 | a0001c0001t0005g0119a0001c0001t0005g0120 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.169-34331dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114500285 | |||||
| chr7:114500472
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.169-34145T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500472 | ||||||
| chr7:114500808
|
C | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-33809C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500808 | ||||||
| chr7:114500894
|
C | G | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-33723C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500894 | ||||||
| chr7:114500919
|
C | T | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-33698C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114500919 | ||||||
| chr7:114501148
|
G | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-33469G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114501148 | ||||||
| chr7:114501731
|
T | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-32886T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114501731 | ||||||
| chr7:114501745
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-32872A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114501745 | ||||||
| chr7:114501802
|
T | C | 1 | a0001c0003t0006g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.169-32815T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114501802 | ||||||
| chr7:114502099
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-32518C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502099 | ||||||
| chr7:114502108
|
T | C | 1 | a0001c0001t0004g0032 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.169-32509T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502108 | ||||||
| chr7:114502195
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-32422A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502195 | ||||||
| chr7:114502333
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.169-32284G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502333 | ||||||
| chr7:114502395
|
T | C | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-32222T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502395 | ||||||
| chr7:114502412
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-32205G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502412 | ||||||
| chr7:114502503
|
G | C | 2 | a0001c0001t0011g0060a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-32114G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114502503 | ||||||
| chr7:114503214
|
A | AT | 6 | a0001c0001t0001g0160a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-31396dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114503214 | |||||
| chr7:114503222
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.169-31395G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503222 | ||||||
| chr7:114503319
|
T | A | 5 | a0001c0001t0001g0144a0001c0001t0004g0129a0001c0001t0004g0131others(2): Show | 5 | HG00140.hp2 HG01361.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-31298T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503319 | ||||||
| chr7:114503352
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-31265C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503352 | ||||||
| chr7:114503467
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.169-31150T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503467 | ||||||
| chr7:114503556
|
C | T | 2 | a0001c0001t0001g0160a0002c0004t0012g0063 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.169-31061C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503556 | ||||||
| chr7:114503596
|
T | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(58): Show | 61 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.169-31021T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503596 | ||||||
| chr7:114503625
|
T | A | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-30992T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503625 | ||||||
| chr7:114503695
|
G | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-30922G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503695 | ||||||
| chr7:114503696
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-30921C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503696 | ||||||
| chr7:114503964
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.169-30653C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114503964 | ||||||
| chr7:114504017
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0004g0014 | 3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.169-30600A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114504017 | ||||||
| chr7:114504519
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-30098C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114504519 | ||||||
| chr7:114504564
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169-30053A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114504564 | ||||||
| chr7:114504635
|
CA | C | 10 | a0001c0001t0001g0118a0001c0001t0001g0160a0001c0001t0015g0092others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-29975delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114504635 | |||||
| chr7:114504636
|
A | C | 1 | a0001c0001t0003g0134 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.169-29981A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114504636 | ||||||
| chr7:114505251
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-29366G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505251 | ||||||
| chr7:114505293
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169-29324C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505293 | ||||||
| chr7:114505313
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0023g0018 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.169-29304G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505313 | ||||||
| chr7:114505470
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.169-29147G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505470 | ||||||
| chr7:114505635
|
C | G | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-28982C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505635 | ||||||
| chr7:114505664
|
G | T | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-28953G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505664 | ||||||
| chr7:114505705
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.169-28912T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505705 | ||||||
| chr7:114505740
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.169-28877T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505740 | ||||||
| chr7:114505801
|
A | C | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-28816A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505801 | ||||||
| chr7:114505914
|
T | C | 1 | a0001c0001t0004g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.169-28703T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505914 | ||||||
| chr7:114505924
|
C | A | 2 | a0001c0001t0015g0092a0001c0001t0016g0169 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169-28693C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114505924 | ||||||
| chr7:114506045
|
A | C | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169-28572A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506045 | ||||||
| chr7:114506050
|
AG | A | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-28566delG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506050 | ||||||
| chr7:114506076
|
G | A | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-28541G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506076 | ||||||
| chr7:114506166
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-28451T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506166 | ||||||
| chr7:114506172
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-28445C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506172 | ||||||
| chr7:114506187
|
T | A | 1 | a0001c0001t0003g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.169-28430T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506187 | ||||||
| chr7:114506237
|
A | G | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-28380A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506237 | ||||||
| chr7:114506416
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-28201A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506416 | ||||||
| chr7:114506941
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-27676C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114506941 | ||||||
| chr7:114507000
|
A | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(18): Show | 21 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.169-27617A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507000 | ||||||
| chr7:114507159
|
C | A | 1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169-27458C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507159 | ||||||
| chr7:114507162
|
C | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.169-27455C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507162 | ||||||
| chr7:114507542
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169-27075A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507542 | ||||||
| chr7:114507603
|
T | C | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.169-27014T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507603 | ||||||
| chr7:114507726
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-26891C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507726 | ||||||
| chr7:114507742
|
A | G | 16 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-26875A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114507742 | ||||||
| chr7:114508031
|
G | A | 1 | a0001c0001t0028g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.169-26586G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508031 | ||||||
| chr7:114508103
|
A | T | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-26514A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508103 | ||||||
| chr7:114508114
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-26503T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508114 | ||||||
| chr7:114508133
|
A | T | 7 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-26484A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508133 | ||||||
| chr7:114508188
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.169-26429A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508188 | ||||||
| chr7:114508276
|
C | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.169-26341C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508276 | ||||||
| chr7:114508479
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.169-26138C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508479 | ||||||
| chr7:114508515
|
G | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-26102G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508515 | ||||||
| chr7:114508637
|
A | ATT | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-25980_169-2597 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508637 | ||||||
| chr7:114508730
|
G | T | 1 | a0001c0001t0003g0050 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.169-25887G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508730 | ||||||
| chr7:114508830
|
T | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-25787T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508830 | ||||||
| chr7:114508914
|
A | G | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-25703A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114508914 | ||||||
| chr7:114509003
|
G | A | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-25614G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114509003 | ||||||
| chr7:114509169
|
C | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-25448C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114509169 | ||||||
| chr7:114509280
|
T | TTTTTG | 32 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(29): Show | 33 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.169-25322_169-2531 others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114509280 | |||||
| chr7:114509521
|
T | C | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-25096T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114509521 | ||||||
| chr7:114509670
|
T | TG | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0046others(68): Show | 71 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-24937dupG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114509670 | |||||
| chr7:114509673
|
G | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-24944G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114509673 | ||||||
| chr7:114510031
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-24586T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114510031 | ||||||
| chr7:114510166
|
A | T | 3 | a0001c0001t0002g0172a0001c0001t0005g0133a0001c0001t0009g0173 | 3 | HG02055.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.169-24451A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114510166 | ||||||
| chr7:114510394
|
A | C | 16 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-24223A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114510394 | ||||||
| chr7:114510467
|
T | A | 1 | a0001c0001t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169-24150T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114510467 | ||||||
| chr7:114510587
|
T | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-24030T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114510587 | ||||||
| chr7:114510669
|
C | G | 16 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-23948C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114510669 | ||||||
| chr7:114511189
|
C | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-23428C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114511189 | ||||||
| chr7:114511216
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0002g0083 | 2 | HG02523.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.169-23401G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114511216 | ||||||
| chr7:114511240
|
G | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-23377G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114511240 | ||||||
| chr7:114511364
|
A | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-23253A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114511364 | ||||||
| chr7:114511597
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.169-23020T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114511597 | ||||||
| chr7:114511966
|
T | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.169-22651T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114511966 | ||||||
| chr7:114512070
|
T | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-22547T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114512070 | ||||||
| chr7:114512411
|
TTAAG | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-22202_169-2219 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114512411 | |||||
| chr7:114512434
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-22183G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114512434 | ||||||
| chr7:114512497
|
C | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-22120C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114512497 | ||||||
| chr7:114512779
|
A | C | 1 | a0001c0001t0003g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169-21838A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114512779 | ||||||
| chr7:114512868
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-21749G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114512868 | ||||||
| chr7:114512919
|
C | T | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-21698C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114512919 | ||||||
| chr7:114513036
|
C | G | 2 | a0001c0001t0003g0091a0001c0001t0004g0074 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.169-21581C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513036 | ||||||
| chr7:114513048
|
T | C | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-21569T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513048 | ||||||
| chr7:114513196
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-21421G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513196 | ||||||
| chr7:114513220
|
A | G | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-21397A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513220 | ||||||
| chr7:114513480
|
G | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-21137G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513480 | ||||||
| chr7:114513624
|
T | G | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-20993T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513624 | ||||||
| chr7:114513718
|
T | C | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-20899T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114513718 | ||||||
| chr7:114514043
|
A | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0002g0077others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.169-20574A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514043 | ||||||
| chr7:114514065
|
T | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-20552T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514065 | ||||||
| chr7:114514086
|
T | TAC | 7 | a0001c0001t0001g0065a0001c0001t0001g0101a0001c0001t0002g0025others(4): Show | 7 | HG02071.hp2 HG02523.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-20500_169-2049 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514086 | |||||
| chr7:114514086
|
TAC | T | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.169-20500_169-2049 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514086 | |||||
| chr7:114514086
|
TACAC | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0152a0001c0001t0001g0153others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-20502_169-2049 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514086 | |||||
| chr7:114514086
|
TACACAC | T | 7 | a0001c0001t0001g0118a0001c0001t0001g0144a0001c0001t0002g0096others(4): Show | 7 | HG01515.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-20504_169-2049 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514086 | |||||
| chr7:114514086
|
TACACACA others(1): Show |
T | 16 | a0001c0001t0001g0127a0001c0001t0002g0082a0001c0001t0002g0087others(13): Show | 16 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.169-20506_169-2049 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514086 | |||||
| chr7:114514086
|
TACACACA others(3): Show |
T | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(39): Show | 42 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.169-20508_169-2049 others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514086 | |||||
| chr7:114514090
|
C | CACACAA | 2 | a0001c0002t0002g0102a0001c0002t0005g0103 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.169-20522_169-2052 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514090 | |||||
| chr7:114514092
|
C | CACAA | 3 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098 | 3 | HG02895.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.169-20522_169-2052 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114514092 | |||||
| chr7:114514138
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.169-20479C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514138 | ||||||
| chr7:114514167
|
T | C | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-20450T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514167 | ||||||
| chr7:114514441
|
C | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-20176C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514441 | ||||||
| chr7:114514477
|
T | TA | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.169-20140_169-2013 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514477 | ||||||
| chr7:114514634
|
G | C | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-19983G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514634 | ||||||
| chr7:114514657
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-19960T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514657 | ||||||
| chr7:114514680
|
A | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-19937A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514680 | ||||||
| chr7:114514758
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.169-19859A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514758 | ||||||
| chr7:114514783
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.169-19834T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514783 | ||||||
| chr7:114514839
|
G | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-19778G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514839 | ||||||
| chr7:114514874
|
C | G | 19 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(16): Show | 20 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.169-19743C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114514874 | ||||||
| chr7:114515265
|
T | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-19352T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515265 | ||||||
| chr7:114515282
|
G | T | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.169-19335G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515282 | ||||||
| chr7:114515288
|
G | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-19329G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515288 | ||||||
| chr7:114515343
|
C | A | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-19274C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515343 | ||||||
| chr7:114515351
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.169-19266C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515351 | ||||||
| chr7:114515403
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-19214T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515403 | ||||||
| chr7:114515404
|
G | A | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-19213G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515404 | ||||||
| chr7:114515405
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-19212C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515405 | ||||||
| chr7:114515433
|
T | G | 3 | a0001c0001t0008g0126a0001c0001t0008g0143a0001c0001t0010g0142 | 3 | HG01515.hp2 HG02293.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.169-19184T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515433 | ||||||
| chr7:114515440
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-19177G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515440 | ||||||
| chr7:114515508
|
G | A | 10 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-19109G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515508 | ||||||
| chr7:114515583
|
A | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-19034A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515583 | ||||||
| chr7:114515642
|
C | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-18975C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114515642 | ||||||
| chr7:114516214
|
A | G | 1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169-18403A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114516214 | ||||||
| chr7:114516557
|
C | G | 1 | a0001c0001t0004g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.169-18060C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114516557 | ||||||
| chr7:114516703
|
GT | G | 12 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-17904delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114516703 | |||||
| chr7:114516739
|
A | C | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-17878A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114516739 | ||||||
| chr7:114516870
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169-17747A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114516870 | ||||||
| chr7:114517017
|
C | CT | 6 | a0001c0001t0005g0119a0001c0001t0019g0095a0001c0002t0001g0097others(3): Show | 6 | HG01243.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-17589dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114517017 | |||||
| chr7:114517216
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.169-17401G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517216 | ||||||
| chr7:114517285
|
C | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-17332C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517285 | ||||||
| chr7:114517538
|
C | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-17079C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517538 | ||||||
| chr7:114517544
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.169-17073G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517544 | ||||||
| chr7:114517551
|
G | C | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-17066G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517551 | ||||||
| chr7:114517599
|
T | G | 32 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(29): Show | 33 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.169-17018T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517599 | ||||||
| chr7:114517857
|
G | A | 9 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-16760G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114517857 | ||||||
| chr7:114518002
|
C | A | 1 | a0001c0001t0003g0134 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.169-16615C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518002 | ||||||
| chr7:114518029
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.169-16588C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518029 | ||||||
| chr7:114518264
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.169-16353C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518264 | ||||||
| chr7:114518265
|
G | A | 1 | a0001c0001t0008g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.169-16352G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518265 | ||||||
| chr7:114518307
|
G | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-16310G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518307 | ||||||
| chr7:114518394
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-16223C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518394 | ||||||
| chr7:114518422
|
T | A | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-16195T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518422 | ||||||
| chr7:114518624
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169-15993T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518624 | ||||||
| chr7:114518687
|
G | C | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-15930G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518687 | ||||||
| chr7:114518695
|
A | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-15922A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518695 | ||||||
| chr7:114518721
|
G | T | 2 | a0001c0001t0002g0055a0001c0001t0003g0086 | 2 | NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.169-15896G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518721 | ||||||
| chr7:114518899
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 157 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.169-15718G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518899 | ||||||
| chr7:114518917
|
T | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-15700T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518917 | ||||||
| chr7:114518933
|
G | T | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-15684G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114518933 | ||||||
| chr7:114519037
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-15580A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114519037 | ||||||
| chr7:114519187
|
G | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-15430G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114519187 | ||||||
| chr7:114519820
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0004g0014 | 3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.169-14797C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114519820 | ||||||
| chr7:114519865
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.169-14752A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114519865 | ||||||
| chr7:114519881
|
C | T | 1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169-14736C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114519881 | ||||||
| chr7:114519882
|
G | A | 9 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-14735G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114519882 | ||||||
| chr7:114520374
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169-14243T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114520374 | ||||||
| chr7:114520687
|
G | A | 22 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0002g0172others(19): Show | 22 | HG00140.hp2 HG00423.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-13930G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114520687 | ||||||
| chr7:114520746
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-13871G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114520746 | ||||||
| chr7:114520816
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.169-13801G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114520816 | ||||||
| chr7:114521437
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-13180G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114521437 | ||||||
| chr7:114521532
|
C | CA | 67 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.169-13064dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114521532 | |||||
| chr7:114521532
|
C | CAA | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(58): Show | 62 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.169-13065_169-1306 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114521532 | |||||
| chr7:114521558
|
A | G | 1 | a0001c0001t0027g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.169-13059A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114521558 | ||||||
| chr7:114521689
|
A | C | 7 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-12928A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114521689 | ||||||
| chr7:114521735
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.169-12882G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114521735 | ||||||
| chr7:114521757
|
T | A | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.169-12860T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114521757 | ||||||
| chr7:114521761
|
T | TAAAG | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.169-12856_169-1285 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114521761 | ||||||
| chr7:114522685
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.169-11932G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114522685 | ||||||
| chr7:114522749
|
G | A | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-11868G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114522749 | ||||||
| chr7:114523295
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-11322A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114523295 | ||||||
| chr7:114523454
|
A | G | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-11163A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114523454 | ||||||
| chr7:114523486
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0029 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.169-11131G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114523486 | ||||||
| chr7:114524110
|
A | G | 5 | a0001c0001t0004g0136a0001c0001t0004g0137a0001c0001t0004g0138others(2): Show | 5 | HG00642.hp2 HG01257.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-10507A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524110 | ||||||
| chr7:114524117
|
G | A | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10500G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524117 | ||||||
| chr7:114524444
|
C | T | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-10173C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524444 | ||||||
| chr7:114524480
|
A | C | 3 | a0001c0001t0008g0126a0001c0001t0008g0143a0001c0001t0010g0142 | 3 | HG01515.hp2 HG02293.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.169-10137A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524480 | ||||||
| chr7:114524481
|
C | T | 3 | a0001c0001t0008g0126a0001c0001t0008g0143a0001c0001t0010g0142 | 3 | HG01515.hp2 HG02293.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.169-10136C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524481 | ||||||
| chr7:114524482
|
C | T | 3 | a0001c0001t0008g0126a0001c0001t0008g0143a0001c0001t0010g0142 | 3 | HG01515.hp2 HG02293.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.169-10135C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524482 | ||||||
| chr7:114524539
|
T | C | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-10078T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524539 | ||||||
| chr7:114524849
|
A | G | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-9768A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524849 | ||||||
| chr7:114524975
|
G | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.169-9642G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524975 | ||||||
| chr7:114524981
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-9636A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114524981 | ||||||
| chr7:114525133
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.169-9484T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114525133 | ||||||
| chr7:114525365
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.169-9252G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114525365 | ||||||
| chr7:114525451
|
C | T | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169-9166C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114525451 | ||||||
| chr7:114525824
|
A | T | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-8793A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114525824 | ||||||
| chr7:114525842
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.169-8775T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114525842 | ||||||
| chr7:114526046
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.169-8571A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526046 | ||||||
| chr7:114526172
|
T | TA | 32 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(29): Show | 32 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.169-8422dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
T | TAA | 7 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0144others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-8423_169-8422d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
T | TAAA | 50 | a0001c0001t0001g0002a0001c0001t0001g0089a0001c0001t0001g0104others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-8424_169-8422d others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
T | TAAAA | 25 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0001g0090others(22): Show | 25 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-8425_169-8422d others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
T | TAAAAA | 9 | a0001c0001t0001g0003a0001c0001t0001g0135a0001c0001t0001g0152others(6): Show | 9 | HG01069.hp2 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-8426_169-8422d others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
T | TAAAAAAA | 8 | a0001c0001t0001g0155a0001c0001t0002g0054a0001c0001t0002g0151others(5): Show | 8 | HG00597.hp2 HG02280.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-8428_169-8422d others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
T | TAAAAAAA others(1): Show |
14 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(11): Show | 15 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-8429_169-8422d others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526172
|
TAAAAA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0100others(7): Show | 10 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-8426_169-8422d others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526172 | |||||
| chr7:114526195
|
A | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-8422A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526195 | ||||||
| chr7:114526229
|
A | T | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.169-8388A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526229 | ||||||
| chr7:114526442
|
C | T | 1 | a0001c0001t0004g0014 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.169-8175C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526442 | ||||||
| chr7:114526483
|
A | AC | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-8134_169-8133i others(3): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526483 | ||||||
| chr7:114526488
|
C | A | 9 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-8129C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526488 | ||||||
| chr7:114526488
|
C | CAA | 7 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-8119_169-8118d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526488 | |||||
| chr7:114526488
|
CA | C | 6 | a0001c0001t0001g0118a0001c0001t0005g0119a0001c0002t0001g0097others(3): Show | 6 | HG01243.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-8118delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526488 | |||||
| chr7:114526489
|
A | C | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-8128A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526489 | ||||||
| chr7:114526519
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.169-8098C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526519 | ||||||
| chr7:114526643
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.169-7974C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526643 | ||||||
| chr7:114526776
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-7841T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526776 | ||||||
| chr7:114526926
|
C | A | 1 | a0001c0001t0005g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169-7691C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114526926 | ||||||
| chr7:114526991
|
A | AT | 11 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0161others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-7609dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526991 | |||||
| chr7:114526991
|
AT | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 73 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.169-7609delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526991 | |||||
| chr7:114526991
|
ATT | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-7610_169-7609d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114526991 | |||||
| chr7:114527283
|
G | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-7334G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114527283 | ||||||
| chr7:114527402
|
G | C | 14 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-7215G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114527402 | ||||||
| chr7:114528015
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-6602A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114528015 | ||||||
| chr7:114528153
|
C | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-6464C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114528153 | ||||||
| chr7:114528315
|
A | T | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-6302A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114528315 | ||||||
| chr7:114529007
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0006g0070a0001c0001t0006g0117others(1): Show | 4 | HG01496.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-5610C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114529007 | ||||||
| chr7:114529824
|
G | GTA | 3 | a0001c0001t0011g0060a0001c0001t0013g0093a0001c0001t0015g0092 | 3 | HG02717.hp2 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-4789_169-4788d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114529824 | |||||
| chr7:114530197
|
A | G | 29 | a0001c0001t0001g0046a0001c0001t0001g0118a0001c0001t0001g0135others(26): Show | 29 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.169-4420A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114530197 | ||||||
| chr7:114530565
|
C | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-4052C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114530565 | ||||||
| chr7:114530654
|
G | T | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169-3963G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114530654 | ||||||
| chr7:114531016
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.169-3601G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531016 | ||||||
| chr7:114531090
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(58): Show | 61 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.169-3527A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531090 | ||||||
| chr7:114531195
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-3422A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531195 | ||||||
| chr7:114531383
|
T | G | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.169-3234T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531383 | ||||||
| chr7:114531427
|
G | T | 1 | a0001c0001t0002g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169-3190G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531427 | ||||||
| chr7:114531436
|
T | A | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-3181T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531436 | ||||||
| chr7:114531523
|
T | C | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.169-3094T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531523 | ||||||
| chr7:114531560
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.169-3057T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531560 | ||||||
| chr7:114531635
|
T | G | 1 | a0001c0001t0004g0156 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.169-2982T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531635 | ||||||
| chr7:114531636
|
A | T | 1 | a0001c0001t0004g0156 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.169-2981A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531636 | ||||||
| chr7:114531718
|
G | T | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.169-2899G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531718 | ||||||
| chr7:114531895
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2722A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114531895 | ||||||
| chr7:114532099
|
G | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0002g0077others(23): Show | 26 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.169-2518G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114532099 | ||||||
| chr7:114532450
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169-2167G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114532450 | ||||||
| chr7:114532552
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169-2065C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114532552 | ||||||
| chr7:114532701
|
T | A | 8 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-1916T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114532701 | ||||||
| chr7:114532759
|
C | G | 1 | a0001c0001t0004g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.169-1858C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114532759 | ||||||
| chr7:114532801
|
T | C | 1 | a0001c0001t0005g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.169-1816T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114532801 | ||||||
| chr7:114533041
|
C | A | 3 | a0001c0001t0004g0081a0001c0001t0004g0088a0001c0001t0029g0079 | 3 | HG00621.hp2 NA18952.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.169-1576C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114533041 | ||||||
| chr7:114533119
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-1498C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114533119 | ||||||
| chr7:114533257
|
T | C | 1 | a0001c0001t0003g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169-1360T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114533257 | ||||||
| chr7:114533710
|
G | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0029 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.169-907G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114533710 | ||||||
| chr7:114533780
|
G | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0029 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.169-837G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114533780 | ||||||
| chr7:114534179
|
T | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-438T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114534179 | ||||||
| chr7:114534293
|
T | C | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-324T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | chr7 | 114534293 | ||||||
| chr7:114534306
|
T | TA | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(58): Show | 61 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.169-309dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 114534306 | |||||
| chr7:114534815
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.258+109T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114534815 | ||||||
| chr7:114534930
|
C | T | 2 | a0001c0001t0004g0081a0001c0001t0004g0088 | 2 | HG00621.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.258+224C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114534930 | ||||||
| chr7:114535350
|
A | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+644A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114535350 | ||||||
| chr7:114535672
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+966G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114535672 | ||||||
| chr7:114536000
|
G | C | 1 | a0001c0001t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.258+1294G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536000 | ||||||
| chr7:114536360
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+1654T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536360 | ||||||
| chr7:114536384
|
T | C | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+1678T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536384 | ||||||
| chr7:114536397
|
CT | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0089others(29): Show | 32 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.258+1712delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114536397 | |||||
| chr7:114536397
|
CTT | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0061others(64): Show | 68 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.258+1711_258+1712d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114536397 | |||||
| chr7:114536397
|
CTTT | C | 31 | a0001c0001t0001g0046a0001c0001t0001g0118a0001c0001t0001g0135others(28): Show | 31 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.258+1710_258+1712d others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114536397 | |||||
| chr7:114536399
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.258+1693T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536399 | ||||||
| chr7:114536400
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.258+1694T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536400 | ||||||
| chr7:114536403
|
T | C | 1 | a0001c0001t0006g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.258+1697T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536403 | ||||||
| chr7:114536416
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0005g0120 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.258+1710T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536416 | ||||||
| chr7:114536471
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.258+1765G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536471 | ||||||
| chr7:114536494
|
A | T | 1 | a0001c0001t0003g0076 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.258+1788A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536494 | ||||||
| chr7:114536578
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.258+1872G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536578 | ||||||
| chr7:114536684
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.258+1978C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536684 | ||||||
| chr7:114536796
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+2090G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114536796 | ||||||
| chr7:114537108
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.258+2402G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114537108 | ||||||
| chr7:114537721
|
A | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+3015A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114537721 | ||||||
| chr7:114538029
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+3323T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538029 | ||||||
| chr7:114538161
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.258+3455C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538161 | ||||||
| chr7:114538224
|
T | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+3518T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538224 | ||||||
| chr7:114538575
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.258+3869G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538575 | ||||||
| chr7:114538598
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(18): Show | 21 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.258+3892A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538598 | ||||||
| chr7:114538918
|
T | A | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.258+4212T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538918 | ||||||
| chr7:114538952
|
A | T | 1 | a0001c0001t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.258+4246A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538952 | ||||||
| chr7:114538975
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(40): Show | 44 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.258+4269A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538975 | ||||||
| chr7:114538999
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.258+4293T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114538999 | ||||||
| chr7:114539169
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.258+4463G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539169 | ||||||
| chr7:114539208
|
T | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4502T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539208 | ||||||
| chr7:114539444
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+4738C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539444 | ||||||
| chr7:114539466
|
T | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+4760T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539466 | ||||||
| chr7:114539486
|
G | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+4780G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539486 | ||||||
| chr7:114539551
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.258+4845C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539551 | ||||||
| chr7:114539559
|
TA | T | 8 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+4862delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114539559 | |||||
| chr7:114539714
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258+5008T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539714 | ||||||
| chr7:114539834
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+5128C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114539834 | ||||||
| chr7:114540007
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.258+5301A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540007 | ||||||
| chr7:114540237
|
C | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+5531C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540237 | ||||||
| chr7:114540540
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+5834G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540540 | ||||||
| chr7:114540656
|
C | A | 1 | a0001c0001t0003g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.258+5950C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540656 | ||||||
| chr7:114540665
|
G | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+5959G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540665 | ||||||
| chr7:114540689
|
G | T | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+5983G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540689 | ||||||
| chr7:114540852
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+6146T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540852 | ||||||
| chr7:114540977
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+6271G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540977 | ||||||
| chr7:114540983
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+6277G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114540983 | ||||||
| chr7:114541286
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+6580G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541286 | ||||||
| chr7:114541360
|
C | T | 1 | a0001c0001t0005g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.258+6654C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541360 | ||||||
| chr7:114541366
|
G | T | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+6660G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541366 | ||||||
| chr7:114541448
|
G | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+6742G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541448 | ||||||
| chr7:114541788
|
C | T | 2 | a0001c0001t0004g0159a0003c0005t0003g0158 | 2 | HG01070.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.258+7082C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541788 | ||||||
| chr7:114541993
|
T | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+7287T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541993 | ||||||
| chr7:114541999
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.258+7293C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114541999 | ||||||
| chr7:114542280
|
C | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+7574C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114542280 | ||||||
| chr7:114542402
|
G | A | 1 | a0001c0001t0010g0142 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.258+7696G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114542402 | ||||||
| chr7:114542794
|
GT | G | 22 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.258+8102delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114542794 | |||||
| chr7:114542794
|
GTT | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(46): Show | 50 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.258+8101_258+8102d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114542794 | |||||
| chr7:114542860
|
C | G | 22 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.258+8154C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114542860 | ||||||
| chr7:114543332
|
A | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+8626A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114543332 | ||||||
| chr7:114543549
|
C | CT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(69): Show | 73 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.258+8849dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114543549 | |||||
| chr7:114543570
|
C | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+8864C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114543570 | ||||||
| chr7:114543678
|
A | T | 1 | a0001c0001t0003g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.258+8972A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114543678 | ||||||
| chr7:114543707
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+9001T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114543707 | ||||||
| chr7:114544043
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.258+9337G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114544043 | ||||||
| chr7:114544536
|
T | C | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+9830T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114544536 | ||||||
| chr7:114544604
|
A | C | 3 | a0001c0001t0005g0073a0001c0001t0006g0071a0001c0001t0006g0130 | 3 | HG02145.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.258+9898A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114544604 | ||||||
| chr7:114544959
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.258+10253T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114544959 | ||||||
| chr7:114545041
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258+10335T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545041 | ||||||
| chr7:114545353
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+10647G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545353 | ||||||
| chr7:114545441
|
A | G | 19 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(16): Show | 20 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.258+10735A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545441 | ||||||
| chr7:114545490
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.258+10784A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545490 | ||||||
| chr7:114545542
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.258+10836T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545542 | ||||||
| chr7:114545589
|
G | C | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.258+10883G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545589 | ||||||
| chr7:114545622
|
A | T | 1 | a0001c0001t0003g0134 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.258+10916A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545622 | ||||||
| chr7:114545751
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+11045G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545751 | ||||||
| chr7:114545855
|
T | C | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.258+11149T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545855 | ||||||
| chr7:114545856
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.258+11150C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545856 | ||||||
| chr7:114545858
|
T | C | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.258+11152T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545858 | ||||||
| chr7:114545872
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.258+11166C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545872 | ||||||
| chr7:114545882
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.258+11176A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114545882 | ||||||
| chr7:114546212
|
A | G | 1 | a0001c0001t0004g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.258+11506A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546212 | ||||||
| chr7:114546294
|
G | A | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.258+11588G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546294 | ||||||
| chr7:114546395
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+11689G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546395 | ||||||
| chr7:114546624
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+11918A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546624 | ||||||
| chr7:114546649
|
C | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+11943C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546649 | ||||||
| chr7:114546808
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.258+12102A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546808 | ||||||
| chr7:114546878
|
C | G | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.258+12172C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546878 | ||||||
| chr7:114546958
|
C | T | 2 | a0001c0001t0006g0010a0003c0005t0003g0158 | 2 | HG01243.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.258+12252C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114546958 | ||||||
| chr7:114547032
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+12326G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547032 | ||||||
| chr7:114547209
|
CT | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+12510delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114547209 | |||||
| chr7:114547421
|
G | C | 25 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0002g0077others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.258+12715G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547421 | ||||||
| chr7:114547533
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+12827G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547533 | ||||||
| chr7:114547758
|
C | CA | 14 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(11): Show | 14 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+13061dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114547758 | |||||
| chr7:114547773
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+13067G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547773 | ||||||
| chr7:114547873
|
A | G | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.258+13167A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547873 | ||||||
| chr7:114547880
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0089a0001c0001t0002g0077others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.258+13174G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547880 | ||||||
| chr7:114547955
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(69): Show | 73 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.258+13249G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547955 | ||||||
| chr7:114547965
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+13259A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114547965 | ||||||
| chr7:114548119
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.258+13413A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114548119 | ||||||
| chr7:114548165
|
G | T | 1 | a0001c0001t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258+13459G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114548165 | ||||||
| chr7:114548434
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+13728A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114548434 | ||||||
| chr7:114548477
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.258+13771A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114548477 | ||||||
| chr7:114548482
|
A | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+13776A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114548482 | ||||||
| chr7:114549194
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.258+14488G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114549194 | ||||||
| chr7:114549323
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+14617T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114549323 | ||||||
| chr7:114549325
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.258+14619C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114549325 | ||||||
| chr7:114549731
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+15025A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114549731 | ||||||
| chr7:114549788
|
TA | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(55): Show | 59 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.258+15091delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114549788 | |||||
| chr7:114549797
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.258+15091A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114549797 | ||||||
| chr7:114550091
|
G | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02572.hp2 HG02818.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+15385G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550091 | ||||||
| chr7:114550112
|
C | CT | 15 | a0001c0001t0001g0089a0001c0001t0002g0082a0001c0001t0002g0087others(12): Show | 15 | HG00423.hp1 HG00423.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+15429dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114550112 | |||||
| chr7:114550112
|
C | CTT | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+15428_258+1542 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114550112 | |||||
| chr7:114550112
|
CT | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0104others(8): Show | 11 | HG01074.hp1 HG01099.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+15429delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114550112 | |||||
| chr7:114550115
|
T | TTC | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+15410_258+1541 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114550115 | |||||
| chr7:114550116
|
T | TC | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(47): Show | 51 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.258+15410_258+1541 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550116 | ||||||
| chr7:114550117
|
T | TC | 2 | a0001c0001t0001g0041a0001c0001t0001g0044 | 2 | HG00140.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.258+15411_258+1541 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550117 | ||||||
| chr7:114550118
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0028g0040 | 2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.258+15412T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550118 | ||||||
| chr7:114550119
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.258+15413T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550119 | ||||||
| chr7:114550148
|
C | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+15442C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550148 | ||||||
| chr7:114550165
|
T | C | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.258+15459T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550165 | ||||||
| chr7:114550279
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+15573G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550279 | ||||||
| chr7:114550328
|
G | T | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.258+15622G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550328 | ||||||
| chr7:114550406
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+15700G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550406 | ||||||
| chr7:114550416
|
T | G | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+15710T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550416 | ||||||
| chr7:114550418
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+15712A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550418 | ||||||
| chr7:114550451
|
A | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+15745A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550451 | ||||||
| chr7:114550497
|
T | C | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.258+15791T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550497 | ||||||
| chr7:114550588
|
T | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+15882T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550588 | ||||||
| chr7:114550674
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+15968A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550674 | ||||||
| chr7:114550982
|
C | CT | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+16283dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114550982 | |||||
| chr7:114550993
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258+16287C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114550993 | ||||||
| chr7:114551012
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+16306A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114551012 | ||||||
| chr7:114551100
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258+16394A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114551100 | ||||||
| chr7:114551103
|
A | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+16397A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114551103 | ||||||
| chr7:114551307
|
TC | T | 2 | a0001c0001t0001g0026a0001c0001t0028g0040 | 2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.258+16603delC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114551307 | |||||
| chr7:114551334
|
A | G | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+16628A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114551334 | ||||||
| chr7:114551498
|
G | A | 7 | a0001c0001t0005g0119a0001c0001t0011g0060a0001c0001t0019g0095others(4): Show | 7 | HG01243.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+16792G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114551498 | ||||||
| chr7:114551697
|
AAAG | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+16993_258+1699 others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114551697 | |||||
| chr7:114551723
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.258+17017A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114551723 | ||||||
| chr7:114552141
|
T | G | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.258+17435T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114552141 | ||||||
| chr7:114552276
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.258+17570A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114552276 | ||||||
| chr7:114552431
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+17725C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114552431 | ||||||
| chr7:114552490
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0061others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.258+17784T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114552490 | ||||||
| chr7:114552741
|
C | G | 4 | a0001c0001t0001g0090a0001c0001t0006g0070a0001c0001t0006g0117others(1): Show | 4 | HG01496.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+18035C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114552741 | ||||||
| chr7:114552993
|
C | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+18287C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114552993 | ||||||
| chr7:114553072
|
TA | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+18375delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114553072 | |||||
| chr7:114553199
|
C | A | 8 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+18493C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114553199 | ||||||
| chr7:114553525
|
A | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+18819A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114553525 | ||||||
| chr7:114553694
|
T | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+18988T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114553694 | ||||||
| chr7:114553914
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+19208G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114553914 | ||||||
| chr7:114554235
|
A | G | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.258+19529A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554235 | ||||||
| chr7:114554290
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.258+19584A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554290 | ||||||
| chr7:114554389
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+19683T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554389 | ||||||
| chr7:114554525
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+19819T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554525 | ||||||
| chr7:114554560
|
T | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.258+19854T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554560 | ||||||
| chr7:114554609
|
A | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0002g0001others(19): Show | 23 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.258+19903A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554609 | ||||||
| chr7:114554766
|
C | A | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+20060C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554766 | ||||||
| chr7:114554768
|
A | G | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+20062A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114554768 | ||||||
| chr7:114555007
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.258+20301G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555007 | ||||||
| chr7:114555069
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+20363G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555069 | ||||||
| chr7:114555255
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.258+20549A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555255 | ||||||
| chr7:114555595
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+20889G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555595 | ||||||
| chr7:114555689
|
C | T | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258+20983C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555689 | ||||||
| chr7:114555952
|
C | G | 4 | a0001c0001t0001g0090a0001c0001t0006g0070a0001c0001t0006g0117others(1): Show | 4 | HG01496.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+21246C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555952 | ||||||
| chr7:114555993
|
G | A | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.258+21287G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114555993 | ||||||
| chr7:114556054
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0003g0009 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.258+21348G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114556054 | ||||||
| chr7:114556194
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+21488C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114556194 | ||||||
| chr7:114556475
|
C | A | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258+21769C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114556475 | ||||||
| chr7:114556487
|
A | C | 2 | a0001c0001t0002g0168a0001c0001t0003g0015 | 2 | HG02040.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.258+21781A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114556487 | ||||||
| chr7:114556834
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.258+22128G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114556834 | ||||||
| chr7:114556854
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+22148C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114556854 | ||||||
| chr7:114557035
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+22329G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557035 | ||||||
| chr7:114557039
|
T | C | 1 | a0001c0001t0009g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.258+22333T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557039 | ||||||
| chr7:114557088
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+22382G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557088 | ||||||
| chr7:114557387
|
T | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+22681T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557387 | ||||||
| chr7:114557417
|
T | C | 5 | a0001c0001t0019g0095a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+22711T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557417 | ||||||
| chr7:114557422
|
C | G | 3 | a0001c0001t0006g0070a0001c0001t0006g0117a0001c0001t0031g0114 | 3 | HG01496.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.258+22716C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557422 | ||||||
| chr7:114557467
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.258+22761G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557467 | ||||||
| chr7:114557498
|
A | AT | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+22799dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557498 | |||||
| chr7:114557575
|
T | TTGTC | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+22872_258+2287 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557575 | |||||
| chr7:114557753
|
GA | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+23049delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557753 | |||||
| chr7:114557787
|
C | CTTTA | 26 | a0001c0001t0001g0033a0001c0001t0001g0090a0001c0001t0001g0164others(23): Show | 26 | HG00642.hp1 HG01106.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.258+23118_258+2312 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557787 | |||||
| chr7:114557787
|
C | CTTTATTT others(1): Show |
5 | a0001c0001t0001g0065a0001c0001t0001g0101a0001c0001t0006g0070others(2): Show | 5 | HG02818.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+23114_258+2312 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557787 | |||||
| chr7:114557787
|
C | CTTTATTT others(5): Show |
5 | a0001c0001t0001g0100a0001c0001t0002g0123a0001c0001t0004g0099others(2): Show | 5 | HG02572.hp2 HG03225.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+23110_258+2312 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557787 | |||||
| chr7:114557787
|
CTTTA | C | 20 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(17): Show | 21 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.258+23118_258+2312 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557787 | |||||
| chr7:114557787
|
CTTTATTT others(1): Show |
C | 11 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0089others(8): Show | 11 | HG01074.hp1 HG01099.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+23114_258+2312 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557787 | |||||
| chr7:114557787
|
CTTTATTT others(9): Show |
C | 8 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+23106_258+2312 others(20): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114557787 | |||||
| chr7:114557835
|
A | G | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.258+23129A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557835 | ||||||
| chr7:114557921
|
G | T | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+23215G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114557921 | ||||||
| chr7:114558245
|
G | T | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+23539G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114558245 | ||||||
| chr7:114558286
|
A | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+23580A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114558286 | ||||||
| chr7:114558342
|
G | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+23636G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114558342 | ||||||
| chr7:114558795
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+24089A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114558795 | ||||||
| chr7:114558861
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258+24155A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114558861 | ||||||
| chr7:114558929
|
C | A | 2 | a0001c0002t0002g0102a0001c0002t0005g0103 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.258+24223C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114558929 | ||||||
| chr7:114559033
|
A | ATT | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.258+24334_258+2433 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114559033 | |||||
| chr7:114559230
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(69): Show | 73 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.258+24524T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559230 | ||||||
| chr7:114559544
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.258+24838A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559544 | ||||||
| chr7:114559610
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0003g0009 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.258+24904C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559610 | ||||||
| chr7:114559654
|
G | T | 2 | a0001c0001t0007g0140a0001c0001t0007g0141 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.258+24948G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559654 | ||||||
| chr7:114559687
|
A | C | 1 | a0001c0001t0003g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.258+24981A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559687 | ||||||
| chr7:114559702
|
G | GA | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+24999dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114559702 | |||||
| chr7:114559886
|
CT | C | 3 | a0001c0001t0001g0033a0001c0001t0006g0010a0001c0001t0025g0012 | 3 | HG02615.hp1 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.258+25182delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114559886 | |||||
| chr7:114559887
|
T | TA | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(22): Show | 25 | HG00423.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.258+25181_258+2518 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559887 | ||||||
| chr7:114559887
|
T | TAA | 79 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 79 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.258+25181_258+2518 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559887 | ||||||
| chr7:114559887
|
T | TAAA | 16 | a0001c0001t0001g0135a0001c0001t0001g0160a0001c0001t0001g0161others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.258+25181_258+2518 others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559887 | ||||||
| chr7:114559887
|
T | TAAAA | 3 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0004g0147 | 3 | HG00642.hp2 HG06807.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.258+25181_258+2518 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559887 | ||||||
| chr7:114559888
|
T | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.258+25182T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559888 | ||||||
| chr7:114559904
|
T | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+25198T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559904 | ||||||
| chr7:114559958
|
A | G | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+25252A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559958 | ||||||
| chr7:114559968
|
G | A | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+25262G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114559968 | ||||||
| chr7:114560014
|
A | T | 2 | a0001c0001t0006g0010a0001c0001t0025g0012 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.258+25308A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114560014 | ||||||
| chr7:114560267
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+25561G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114560267 | ||||||
| chr7:114560479
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.258+25773G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114560479 | ||||||
| chr7:114560619
|
G | A | 1 | a0001c0002t0002g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.258+25913G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114560619 | ||||||
| chr7:114561004
|
G | C | 9 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02572.hp2 HG02818.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+26298G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561004 | ||||||
| chr7:114561117
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.258+26411G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561117 | ||||||
| chr7:114561425
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.258+26719C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561425 | ||||||
| chr7:114561630
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(57): Show | 61 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.258+26924C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561630 | ||||||
| chr7:114561640
|
A | G | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+26934A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561640 | ||||||
| chr7:114561738
|
A | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+27032A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561738 | ||||||
| chr7:114561748
|
A | G | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+27042A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561748 | ||||||
| chr7:114561789
|
T | TTTTG | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+27095_258+2709 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114561789 | |||||
| chr7:114561974
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0013g0093 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+27268C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114561974 | ||||||
| chr7:114562360
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.258+27654C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562360 | ||||||
| chr7:114562361
|
A | G | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+27655A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562361 | ||||||
| chr7:114562406
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+27700G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562406 | ||||||
| chr7:114562452
|
T | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+27746T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562452 | ||||||
| chr7:114562682
|
T | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02572.hp2 HG02818.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+27976T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562682 | ||||||
| chr7:114562709
|
C | T | 23 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(20): Show | 24 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.258+28003C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562709 | ||||||
| chr7:114562758
|
C | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+28052C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562758 | ||||||
| chr7:114562774
|
GT | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.258+28078delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114562774 | |||||
| chr7:114562900
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.258+28194A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114562900 | ||||||
| chr7:114563559
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.258+28853C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114563559 | ||||||
| chr7:114563815
|
G | A | 1 | a0001c0001t0005g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.258+29109G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114563815 | ||||||
| chr7:114563862
|
C | T | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+29156C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114563862 | ||||||
| chr7:114563882
|
C | CTCAG | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+29179_258+2918 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114563882 | |||||
| chr7:114563894
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(73): Show | 77 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.258+29188A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114563894 | ||||||
| chr7:114564010
|
G | C | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+29304G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564010 | ||||||
| chr7:114564074
|
T | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.258+29368T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564074 | ||||||
| chr7:114564243
|
GT | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.258+29546delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114564243 | |||||
| chr7:114564309
|
T | C | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+29603T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564309 | ||||||
| chr7:114564324
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0104others(7): Show | 10 | HG01074.hp1 HG01099.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.258+29618T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564324 | ||||||
| chr7:114564352
|
G | A | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+29646G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564352 | ||||||
| chr7:114564358
|
C | T | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+29652C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564358 | ||||||
| chr7:114564463
|
T | C | 1 | a0001c0001t0002g0025 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.258+29757T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564463 | ||||||
| chr7:114564480
|
C | T | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.258+29774C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564480 | ||||||
| chr7:114564799
|
T | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+30093T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564799 | ||||||
| chr7:114564800
|
G | T | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.258+30094G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564800 | ||||||
| chr7:114564878
|
C | CA | 41 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(38): Show | 42 | HG00609.hp1 HG00673.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.258+30190dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114564878 | |||||
| chr7:114564878
|
CA | C | 30 | a0001c0001t0001g0046a0001c0001t0001g0118a0001c0001t0001g0135others(27): Show | 30 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.258+30190delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114564878 | |||||
| chr7:114564976
|
A | G | 2 | a0001c0001t0004g0136a0001c0001t0004g0138 | 2 | HG01257.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.258+30270A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114564976 | ||||||
| chr7:114566056
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258+31350C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566056 | ||||||
| chr7:114566185
|
T | C | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+31479T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566185 | ||||||
| chr7:114566383
|
G | A | 2 | a0001c0001t0003g0148a0001c0001t0004g0048 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.258+31677G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566383 | ||||||
| chr7:114566431
|
G | GTGAT | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+31726_258+3172 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114566431 | |||||
| chr7:114566466
|
T | A | 1 | a0001c0001t0006g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.258+31760T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566466 | ||||||
| chr7:114566509
|
C | T | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+31803C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566509 | ||||||
| chr7:114566531
|
C | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+31825C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566531 | ||||||
| chr7:114566619
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+31913G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566619 | ||||||
| chr7:114566724
|
A | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+32018A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114566724 | ||||||
| chr7:114567092
|
A | G | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+32386A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114567092 | ||||||
| chr7:114567265
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.258+32559A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114567265 | ||||||
| chr7:114567340
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0013g0093 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+32634C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114567340 | ||||||
| chr7:114567579
|
C | G | 28 | a0001c0001t0001g0046a0001c0001t0001g0118a0001c0001t0001g0135others(25): Show | 28 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.258+32873C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114567579 | ||||||
| chr7:114568219
|
T | C | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+33513T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568219 | ||||||
| chr7:114568413
|
T | C | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.258+33707T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568413 | ||||||
| chr7:114568432
|
T | TG | 2 | a0001c0001t0001g0118a0001c0001t0013g0093 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+33726_258+3372 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568432 | ||||||
| chr7:114568433
|
T | G | 14 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0152others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+33727T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568433 | ||||||
| chr7:114568433
|
T | TG | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0144others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+33736dupG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114568433 | |||||
| chr7:114568463
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+33757T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568463 | ||||||
| chr7:114568492
|
C | T | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+33786C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568492 | ||||||
| chr7:114568493
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.258+33787G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568493 | ||||||
| chr7:114568533
|
A | G | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+33827A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568533 | ||||||
| chr7:114568608
|
C | T | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258+33902C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568608 | ||||||
| chr7:114568741
|
T | C | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+34035T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568741 | ||||||
| chr7:114568742
|
G | A | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+34036G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114568742 | ||||||
| chr7:114569031
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.258+34325A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114569031 | ||||||
| chr7:114569047
|
G | A | 1 | a0001c0001t0028g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+34341G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114569047 | ||||||
| chr7:114569062
|
A | G | 1 | a0001c0001t0004g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258+34356A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114569062 | ||||||
| chr7:114569627
|
A | C | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+34921A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114569627 | ||||||
| chr7:114569642
|
C | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+34936C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114569642 | ||||||
| chr7:114569997
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.258+35291T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114569997 | ||||||
| chr7:114570056
|
G | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0024others(2): Show | 5 | HG00597.hp2 NA18951.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+35350G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114570056 | ||||||
| chr7:114570540
|
C | A | 1 | a0001c0001t0002g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.258+35834C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114570540 | ||||||
| chr7:114570546
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.258+35840C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114570546 | ||||||
| chr7:114570548
|
T | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.258+35842T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114570548 | ||||||
| chr7:114570754
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0013g0093 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+36048A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114570754 | ||||||
| chr7:114570759
|
T | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.258+36053T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114570759 | ||||||
| chr7:114571392
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 77 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.258+36686A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114571392 | ||||||
| chr7:114571651
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0029 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.258+36945C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114571651 | ||||||
| chr7:114571857
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.258+37151G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114571857 | ||||||
| chr7:114572048
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0013g0093 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+37342C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114572048 | ||||||
| chr7:114572202
|
A | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.258+37496A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114572202 | ||||||
| chr7:114572244
|
C | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+37538C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114572244 | ||||||
| chr7:114572244
|
C | CA | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(41): Show | 45 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.258+37548dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114572244 | |||||
| chr7:114572259
|
TAATG | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.258+37558_258+3756 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114572259 | |||||
| chr7:114572597
|
T | C | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.258+37891T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114572597 | ||||||
| chr7:114572959
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+38253G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114572959 | ||||||
| chr7:114573043
|
C | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+38337C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573043 | ||||||
| chr7:114573188
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+38482C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573188 | ||||||
| chr7:114573470
|
G | A | 1 | a0001c0001t0004g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+38764G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573470 | ||||||
| chr7:114573478
|
A | C | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.258+38772A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573478 | ||||||
| chr7:114573525
|
A | T | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+38819A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573525 | ||||||
| chr7:114573621
|
CAT | C | 15 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+38918_258+3891 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114573621 | |||||
| chr7:114573696
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(57): Show | 61 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.258+38990G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573696 | ||||||
| chr7:114573989
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.258+39283G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114573989 | ||||||
| chr7:114574065
|
A | T | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+39359A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574065 | ||||||
| chr7:114574111
|
C | A | 1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.258+39405C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574111 | ||||||
| chr7:114574207
|
A | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+39501A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574207 | ||||||
| chr7:114574299
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(55): Show | 59 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.258+39593A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574299 | ||||||
| chr7:114574436
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(55): Show | 59 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.258+39730A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574436 | ||||||
| chr7:114574437
|
C | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+39731C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574437 | ||||||
| chr7:114574622
|
A | C | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+39916A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574622 | ||||||
| chr7:114574654
|
G | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(67): Show | 71 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+39948G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114574654 | ||||||
| chr7:114575150
|
T | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+40444T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575150 | ||||||
| chr7:114575228
|
C | G | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+40522C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575228 | ||||||
| chr7:114575651
|
A | T | 1 | a0001c0001t0002g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.258+40945A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575651 | ||||||
| chr7:114575682
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+40976A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575682 | ||||||
| chr7:114575749
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(67): Show | 71 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+41043G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575749 | ||||||
| chr7:114575771
|
C | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(67): Show | 71 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+41065C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575771 | ||||||
| chr7:114575865
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(67): Show | 71 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+41159A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114575865 | ||||||
| chr7:114576072
|
TTAAGATA others(1): Show |
T | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+41368_258+4137 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114576072 | |||||
| chr7:114576135
|
T | C | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+41429T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576135 | ||||||
| chr7:114576179
|
A | T | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+41473A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576179 | ||||||
| chr7:114576321
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0118 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+41615A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576321 | ||||||
| chr7:114576375
|
C | G | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.258+41669C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576375 | ||||||
| chr7:114576473
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+41767G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576473 | ||||||
| chr7:114576679
|
T | G | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.258+41973T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576679 | ||||||
| chr7:114576694
|
A | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+41988A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576694 | ||||||
| chr7:114576913
|
G | T | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+42207G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576913 | ||||||
| chr7:114576955
|
A | C | 1 | a0001c0001t0004g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.258+42249A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576955 | ||||||
| chr7:114576978
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+42272G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576978 | ||||||
| chr7:114576996
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(67): Show | 71 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+42290G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114576996 | ||||||
| chr7:114577020
|
A | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.258+42314A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577020 | ||||||
| chr7:114577064
|
AT | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+42361delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114577064 | |||||
| chr7:114577086
|
G | A | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+42380G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577086 | ||||||
| chr7:114577324
|
A | T | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.258+42618A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577324 | ||||||
| chr7:114577434
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+42728A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577434 | ||||||
| chr7:114577499
|
C | A | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258+42793C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577499 | ||||||
| chr7:114577680
|
A | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+42974A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577680 | ||||||
| chr7:114577709
|
C | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+43003C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577709 | ||||||
| chr7:114577820
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+43114C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577820 | ||||||
| chr7:114577851
|
G | A | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+43145G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577851 | ||||||
| chr7:114577854
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(67): Show | 71 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.258+43148A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577854 | ||||||
| chr7:114577855
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+43149T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577855 | ||||||
| chr7:114577963
|
GA | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.258+43258delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577963 | ||||||
| chr7:114577983
|
A | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+43277A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114577983 | ||||||
| chr7:114578027
|
A | G | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258+43321A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578027 | ||||||
| chr7:114578073
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.258+43367G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578073 | ||||||
| chr7:114578234
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0004g0014 | 3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.258+43528G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578234 | ||||||
| chr7:114578295
|
G | A | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.258+43589G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578295 | ||||||
| chr7:114578527
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.258+43821C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578527 | ||||||
| chr7:114578551
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.258+43845T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578551 | ||||||
| chr7:114578836
|
T | C | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+44130T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114578836 | ||||||
| chr7:114579077
|
C | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+44371C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579077 | ||||||
| chr7:114579386
|
T | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+44680T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579386 | ||||||
| chr7:114579615
|
C | T | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+44909C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579615 | ||||||
| chr7:114579616
|
G | A | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+44910G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579616 | ||||||
| chr7:114579852
|
A | G | 1 | a0001c0003t0006g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.258+45146A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579852 | ||||||
| chr7:114579882
|
G | T | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.258+45176G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579882 | ||||||
| chr7:114579927
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+45221G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579927 | ||||||
| chr7:114579993
|
A | T | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.258+45287A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114579993 | ||||||
| chr7:114580054
|
T | A | 1 | a0001c0001t0002g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.258+45348T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580054 | ||||||
| chr7:114580199
|
A | G | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258+45493A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580199 | ||||||
| chr7:114580282
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258+45576G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580282 | ||||||
| chr7:114580519
|
A | G | 1 | a0001c0001t0005g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.258+45813A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580519 | ||||||
| chr7:114580580
|
C | CAAAACA | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+45890_258+4589 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114580580 | |||||
| chr7:114580633
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00642.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.258+45927T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580633 | ||||||
| chr7:114580663
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.258+45957A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580663 | ||||||
| chr7:114580726
|
G | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+46020G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580726 | ||||||
| chr7:114580804
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+46098G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580804 | ||||||
| chr7:114580820
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+46114T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580820 | ||||||
| chr7:114580821
|
G | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+46115G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114580821 | ||||||
| chr7:114581008
|
C | A | 1 | a0001c0001t0004g0088 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.258+46302C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581008 | ||||||
| chr7:114581044
|
G | A | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+46338G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581044 | ||||||
| chr7:114581075
|
G | GCA | 12 | a0001c0001t0001g0100a0001c0001t0002g0087a0001c0001t0004g0005others(9): Show | 12 | HG00099.hp2 HG00642.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.258+46400_258+4640 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581075
|
G | GCACA | 101 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0056others(98): Show | 102 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.258+46398_258+4640 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581075
|
G | GCACACA | 30 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0046others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.258+46396_258+4640 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581075
|
G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(1): Show | 4 | HG00642.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+46394_258+4640 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581075
|
G | GCACACAC others(3): Show |
2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.258+46392_258+4640 others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581075
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0004g0156 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.258+46390_258+4640 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581075
|
GCACACA | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+46396_258+4640 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581075 | |||||
| chr7:114581136
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.258+46430T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581136 | ||||||
| chr7:114581149
|
G | GTTTA | 2 | a0001c0001t0004g0139a0001c0001t0006g0071 | 2 | HG00642.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.258+46491_258+4649 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581149 | |||||
| chr7:114581149
|
GTTTA | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0033others(63): Show | 66 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.258+46491_258+4649 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581149 | |||||
| chr7:114581149
|
GTTTATTT others(1): Show |
G | 46 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(43): Show | 47 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.258+46487_258+4649 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581149 | |||||
| chr7:114581149
|
GTTTATTT others(5): Show |
G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.258+46483_258+4649 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581149 | |||||
| chr7:114581149
|
GTTTATTT others(9): Show |
G | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+46479_258+4649 others(20): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114581149 | |||||
| chr7:114581479
|
T | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+46773T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581479 | ||||||
| chr7:114581578
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+46872G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581578 | ||||||
| chr7:114581653
|
C | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-46887C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581653 | ||||||
| chr7:114581683
|
A | T | 1 | a0001c0001t0004g0156 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.259-46857A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581683 | ||||||
| chr7:114581698
|
C | T | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-46842C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581698 | ||||||
| chr7:114581789
|
C | T | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.259-46751C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114581789 | ||||||
| chr7:114582373
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.259-46167T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114582373 | ||||||
| chr7:114582690
|
T | A | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-45850T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114582690 | ||||||
| chr7:114582855
|
A | G | 1 | a0001c0001t0006g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.259-45685A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114582855 | ||||||
| chr7:114583304
|
G | A | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-45236G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583304 | ||||||
| chr7:114583360
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.259-45180A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583360 | ||||||
| chr7:114583367
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-45173G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583367 | ||||||
| chr7:114583481
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.259-45059G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583481 | ||||||
| chr7:114583590
|
C | T | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-44950C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583590 | ||||||
| chr7:114583668
|
C | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.259-44872C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583668 | ||||||
| chr7:114583758
|
T | C | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.259-44782T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583758 | ||||||
| chr7:114583806
|
T | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-44734T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114583806 | ||||||
| chr7:114584108
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.259-44432A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114584108 | ||||||
| chr7:114584245
|
T | A | 2 | a0001c0001t0007g0140a0001c0001t0007g0141 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.259-44295T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114584245 | ||||||
| chr7:114585115
|
A | G | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.259-43425A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585115 | ||||||
| chr7:114585131
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.259-43409C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585131 | ||||||
| chr7:114585510
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0003g0009 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.259-43030G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585510 | ||||||
| chr7:114585569
|
T | TA | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-42956dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114585569 | |||||
| chr7:114585569
|
TA | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.259-42956delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114585569 | |||||
| chr7:114585585
|
G | A | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-42955G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585585 | ||||||
| chr7:114585641
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.259-42899G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585641 | ||||||
| chr7:114585684
|
A | G | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-42856A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585684 | ||||||
| chr7:114585694
|
G | A | 2 | a0001c0001t0004g0137a0001c0001t0004g0139 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.259-42846G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585694 | ||||||
| chr7:114585836
|
A | T | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-42704A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114585836 | ||||||
| chr7:114586172
|
C | T | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-42368C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114586172 | ||||||
| chr7:114586262
|
T | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.259-42278T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114586262 | ||||||
| chr7:114586971
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.259-41569G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114586971 | ||||||
| chr7:114587055
|
A | G | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259-41485A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587055 | ||||||
| chr7:114587059
|
C | CT | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(44): Show | 48 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.259-41469dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114587059 | |||||
| chr7:114587062
|
T | TG | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-41478_259-4147 others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587062 | ||||||
| chr7:114587137
|
G | A | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259-41403G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587137 | ||||||
| chr7:114587401
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.259-41139G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587401 | ||||||
| chr7:114587451
|
T | A | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-41089T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587451 | ||||||
| chr7:114587499
|
C | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.259-41041C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587499 | ||||||
| chr7:114587842
|
T | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-40698T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587842 | ||||||
| chr7:114587876
|
A | T | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.259-40664A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587876 | ||||||
| chr7:114587877
|
T | A | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.259-40663T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587877 | ||||||
| chr7:114587879
|
A | ATATATAT others(29): Show |
2 | a0001c0001t0002g0029a0001c0001t0030g0068 | 2 | HG02523.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.259-40661_259-4066 others(40): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.259-40661_259-4066 others(50): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.259-40661_259-4066 others(52): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(43): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0105others(5): Show | 8 | HG01074.hp1 HG01099.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(54): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0001g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.259-40661_259-4066 others(60): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(53): Show |
7 | a0001c0001t0001g0026a0001c0001t0002g0083a0001c0001t0003g0091others(4): Show | 7 | HG00639.hp2 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(64): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(55): Show |
2 | a0001c0001t0004g0074a0001c0001t0005g0133 | 2 | HG03490.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.259-40661_259-4066 others(66): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(57): Show |
1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.259-40661_259-4066 others(68): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(59): Show |
7 | a0001c0001t0001g0144a0001c0001t0002g0082a0001c0001t0002g0168others(4): Show | 7 | HG00423.hp1 HG01069.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(70): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(57): Show |
1 | a0001c0001t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.259-40661_259-4066 others(68): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(61): Show |
5 | a0001c0001t0001g0127a0001c0001t0002g0087a0001c0001t0003g0009others(2): Show | 5 | HG00621.hp1 HG02622.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(72): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(63): Show |
5 | a0001c0001t0003g0069a0001c0001t0003g0148a0001c0001t0004g0081others(2): Show | 5 | HG00621.hp2 HG01106.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(74): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(62): Show |
1 | a0001c0001t0029g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.259-40661_259-4066 others(73): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(61): Show |
1 | a0001c0001t0004g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.259-40661_259-4066 others(72): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(65): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0002g0077others(9): Show | 12 | HG00609.hp2 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(76): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(67): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0003g0015others(3): Show | 6 | HG00597.hp1 HG00642.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(78): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(69): Show |
9 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0053others(6): Show | 9 | HG00140.hp2 HG01361.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-40661_259-4066 others(80): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(71): Show |
1 | a0001c0001t0004g0075 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.259-40661_259-4066 others(82): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(73): Show |
1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.259-40661_259-4066 others(84): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(72): Show |
1 | a0001c0001t0004g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.259-40661_259-4066 others(83): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(75): Show |
1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.259-40661_259-4066 others(86): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(79): Show |
2 | a0001c0001t0004g0048a0001c0001t0004g0088 | 2 | HG01496.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.259-40661_259-4066 others(90): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587879
|
A | ATATATAT others(62): Show |
1 | a0001c0001t0003g0039 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.259-40661_259-4066 others(73): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587879 | ||||||
| chr7:114587882
|
T | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 77 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-40658T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587882 | ||||||
| chr7:114587883
|
C | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 77 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-40657C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587883 | ||||||
| chr7:114587930
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-40610T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587930 | ||||||
| chr7:114587984
|
T | A | 1 | a0001c0001t0003g0134 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.259-40556T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114587984 | ||||||
| chr7:114588032
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.259-40508G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588032 | ||||||
| chr7:114588032
|
G | T | 1 | a0001c0001t0002g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.259-40508G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588032 | ||||||
| chr7:114588164
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.259-40376G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588164 | ||||||
| chr7:114588169
|
G | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02572.hp2 HG02818.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-40371G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588169 | ||||||
| chr7:114588263
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.259-40277C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588263 | ||||||
| chr7:114588345
|
C | A | 1 | a0001c0001t0003g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.259-40195C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588345 | ||||||
| chr7:114588750
|
C | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.259-39790C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588750 | ||||||
| chr7:114588806
|
T | A | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.259-39734T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114588806 | ||||||
| chr7:114589078
|
A | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-39462A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589078 | ||||||
| chr7:114589084
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 77 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-39456G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589084 | ||||||
| chr7:114589136
|
A | T | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.259-39404A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589136 | ||||||
| chr7:114589621
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.259-38919T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589621 | ||||||
| chr7:114589709
|
A | G | 2 | a0001c0001t0013g0093a0001c0001t0019g0095 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.259-38831A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589709 | ||||||
| chr7:114589914
|
T | G | 1 | a0001c0001t0006g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.259-38626T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589914 | ||||||
| chr7:114589949
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0002g0083a0001c0001t0027g0030 | 3 | HG02523.hp1 NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.259-38591A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114589949 | ||||||
| chr7:114590154
|
C | CA | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-38379dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114590154 | |||||
| chr7:114590331
|
G | T | 1 | a0001c0001t0002g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.259-38209G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114590331 | ||||||
| chr7:114590699
|
T | C | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-37841T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114590699 | ||||||
| chr7:114590907
|
G | A | 1 | a0001c0001t0004g0005 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259-37633G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114590907 | ||||||
| chr7:114591506
|
A | G | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-37034A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114591506 | ||||||
| chr7:114591528
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-37012C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114591528 | ||||||
| chr7:114591558
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.259-36982G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114591558 | ||||||
| chr7:114591846
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-36694A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114591846 | ||||||
| chr7:114592133
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-36407T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592133 | ||||||
| chr7:114592229
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.259-36311C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592229 | ||||||
| chr7:114592251
|
A | G | 1 | a0001c0001t0022g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.259-36289A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592251 | ||||||
| chr7:114592429
|
T | G | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.259-36111T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592429 | ||||||
| chr7:114592460
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.259-36080T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592460 | ||||||
| chr7:114592678
|
A | G | 6 | a0001c0001t0002g0145a0001c0001t0002g0151a0001c0001t0002g0167others(3): Show | 6 | HG01168.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-35862A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592678 | ||||||
| chr7:114592737
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-35803A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592737 | ||||||
| chr7:114592824
|
A | G | 2 | a0001c0001t0006g0010a0001c0001t0025g0012 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.259-35716A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114592824 | ||||||
| chr7:114593058
|
A | G | 5 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(2): Show | 5 | HG01168.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-35482A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593058 | ||||||
| chr7:114593063
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-35477T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593063 | ||||||
| chr7:114593241
|
G | GA | 19 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0090others(16): Show | 19 | HG01074.hp1 HG01099.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.259-35290dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114593241 | |||||
| chr7:114593242
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-35298A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593242 | ||||||
| chr7:114593325
|
T | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-35215T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593325 | ||||||
| chr7:114593363
|
T | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-35177T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593363 | ||||||
| chr7:114593418
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-35122G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593418 | ||||||
| chr7:114593622
|
T | C | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-34918T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593622 | ||||||
| chr7:114593711
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-34829C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593711 | ||||||
| chr7:114593759
|
A | C | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-34781A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593759 | ||||||
| chr7:114593867
|
C | T | 1 | a0001c0001t0005g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-34673C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593867 | ||||||
| chr7:114593946
|
C | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-34594C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114593946 | ||||||
| chr7:114594264
|
T | C | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-34276T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594264 | ||||||
| chr7:114594287
|
G | C | 1 | a0001c0001t0004g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.259-34253G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594287 | ||||||
| chr7:114594352
|
C | T | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.259-34188C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594352 | ||||||
| chr7:114594355
|
C | T | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-34185C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594355 | ||||||
| chr7:114594384
|
T | G | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-34156T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594384 | ||||||
| chr7:114594515
|
G | C | 3 | a0001c0001t0005g0119a0001c0001t0011g0060a0001c0001t0024g0132 | 3 | HG01243.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-34025G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594515 | ||||||
| chr7:114594606
|
T | C | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-33934T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594606 | ||||||
| chr7:114594680
|
G | A | 3 | a0001c0001t0005g0119a0001c0001t0011g0060a0001c0001t0024g0132 | 3 | HG01243.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-33860G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114594680 | ||||||
| chr7:114595001
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0084 | 2 | NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.259-33539G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595001 | ||||||
| chr7:114595027
|
A | C | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-33513A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595027 | ||||||
| chr7:114595032
|
C | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-33508C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595032 | ||||||
| chr7:114595136
|
G | T | 1 | a0001c0001t0006g0071 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-33404G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595136 | ||||||
| chr7:114595369
|
G | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG02572.hp2 HG03098.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-33171G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595369 | ||||||
| chr7:114595395
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259-33145T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595395 | ||||||
| chr7:114595987
|
C | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-32553C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595987 | ||||||
| chr7:114595998
|
G | A | 2 | a0001c0001t0015g0092a0001c0001t0019g0095 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.259-32542G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114595998 | ||||||
| chr7:114596107
|
T | TA | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(46): Show | 50 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.259-32428dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114596107 | |||||
| chr7:114596454
|
C | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-32086C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114596454 | ||||||
| chr7:114596496
|
C | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-32044C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114596496 | ||||||
| chr7:114596502
|
A | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-32038A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114596502 | ||||||
| chr7:114596648
|
T | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-31892T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114596648 | ||||||
| chr7:114596825
|
G | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.259-31715G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114596825 | ||||||
| chr7:114597058
|
A | C | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.259-31482A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114597058 | ||||||
| chr7:114597759
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-30781T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114597759 | ||||||
| chr7:114598108
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.259-30432A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114598108 | ||||||
| chr7:114598229
|
T | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0002g0001others(19): Show | 23 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.259-30311T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114598229 | ||||||
| chr7:114598471
|
G | C | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259-30069G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114598471 | ||||||
| chr7:114598777
|
A | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093 | 3 | HG01168.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.259-29763A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114598777 | ||||||
| chr7:114598809
|
A | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-29731A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114598809 | ||||||
| chr7:114598822
|
A | G | 1 | a0001c0001t0005g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-29718A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114598822 | ||||||
| chr7:114599083
|
G | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-29457G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599083 | ||||||
| chr7:114599089
|
C | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-29451C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599089 | ||||||
| chr7:114599136
|
A | AT | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-29403dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114599136 | |||||
| chr7:114599393
|
G | A | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-29147G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599393 | ||||||
| chr7:114599595
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.259-28945G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599595 | ||||||
| chr7:114599745
|
T | A | 2 | a0001c0001t0006g0010a0001c0001t0025g0012 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.259-28795T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599745 | ||||||
| chr7:114599755
|
A | G | 3 | a0001c0001t0005g0119a0001c0001t0006g0010a0001c0001t0011g0060 | 3 | HG01243.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-28785A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599755 | ||||||
| chr7:114599873
|
T | C | 3 | a0001c0001t0005g0073a0001c0001t0006g0071a0001c0001t0006g0130 | 3 | HG02145.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.259-28667T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599873 | ||||||
| chr7:114599960
|
C | T | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.259-28580C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114599960 | ||||||
| chr7:114600061
|
T | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-28479T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114600061 | ||||||
| chr7:114600231
|
G | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-28309G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114600231 | ||||||
| chr7:114600371
|
A | C | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-28169A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114600371 | ||||||
| chr7:114600439
|
G | T | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-28101G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114600439 | ||||||
| chr7:114600675
|
T | C | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-27865T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114600675 | ||||||
| chr7:114600695
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-27845A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114600695 | ||||||
| chr7:114600958
|
CT | C | 40 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(37): Show | 40 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.259-27567delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114600958 | |||||
| chr7:114601162
|
C | T | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-27378C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114601162 | ||||||
| chr7:114601310
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-27230C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114601310 | ||||||
| chr7:114601405
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-27135G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114601405 | ||||||
| chr7:114601563
|
A | C | 1 | a0001c0001t0002g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-26977A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114601563 | ||||||
| chr7:114601657
|
C | T | 1 | a0001c0001t0021g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-26883C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114601657 | ||||||
| chr7:114601876
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-26664T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114601876 | ||||||
| chr7:114602045
|
A | T | 1 | a0001c0001t0018g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.259-26495A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602045 | ||||||
| chr7:114602049
|
A | G | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.259-26491A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602049 | ||||||
| chr7:114602250
|
A | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0152others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-26290A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602250 | ||||||
| chr7:114602486
|
A | G | 5 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0170others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-26054A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602486 | ||||||
| chr7:114602621
|
C | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-25919C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602621 | ||||||
| chr7:114602735
|
C | T | 5 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0170others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-25805C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602735 | ||||||
| chr7:114602810
|
C | T | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.259-25730C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602810 | ||||||
| chr7:114602995
|
A | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-25545A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114602995 | ||||||
| chr7:114603535
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259-25005T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603535 | ||||||
| chr7:114603551
|
G | A | 20 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(17): Show | 21 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.259-24989G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603551 | ||||||
| chr7:114603672
|
A | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093 | 3 | HG01168.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.259-24868A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603672 | ||||||
| chr7:114603829
|
C | T | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.259-24711C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603829 | ||||||
| chr7:114603897
|
G | A | 1 | a0001c0001t0009g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-24643G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603897 | ||||||
| chr7:114603978
|
A | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-24562A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603978 | ||||||
| chr7:114603987
|
A | T | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-24553A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114603987 | ||||||
| chr7:114604077
|
C | T | 2 | a0001c0001t0004g0081a0001c0001t0004g0088 | 2 | HG00621.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.259-24463C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604077 | ||||||
| chr7:114604316
|
G | A | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-24224G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604316 | ||||||
| chr7:114604441
|
A | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-24099A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604441 | ||||||
| chr7:114604527
|
A | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-24013A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604527 | ||||||
| chr7:114604674
|
G | A | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-23866G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604674 | ||||||
| chr7:114604709
|
G | T | 7 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG02572.hp2 HG03098.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-23831G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604709 | ||||||
| chr7:114604724
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-23816C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604724 | ||||||
| chr7:114604851
|
T | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-23689T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114604851 | ||||||
| chr7:114605202
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-23338C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114605202 | ||||||
| chr7:114605592
|
C | T | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-22948C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114605592 | ||||||
| chr7:114605679
|
A | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-22861A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114605679 | ||||||
| chr7:114605694
|
T | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.259-22846T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114605694 | ||||||
| chr7:114605839
|
C | T | 2 | a0001c0001t0004g0136a0001c0001t0004g0138 | 2 | HG01257.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.259-22701C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114605839 | ||||||
| chr7:114606421
|
A | T | 10 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0152others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-22119A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114606421 | ||||||
| chr7:114606971
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259-21569A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114606971 | ||||||
| chr7:114607093
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.259-21447T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114607093 | ||||||
| chr7:114607557
|
GA | G | 2 | a0001c0001t0015g0092a0001c0001t0019g0095 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.259-20981delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114607557 | |||||
| chr7:114607562
|
A | T | 2 | a0001c0001t0015g0092a0001c0001t0019g0095 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.259-20978A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114607562 | ||||||
| chr7:114607792
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259-20748C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114607792 | ||||||
| chr7:114607900
|
T | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-20640T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114607900 | ||||||
| chr7:114607919
|
T | A | 3 | a0001c0001t0005g0119a0001c0001t0011g0060a0001c0001t0024g0132 | 3 | HG01243.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-20621T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114607919 | ||||||
| chr7:114608069
|
A | G | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-20471A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608069 | ||||||
| chr7:114608375
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-20165G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608375 | ||||||
| chr7:114608529
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.259-20011A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608529 | ||||||
| chr7:114608677
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.259-19863C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608677 | ||||||
| chr7:114608796
|
A | G | 14 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0057others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.259-19744A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608796 | ||||||
| chr7:114608809
|
C | A | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-19731C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608809 | ||||||
| chr7:114608864
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259-19676C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114608864 | ||||||
| chr7:114609028
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.259-19512G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609028 | ||||||
| chr7:114609090
|
G | T | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-19450G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609090 | ||||||
| chr7:114609251
|
T | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-19289T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609251 | ||||||
| chr7:114609353
|
G | T | 2 | a0001c0001t0004g0072a0001c0001t0004g0129 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.259-19187G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609353 | ||||||
| chr7:114609467
|
A | G | 3 | a0001c0001t0001g0057a0001c0001t0003g0058a0001c0001t0022g0043 | 3 | HG01099.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.259-19073A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609467 | ||||||
| chr7:114609521
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-19019C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609521 | ||||||
| chr7:114609649
|
A | G | 20 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(17): Show | 21 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.259-18891A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609649 | ||||||
| chr7:114609678
|
T | G | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-18862T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609678 | ||||||
| chr7:114609686
|
T | C | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.259-18854T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609686 | ||||||
| chr7:114609741
|
C | T | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.259-18799C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609741 | ||||||
| chr7:114609803
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-18737G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114609803 | ||||||
| chr7:114610175
|
G | A | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.259-18365G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114610175 | ||||||
| chr7:114610236
|
T | C | 2 | a0001c0001t0015g0092a0001c0001t0019g0095 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.259-18304T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114610236 | ||||||
| chr7:114610676
|
G | GT | 11 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0152others(8): Show | 11 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-17854dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114610676 | |||||
| chr7:114610677
|
T | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-17863T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114610677 | ||||||
| chr7:114610833
|
C | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-17707C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114610833 | ||||||
| chr7:114610872
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.259-17668C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114610872 | ||||||
| chr7:114611042
|
T | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-17498T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114611042 | ||||||
| chr7:114611231
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-17309C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114611231 | ||||||
| chr7:114611254
|
G | A | 5 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(2): Show | 5 | HG01168.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-17286G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114611254 | ||||||
| chr7:114611857
|
C | T | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.259-16683C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114611857 | ||||||
| chr7:114611966
|
A | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-16574A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114611966 | ||||||
| chr7:114612025
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0106 | 2 | HG01074.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.259-16515T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114612025 | ||||||
| chr7:114612388
|
T | TATACGTA others(43): Show |
32 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(29): Show | 32 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.259-16149_259-1614 others(54): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114612388 | |||||
| chr7:114612392
|
T | C | 35 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(32): Show | 35 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.259-16148T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114612392 | ||||||
| chr7:114612392
|
T | TGTATATA others(43): Show |
2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-16099_259-1609 others(54): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114612392 | |||||
| chr7:114612426
|
C | CACACACA others(41): Show |
3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-16099_259-1609 others(52): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114612426 | |||||
| chr7:114612612
|
ACT | A | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-15925_259-1592 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114612612 | |||||
| chr7:114612777
|
T | C | 2 | a0001c0001t0003g0091a0001c0001t0004g0074 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.259-15763T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114612777 | ||||||
| chr7:114612851
|
C | T | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-15689C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114612851 | ||||||
| chr7:114613001
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0009g0064 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-15539A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613001 | ||||||
| chr7:114613455
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.259-15085C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613455 | ||||||
| chr7:114613477
|
C | A | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-15063C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613477 | ||||||
| chr7:114613500
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.259-15040C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613500 | ||||||
| chr7:114613527
|
T | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-15013T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613527 | ||||||
| chr7:114613689
|
T | G | 2 | a0001c0001t0006g0121a0001c0001t0006g0122 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259-14851T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613689 | ||||||
| chr7:114613690
|
G | GTA | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(30): Show | 34 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-14834_259-1483 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114613690 | |||||
| chr7:114613774
|
A | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0014g0146 | 3 | HG01168.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.259-14766A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613774 | ||||||
| chr7:114613952
|
C | T | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-14588C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114613952 | ||||||
| chr7:114614075
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0006g0070a0001c0001t0006g0117others(3): Show | 6 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-14465G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614075 | ||||||
| chr7:114614168
|
T | G | 3 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093 | 3 | HG01168.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.259-14372T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614168 | ||||||
| chr7:114614308
|
T | TA | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-14230dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114614308 | |||||
| chr7:114614352
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-14188G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614352 | ||||||
| chr7:114614490
|
T | C | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-14050T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614490 | ||||||
| chr7:114614673
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0089others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-13867G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614673 | ||||||
| chr7:114614703
|
A | G | 2 | a0001c0001t0004g0159a0003c0005t0003g0158 | 2 | HG01070.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.259-13837A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614703 | ||||||
| chr7:114614922
|
T | C | 3 | a0001c0001t0003g0039a0001c0001t0027g0030a0001c0001t0029g0079 | 3 | HG00423.hp2 NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.259-13618T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614922 | ||||||
| chr7:114614931
|
A | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093 | 3 | HG01168.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.259-13609A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614931 | ||||||
| chr7:114614995
|
C | T | 1 | a0001c0001t0028g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-13545C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114614995 | ||||||
| chr7:114615102
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259-13438C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114615102 | ||||||
| chr7:114615111
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0003g0050 | 2 | NA18951.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.259-13429C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114615111 | ||||||
| chr7:114615113
|
T | C | 123 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.259-13427T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114615113 | ||||||
| chr7:114615129
|
A | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-13411A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114615129 | ||||||
| chr7:114615151
|
G | A | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.259-13389G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114615151 | ||||||
| chr7:114615683
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-12857A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114615683 | ||||||
| chr7:114616097
|
G | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-12443G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616097 | ||||||
| chr7:114616140
|
G | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-12400G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616140 | ||||||
| chr7:114616171
|
GT | G | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-12360delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114616171 | |||||
| chr7:114616286
|
T | C | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-12254T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616286 | ||||||
| chr7:114616307
|
C | T | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.259-12233C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616307 | ||||||
| chr7:114616415
|
T | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-12125T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616415 | ||||||
| chr7:114616453
|
A | G | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-12087A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616453 | ||||||
| chr7:114616873
|
A | G | 1 | a0001c0001t0004g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.259-11667A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114616873 | ||||||
| chr7:114617103
|
T | G | 1 | a0001c0001t0018g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.259-11437T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617103 | ||||||
| chr7:114617486
|
CCCTACTC others(6): Show |
C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-11051_259-1103 others(17): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114617486 | |||||
| chr7:114617619
|
C | G | 1 | a0001c0001t0004g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.259-10921C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617619 | ||||||
| chr7:114617802
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.259-10738A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617802 | ||||||
| chr7:114617824
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-10716T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617824 | ||||||
| chr7:114617955
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.259-10585C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617955 | ||||||
| chr7:114617959
|
C | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-10581C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617959 | ||||||
| chr7:114617992
|
C | A | 1 | a0001c0003t0006g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.259-10548C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114617992 | ||||||
| chr7:114618058
|
C | T | 31 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(28): Show | 31 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.259-10482C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618058 | ||||||
| chr7:114618210
|
G | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-10330G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618210 | ||||||
| chr7:114618307
|
C | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-10233C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618307 | ||||||
| chr7:114618402
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-10138T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618402 | ||||||
| chr7:114618446
|
A | G | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-10094A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618446 | ||||||
| chr7:114618856
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-9684C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618856 | ||||||
| chr7:114618961
|
T | C | 1 | a0001c0001t0018g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.259-9579T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618961 | ||||||
| chr7:114618980
|
T | C | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.259-9560T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114618980 | ||||||
| chr7:114619012
|
G | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-9528G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114619012 | ||||||
| chr7:114619219
|
GA | G | 14 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0057others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.259-9315delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114619219 | |||||
| chr7:114619534
|
T | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-9006T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114619534 | ||||||
| chr7:114619708
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-8832T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114619708 | ||||||
| chr7:114620794
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.259-7746A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114620794 | ||||||
| chr7:114621236
|
T | A | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-7304T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114621236 | ||||||
| chr7:114621307
|
G | A | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-7233G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114621307 | ||||||
| chr7:114621389
|
A | T | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.259-7151A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114621389 | ||||||
| chr7:114621855
|
C | G | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.259-6685C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114621855 | ||||||
| chr7:114621918
|
T | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-6622T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114621918 | ||||||
| chr7:114621932
|
A | G | 1 | a0001c0001t0005g0073 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259-6608A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114621932 | ||||||
| chr7:114622004
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259-6536G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114622004 | ||||||
| chr7:114622113
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0002g0083 | 2 | HG02523.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.259-6427G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114622113 | ||||||
| chr7:114622142
|
A | C | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259-6398A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114622142 | ||||||
| chr7:114622564
|
C | A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259-5976C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114622564 | ||||||
| chr7:114622842
|
A | C | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-5698A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114622842 | ||||||
| chr7:114622918
|
C | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-5622C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114622918 | ||||||
| chr7:114623109
|
A | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0002g0027others(13): Show | 16 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.259-5431A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114623109 | ||||||
| chr7:114623555
|
G | A | 5 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0170others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-4985G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114623555 | ||||||
| chr7:114623877
|
T | C | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259-4663T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114623877 | ||||||
| chr7:114624243
|
C | G | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-4297C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114624243 | ||||||
| chr7:114624286
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.259-4254C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114624286 | ||||||
| chr7:114624451
|
A | G | 5 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(2): Show | 5 | HG01168.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-4089A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114624451 | ||||||
| chr7:114625095
|
A | T | 34 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-3445A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625095 | ||||||
| chr7:114625138
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.259-3402A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625138 | ||||||
| chr7:114625302
|
T | C | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-3238T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625302 | ||||||
| chr7:114625426
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0046others(32): Show | 35 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.259-3114C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625426 | ||||||
| chr7:114625680
|
A | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-2860A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625680 | ||||||
| chr7:114625715
|
C | T | 5 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(2): Show | 5 | HG01168.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-2825C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625715 | ||||||
| chr7:114625886
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.259-2654T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114625886 | ||||||
| chr7:114626343
|
A | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-2197A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626343 | ||||||
| chr7:114626351
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093 | 3 | HG01168.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.259-2189C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626351 | ||||||
| chr7:114626448
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.259-2092G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626448 | ||||||
| chr7:114626491
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.259-2049C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626491 | ||||||
| chr7:114626531
|
A | ATC | 15 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0057others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-1989_259-1988d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114626531 | |||||
| chr7:114626553
|
G | C | 5 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(2): Show | 5 | HG01168.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1987G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626553 | ||||||
| chr7:114626553
|
GTCTC | G | 28 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(25): Show | 28 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.259-1979_259-1976d others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114626553 | |||||
| chr7:114626557
|
C | CTG | 5 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(2): Show | 5 | HG01168.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1982_259-1981i others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114626557 | |||||
| chr7:114626700
|
A | G | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-1840A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626700 | ||||||
| chr7:114626711
|
G | A | 3 | a0001c0001t0002g0151a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.259-1829G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626711 | ||||||
| chr7:114626740
|
A | AT | 33 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.259-1792dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114626740 | |||||
| chr7:114626785
|
G | A | 33 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.259-1755G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626785 | ||||||
| chr7:114626916
|
A | G | 1 | a0001c0001t0003g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.259-1624A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626916 | ||||||
| chr7:114626982
|
T | A | 33 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.259-1558T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114626982 | ||||||
| chr7:114627142
|
CT | C | 33 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.259-1386delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114627142 | |||||
| chr7:114627155
|
C | A | 1 | a0001c0001t0004g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259-1385C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627155 | ||||||
| chr7:114627180
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.259-1360A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627180 | ||||||
| chr7:114627184
|
T | C | 20 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(17): Show | 21 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.259-1356T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627184 | ||||||
| chr7:114627504
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.259-1036A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627504 | ||||||
| chr7:114627578
|
T | C | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-962T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627578 | ||||||
| chr7:114627625
|
T | C | 6 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(3): Show | 6 | HG01168.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-915T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627625 | ||||||
| chr7:114627872
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.259-668G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627872 | ||||||
| chr7:114627939
|
C | T | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.259-601C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627939 | ||||||
| chr7:114627939
|
CAT | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.259-588_259-587del others(2): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 114627939 | |||||
| chr7:114627941
|
T | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(63): Show | 66 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.259-599T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627941 | ||||||
| chr7:114627952
|
A | C | 3 | a0001c0001t0006g0010a0001c0001t0025g0012a0001c0001t0031g0114 | 3 | HG02615.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.259-588A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627952 | ||||||
| chr7:114627999
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259-541C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114627999 | ||||||
| chr7:114628056
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.259-484A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114628056 | ||||||
| chr7:114628108
|
T | C | 2 | a0001c0001t0005g0125a0001c0001t0009g0173 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.259-432T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 3/16 | chr7 | 114628108 | ||||||
| chr7:114628686
|
G | C | 1 | a0001c0001t0031g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.396+9G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 4/16 | chr7 | 114628686 | ||||||
| chr7:114628950
|
A | G | 1 | a0001c0001t0030g0068 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.396+273A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 4/16 | chr7 | 114628950 | ||||||
| chr7:114629408
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.397-397A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 4/16 | chr7 | 114629408 | ||||||
| chr7:114630022
|
T | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.597+17T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114630022 | ||||||
| chr7:114630202
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.597+197A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114630202 | ||||||
| chr7:114630306
|
G | T | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.597+301G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114630306 | ||||||
| chr7:114630921
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.598-607C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114630921 | ||||||
| chr7:114630999
|
T | A | 2 | a0001c0001t0003g0091a0001c0001t0004g0074 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.598-529T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114630999 | ||||||
| chr7:114631000
|
A | T | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.598-528A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114631000 | ||||||
| chr7:114631195
|
A | G | 3 | a0001c0001t0005g0073a0001c0001t0006g0071a0001c0001t0006g0130 | 3 | HG02145.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.598-333A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114631195 | ||||||
| chr7:114631239
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.598-289T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 5/16 | chr7 | 114631239 | ||||||
| chr7:114631854
|
A | G | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.775+149A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114631854 | ||||||
| chr7:114632009
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.775+304G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114632009 | ||||||
| chr7:114632100
|
A | G | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.775+395A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114632100 | ||||||
| chr7:114632201
|
C | A | 1 | a0001c0001t0004g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.775+496C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114632201 | ||||||
| chr7:114632438
|
C | A | 1 | a0001c0001t0020g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.775+733C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114632438 | ||||||
| chr7:114632468
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.775+763T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114632468 | ||||||
| chr7:114633669
|
G | A | 1 | a0001c0001t0031g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.775+1964G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114633669 | ||||||
| chr7:114633674
|
A | G | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+1969A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114633674 | ||||||
| chr7:114633698
|
T | C | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.775+1993T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114633698 | ||||||
| chr7:114633941
|
C | T | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.775+2236C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114633941 | ||||||
| chr7:114634005
|
C | T | 9 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0011g0060others(6): Show | 9 | HG01168.hp1 HG02280.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.775+2300C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634005 | ||||||
| chr7:114634054
|
A | G | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.775+2349A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634054 | ||||||
| chr7:114634072
|
G | C | 1 | a0001c0001t0004g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.775+2367G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634072 | ||||||
| chr7:114634276
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.775+2571A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634276 | ||||||
| chr7:114634734
|
A | G | 2 | a0001c0001t0004g0171a0001c0001t0021g0128 | 2 | HG01169.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.775+3029A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634734 | ||||||
| chr7:114634754
|
T | G | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.775+3049T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634754 | ||||||
| chr7:114634870
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.775+3165C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634870 | ||||||
| chr7:114634931
|
G | C | 6 | a0001c0001t0006g0085a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+3226G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114634931 | ||||||
| chr7:114635299
|
C | A | 5 | a0001c0001t0003g0039a0001c0001t0008g0126a0001c0001t0018g0080others(2): Show | 5 | HG00423.hp2 HG02293.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+3594C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114635299 | ||||||
| chr7:114635327
|
G | A | 5 | a0001c0001t0003g0039a0001c0001t0008g0126a0001c0001t0018g0080others(2): Show | 5 | HG00423.hp2 HG02293.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+3622G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114635327 | ||||||
| chr7:114635514
|
A | G | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.775+3809A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114635514 | ||||||
| chr7:114635576
|
C | T | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.775+3871C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114635576 | ||||||
| chr7:114635770
|
C | A | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.775+4065C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114635770 | ||||||
| chr7:114635878
|
G | A | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.775+4173G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114635878 | ||||||
| chr7:114636191
|
G | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.775+4486G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636191 | ||||||
| chr7:114636222
|
C | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0160others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.775+4517C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636222 | ||||||
| chr7:114636256
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.775+4551T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636256 | ||||||
| chr7:114636312
|
T | C | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.775+4607T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636312 | ||||||
| chr7:114636624
|
CT | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(73): Show | 76 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.775+4934delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 114636624 | |||||
| chr7:114636822
|
C | A | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.775+5117C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636822 | ||||||
| chr7:114636858
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.775+5153A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636858 | ||||||
| chr7:114636967
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.775+5262C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114636967 | ||||||
| chr7:114637152
|
C | T | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-5258C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637152 | ||||||
| chr7:114637258
|
C | A | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-5152C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637258 | ||||||
| chr7:114637470
|
A | G | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.776-4940A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637470 | ||||||
| chr7:114637500
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.776-4910G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637500 | ||||||
| chr7:114637506
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.776-4904G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637506 | ||||||
| chr7:114637537
|
A | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776-4873A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637537 | ||||||
| chr7:114637559
|
T | A | 29 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(26): Show | 29 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.776-4851T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637559 | ||||||
| chr7:114637680
|
A | G | 4 | a0001c0001t0002g0145a0001c0001t0002g0167a0001c0001t0013g0093others(1): Show | 4 | HG01168.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-4730A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637680 | ||||||
| chr7:114637868
|
C | T | 2 | a0001c0002t0002g0102a0001c0002t0005g0103 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.776-4542C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114637868 | ||||||
| chr7:114638105
|
C | T | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-4305C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638105 | ||||||
| chr7:114638176
|
CT | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00642.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.776-4233delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638176 | ||||||
| chr7:114638205
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.776-4205C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638205 | ||||||
| chr7:114638235
|
T | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776-4175T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638235 | ||||||
| chr7:114638247
|
G | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776-4163G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638247 | ||||||
| chr7:114638322
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.776-4088T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638322 | ||||||
| chr7:114638512
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.776-3898A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638512 | ||||||
| chr7:114638819
|
G | T | 6 | a0001c0001t0006g0085a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-3591G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638819 | ||||||
| chr7:114638963
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.776-3447T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638963 | ||||||
| chr7:114638970
|
C | G | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776-3440C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638970 | ||||||
| chr7:114638980
|
T | C | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.776-3430T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114638980 | ||||||
| chr7:114639015
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.776-3395A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114639015 | ||||||
| chr7:114639398
|
G | T | 1 | a0001c0001t0004g0156 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.776-3012G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114639398 | ||||||
| chr7:114639540
|
T | A | 4 | a0001c0001t0005g0119a0001c0001t0011g0060a0001c0003t0006g0149others(1): Show | 4 | HG01243.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-2870T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114639540 | ||||||
| chr7:114639593
|
A | G | 2 | a0001c0001t0013g0093a0001c0001t0024g0132 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.776-2817A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114639593 | ||||||
| chr7:114639834
|
T | G | 4 | a0001c0001t0005g0119a0001c0001t0011g0060a0001c0003t0006g0149others(1): Show | 4 | HG01243.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-2576T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114639834 | ||||||
| chr7:114639853
|
CTGT | C | 3 | a0001c0001t0002g0013a0001c0001t0015g0092a0001c0001t0019g0095 | 3 | HG02615.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.776-2543_776-2541d others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 114639853 | |||||
| chr7:114640127
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0004g0014 | 3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.776-2283A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640127 | ||||||
| chr7:114640232
|
C | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-2178C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640232 | ||||||
| chr7:114640269
|
A | G | 1 | a0001c0001t0022g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.776-2141A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640269 | ||||||
| chr7:114640319
|
A | G | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-2091A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640319 | ||||||
| chr7:114640366
|
T | C | 1 | a0001c0001t0009g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-2044T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640366 | ||||||
| chr7:114640747
|
A | C | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.776-1663A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640747 | ||||||
| chr7:114640825
|
A | G | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776-1585A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640825 | ||||||
| chr7:114640839
|
G | C | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.776-1571G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640839 | ||||||
| chr7:114640989
|
T | C | 6 | a0001c0001t0006g0085a0001c0002t0001g0097a0001c0002t0001g0098others(3): Show | 6 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-1421T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114640989 | ||||||
| chr7:114641070
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.776-1340A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114641070 | ||||||
| chr7:114641560
|
T | G | 3 | a0001c0001t0002g0013a0001c0001t0015g0092a0001c0001t0019g0095 | 3 | HG02615.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.776-850T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114641560 | ||||||
| chr7:114641590
|
T | C | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-820T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114641590 | ||||||
| chr7:114641807
|
T | A | 2 | a0001c0001t0013g0093a0001c0001t0024g0132 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.776-603T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114641807 | ||||||
| chr7:114641919
|
C | T | 3 | a0001c0001t0004g0032a0001c0001t0008g0143a0001c0001t0010g0142 | 3 | HG01515.hp2 HG02293.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.776-491C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114641919 | ||||||
| chr7:114641987
|
G | A | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-423G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114641987 | ||||||
| chr7:114642172
|
T | A | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.776-238T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114642172 | ||||||
| chr7:114642202
|
C | G | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776-208C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114642202 | ||||||
| chr7:114642206
|
T | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0101a0001c0001t0009g0064 | 3 | HG03098.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.776-204T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 6/16 | chr7 | 114642206 | ||||||
| chr7:114642705
|
G | C | 3 | a0001c0001t0002g0013a0001c0001t0015g0092a0001c0001t0019g0095 | 3 | HG02615.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.989+82G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642705 | ||||||
| chr7:114642779
|
A | AATATAT | 1 | a0001c0001t0002g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.989+185_989+190dup others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
A | AATATATA others(1): Show |
3 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0004g0051 | 3 | HG02602.hp1 HG03688.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.989+183_989+190dup others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
A | AATATATA others(3): Show |
4 | a0001c0001t0002g0028a0001c0001t0002g0054a0001c0001t0003g0045others(1): Show | 4 | HG00597.hp2 HG00673.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.989+181_989+190dup others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
A | AATATATA others(5): Show |
1 | a0001c0001t0002g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.989+179_989+190dup others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
A | AATATATA others(7): Show |
4 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0002g0084others(1): Show | 4 | HG00609.hp1 HG03710.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.989+177_989+190dup others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
A | AATATATA others(9): Show |
1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.989+175_989+190dup others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
A | ATAATATA others(5): Show |
1 | a0001c0003t0006g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.989+156_989+157ins others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642779 | ||||||
| chr7:114642779
|
A | T | 2 | a0001c0001t0007g0140a0001c0001t0007g0141 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.989+156A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642779 | ||||||
| chr7:114642779
|
AAT | A | 11 | a0001c0001t0002g0096a0001c0001t0002g0172a0001c0001t0003g0015others(8): Show | 11 | HG01069.hp1 HG01257.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.989+189_989+190del others(2): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
AATAT | A | 32 | a0001c0001t0001g0056a0001c0001t0001g0089a0001c0001t0001g0127others(29): Show | 32 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.989+187_989+190del others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
AATATAT | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0037a0001c0001t0024g0132 | 3 | HG00621.hp1 HG01168.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.989+185_989+190del others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642779
|
AATATATA others(3): Show |
A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0002g0102others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.989+181_989+190del others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642779 | |||||
| chr7:114642799
|
TATA | T | 4 | a0001c0001t0002g0168a0001c0001t0003g0078a0001c0001t0003g0148others(1): Show | 4 | HG01106.hp1 HG01981.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.989+177_989+179del others(3): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642799 | ||||||
| chr7:114642799
|
TATATA | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0002g0027others(11): Show | 14 | HG02040.hp2 HG02071.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.989+177_989+181del others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642799 | ||||||
| chr7:114642801
|
TATATA | T | 2 | a0001c0001t0004g0081a0001c0001t0004g0131 | 2 | HG00140.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.989+179_989+183del others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642801 | ||||||
| chr7:114642801
|
TATATATA | T | 14 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0044others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.989+179_989+185del others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642801 | ||||||
| chr7:114642801
|
TATATATA others(4): Show |
T | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.989+179_989+189del others(11): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642801 | ||||||
| chr7:114642802
|
A | T | 1 | a0001c0001t0003g0015 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.989+179A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642802 | ||||||
| chr7:114642802
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0006g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.989+181_989+191del others(11): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642802 | |||||
| chr7:114642804
|
A | T | 34 | a0001c0001t0001g0056a0001c0001t0001g0089a0001c0001t0002g0025others(31): Show | 34 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.989+181A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642804 | ||||||
| chr7:114642806
|
A | T | 59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0056others(56): Show | 59 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.989+183A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642806 | ||||||
| chr7:114642808
|
A | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0056others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.989+185A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642808 | ||||||
| chr7:114642810
|
A | AT | 4 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0164others(1): Show | 4 | HG00642.hp1 HG01257.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.989+188dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642810 | |||||
| chr7:114642810
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0005g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.989+188_989+189ins others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642810 | |||||
| chr7:114642810
|
A | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.989+187A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642810 | ||||||
| chr7:114642811
|
TA | T | 2 | a0001c0001t0006g0010a0002c0004t0012g0063 | 2 | HG02615.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.989+189delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642811 | ||||||
| chr7:114642812
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.989+190_989+191ins others(15): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642812 | |||||
| chr7:114642812
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.989+190_989+191ins others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642812 | |||||
| chr7:114642812
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.989+190_989+191ins others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642812 | |||||
| chr7:114642812
|
A | ATT | 5 | a0001c0001t0001g0101a0001c0001t0002g0123a0001c0001t0002g0167others(2): Show | 5 | HG02723.hp2 HG03098.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.989+203_989+204dup others(2): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642812 | |||||
| chr7:114642812
|
A | ATTT | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.989+202_989+204dup others(3): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 114642812 | |||||
| chr7:114642812
|
A | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.989+189A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642812 | ||||||
| chr7:114642813
|
T | TA | 5 | a0001c0001t0001g0090a0001c0001t0005g0115a0001c0001t0005g0116others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.989+190_989+191ins others(1): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642813 | ||||||
| chr7:114642813
|
T | TATATATA others(2): Show |
2 | a0001c0001t0007g0140a0001c0001t0007g0141 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.989+190_989+191ins others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642813 | ||||||
| chr7:114642813
|
T | TATATATA others(4): Show |
1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.989+190_989+191ins others(11): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642813 | ||||||
| chr7:114642815
|
T | A | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989+192T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642815 | ||||||
| chr7:114642817
|
T | A | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989+194T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642817 | ||||||
| chr7:114642819
|
T | A | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989+196T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642819 | ||||||
| chr7:114642821
|
T | A | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989+198T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642821 | ||||||
| chr7:114642877
|
T | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989+254T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642877 | ||||||
| chr7:114642895
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0015g0092a0001c0001t0019g0095 | 3 | HG02615.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.989+272G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642895 | ||||||
| chr7:114642963
|
C | A | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989+340C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642963 | ||||||
| chr7:114642984
|
A | T | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.989+361A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114642984 | ||||||
| chr7:114643005
|
G | A | 1 | a0001c0001t0006g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.989+382G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114643005 | ||||||
| chr7:114643488
|
G | C | 3 | a0001c0001t0002g0013a0001c0001t0015g0092a0001c0001t0019g0095 | 3 | HG02615.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.989+865G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114643488 | ||||||
| chr7:114643647
|
G | T | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.989+1024G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114643647 | ||||||
| chr7:114643732
|
G | A | 5 | a0001c0001t0006g0085a0001c0002t0001g0097a0001c0002t0001g0098others(2): Show | 5 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.990-953G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114643732 | ||||||
| chr7:114643954
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.990-731A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114643954 | ||||||
| chr7:114644345
|
G | A | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.990-340G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114644345 | ||||||
| chr7:114644607
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0077 | 2 | HG00609.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.990-78G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 7/16 | chr7 | 114644607 | ||||||
| chr7:114644964
|
A | G | 1 | a0001c0001t0006g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1094+175A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114644964 | ||||||
| chr7:114645126
|
CCTAATAT others(42): Show |
C | 1 | a0001c0001t0013g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1094+338_1094+386d others(51): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645126 | ||||||
| chr7:114645128
|
TAATATAT others(25): Show |
T | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1094+340_1094+371d others(34): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645128 | ||||||
| chr7:114645129
|
A | AAT | 12 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0061others(9): Show | 12 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1094+389_1094+390d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
A | AATAT | 3 | a0001c0001t0003g0045a0001c0001t0003g0052a0001c0001t0010g0142 | 3 | HG00673.hp1 HG01515.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1094+387_1094+390d others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
A | AATATAT | 3 | a0001c0001t0002g0084a0001c0001t0005g0120a0001c0001t0028g0040 | 3 | HG00639.hp1 HG02258.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1094+385_1094+390d others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
A | T | 1 | a0001c0001t0002g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1094+340A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645129 | ||||||
| chr7:114645129
|
AAT | A | 23 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0100others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094+389_1094+390d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATAT | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0089others(25): Show | 28 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1094+387_1094+390d others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATAT | A | 22 | a0001c0001t0001g0104a0001c0001t0002g0001a0001c0001t0002g0017others(19): Show | 23 | HG00597.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1094+385_1094+390d others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(1): Show |
A | 23 | a0001c0001t0001g0007a0001c0001t0001g0065a0001c0001t0001g0101others(20): Show | 23 | HG00642.hp2 HG01106.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094+383_1094+390d others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(3): Show |
A | 10 | a0001c0001t0002g0077a0001c0001t0002g0168a0001c0001t0003g0015others(7): Show | 10 | HG00609.hp2 HG01192.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1094+381_1094+390d others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(5): Show |
A | 11 | a0001c0001t0002g0025a0001c0001t0002g0123a0001c0001t0002g0172others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1094+379_1094+390d others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(7): Show |
A | 3 | a0001c0001t0002g0013a0001c0003t0006g0149a0001c0003t0006g0150 | 3 | HG02280.hp2 HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1094+377_1094+390d others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0003g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1094+375_1094+390d others(18): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0024g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1094+373_1094+390d others(20): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1094+369_1094+390d others(24): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645129
|
AATATATA others(25): Show |
A | 1 | a0001c0001t0026g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1094+359_1094+390d others(34): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645129 | |||||
| chr7:114645168
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0003g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1094+381_1094+391d others(13): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645168 | |||||
| chr7:114645172
|
ATATATAT | A | 3 | a0001c0001t0001g0056a0001c0001t0002g0167a0001c0001t0004g0088 | 3 | HG02723.hp2 NA19083.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1094+385_1094+391d others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645172 | |||||
| chr7:114645174
|
ATATAT | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0006 | 2 | HG02523.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1094+387_1094+391d others(7): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645174 | |||||
| chr7:114645178
|
AT | A | 4 | a0001c0001t0001g0026a0001c0001t0004g0081a0001c0001t0006g0121others(1): Show | 4 | HG00621.hp2 HG00639.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1094+392delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114645178 | |||||
| chr7:114645179
|
T | TATA | 4 | a0001c0001t0002g0055a0001c0001t0004g0072a0001c0001t0006g0010others(1): Show | 4 | HG02145.hp1 HG02615.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+390_1094+391i others(5): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645179 | ||||||
| chr7:114645180
|
T | A | 1 | a0001c0001t0002g0019 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1094+391T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645180 | ||||||
| chr7:114645200
|
A | G | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1094+411A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645200 | ||||||
| chr7:114645204
|
C | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1094+415C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645204 | ||||||
| chr7:114645209
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1094+420T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645209 | ||||||
| chr7:114645481
|
T | C | 3 | a0001c0001t0006g0010a0001c0001t0025g0012a0001c0001t0031g0114 | 3 | HG02615.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1094+692T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645481 | ||||||
| chr7:114645623
|
A | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1094+834A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645623 | ||||||
| chr7:114645887
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1094+1098G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645887 | ||||||
| chr7:114645928
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1094+1139G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114645928 | ||||||
| chr7:114646060
|
T | TA | 6 | a0001c0001t0001g0003a0001c0001t0002g0017a0001c0001t0002g0022others(3): Show | 6 | HG00597.hp2 HG00609.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1094+1293dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114646060 | |||||
| chr7:114646060
|
T | TAAAA | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1094+1290_1094+129 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114646060 | |||||
| chr7:114646060
|
T | TAAAAA | 62 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0089others(59): Show | 62 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1094+1289_1094+129 others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114646060 | |||||
| chr7:114646060
|
T | TAAAAAA | 24 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0135others(21): Show | 24 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1094+1288_1094+129 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114646060 | |||||
| chr7:114646060
|
TA | T | 6 | a0001c0001t0006g0085a0001c0001t0014g0146a0001c0002t0001g0097others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1094+1293delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114646060 | |||||
| chr7:114646072
|
A | G | 1 | a0002c0004t0012g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1094+1283A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114646072 | ||||||
| chr7:114646472
|
TG | T | 9 | a0001c0001t0001g0065a0001c0001t0001g0101a0001c0001t0001g0110others(6): Show | 9 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1094+1684delG | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114646472 | ||||||
| chr7:114646556
|
T | C | 27 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1094+1767T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114646556 | ||||||
| chr7:114646646
|
T | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0084 | 2 | NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1094+1857T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114646646 | ||||||
| chr7:114646700
|
A | T | 2 | a0001c0001t0013g0093a0001c0001t0024g0132 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1094+1911A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114646700 | ||||||
| chr7:114646826
|
CA | C | 4 | a0001c0001t0006g0070a0001c0001t0006g0117a0001c0001t0006g0121others(1): Show | 4 | HG01496.hp2 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1094+2044delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114646826 | |||||
| chr7:114647061
|
T | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0044others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1094+2272T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114647061 | ||||||
| chr7:114647312
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1094+2523T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114647312 | ||||||
| chr7:114647595
|
G | C | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1094+2806G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114647595 | ||||||
| chr7:114647862
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1094+3073T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114647862 | ||||||
| chr7:114647878
|
A | T | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1094+3089A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114647878 | ||||||
| chr7:114648109
|
C | T | 2 | a0001c0003t0006g0149a0001c0003t0006g0150 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1094+3320C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114648109 | ||||||
| chr7:114648372
|
C | G | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1094+3583C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114648372 | ||||||
| chr7:114648934
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1095-3269G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114648934 | ||||||
| chr7:114648941
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1095-3262A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114648941 | ||||||
| chr7:114649384
|
A | T | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1095-2819A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114649384 | ||||||
| chr7:114649566
|
G | A | 2 | a0001c0001t0005g0119a0001c0001t0011g0060 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1095-2637G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114649566 | ||||||
| chr7:114649586
|
T | A | 7 | a0001c0001t0002g0013a0001c0001t0005g0119a0001c0001t0011g0060others(4): Show | 7 | HG01243.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1095-2617T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114649586 | ||||||
| chr7:114650158
|
A | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0118others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1095-2045A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650158 | ||||||
| chr7:114650314
|
T | G | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1095-1889T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650314 | ||||||
| chr7:114650360
|
T | C | 39 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1095-1843T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650360 | ||||||
| chr7:114650428
|
G | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.1095-1775G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650428 | ||||||
| chr7:114650428
|
GA | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0089others(88): Show | 92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1095-1762delA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 114650428 | |||||
| chr7:114650436
|
A | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.1095-1767A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650436 | ||||||
| chr7:114650612
|
C | T | 4 | a0001c0001t0005g0073a0001c0001t0006g0071a0001c0001t0006g0085others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095-1591C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650612 | ||||||
| chr7:114650693
|
A | G | 33 | a0001c0001t0001g0026a0001c0001t0001g0057a0001c0001t0001g0065others(30): Show | 33 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1095-1510A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650693 | ||||||
| chr7:114650963
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1095-1240T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650963 | ||||||
| chr7:114650997
|
C | T | 20 | a0001c0001t0003g0049a0001c0001t0004g0005a0001c0001t0004g0008others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1095-1206C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114650997 | ||||||
| chr7:114651106
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1095-1097T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651106 | ||||||
| chr7:114651298
|
A | C | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1095-905A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651298 | ||||||
| chr7:114651341
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1095-862A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651341 | ||||||
| chr7:114651345
|
C | G | 5 | a0001c0001t0005g0107a0001c0001t0005g0116a0001c0001t0016g0169others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095-858C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651345 | ||||||
| chr7:114651380
|
G | A | 75 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0100others(72): Show | 76 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1095-823G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651380 | ||||||
| chr7:114651381
|
T | C | 19 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0155others(16): Show | 19 | HG01243.hp1 HG01496.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095-822T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651381 | ||||||
| chr7:114651500
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1095-703G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651500 | ||||||
| chr7:114651663
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1095-540T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651663 | ||||||
| chr7:114651681
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1095-522A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651681 | ||||||
| chr7:114651946
|
G | T | 4 | a0001c0001t0001g0057a0001c0001t0002g0013a0001c0001t0002g0096others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095-257G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 8/16 | chr7 | 114651946 | ||||||
| chr7:114652477
|
A | C | 1 | a0001c0001t0002g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1182+187A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 9/16 | chr7 | 114652477 | ||||||
| chr7:114652674
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1182+384A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 9/16 | chr7 | 114652674 | ||||||
| chr7:114652693
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1182+403A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 9/16 | chr7 | 114652693 | ||||||
| chr7:114652706
|
T | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0101 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1182+416T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 9/16 | chr7 | 114652706 | ||||||
| chr7:114653804
|
G | T | 35 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0104others(32): Show | 36 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1183-122G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 9/16 | chr7 | 114653804 | ||||||
| chr7:114653854
|
G | T | 1 | a0001c0001t0005g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1183-72G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 9/16 | chr7 | 114653854 | ||||||
| chr7:114654146
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1266+137G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114654146 | ||||||
| chr7:114654229
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1266+220A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114654229 | ||||||
| chr7:114654350
|
G | C | 36 | a0001c0001t0001g0057a0001c0001t0002g0013a0001c0001t0002g0096others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1266+341G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114654350 | ||||||
| chr7:114654721
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1266+712A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114654721 | ||||||
| chr7:114654884
|
C | T | 3 | a0001c0001t0002g0123a0001c0001t0002g0172a0001c0001t0024g0132 | 3 | HG02622.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+875C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114654884 | ||||||
| chr7:114654887
|
C | T | 33 | a0001c0001t0001g0057a0001c0001t0002g0013a0001c0001t0002g0096others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1266+878C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114654887 | ||||||
| chr7:114655009
|
A | G | 35 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0104others(32): Show | 36 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1266+1000A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114655009 | ||||||
| chr7:114655087
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1266+1078C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114655087 | ||||||
| chr7:114655109
|
T | G | 10 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0104others(7): Show | 10 | HG00642.hp1 HG01257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1266+1100T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114655109 | ||||||
| chr7:114655539
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1266+1530G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114655539 | ||||||
| chr7:114655625
|
T | G | 24 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(21): Show | 25 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1266+1616T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114655625 | ||||||
| chr7:114656018
|
A | C | 35 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0104others(32): Show | 36 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1266+2009A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656018 | ||||||
| chr7:114656047
|
T | C | 71 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0100others(68): Show | 72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1267-2019T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656047 | ||||||
| chr7:114656049
|
C | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0155others(16): Show | 19 | HG01243.hp1 HG01496.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1267-2017C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656049 | ||||||
| chr7:114656279
|
A | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1267-1787A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656279 | ||||||
| chr7:114656313
|
GT | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0057a0001c0001t0001g0101others(36): Show | 39 | HG01168.hp1 HG01243.hp1 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.1267-1741delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 114656313 | |||||
| chr7:114656431
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1267-1635A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656431 | ||||||
| chr7:114656490
|
A | C | 36 | a0001c0001t0001g0057a0001c0001t0002g0013a0001c0001t0002g0096others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1267-1576A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656490 | ||||||
| chr7:114656535
|
A | C | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1267-1531A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114656535 | ||||||
| chr7:114657125
|
G | A | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1267-941G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114657125 | ||||||
| chr7:114657303
|
C | A | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1267-763C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114657303 | ||||||
| chr7:114657765
|
G | A | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.1267-301G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114657765 | ||||||
| chr7:114657945
|
T | C | 1 | a0001c0001t0005g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1267-121T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114657945 | ||||||
| chr7:114658004
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0013g0093 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1267-62C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 10/16 | chr7 | 114658004 | ||||||
| chr7:114658632
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+365G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 11/16 | chr7 | 114658632 | ||||||
| chr7:114658653
|
C | T | 4 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0058others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+386C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 11/16 | chr7 | 114658653 | ||||||
| chr7:114659152
|
G | A | 1 | a0001c0001t0002g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1469-204G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 11/16 | chr7 | 114659152 | ||||||
| chr7:114659703
|
C | G | 3 | a0001c0001t0004g0072a0001c0001t0004g0129a0001c0001t0004g0156 | 3 | HG01361.hp1 HG01517.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1647+30C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114659703 | ||||||
| chr7:114659719
|
A | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1647+46A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114659719 | ||||||
| chr7:114659849
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1647+176T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114659849 | ||||||
| chr7:114660494
|
T | C | 1 | a0001c0001t0005g0073 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1647+821T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114660494 | ||||||
| chr7:114660537
|
G | T | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1647+864G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114660537 | ||||||
| chr7:114660662
|
T | C | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1647+989T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114660662 | ||||||
| chr7:114660757
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1647+1084A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114660757 | ||||||
| chr7:114660887
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1648-1178G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114660887 | ||||||
| chr7:114661052
|
C | CT | 50 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1648-998dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 114661052 | |||||
| chr7:114661052
|
C | CTT | 54 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0017others(51): Show | 55 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1648-999_1648-998d others(4): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 114661052 | |||||
| chr7:114661472
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1648-593T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114661472 | ||||||
| chr7:114661492
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1648-573A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114661492 | ||||||
| chr7:114662017
|
T | C | 1 | a0001c0001t0015g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1648-48T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 13/16 | chr7 | 114662017 | ||||||
| chr7:114662210
|
T | C | 1 | a0003c0005t0003g0158 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1769+24T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662210 | ||||||
| chr7:114662514
|
C | T | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+328C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662514 | ||||||
| chr7:114662778
|
T | G | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.1769+592T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662778 | ||||||
| chr7:114662799
|
C | T | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1769+613C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662799 | ||||||
| chr7:114662800
|
A | G | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+614A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662800 | ||||||
| chr7:114662848
|
T | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0123others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1770-602T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662848 | ||||||
| chr7:114662995
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1770-455G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114662995 | ||||||
| chr7:114663074
|
A | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1770-376A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114663074 | ||||||
| chr7:114663134
|
G | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1770-316G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114663134 | ||||||
| chr7:114663301
|
C | G | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1770-149C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114663301 | ||||||
| chr7:114663305
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1770-145A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114663305 | ||||||
| chr7:114663352
|
T | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0084 | 2 | NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1770-98T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114663352 | ||||||
| chr7:114663389
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1770-61T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | chr7 | 114663389 | ||||||
| chr7:114663436
|
A | AT | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1770-4dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 114663436 | |||||
| chr7:114663562
|
CT | C | 67 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1839+58delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr7 | 114663562 | |||||
| chr7:114663778
|
G | A | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1839+259G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 15/16 | chr7 | 114663778 | ||||||
| chr7:114663902
|
A | T | 1 | a0001c0001t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1840-371A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 15/16 | chr7 | 114663902 | ||||||
| chr7:114664126
|
G | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(31): Show | 35 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1840-147G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 15/16 | chr7 | 114664126 | ||||||
| chr7:114664508
|
C | T | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2003+72C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114664508 | ||||||
| chr7:114664575
|
A | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2003+139A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114664575 | ||||||
| chr7:114664599
|
G | A | 34 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(31): Show | 35 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.2003+163G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114664599 | ||||||
| chr7:114664791
|
T | C | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2003+355T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114664791 | ||||||
| chr7:114664914
|
T | C | 39 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0123others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.2003+478T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114664914 | ||||||
| chr7:114665467
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2003+1031C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114665467 | ||||||
| chr7:114665532
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2003+1096T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114665532 | ||||||
| chr7:114665985
|
G | A | 11 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(8): Show | 11 | HG00642.hp1 HG01257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2003+1549G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114665985 | ||||||
| chr7:114666792
|
C | T | 1 | a0001c0001t0005g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2003+2356C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114666792 | ||||||
| chr7:114667095
|
C | G | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2003+2659C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114667095 | ||||||
| chr7:114667365
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2003+2929G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114667365 | ||||||
| chr7:114667703
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2003+3267A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114667703 | ||||||
| chr7:114667760
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2003+3324C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114667760 | ||||||
| chr7:114668583
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2003+4147C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114668583 | ||||||
| chr7:114668626
|
A | G | 1 | a0001c0001t0027g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2003+4190A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114668626 | ||||||
| chr7:114668653
|
G | A | 7 | a0001c0001t0003g0052a0001c0001t0003g0066a0001c0001t0003g0067others(4): Show | 7 | HG00597.hp1 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+4217G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114668653 | ||||||
| chr7:114669060
|
T | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2003+4624T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114669060 | ||||||
| chr7:114669456
|
C | T | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2003+5020C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114669456 | ||||||
| chr7:114669472
|
C | T | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2003+5036C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114669472 | ||||||
| chr7:114669905
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2003+5469C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114669905 | ||||||
| chr7:114669977
|
C | T | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2003+5541C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114669977 | ||||||
| chr7:114669998
|
G | T | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2003+5562G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114669998 | ||||||
| chr7:114670183
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2003+5747C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114670183 | ||||||
| chr7:114670234
|
A | G | 2 | a0001c0001t0005g0119a0001c0001t0005g0120 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2003+5798A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114670234 | ||||||
| chr7:114671082
|
T | A | 1 | a0001c0001t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2003+6646T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114671082 | ||||||
| chr7:114671671
|
A | G | 26 | a0001c0001t0005g0073a0001c0001t0005g0094a0001c0001t0005g0107others(23): Show | 26 | HG01243.hp1 HG01496.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.2003+7235A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114671671 | ||||||
| chr7:114671681
|
A | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2003+7245A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114671681 | ||||||
| chr7:114671939
|
C | T | 1 | a0001c0001t0002g0019 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2003+7503C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114671939 | ||||||
| chr7:114672077
|
A | G | 1 | a0001c0001t0004g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2003+7641A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114672077 | ||||||
| chr7:114672360
|
A | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2003+7924A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114672360 | ||||||
| chr7:114672401
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2003+7965G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114672401 | ||||||
| chr7:114672500
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2003+8064G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114672500 | ||||||
| chr7:114672584
|
C | CA | 39 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(36): Show | 40 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.2003+8159dupA | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114672584 | |||||
| chr7:114672596
|
T | A | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2003+8160T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114672596 | ||||||
| chr7:114672619
|
T | TC | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.2003+8184dupC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114672619 | |||||
| chr7:114672914
|
T | C | 8 | a0001c0001t0001g0046a0001c0001t0001g0127a0001c0001t0001g0135others(5): Show | 8 | HG00642.hp1 HG01257.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.2003+8478T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114672914 | ||||||
| chr7:114673007
|
A | G | 2 | a0001c0001t0005g0125a0001c0001t0005g0133 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2003+8571A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114673007 | ||||||
| chr7:114673144
|
A | G | 35 | a0001c0001t0002g0123a0001c0001t0002g0172a0001c0001t0004g0005others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.2003+8708A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114673144 | ||||||
| chr7:114673163
|
A | G | 104 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2003+8727A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114673163 | ||||||
| chr7:114673537
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2003+9101G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114673537 | ||||||
| chr7:114673845
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2003+9409G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114673845 | ||||||
| chr7:114673861
|
G | A | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2003+9425G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114673861 | ||||||
| chr7:114674291
|
A | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2003+9855A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114674291 | ||||||
| chr7:114674356
|
C | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2003+9920C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114674356 | ||||||
| chr7:114674453
|
A | T | 1 | a0001c0001t0004g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2003+10017A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114674453 | ||||||
| chr7:114674508
|
C | T | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2003+10072C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114674508 | ||||||
| chr7:114674601
|
GAAAGA | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0172a0001c0001t0024g0132 | 3 | HG02622.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2003+10166_2003+10 others(11): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114674601 | ||||||
| chr7:114675441
|
T | A | 34 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(31): Show | 35 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.2003+11005T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675441 | ||||||
| chr7:114675471
|
T | G | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2003+11035T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675471 | ||||||
| chr7:114675550
|
T | G | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2003+11114T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675550 | ||||||
| chr7:114675559
|
A | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2003+11123A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675559 | ||||||
| chr7:114675626
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2003+11190G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675626 | ||||||
| chr7:114675631
|
C | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2003+11195C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675631 | ||||||
| chr7:114675639
|
A | T | 2 | a0001c0001t0002g0025a0001c0001t0002g0036 | 2 | NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2003+11203A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675639 | ||||||
| chr7:114675835
|
G | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(8): Show | 11 | HG00642.hp1 HG01257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2003+11399G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675835 | ||||||
| chr7:114675901
|
T | A | 1 | a0001c0001t0027g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2003+11465T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675901 | ||||||
| chr7:114675918
|
A | T | 1 | a0001c0001t0004g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2003+11482A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675918 | ||||||
| chr7:114675921
|
A | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0131a0001c0001t0004g0171 | 3 | HG00099.hp2 HG00140.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+11485A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114675921 | ||||||
| chr7:114676075
|
A | AT | 35 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0056others(32): Show | 36 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2003+11664dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114676075 | |||||
| chr7:114676075
|
A | ATT | 5 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0053others(2): Show | 5 | HG00597.hp2 HG02040.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003+11663_2003+11 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114676075 | |||||
| chr7:114676075
|
AT | A | 20 | a0001c0001t0001g0106a0001c0001t0001g0118a0001c0001t0003g0091others(17): Show | 20 | HG01074.hp1 HG01496.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2003+11664delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114676075 | |||||
| chr7:114676075
|
ATT | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0041others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2003+11663_2003+11 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114676075 | |||||
| chr7:114676098
|
T | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0041others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.2003+11662T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114676098 | ||||||
| chr7:114676209
|
G | T | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2003+11773G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114676209 | ||||||
| chr7:114676230
|
A | G | 2 | a0001c0001t0009g0064a0001c0001t0009g0173 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2003+11794A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114676230 | ||||||
| chr7:114676385
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0172a0001c0001t0024g0132 | 3 | HG02622.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2003+11949G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114676385 | ||||||
| chr7:114676498
|
G | A | 1 | a0001c0002t0002g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2003+12062G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114676498 | ||||||
| chr7:114677030
|
G | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(8): Show | 11 | HG00642.hp1 HG01257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2003+12594G>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677030 | ||||||
| chr7:114677179
|
A | C | 1 | a0001c0001t0008g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2004-12603A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677179 | ||||||
| chr7:114677180
|
A | AAAAAAAC | 33 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(30): Show | 34 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2004-12595_2004-12 others(13): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114677180 | |||||
| chr7:114677180
|
A | AAAAAAC | 28 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.2004-12597_2004-12 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114677180 | |||||
| chr7:114677180
|
A | C | 5 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0123others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-12602A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677180 | ||||||
| chr7:114677181
|
A | C | 1 | a0001c0001t0003g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2004-12601A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677181 | ||||||
| chr7:114677200
|
CTT | C | 2 | a0001c0001t0002g0172a0001c0001t0024g0132 | 2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2004-12581_2004-12 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677200 | ||||||
| chr7:114677598
|
T | C | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2004-12184T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677598 | ||||||
| chr7:114677725
|
T | C | 2 | a0001c0001t0004g0072a0001c0001t0004g0129 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2004-12057T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677725 | ||||||
| chr7:114677833
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-11949C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114677833 | ||||||
| chr7:114678016
|
G | A | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2004-11766G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678016 | ||||||
| chr7:114678042
|
C | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-11740C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678042 | ||||||
| chr7:114678234
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2004-11548G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678234 | ||||||
| chr7:114678375
|
G | C | 1 | a0001c0001t0002g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2004-11407G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678375 | ||||||
| chr7:114678380
|
G | A | 1 | a0001c0001t0005g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2004-11402G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678380 | ||||||
| chr7:114678391
|
C | A | 2 | a0001c0001t0011g0060a0001c0001t0019g0095 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2004-11391C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678391 | ||||||
| chr7:114678547
|
C | CT | 23 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0061others(20): Show | 23 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-11209dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114678547 | |||||
| chr7:114678547
|
C | CTT | 16 | a0001c0001t0003g0023a0001c0001t0003g0069a0001c0001t0004g0014others(13): Show | 16 | HG00642.hp2 HG01070.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2004-11210_2004-11 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114678547 | |||||
| chr7:114678547
|
C | CTTT | 10 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0051others(7): Show | 10 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-11211_2004-11 others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114678547 | |||||
| chr7:114678547
|
C | CTTTT | 6 | a0001c0001t0004g0072a0001c0001t0004g0099a0001c0001t0004g0156others(3): Show | 6 | HG00423.hp1 HG01169.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-11212_2004-11 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114678547 | |||||
| chr7:114678547
|
CT | C | 10 | a0001c0001t0002g0019a0001c0001t0002g0053a0001c0001t0002g0055others(7): Show | 10 | HG00423.hp2 HG01168.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.2004-11209delT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114678547 | |||||
| chr7:114678547
|
CTT | C | 21 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0020others(18): Show | 22 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.2004-11210_2004-11 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114678547 | |||||
| chr7:114678627
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2004-11155A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678627 | ||||||
| chr7:114678628
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2004-11154T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678628 | ||||||
| chr7:114678800
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2004-10982A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114678800 | ||||||
| chr7:114679759
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2004-10023C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114679759 | ||||||
| chr7:114680164
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2004-9618C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114680164 | ||||||
| chr7:114680167
|
A | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-9615A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114680167 | ||||||
| chr7:114680176
|
A | C | 1 | a0001c0001t0003g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2004-9606A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114680176 | ||||||
| chr7:114681349
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2004-8433G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114681349 | ||||||
| chr7:114681888
|
A | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.2004-7894A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114681888 | ||||||
| chr7:114682069
|
C | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-7713C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114682069 | ||||||
| chr7:114682243
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2004-7539C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114682243 | ||||||
| chr7:114682441
|
G | A | 3 | a0001c0001t0003g0039a0001c0001t0003g0062a0001c0001t0003g0086 | 3 | HG00423.hp2 NA18961.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2004-7341G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114682441 | ||||||
| chr7:114682535
|
A | G | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2004-7247A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114682535 | ||||||
| chr7:114682562
|
C | T | 3 | a0001c0001t0002g0123a0001c0001t0002g0172a0001c0001t0024g0132 | 3 | HG02622.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2004-7220C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114682562 | ||||||
| chr7:114682866
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2004-6916T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114682866 | ||||||
| chr7:114683017
|
T | A | 2 | a0001c0001t0011g0060a0001c0001t0019g0095 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2004-6765T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683017 | ||||||
| chr7:114683151
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2004-6631A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683151 | ||||||
| chr7:114683365
|
G | A | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2004-6417G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683365 | ||||||
| chr7:114683513
|
C | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0123others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2004-6269C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683513 | ||||||
| chr7:114683569
|
GC | G | 2 | a0001c0001t0011g0060a0001c0001t0019g0095 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2004-6212delC | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683569 | ||||||
| chr7:114683662
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2004-6120G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683662 | ||||||
| chr7:114683664
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0029 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2004-6118A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683664 | ||||||
| chr7:114683850
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2004-5932G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683850 | ||||||
| chr7:114683904
|
C | T | 27 | a0001c0001t0001g0118a0001c0001t0005g0073a0001c0001t0005g0094others(24): Show | 27 | HG01243.hp1 HG01496.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.2004-5878C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683904 | ||||||
| chr7:114683916
|
C | CCT | 162 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.2004-5866_2004-586 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114683916 | ||||||
| chr7:114684021
|
T | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0123others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2004-5761T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114684021 | ||||||
| chr7:114684087
|
C | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0017others(31): Show | 35 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.2004-5695C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114684087 | ||||||
| chr7:114684105
|
A | G | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2004-5677A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114684105 | ||||||
| chr7:114684259
|
C | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2004-5523C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114684259 | ||||||
| chr7:114684757
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2004-5025T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114684757 | ||||||
| chr7:114684762
|
G | C | 1 | a0001c0001t0006g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2004-5020G>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114684762 | ||||||
| chr7:114685128
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2004-4654C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685128 | ||||||
| chr7:114685227
|
T | C | 2 | a0001c0001t0003g0009a0001c0001t0003g0076 | 2 | HG00621.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2004-4555T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685227 | ||||||
| chr7:114685332
|
G | A | 2 | a0001c0001t0009g0064a0001c0001t0009g0173 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2004-4450G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685332 | ||||||
| chr7:114685382
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2004-4400T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685382 | ||||||
| chr7:114685490
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2004-4292A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685490 | ||||||
| chr7:114685760
|
A | C | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2004-4022A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685760 | ||||||
| chr7:114685853
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2004-3929A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685853 | ||||||
| chr7:114685970
|
G | GT | 5 | a0001c0001t0001g0056a0001c0001t0002g0013a0001c0001t0002g0096others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-3801dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114685970 | |||||
| chr7:114685981
|
T | A | 1 | a0001c0001t0025g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2004-3801T>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685981 | ||||||
| chr7:114685982
|
A | T | 5 | a0001c0001t0001g0155a0001c0001t0004g0032a0001c0001t0005g0119others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-3800A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114685982 | ||||||
| chr7:114686051
|
GTATTA | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0124others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004-3730_2004-372 others(9): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686051 | ||||||
| chr7:114686301
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2004-3481T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686301 | ||||||
| chr7:114686420
|
A | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0157 | 2 | HG01069.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2004-3362A>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686420 | ||||||
| chr7:114686457
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2004-3325G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686457 | ||||||
| chr7:114686640
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2004-3142T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686640 | ||||||
| chr7:114686758
|
A | G | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-3024A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686758 | ||||||
| chr7:114686785
|
C | T | 1 | a0001c0001t0017g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2004-2997C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686785 | ||||||
| chr7:114686786
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0167 | 2 | HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2004-2996G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686786 | ||||||
| chr7:114686860
|
G | A | 3 | a0001c0001t0001g0110a0001c0002t0001g0097a0001c0002t0001g0098 | 3 | HG02572.hp1 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2004-2922G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114686860 | ||||||
| chr7:114688003
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0124others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004-1779T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688003 | ||||||
| chr7:114688105
|
T | G | 32 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2004-1677T>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688105 | ||||||
| chr7:114688208
|
T | TAC | 38 | a0001c0001t0001g0154a0001c0001t0002g0027a0001c0001t0003g0015others(35): Show | 38 | HG00597.hp1 HG01069.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.2004-1536_2004-153 others(6): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
T | TACAC | 44 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0044others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-1538_2004-153 others(8): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
T | TACACAC | 22 | a0001c0001t0001g0026a0001c0001t0001g0104a0001c0001t0001g0127others(19): Show | 23 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-1540_2004-153 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
T | TACACACA others(1): Show |
7 | a0001c0001t0002g0017a0001c0001t0002g0082a0001c0001t0002g0087others(4): Show | 7 | HG02258.hp1 HG02602.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2004-1542_2004-153 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
T | TACACACA others(3): Show |
3 | a0001c0001t0002g0028a0001c0001t0005g0107a0001c0001t0005g0116 | 3 | HG02257.hp2 HG02976.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2004-1544_2004-153 others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
T | TACACACA others(5): Show |
1 | a0001c0002t0005g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2004-1546_2004-153 others(16): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
TACACAC | T | 3 | a0001c0001t0003g0091a0001c0001t0011g0060a0001c0001t0019g0095 | 3 | HG03225.hp2 HG03239.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2004-1540_2004-153 others(10): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
TACACACA others(1): Show |
T | 2 | a0001c0001t0004g0042a0001c0001t0004g0171 | 2 | HG01169.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2004-1542_2004-153 others(12): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688208
|
TACACACA others(3): Show |
T | 27 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.2004-1544_2004-153 others(14): Show |
FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688208 | |||||
| chr7:114688246
|
C | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-1536C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688246 | ||||||
| chr7:114688247
|
A | C | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-1535A>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688247 | ||||||
| chr7:114688249
|
C | CT | 46 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0100others(43): Show | 47 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2004-1520dupT | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 114688249 | |||||
| chr7:114688249
|
C | T | 29 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0014others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2004-1533C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688249 | ||||||
| chr7:114688294
|
C | G | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2004-1488C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688294 | ||||||
| chr7:114688764
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2004-1018A>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114688764 | ||||||
| chr7:114689000
|
T | C | 1 | a0001c0001t0018g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2004-782T>C | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114689000 | ||||||
| chr7:114689251
|
C | A | 25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0019others(22): Show | 26 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2004-531C>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114689251 | ||||||
| chr7:114689458
|
C | G | 2 | a0001c0001t0009g0064a0001c0001t0009g0173 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2004-324C>G | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114689458 | ||||||
| chr7:114689471
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2004-311C>T | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114689471 | ||||||
| chr7:114689763
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2004-19G>A | FOXP2 | ENSG00000128573.28 | transcript | ENST00000350908.9 | protein_coding | 16/16 | chr7 | 114689763 |