Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MMQES others(710): Show |
chr7 | 114409815 | 114698765 |
| a0002 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | MMQES others(710): Show |
chr7 | 114409815 | 114698765 |
| a0003 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | MMQES others(710): Show |
chr7 | 114409815 | 114698765 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2145 | 165 | 55 | 33 | 42 | 8 | 25 | FOXP2_chr7_114409815_114698765 | FOXP2 | ATGAT others(2140): Show |
chr7 | 114409815 | 114698765 | ||
| a0001c0002 | 0/0 | 2145 | 5 | 5 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ATGAT others(2140): Show |
chr7 | 114409815 | 114698765 | ||
| a0001c0003 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ATGAT others(2140): Show |
chr7 | 114409815 | 114698765 | ||
| a0002c0005 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ATGAT others(2140): Show |
chr7 | 114409815 | 114698765 | ||
| a0003c0004 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | ATGAT others(2140): Show |
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 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0002 | 0/0 | 6542 | 29 | 7 | 3 | 16 | 0 | 3 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0003 | 0/0 | 6543 | 27 | 1 | 8 | 13 | 2 | 3 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0004 | 0/1 | 6540 | 24 | 3 | 8 | 3 | 3 | 6 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6535): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0005 | 0/0 | 6543 | 9 | 8 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0006 | 0/0 | 6544 | 8 | 7 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0007 | 0/0 | 6540 | 2 | 0 | 0 | 0 | 0 | 2 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6535): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0008 | 0/0 | 6541 | 2 | 0 | 1 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6536): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0009 | 0/0 | 6544 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0010 | 0/0 | 6538 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6533): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0011 | 0/0 | 6541 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6536): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0013 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0014 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0015 | 0/0 | 6544 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0016 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0017 | 0/0 | 6540 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6535): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0018 | 0/0 | 6541 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6536): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0019 | 0/0 | 6541 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6536): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0020 | 0/0 | 6540 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6535): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0021 | 0/0 | 6540 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6535): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0022 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0023 | 0/0 | 6542 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0024 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0025 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0026 | 0/0 | 6542 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0027 | 0/0 | 6543 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0028 | 0/0 | 6543 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0029 | 0/0 | 6544 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0030 | 0/0 | 6544 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0001c0001t0031 | 0/0 | 6544 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0001c0002t0001 | 0/0 | 6543 | 3 | 3 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0002t0002 | 0/0 | 6542 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6537): Show |
chr7 | 114409815 | 114698765 |
| a0001c0002t0005 | 0/0 | 6543 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0001c0003t0006 | 0/0 | 6544 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6539): Show |
chr7 | 114409815 | 114698765 |
| a0002c0005t0003 | 0/0 | 6543 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6538): Show |
chr7 | 114409815 | 114698765 |
| a0003c0004t0012 | 0/0 | 6540 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP2_chr7_114409815_114698765 | FOXP2 | ACAGA others(6535): Show |
chr7 | 114409815 | 114698765 |
| actghapid | grch38/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 |
| a0002c0005t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP2_chr7_114409815_114698765 | FOXP2 | chr7 | 114409815 | 114698765 |
| a0003c0004t0012g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | a0002 | 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 | a0003 | 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 |
| view | 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 | a0003 | 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 | a0002 | 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 |
| view | 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 |
| view | 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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 |
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 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0014 others(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 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0029 others(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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0022 others(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 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(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 | a0001c0001t0026 a0001c0001t0028 |
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 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0017 others(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 | a0001c0001t0026 a0001c0001t0028 |
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 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(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 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0027 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(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 |
| view | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0057 a0001c0001t0003g0058 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0003g0059 others(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 | a0001c0001t0001g0056 a0001c0001t0002g0053 a0001c0001t0002g0054 others(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 | a0001c0001t0002g0172 a0001c0001t0009g0173 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0015g0092 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0015g0092 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0015g0092 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0046 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0006 a0001c0001t0005g0094 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0172 a0001c0001t0009g0173 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0015g0092 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0033 a0001c0001t0014g0146 |
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 | a0001c0001t0002g0036 a0001c0001t0003g0052 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0144 others(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 | a0001c0001t0014g0146 a0003c0004t0012g0063 |
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 | a0001c0001t0014g0146 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0002g0172 a0001c0001t0009g0173 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0049 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | a0001c0001t0002g0172 a0001c0001t0009g0173 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0011g0060 a0001c0001t0015g0092 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0056 a0001c0001t0004g0008 a0001c0001t0004g0032 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0002g0025 a0001c0001t0003g0009 |
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 | a0001c0001t0003g0039 a0001c0001t0020g0047 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0113 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0101 a0001c0001t0011g0060 a0001c0001t0013g0093 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0015g0092 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0002g0001 a0001c0001t0004g0014 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0008g0126 others(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 | a0001c0001t0001g0101 a0001c0001t0011g0060 a0001c0001t0013g0093 others(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 | a0001c0001t0001g0160 a0001c0001t0003g0157 a0001c0001t0004g0156 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0016g0169 a0001c0001t0019g0095 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0135 a0001c0001t0003g0134 a0001c0001t0004g0136 others(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 | a0001c0001t0004g0072 a0001c0001t0005g0073 a0001c0001t0006g0071 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0144 a0001c0001t0004g0129 a0001c0001t0004g0131 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0002g0145 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0002g0172 a0001c0001t0009g0173 |
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 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0008g0126 others(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 | a0001c0001t0001g0046 a0001c0001t0003g0034 a0001c0001t0003g0035 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0003g0091 a0001c0001t0004g0074 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0046 a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0046 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0046 a0001c0001t0002g0172 a0001c0001t0003g0035 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | a0001c0002t0002g0102 a0001c0002t0005g0103 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0014g0146 others(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 | a0001c0001t0002g0001 a0001c0001t0004g0014 |
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 | a0001c0001t0002g0096 a0001c0001t0002g0172 a0001c0001t0009g0173 |
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 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0006g0070 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0014g0146 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0166 a0001c0001t0003g0148 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 a0001c0001t0019g0095 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0024g0132 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0002g0123 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0014g0146 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0024g0132 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0014g0146 others(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 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0006g0070 others(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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0004g0129 a0001c0001t0006g0130 a0001c0001t0011g0060 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0001g0044 a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0028g0040 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0135 a0001c0001t0004g0136 a0001c0001t0004g0137 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0011g0060 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0101 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0041 a0001c0001t0014g0146 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0014g0146 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0004g0129 a0001c0001t0006g0130 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0041 others(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 | a0001c0001t0002g0145 a0001c0001t0004g0016 a0001c0001t0014g0146 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0006 a0001c0001t0002g0083 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0003g0148 others(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 | a0001c0001t0001g0118 a0001c0001t0015g0092 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0090 a0001c0001t0006g0070 a0001c0001t0006g0117 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0029g0079 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0002g0017 a0001c0001t0023g0018 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0089 a0001c0001t0003g0076 |
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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0101 a0001c0001t0006g0121 a0001c0001t0006g0122 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0004g0081 a0001c0001t0004g0088 |
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 | a0001c0001t0001g0118 a0001c0001t0015g0092 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0004g0159 a0002c0005t0003g0158 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0002g0082 a0001c0001t0003g0059 a0001c0001t0004g0075 |
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 | a0001c0001t0003g0039 a0001c0001t0020g0047 |
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 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0056 a0001c0001t0004g0032 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0111 a0001c0001t0001g0135 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0002g0027 a0001c0001t0003g0015 a0001c0001t0003g0067 others(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 | a0001c0001t0001g0118 a0001c0001t0015g0092 a0001c0001t0016g0169 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0118 a0001c0001t0015g0092 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0002g0084 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0006g0117 a0001c0001t0031g0114 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0006g0117 a0001c0001t0031g0114 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0003g0039 others(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 | a0001c0001t0003g0134 a0001c0001t0004g0136 a0001c0001t0004g0137 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0164 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0003g0050 a0001c0001t0004g0051 a0001c0001t0011g0060 others(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 | a0001c0001t0003g0091 a0001c0001t0004g0074 |
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 | a0001c0001t0016g0169 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0127 others(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 | a0001c0002t0002g0102 a0001c0002t0005g0103 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0002g0084 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0004g0131 a0001c0001t0021g0128 |
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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0004g0131 a0001c0001t0021g0128 |
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 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0138 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0002g0172 a0001c0001t0003g0134 a0001c0001t0004g0136 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0029g0079 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0106 |
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 | a0001c0001t0005g0119 a0001c0001t0005g0120 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0160 a0001c0001t0003g0157 a0001c0002t0001g0097 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0024 others(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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0164 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0100 a0001c0001t0005g0094 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0002g0019 a0001c0001t0003g0045 a0001c0001t0003g0049 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0105 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0005g0107 |
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 | a0001c0001t0004g0088 a0001c0001t0004g0171 |
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 | a0001c0001t0004g0131 a0001c0001t0021g0128 |
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 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0029g0079 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0002g0053 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0165 a0001c0001t0004g0042 |
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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0003g0091 a0001c0001t0004g0074 |
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 | a0001c0001t0001g0090 a0001c0001t0006g0070 a0001c0001t0006g0117 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0152 others(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 | a0001c0001t0005g0119 a0001c0001t0005g0120 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0160 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0144 a0001c0001t0004g0129 a0001c0001t0004g0131 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0160 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0001 a0001c0001t0004g0014 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0160 a0001c0001t0015g0092 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0002g0017 a0001c0001t0023g0018 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0015g0092 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0118 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0172 a0001c0001t0005g0133 a0001c0001t0009g0173 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0006 a0001c0001t0002g0083 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0003g0091 a0001c0001t0004g0074 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0002g0077 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0101 a0001c0001t0002g0025 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0144 a0001c0001t0002g0096 others(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 | a0001c0001t0001g0127 a0001c0001t0002g0082 a0001c0001t0002g0087 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0002t0002g0102 a0001c0002t0005g0103 |
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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0008g0126 a0001c0001t0008g0143 a0001c0001t0010g0142 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0005g0119 a0001c0001t0019g0095 a0001c0002t0001g0097 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0055 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0002g0001 a0001c0001t0004g0014 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0002g0172 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0029 |
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 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0138 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0008g0126 a0001c0001t0008g0143 a0001c0001t0010g0142 |
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 | a0001c0001t0008g0126 a0001c0001t0008g0143 a0001c0001t0010g0142 |
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 | a0001c0001t0008g0126 a0001c0001t0008g0143 a0001c0001t0010g0142 |
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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0111 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0155 a0001c0001t0002g0054 a0001c0001t0002g0151 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0118 a0001c0001t0005g0119 a0001c0002t0001g0097 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0090 a0001c0001t0006g0070 a0001c0001t0006g0117 others(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 | a0001c0001t0011g0060 a0001c0001t0013g0093 a0001c0001t0015g0092 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0118 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0004g0081 a0001c0001t0004g0088 a0001c0001t0029g0079 |
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 | a0001c0001t0002g0027 a0001c0001t0002g0029 |
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 | a0001c0001t0002g0027 a0001c0001t0002g0029 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0004g0081 a0001c0001t0004g0088 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0118 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0033 a0001c0001t0005g0120 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0004g0159 a0002c0005t0003g0158 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0005g0073 a0001c0001t0006g0071 a0001c0001t0006g0130 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0006g0010 a0002c0005t0003g0158 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0089 a0001c0001t0002g0082 a0001c0001t0002g0087 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0026 a0001c0001t0028g0040 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0026 a0001c0001t0028g0040 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 a0001c0001t0019g0095 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0090 a0001c0001t0006g0070 a0001c0001t0006g0117 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0002g0001 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0090 a0001c0001t0006g0070 a0001c0001t0006g0117 others(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 | a0001c0001t0002g0025 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0002g0168 a0001c0001t0003g0015 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0019g0095 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0006g0070 a0001c0001t0006g0117 a0001c0001t0031g0114 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0090 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0101 a0001c0001t0006g0070 others(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 | a0001c0001t0001g0100 a0001c0001t0002g0123 a0001c0001t0004g0099 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0002t0002g0102 a0001c0002t0005g0103 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0002g0025 a0001c0001t0003g0009 |
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 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0033 a0001c0001t0006g0010 a0001c0001t0025g0012 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0160 a0001c0001t0001g0161 others(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 | a0001c0001t0004g0137 a0001c0001t0004g0139 a0001c0001t0004g0147 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0006g0010 a0001c0001t0025g0012 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0118 a0001c0001t0013g0093 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0118 a0001c0001t0001g0135 others(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 | a0001c0001t0004g0136 a0001c0001t0004g0138 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0003g0148 a0001c0001t0004g0048 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0001g0118 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0118 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0118 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0118 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0024 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0118 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0029 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0118 a0001c0001t0013g0093 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0002g0001 a0001c0001t0004g0014 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0100 a0001c0001t0002g0087 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0004g0139 a0001c0001t0006g0071 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
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 | a0001c0001t0002g0025 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0004g0137 a0001c0001t0004g0139 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0029 a0001c0001t0030g0068 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0026 a0001c0001t0002g0083 a0001c0001t0003g0091 others(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 | a0001c0001t0004g0074 a0001c0001t0005g0133 |
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 | a0001c0001t0001g0144 a0001c0001t0002g0082 a0001c0001t0002g0168 others(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 | a0001c0001t0001g0127 a0001c0001t0002g0087 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0069 a0001c0001t0003g0148 a0001c0001t0004g0081 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0003g0015 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0053 others(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 | a0001c0001t0004g0048 a0001c0001t0004g0088 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0013g0093 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0006 a0001c0001t0002g0083 a0001c0001t0027g0030 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0151 a0001c0001t0002g0167 others(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 | a0001c0001t0006g0010 a0001c0001t0025g0012 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0090 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 a0001c0001t0024g0132 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 a0001c0001t0024g0132 |
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 | a0001c0001t0002g0055 a0001c0001t0002g0084 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0002g0001 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0006g0010 a0001c0001t0025g0012 |
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 | a0001c0001t0005g0119 a0001c0001t0006g0010 a0001c0001t0011g0060 |
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 | a0001c0001t0005g0073 a0001c0001t0006g0071 a0001c0001t0006g0130 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0118 a0001c0001t0001g0152 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0170 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0170 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0004g0081 a0001c0001t0004g0088 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0004g0136 a0001c0001t0004g0138 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0118 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0057 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0004g0072 a0001c0001t0004g0129 |
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 | a0001c0001t0001g0057 a0001c0001t0003g0058 a0001c0001t0022g0043 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0118 a0001c0001t0001g0152 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0106 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0003g0091 a0001c0001t0004g0074 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0065 a0001c0001t0009g0064 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0006g0121 a0001c0001t0006g0122 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0033 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0014g0146 |
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 | a0001c0001t0001g0090 a0001c0001t0006g0070 a0001c0001t0006g0117 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0089 others(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 | a0001c0001t0004g0159 a0002c0005t0003g0158 |
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 | a0001c0001t0003g0039 a0001c0001t0027g0030 a0001c0001t0029g0079 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 |
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 | a0001c0001t0003g0021 a0001c0001t0003g0050 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0006 a0001c0001t0002g0083 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0002g0027 others(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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0170 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0057 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0151 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0006g0010 a0001c0001t0025g0012 a0001c0001t0031g0114 |
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 | a0001c0001t0005g0125 a0001c0001t0009g0173 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0003g0091 a0001c0001t0004g0074 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0005g0073 a0001c0001t0006g0071 a0001c0001t0006g0130 |
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 | a0003c0004t0012g0063 | 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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0011g0060 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0004g0171 a0001c0001t0021g0128 |
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 | a0001c0001t0006g0085 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0003g0039 a0001c0001t0008g0126 a0001c0001t0018g0080 others(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 | a0001c0001t0003g0039 a0001c0001t0008g0126 a0001c0001t0018g0080 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0003c0004t0012g0063 | 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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0160 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 a0001c0001t0013g0093 others(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 | a0001c0002t0002g0102 a0001c0002t0005g0103 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0006g0085 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0005g0119 a0001c0001t0011g0060 a0001c0003t0006g0149 others(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 | a0001c0001t0013g0093 a0001c0001t0024g0132 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 a0001c0003t0006g0149 others(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 | a0001c0001t0002g0013 a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0002g0001 a0001c0001t0004g0014 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0006g0085 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0002g0013 a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0013g0093 a0001c0001t0024g0132 |
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 | a0001c0001t0004g0032 a0001c0001t0008g0143 a0001c0001t0010g0142 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0101 a0001c0001t0009g0064 |
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 | a0001c0001t0002g0013 a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0019 a0001c0001t0004g0051 |
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 | a0001c0001t0002g0028 a0001c0001t0002g0054 a0001c0001t0003g0045 others(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 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0084 others(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 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
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 | a0001c0001t0002g0096 a0001c0001t0002g0172 a0001c0001t0003g0015 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0127 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0037 a0001c0001t0024g0132 |
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 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0002g0102 others(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 | a0001c0001t0002g0168 a0001c0001t0003g0078 a0001c0001t0003g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0002g0027 others(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 | a0001c0001t0004g0081 a0001c0001t0004g0131 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0002g0025 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0006g0010 a0003c0004t0012g0063 |
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 | a0001c0001t0001g0101 a0001c0001t0002g0123 a0001c0001t0002g0167 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0090 a0001c0001t0005g0115 a0001c0001t0005g0116 others(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 | a0001c0001t0007g0140 a0001c0001t0007g0141 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0013 a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0002g0013 a0001c0001t0015g0092 a0001c0001t0019g0095 |
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 | a0001c0001t0006g0085 a0001c0002t0001g0097 a0001c0002t0001g0098 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0077 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0061 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0052 a0001c0001t0010g0142 |
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 | a0001c0001t0002g0084 a0001c0001t0005g0120 a0001c0001t0028g0040 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0104 a0001c0001t0002g0001 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0101 others(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 | a0001c0001t0002g0077 a0001c0001t0002g0168 a0001c0001t0003g0015 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0123 a0001c0001t0002g0172 others(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 | a0001c0001t0002g0013 a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0056 a0001c0001t0002g0167 a0001c0001t0004g0088 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0026 a0001c0001t0004g0081 a0001c0001t0006g0121 others(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 | a0001c0001t0002g0055 a0001c0001t0004g0072 a0001c0001t0006g0010 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0006g0010 a0001c0001t0025g0012 a0001c0001t0031g0114 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0003 a0001c0001t0002g0017 a0001c0001t0002g0022 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0056 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0135 others(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 | a0001c0001t0006g0085 a0001c0001t0014g0146 a0001c0002t0001g0097 others(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 | a0003c0004t0012g0063 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0101 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0084 |
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 | a0001c0001t0013g0093 a0001c0001t0024g0132 |
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 | a0001c0001t0006g0070 a0001c0001t0006g0117 a0001c0001t0006g0121 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0044 others(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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0003t0006g0149 a0001c0003t0006g0150 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0005g0119 a0001c0001t0011g0060 |
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 | a0001c0001t0002g0013 a0001c0001t0005g0119 a0001c0001t0011g0060 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0033 others(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 | a0001c0001t0005g0073 a0001c0001t0006g0071 a0001c0001t0006g0085 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0057 a0001c0001t0001g0065 others(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 | a0001c0001t0003g0049 a0001c0001t0004g0005 a0001c0001t0004g0008 others(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 | a0001c0001t0005g0107 a0001c0001t0005g0116 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0118 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0013 a0001c0001t0002g0096 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0100 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0013 a0001c0001t0002g0096 others(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 | a0001c0001t0002g0123 a0001c0001t0002g0172 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0057 a0001c0001t0002g0013 a0001c0001t0002g0096 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0100 a0001c0001t0001g0104 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0100 a0001c0001t0001g0104 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0100 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0118 a0001c0001t0001g0155 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0013 a0001c0001t0002g0096 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0155 a0001c0001t0013g0093 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0058 others(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 | a0001c0001t0004g0072 a0001c0001t0004g0129 a0001c0001t0004g0156 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0002c0005t0003g0158 | 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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0123 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0084 |
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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0003g0052 a0001c0001t0003g0066 a0001c0001t0003g0067 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0005g0119 a0001c0001t0005g0120 |
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 | a0001c0001t0005g0073 a0001c0001t0005g0094 a0001c0001t0005g0107 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0127 a0001c0001t0001g0135 others(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 | a0001c0001t0005g0125 a0001c0001t0005g0133 |
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 | a0001c0001t0002g0123 a0001c0001t0002g0172 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0123 a0001c0001t0002g0172 a0001c0001t0024g0132 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0036 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0171 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0056 others(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 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0053 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0118 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0041 others(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 | a0001c0001t0009g0064 a0001c0001t0009g0173 |
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 | a0001c0001t0002g0123 a0001c0001t0002g0172 a0001c0001t0024g0132 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0123 others(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 | a0001c0001t0002g0172 a0001c0001t0024g0132 |
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 | a0001c0001t0004g0072 a0001c0001t0004g0129 |
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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | a0001c0001t0011g0060 a0001c0001t0019g0095 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0061 others(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 | a0001c0001t0003g0023 a0001c0001t0003g0069 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0051 others(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 | a0001c0001t0004g0072 a0001c0001t0004g0099 a0001c0001t0004g0156 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0020 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0003g0039 a0001c0001t0003g0062 a0001c0001t0003g0086 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0002g0123 a0001c0001t0002g0172 a0001c0001t0024g0132 |
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 | a0001c0001t0011g0060 a0001c0001t0019g0095 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0123 others(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 | a0001c0001t0011g0060 a0001c0001t0019g0095 |
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 | a0001c0001t0002g0027 a0001c0001t0002g0029 |
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 | a0001c0001t0001g0118 a0001c0001t0005g0073 a0001c0001t0005g0094 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0123 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0003g0009 a0001c0001t0003g0076 |
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 | a0001c0001t0009g0064 a0001c0001t0009g0173 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0056 a0001c0001t0002g0013 a0001c0001t0002g0096 others(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 | a0001c0001t0001g0155 a0001c0001t0004g0032 a0001c0001t0005g0119 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0124 others(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 | a0001c0001t0003g0134 a0001c0001t0003g0157 |
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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0145 a0001c0001t0002g0167 |
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 | a0001c0001t0001g0110 a0001c0002t0001g0097 a0001c0002t0001g0098 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0096 a0001c0001t0002g0124 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0154 a0001c0001t0002g0027 a0001c0001t0003g0015 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0104 a0001c0001t0001g0127 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0082 a0001c0001t0002g0087 others(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 | a0001c0001t0002g0028 a0001c0001t0005g0107 a0001c0001t0005g0116 |
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 | a0001c0001t0003g0091 a0001c0001t0011g0060 a0001c0001t0019g0095 |
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 | a0001c0001t0004g0042 a0001c0001t0004g0171 |
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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0100 others(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 | a0001c0001t0004g0005 a0001c0001t0004g0008 a0001c0001t0004g0014 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(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 | a0001c0001t0009g0064 a0001c0001t0009g0173 |
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 |