Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 728577 |
|---|---|
| ensemblid | ENSG00000154529.15 |
| hgncid | 32035 |
| symbol | CNTNAP3B |
| name | contactin associated protein family member 3B |
| refseq_nuc | NM_001201380.3 |
| refseq_prot | NP_001188309.2 |
| ensembl_nuc | ENST00000377561.7 |
| ensembl_prot | ENSP00000478671.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 41890536 |
| end | 42129426 |
| strand | - |
| ver | v1.2 |
| region | chr9:41890536-42129426 |
| region5000 | chr9:41885536-42134426 |
| regionname0 | CNTNAP3B_chr9_41890536_42129426 |
| regionname5000 | CNTNAP3B_chr9_41885536_42134426 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 675 | 25 | 2 | 9 | 8 | 2 | 4 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002 | 0/1 | 1288 | 24 | 2 | 8 | 6 | 1 | 6 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003 | 0/0 | 1288 | 10 | 3 | 1 | 3 | 1 | 2 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0004 | 0/0 | 1288 | 5 | 0 | 1 | 1 | 1 | 2 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0005 | 0/0 | 1288 | 4 | 2 | 0 | 0 | 1 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0006 | 0/0 | 675 | 4 | 1 | 0 | 2 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0007 | 0/0 | 1288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0008 | 0/0 | 1288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0009 | 0/0 | 1288 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0010 | 0/0 | 675 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0011 | 0/0 | 1288 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0012 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0013 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0014 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0015 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0016 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0017 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0018 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0019 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0020 | 1/0 | 1288 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0021 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0022 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0023 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0024 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0025 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0026 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0027 | 0/0 | 1270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0028 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0029 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0030 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0031 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0032 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0033 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0034 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3867 | 20 | 0 | 8 | 6 | 2 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0002 | 0/1 | 3867 | 19 | 1 | 7 | 4 | 0 | 6 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0003 | 0/0 | 3867 | 8 | 2 | 1 | 2 | 1 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0004 | 0/0 | 3867 | 5 | 0 | 1 | 1 | 1 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0005 | 0/0 | 3867 | 4 | 2 | 0 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0006 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0007 | 0/0 | 3867 | 3 | 1 | 0 | 1 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0008 | 0/0 | 3867 | 3 | 0 | 2 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0009 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0010 | 0/0 | 3867 | 2 | 0 | 1 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0011 | 0/0 | 3867 | 2 | 1 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0012 | 0/0 | 3867 | 2 | 0 | 1 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0013 | 0/0 | 3867 | 2 | 0 | 0 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0014 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0015 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0016 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0017 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0018 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0019 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0020 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0021 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0022 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0023 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0024 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0025 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0026 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0027 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0028 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0029 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0030 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0031 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0032 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0033 | 1/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0034 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0035 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0036 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0037 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0038 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0039 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0040 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0041 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0042 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0043 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0044 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0045 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| c0046 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3790 | 26 | 5 | 8 | 6 | 2 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0002 | 0/0 | 3811 | 14 | 1 | 5 | 7 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0003 | 0/0 | 3811 | 11 | 0 | 4 | 1 | 2 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0004 | 0/0 | 3790 | 7 | 2 | 0 | 4 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0005 | 0/0 | 3811 | 6 | 0 | 1 | 2 | 1 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0006 | 0/0 | 3790 | 6 | 4 | 1 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0007 | 0/0 | 3811 | 4 | 0 | 0 | 4 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0008 | 0/0 | 3790 | 4 | 0 | 1 | 0 | 2 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0009 | 0/0 | 3811 | 4 | 0 | 2 | 0 | 0 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0010 | 0/0 | 3790 | 3 | 3 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0011 | 0/0 | 3811 | 2 | 1 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0012 | 0/0 | 3790 | 2 | 0 | 1 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0013 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0014 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0015 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0016 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0017 | 0/0 | 3811 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0018 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0019 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0020 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0021 | 0/0 | 3790 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0022 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0023 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0024 | 0/0 | 3790 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0025 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0026 | 1/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0027 | 0/0 | 3790 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0028 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0029 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0030 | 0/0 | 3790 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| t0031 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3867 | 20 | 0 | 8 | 6 | 2 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0012 | 0/0 | 3867 | 2 | 0 | 1 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0042 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0043 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0046 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0002 | 0/1 | 3867 | 19 | 1 | 7 | 4 | 0 | 6 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0010 | 0/0 | 3867 | 2 | 0 | 1 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0015 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0020 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0023 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0003 | 0/0 | 3867 | 8 | 2 | 1 | 2 | 1 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0011 | 0/0 | 3867 | 2 | 1 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0004c0004 | 0/0 | 3867 | 5 | 0 | 1 | 1 | 1 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0005c0005 | 0/0 | 3867 | 4 | 2 | 0 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0006c0007 | 0/0 | 3867 | 3 | 1 | 0 | 1 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0006c0041 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0007c0009 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0007c0016 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0008c0006 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0009c0008 | 0/0 | 3867 | 3 | 0 | 2 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0010c0013 | 0/0 | 3867 | 2 | 0 | 0 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0011c0037 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0011c0040 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0012c0022 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0013c0021 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0014c0018 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0015c0019 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0016c0017 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0017c0014 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0018c0024 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0019c0031 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0020c0033 | 1/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0021c0032 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0022c0030 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0023c0028 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0024c0029 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0025c0034 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0026c0025 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0027c0026 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0028c0027 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0029c0045 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0030c0035 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0031c0044 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0032c0039 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0033c0036 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0034c0038 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 7677 | 8 | 0 | 3 | 4 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0001t0003 | 0/0 | 7677 | 9 | 0 | 4 | 1 | 1 | 3 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0001t0017 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0001t0018 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0001t0031 | 0/0 | 7677 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0012t0002 | 0/0 | 7677 | 2 | 0 | 1 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0042t0013 | 0/0 | 7677 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0043t0015 | 0/0 | 7673 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0001c0046t0016 | 0/0 | 7677 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0002t0001 | 0/1 | 7656 | 15 | 0 | 6 | 4 | 0 | 4 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0002t0012 | 0/0 | 7656 | 2 | 0 | 1 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0002t0022 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0002t0024 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0010t0001 | 0/0 | 7656 | 2 | 0 | 1 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0015t0001 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0020t0001 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0002c0023t0001 | 0/0 | 7656 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0003t0004 | 0/0 | 7656 | 3 | 1 | 0 | 2 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0003t0008 | 0/0 | 7656 | 3 | 0 | 1 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0003t0021 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0003t0029 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0003c0011t0004 | 0/0 | 7656 | 2 | 1 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0004c0004t0005 | 0/0 | 7677 | 5 | 0 | 1 | 1 | 1 | 2 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0005c0005t0006 | 0/0 | 7656 | 3 | 2 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0005c0005t0030 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0006c0007t0002 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0006c0007t0011 | 0/0 | 7677 | 2 | 1 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0006c0041t0002 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0007c0009t0023 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0007c0009t0025 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0007c0016t0001 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0008c0006t0010 | 0/0 | 7656 | 3 | 3 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0009c0008t0009 | 0/0 | 7677 | 3 | 0 | 2 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0010c0013t0003 | 0/0 | 7677 | 2 | 0 | 0 | 0 | 1 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0011c0037t0007 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0011c0040t0007 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0012c0022t0001 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0013c0021t0027 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0014c0018t0001 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0015c0019t0001 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0016c0017t0001 | 0/0 | 7656 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0017c0014t0001 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0018c0024t0008 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0019c0031t0028 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0020c0033t0026 | 1/0 | 7652 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0021c0032t0004 | 0/0 | 7656 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0022c0030t0006 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0023c0028t0006 | 0/0 | 7656 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0024c0029t0006 | 0/0 | 7656 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0025c0034t0004 | 0/0 | 7656 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0026c0025t0019 | 0/0 | 7677 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0027c0026t0020 | 0/0 | 7677 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0028c0027t0005 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0029c0045t0002 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0030c0035t0007 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0031c0044t0009 | 0/0 | 7677 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0032c0039t0014 | 0/0 | 7677 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0033c0036t0007 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| a0034c0038t0002 | 0/0 | 7677 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | copy fasta | chr9 | 41885536 | 42134426 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0017g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0018g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0001t0031g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0012t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0012t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0042t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0043t0015g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0001c0046t0016g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0012g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0012g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0022g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0002t0024g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0010t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0015t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0020t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0002c0023t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0008g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0008g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0008g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0021g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0003t0029g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0011t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0003c0011t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0004c0004t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0004c0004t0005g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0004c0004t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0004c0004t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0004c0004t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0005c0005t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0005c0005t0006g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0005c0005t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0005c0005t0030g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0006c0007t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0006c0007t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0006c0007t0011g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0006c0041t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0007c0009t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0007c0009t0025g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0007c0016t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0008c0006t0010g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0008c0006t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0008c0006t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0009c0008t0009g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0009c0008t0009g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0009c0008t0009g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0010c0013t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0010c0013t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0011c0037t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0011c0040t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0012c0022t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0013c0021t0027g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0014c0018t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0015c0019t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0016c0017t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0017c0014t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0018c0024t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0019c0031t0028g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0020c0033t0026g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0021c0032t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0022c0030t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0023c0028t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0024c0029t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0025c0034t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0026c0025t0019g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0027c0026t0020g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0028c0027t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0029c0045t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0030c0035t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0031c0044t0009g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0032c0039t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0033c0036t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| a0034c0038t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0025 | c0034 | t0004 | g0090 | EUR | GBR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00099 | hp2 | a0001 | c0001 | t0031 | g0098 | EUR | GBR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00140 | hp1 | a0003 | c0003 | t0008 | g0077 | EUR | GBR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00140 | hp2 | a0002 | c0020 | t0001 | g0060 | EUR | GBR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0096 | EUR | FIN | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00280 | hp2 | a0004 | c0004 | t0005 | g0031 | EUR | FIN | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00323 | hp1 | a0012 | c0022 | t0001 | g0055 | EUR | FIN | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00323 | hp2 | a0018 | c0024 | t0008 | g0080 | EUR | FIN | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00558 | hp1 | a0001 | c0043 | t0015 | g0013 | EAS | CHS | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00558 | hp2 | a0003 | c0003 | t0004 | g0082 | EAS | CHS | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00642 | hp1 | a0003 | c0003 | t0008 | g0083 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00642 | hp2 | a0001 | c0001 | t0017 | g0012 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00735 | hp1 | a0009 | c0008 | t0009 | g0106 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01071 | hp1 | a0002 | c0002 | t0012 | g0043 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01081 | hp1 | a0016 | c0017 | t0001 | g0042 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01106 | hp2 | a0009 | c0008 | t0009 | g0107 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01175 | hp2 | a0004 | c0004 | t0005 | g0032 | AMR | PUR | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01255 | hp1 | a0029 | c0045 | t0002 | g0019 | AMR | CLM | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | CLM | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01516 | hp1 | a0005 | c0005 | t0006 | g0076 | EUR | IBS | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01516 | hp2 | a0010 | c0013 | t0003 | g0103 | EUR | IBS | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01934 | hp1 | a0023 | c0028 | t0006 | g0084 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01943 | hp2 | a0001 | c0012 | t0002 | g0009 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01952 | hp1 | a0002 | c0010 | t0001 | g0057 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02040 | hp2 | a0006 | c0041 | t0002 | g0020 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02056 | hp1 | a0003 | c0011 | t0004 | g0078 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02083 | hp1 | a0033 | c0036 | t0007 | g0010 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02135 | hp2 | a0002 | c0023 | t0001 | g0054 | EAS | KHV | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02145 | hp1 | a0002 | c0015 | t0001 | g0046 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02145 | hp2 | a0006 | c0007 | t0011 | g0017 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02572 | hp1 | a0002 | c0002 | t0022 | g0068 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02572 | hp2 | a0005 | c0005 | t0006 | g0073 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02622 | hp1 | a0017 | c0014 | t0001 | g0038 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02622 | hp2 | a0026 | c0025 | t0019 | g0028 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02717 | hp1 | a0001 | c0042 | t0013 | g0001 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02717 | hp2 | a0003 | c0011 | t0004 | g0074 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02738 | hp1 | a0005 | c0005 | t0030 | g0092 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02738 | hp2 | a0002 | c0002 | t0024 | g0061 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02886 | hp1 | a0003 | c0003 | t0004 | g0075 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02886 | hp2 | a0008 | c0006 | t0010 | g0070 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02922 | hp1 | a0003 | c0003 | t0029 | g0072 | AFR | ESN | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02922 | hp2 | a0019 | c0031 | t0028 | g0088 | AFR | ESN | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03041 | hp1 | a0015 | c0019 | t0001 | g0066 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03041 | hp2 | a0022 | c0030 | t0006 | g0085 | AFR | GWD | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03239 | hp2 | a0003 | c0003 | t0008 | g0086 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03453 | hp1 | a0008 | c0006 | t0010 | g0071 | AFR | MSL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03453 | hp2 | a0034 | c0038 | t0002 | g0016 | AFR | MSL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03486 | hp1 | a0007 | c0009 | t0025 | g0037 | AFR | MSL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03486 | hp2 | a0005 | c0005 | t0006 | g0091 | AFR | MSL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03490 | hp1 | a0004 | c0004 | t0005 | g0029 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03669 | hp2 | a0006 | c0007 | t0011 | g0021 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03704 | hp1 | a0004 | c0004 | t0005 | g0030 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | BEB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03831 | hp2 | a0010 | c0013 | t0003 | g0108 | SAS | BEB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03834 | hp1 | a0009 | c0008 | t0009 | g0105 | SAS | BEB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03942 | hp1 | a0002 | c0002 | t0012 | g0051 | SAS | BEB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG03942 | hp2 | a0031 | c0044 | t0009 | g0094 | SAS | BEB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG04115 | hp1 | a0013 | c0021 | t0027 | g0064 | SAS | STU | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0065 | SAS | STU | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18947 | hp1 | a0001 | c0001 | t0018 | g0026 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18947 | hp2 | a0006 | c0007 | t0002 | g0014 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18949 | hp1 | a0002 | c0010 | t0001 | g0058 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18949 | hp2 | a0011 | c0037 | t0007 | g0008 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18968 | hp1 | a0001 | c0012 | t0002 | g0007 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18968 | hp2 | a0011 | c0040 | t0007 | g0003 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18970 | hp1 | a0003 | c0003 | t0004 | g0081 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18974 | hp1 | a0030 | c0035 | t0007 | g0023 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA18998 | hp2 | a0021 | c0032 | t0004 | g0079 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA19030 | hp1 | a0007 | c0016 | t0001 | g0036 | AFR | LWK | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA19030 | hp2 | a0024 | c0029 | t0006 | g0087 | AFR | LWK | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA19086 | hp2 | a0028 | c0027 | t0005 | g0033 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA19090 | hp2 | a0004 | c0004 | t0005 | g0034 | EAS | JPT | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA20905 | hp1 | a0003 | c0003 | t0021 | g0035 | SAS | GIH | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | GIH | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02109 | hp1 | a0007 | c0009 | t0023 | g0039 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02109 | hp2 | a0027 | c0026 | t0020 | g0027 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02486 | hp1 | a0032 | c0039 | t0014 | g0025 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02486 | hp2 | a0001 | c0046 | t0016 | g0015 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02559 | hp1 | a0014 | c0018 | t0001 | g0067 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| HG02559 | hp2 | a0008 | c0006 | t0010 | g0069 | AFR | ACB | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0047 | REF | REF | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| homoSapiens_grch38 | hp1 | a0020 | c0033 | t0026 | g0089 | REF | REF | CNTNAP3B_chr9_41885536_42134426 | CNTNAP3B | chr9 | 41885536 | 42134426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41894003
|
T | C | 1 | a0023 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.3853A>G | p.Lys1285Glu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 4185/7652 | 3853/3867 | 1285/1288 | chr9 | 41894003 | ||
| chr9:41894045
|
G | A | 1 | a0027 | 1 | HG02109.hp2 | stop_gained | HIGH | c.3811C>T | p.Gln1271* | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 4143/7652 | 3811/3867 | 1271/1288 | chr9 | 41894045 | ||
| chr9:41894068
|
G | A | 1 | a0021 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.3788C>T | p.Ala1263Val | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 4120/7652 | 3788/3867 | 1263/1288 | chr9 | 41894068 | ||
| chr9:41894095
|
T | A | 33 | a0001a0002a0003others(30): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
missense_variant | MODERATE | c.3761A>T | p.Glu1254Val | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 4093/7652 | 3761/3867 | 1254/1288 | chr9 | 41894095 | ||
| chr9:41898466
|
G | C | 21 | a0002a0003a0005others(18): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
missense_variant | MODERATE | c.3741C>G | p.Ile1247Met | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/24 | 4073/7652 | 3741/3867 | 1247/1288 | chr9 | 41898466 | ||
| chr9:41898859
|
C | G | 6 | a0001a0006a0010others(3): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
missense_variant | MODERATE | c.3583G>C | p.Gly1195Arg | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 22/24 | 3915/7652 | 3583/3867 | 1195/1288 | chr9 | 41898859 | ||
| chr9:41898919
|
A | G | 33 | a0001a0002a0003others(30): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
missense_variant | MODERATE | c.3523T>C | p.Cys1175Arg | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 22/24 | 3855/7652 | 3523/3867 | 1175/1288 | chr9 | 41898919 | ||
| chr9:41898954
|
C | T | 3 | a0002a0012a0016 | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
missense_variant | MODERATE | c.3488G>A | p.Gly1163Asp | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 22/24 | 3820/7652 | 3488/3867 | 1163/1288 | chr9 | 41898954 | ||
| chr9:41898963
|
G | A | 1 | a0015 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.3479C>T | p.Ala1160Val | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 22/24 | 3811/7652 | 3479/3867 | 1160/1288 | chr9 | 41898963 | ||
| chr9:41905943
|
C | T | 2 | a0001a0006 | 2 | HG02040.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.3367G>A | p.Ala1123Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/24 | 3699/7652 | 3367/3867 | 1123/1288 | chr9 | 41905943 | ||
| chr9:41906870
|
G | A | 1 | a0024 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3338C>T | p.Ala1113Val | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/24 | 3670/7652 | 3338/3867 | 1113/1288 | chr9 | 41906870 | ||
| chr9:41906984
|
C | A | 1 | a0022 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3224G>T | p.Ser1075Ile | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/24 | 3556/7652 | 3224/3867 | 1075/1288 | chr9 | 41906984 | ||
| chr9:41908622
|
G | A | 1 | a0008 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.3155C>T | p.Pro1052Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/24 | 3487/7652 | 3155/3867 | 1052/1288 | chr9 | 41908622 | ||
| chr9:41908626
|
T | A | 33 | a0001a0002a0003others(30): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
missense_variant | MODERATE | c.3151A>T | p.Thr1051Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/24 | 3483/7652 | 3151/3867 | 1051/1288 | chr9 | 41908626 | ||
| chr9:41908683
|
G | A | 33 | a0001a0002a0003others(30): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
missense_variant | MODERATE | c.3094C>T | p.His1032Tyr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/24 | 3426/7652 | 3094/3867 | 1032/1288 | chr9 | 41908683 | ||
| chr9:41920084
|
G | A | 2 | a0011a0028 | 3 | NA18949.hp2 NA18968.hp2 NA19086.hp2 |
missense_variant | MODERATE | c.2981C>T | p.Pro994Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/24 | 3313/7652 | 2981/3867 | 994/1288 | chr9 | 41920084 | ||
| chr9:41920157
|
G | A | 2 | a0001a0017 | 2 | HG02486.hp2 HG02622.hp1 |
missense_variant | MODERATE | c.2908C>T | p.Arg970Cys | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/24 | 3240/7652 | 2908/3867 | 970/1288 | chr9 | 41920157 | ||
| chr9:41920210
|
G | A | 1 | a0027 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2855C>T | p.Pro952Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/24 | 3187/7652 | 2855/3867 | 952/1288 | chr9 | 41920210 | ||
| chr9:41920213
|
G | A | 2 | a0014a0015 | 2 | HG02559.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.2852C>T | p.Thr951Met | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/24 | 3184/7652 | 2852/3867 | 951/1288 | chr9 | 41920213 | ||
| chr9:41922706
|
C | T | 1 | a0001 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.2726G>A | p.Arg909His | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/24 | 3058/7652 | 2726/3867 | 909/1288 | chr9 | 41922706 | ||
| chr9:41924065
|
G | C | 1 | a0027 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2394C>G | p.Asn798Lys | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/24 | 2726/7652 | 2394/3867 | 798/1288 | chr9 | 41924065 | ||
| chr9:41938253
|
T | C | 27 | a0001a0002a0004others(24): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
missense_variant | MODERATE | c.2228A>G | p.Gln743Arg | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/24 | 2560/7652 | 2228/3867 | 743/1288 | chr9 | 41938253 | ||
| chr9:41938349
|
G | T | 13 | a0001a0004a0006others(10): Show | 46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
missense_variant | MODERATE | c.2132C>A | p.Ser711Tyr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/24 | 2464/7652 | 2132/3867 | 711/1288 | chr9 | 41938349 | ||
| chr9:41953185
|
C | T | 6 | a0001a0006a0010others(3): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
missense_variant&splice_region_variant | MODERATE | c.2078G>A | p.Arg693Gln | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2410/7652 | 2078/3867 | 693/1288 | chr9 | 41953185 | ||
| chr9:41953215
|
C | A | 6 | a0001a0006a0010others(3): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
missense_variant | MODERATE | c.2048G>T | p.Arg683Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2380/7652 | 2048/3867 | 683/1288 | chr9 | 41953215 | ||
| chr9:41953225
|
G | T | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2038C>A | p.Leu680Met | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2370/7652 | 2038/3867 | 680/1288 | chr9 | 41953225 | ||
| chr9:41953227
|
C | T | 1 | a0034 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2036G>A | p.Arg679Gln | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2368/7652 | 2036/3867 | 679/1288 | chr9 | 41953227 | ||
| chr9:41953233
|
T | C | 6 | a0001a0006a0010others(3): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
missense_variant | MODERATE | c.2030A>G | p.Glu677Gly | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2362/7652 | 2030/3867 | 677/1288 | chr9 | 41953233 | ||
| chr9:41953235
|
G | T | 6 | a0001a0006a0010others(3): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
stop_gained | HIGH | c.2028C>A | p.Cys676* | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2360/7652 | 2028/3867 | 676/1288 | chr9 | 41953235 | ||
| chr9:41953308
|
A | C | 12 | a0001a0004a0006others(9): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
missense_variant | MODERATE | c.1955T>G | p.Leu652Arg | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2287/7652 | 1955/3867 | 652/1288 | chr9 | 41953308 | ||
| chr9:41953377
|
G | A | 1 | a0025 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1886C>T | p.Ala629Val | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2218/7652 | 1886/3867 | 629/1288 | chr9 | 41953377 | ||
| chr9:41964553
|
C | T | 1 | a0016 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1741G>A | p.Glu581Lys | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/24 | 2073/7652 | 1741/3867 | 581/1288 | chr9 | 41964553 | ||
| chr9:41964578
|
G | T | 1 | a0010 | 2 | HG01516.hp2 HG03831.hp2 |
missense_variant | MODERATE | c.1716C>A | p.Asp572Glu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/24 | 2048/7652 | 1716/3867 | 572/1288 | chr9 | 41964578 | ||
| chr9:41970108
|
C | G | 2 | a0007a0017 | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.1615G>C | p.Asp539His | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/24 | 1947/7652 | 1615/3867 | 539/1288 | chr9 | 41970108 | ||
| chr9:41970109
|
C | G | 1 | a0019 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1614G>C | p.Arg538Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/24 | 1946/7652 | 1614/3867 | 538/1288 | chr9 | 41970109 | ||
| chr9:41986185
|
T | C | 1 | a0034 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1460A>G | p.Asp487Gly | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/24 | 1792/7652 | 1460/3867 | 487/1288 | chr9 | 41986185 | ||
| chr9:41991640
|
C | T | 1 | a0006 | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.1303G>A | p.Ala435Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/24 | 1635/7652 | 1303/3867 | 435/1288 | chr9 | 41991640 | ||
| chr9:41991721
|
G | A | 8 | a0001a0006a0008others(5): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
missense_variant | MODERATE | c.1222C>T | p.Leu408Phe | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/24 | 1554/7652 | 1222/3867 | 408/1288 | chr9 | 41991721 | ||
| chr9:41991862
|
A | T | 1 | a0008 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1081T>A | p.Ser361Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/24 | 1413/7652 | 1081/3867 | 361/1288 | chr9 | 41991862 | ||
| chr9:41996327
|
A | T | 23 | a0001a0002a0004others(20): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
missense_variant | MODERATE | c.949T>A | p.Ser317Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/24 | 1281/7652 | 949/3867 | 317/1288 | chr9 | 41996327 | ||
| chr9:41996341
|
A | G | 1 | a0017 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.935T>C | p.Phe312Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/24 | 1267/7652 | 935/3867 | 312/1288 | chr9 | 41996341 | ||
| chr9:41997672
|
C | T | 1 | a0034 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.823G>A | p.Val275Ile | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/24 | 1155/7652 | 823/3867 | 275/1288 | chr9 | 41997672 | ||
| chr9:41997689
|
T | G | 1 | a0019 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.806A>C | p.Asp269Ala | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/24 | 1138/7652 | 806/3867 | 269/1288 | chr9 | 41997689 | ||
| chr9:41997728
|
A | G | 1 | a0034 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.767T>C | p.Ile256Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/24 | 1099/7652 | 767/3867 | 256/1288 | chr9 | 41997728 | ||
| chr9:42013449
|
C | T | 1 | a0030 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.467G>A | p.Arg156His | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/24 | 799/7652 | 467/3867 | 156/1288 | chr9 | 42013449 | ||
| chr9:42076931
|
G | A | 1 | a0012 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.328C>T | p.Leu110Phe | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/24 | 660/7652 | 328/3867 | 110/1288 | chr9 | 42076931 | ||
| chr9:42104637
|
C | G | 1 | a0018 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.188G>C | p.Arg63Pro | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/24 | 520/7652 | 188/3867 | 63/1288 | chr9 | 42104637 | ||
| chr9:42104658
|
G | A | 1 | a0029 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.167C>T | p.Pro56Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/24 | 499/7652 | 167/3867 | 56/1288 | chr9 | 42104658 | ||
| chr9:42104728
|
A | C | 11 | a0001a0006a0009others(8): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
missense_variant | MODERATE | c.97T>G | p.Ser33Ala | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/24 | 429/7652 | 97/3867 | 33/1288 | chr9 | 42104728 | ||
| chr9:42129032
|
G | T | 9 | a0002a0007a0008others(6): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
missense_variant | MODERATE | c.63C>A | p.Ser21Arg | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 395/7652 | 63/3867 | 21/1288 | chr9 | 42129032 | ||
| chr9:42129091
|
C | A | 11 | a0001a0006a0009others(8): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
missense_variant | MODERATE | c.4G>T | p.Ala2Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 336/7652 | 4/3867 | 2/1288 | chr9 | 42129091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41906917
|
G | A | 43 | a0001c0001a0001c0012a0001c0042others(40): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
synonymous_variant | LOW | c.3291C>T | p.Asn1097Asn | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/24 | 3623/7652 | 3291/3867 | 1097/1288 | chr9 | 41906917 | ||
| chr9:41908765
|
G | A | 44 | a0001c0001a0001c0012a0001c0042others(41): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
synonymous_variant | LOW | c.3012C>T | p.Phe1004Phe | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/24 | 3344/7652 | 3012/3867 | 1004/1288 | chr9 | 41908765 | ||
| chr9:41920163
|
A | G | 6 | a0004c0004a0011c0037a0011c0040others(3): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
synonymous_variant | LOW | c.2902T>C | p.Leu968Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/24 | 3234/7652 | 2902/3867 | 968/1288 | chr9 | 41920163 | ||
| chr9:41920212
|
C | T | 1 | a0019c0031 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.2853G>A | p.Thr951Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/24 | 3185/7652 | 2853/3867 | 951/1288 | chr9 | 41920212 | ||
| chr9:41922726
|
G | A | 11 | a0001c0001a0001c0012a0001c0042others(8): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
synonymous_variant | LOW | c.2706C>T | p.Ala902Ala | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/24 | 3038/7652 | 2706/3867 | 902/1288 | chr9 | 41922726 | ||
| chr9:41922750
|
C | T | 9 | a0002c0002a0002c0010a0002c0015others(6): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
synonymous_variant | LOW | c.2682G>A | p.Gln894Gln | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/24 | 3014/7652 | 2682/3867 | 894/1288 | chr9 | 41922750 | ||
| chr9:41922768
|
C | T | 1 | a0032c0039 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2664G>A | p.Ala888Ala | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/24 | 2996/7652 | 2664/3867 | 888/1288 | chr9 | 41922768 | ||
| chr9:41922879
|
T | G | 12 | a0001c0001a0001c0012a0001c0042others(9): Show | 35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
synonymous_variant | LOW | c.2553A>C | p.Thr851Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/24 | 2885/7652 | 2553/3867 | 851/1288 | chr9 | 41922879 | ||
| chr9:41923978
|
A | G | 1 | a0003c0011 | 2 | HG02056.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.2481T>C | p.Ser827Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/24 | 2813/7652 | 2481/3867 | 827/1288 | chr9 | 41923978 | ||
| chr9:41924086
|
A | G | 1 | a0021c0032 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.2373T>C | p.Phe791Phe | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/24 | 2705/7652 | 2373/3867 | 791/1288 | chr9 | 41924086 | ||
| chr9:41938351
|
A | G | 1 | a0032c0039 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2130T>C | p.Thr710Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/24 | 2462/7652 | 2130/3867 | 710/1288 | chr9 | 41938351 | ||
| chr9:41953205
|
T | C | 1 | a0002c0023 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.2058A>G | p.Thr686Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2390/7652 | 2058/3867 | 686/1288 | chr9 | 41953205 | ||
| chr9:41953211
|
G | A | 11 | a0001c0001a0001c0012a0001c0042others(8): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
synonymous_variant | LOW | c.2052C>T | p.Cys684Cys | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2384/7652 | 2052/3867 | 684/1288 | chr9 | 41953211 | ||
| chr9:41953319
|
G | A | 11 | a0001c0001a0001c0012a0001c0042others(8): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
synonymous_variant | LOW | c.1944C>T | p.Ser648Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/24 | 2276/7652 | 1944/3867 | 648/1288 | chr9 | 41953319 | ||
| chr9:41964554
|
G | A | 6 | a0004c0004a0011c0037a0011c0040others(3): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
synonymous_variant | LOW | c.1740C>T | p.Gly580Gly | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/24 | 2072/7652 | 1740/3867 | 580/1288 | chr9 | 41964554 | ||
| chr9:41964572
|
T | C | 18 | a0001c0001a0001c0012a0001c0042others(15): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
synonymous_variant | LOW | c.1722A>G | p.Leu574Leu | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/24 | 2054/7652 | 1722/3867 | 574/1288 | chr9 | 41964572 | ||
| chr9:41964599
|
C | T | 1 | a0007c0016 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1695G>A | p.Ser565Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/24 | 2027/7652 | 1695/3867 | 565/1288 | chr9 | 41964599 | ||
| chr9:41986235
|
A | G | 19 | a0001c0001a0001c0012a0001c0042others(16): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
synonymous_variant | LOW | c.1410T>C | p.Asp470Asp | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/24 | 1742/7652 | 1410/3867 | 470/1288 | chr9 | 41986235 | ||
| chr9:41986277
|
T | C | 19 | a0001c0001a0001c0012a0001c0042others(16): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
synonymous_variant | LOW | c.1368A>G | p.Val456Val | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/24 | 1700/7652 | 1368/3867 | 456/1288 | chr9 | 41986277 | ||
| chr9:41991743
|
C | T | 1 | a0002c0015 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1200G>A | p.Thr400Thr | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/24 | 1532/7652 | 1200/3867 | 400/1288 | chr9 | 41991743 | ||
| chr9:41997703
|
G | A | 1 | a0002c0023 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.792C>T | p.Gly264Gly | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/24 | 1124/7652 | 792/3867 | 264/1288 | chr9 | 41997703 | ||
| chr9:41997733
|
A | G | 39 | a0001c0001a0001c0012a0001c0042others(36): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
synonymous_variant | LOW | c.762T>C | p.Ser254Ser | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/24 | 1094/7652 | 762/3867 | 254/1288 | chr9 | 41997733 | ||
| chr9:42104657
|
C | T | 4 | a0001c0012a0011c0037a0030c0035others(1): Show | 5 | HG01943.hp2 HG02083.hp1 NA18949.hp2 others(2): Show |
synonymous_variant | LOW | c.168G>A | p.Pro56Pro | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/24 | 500/7652 | 168/3867 | 56/1288 | chr9 | 42104657 | ||
| chr9:42104663
|
G | A | 3 | a0001c0046a0002c0010a0002c0023 | 4 | HG01952.hp1 HG02135.hp2 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.162C>T | p.His54His | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/24 | 494/7652 | 162/3867 | 54/1288 | chr9 | 42104663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41890723
|
T | C | 1 | a0001c0001t0017 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 3266 | chr9 | 41890723 | |||||
| chr9:41890975
|
G | T | 1 | a0007c0009t0023 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3014C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 3014 | chr9 | 41890975 | |||||
| chr9:41890999
|
A | G | 41 | a0001c0046t0016a0002c0002t0001a0002c0002t0012others(38): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2990T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2990 | chr9 | 41890999 | |||||
| chr9:41891099
|
G | A | 1 | a0002c0002t0012 | 2 | HG01071.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2890C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2890 | chr9 | 41891099 | |||||
| chr9:41891287
|
T | C | 6 | a0004c0004t0005a0011c0037t0007a0011c0040t0007others(3): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2702A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2702 | chr9 | 41891287 | |||||
| chr9:41891376
|
G | A | 1 | a0001c0001t0031 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2613C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2613 | chr9 | 41891376 | |||||
| chr9:41891418
|
G | A | 1 | a0019c0031t0028 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2571C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2571 | chr9 | 41891418 | |||||
| chr9:41891458
|
C | T | 57 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(54): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2531G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2531 | chr9 | 41891458 | |||||
| chr9:41891572
|
T | C | 1 | a0006c0007t0011 | 2 | HG02145.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2417A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2417 | chr9 | 41891572 | |||||
| chr9:41891633
|
C | T | 1 | a0027c0026t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2356G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2356 | chr9 | 41891633 | |||||
| chr9:41891739
|
C | T | 1 | a0003c0003t0029 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2250G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 2250 | chr9 | 41891739 | |||||
| chr9:41892212
|
G | A | 1 | a0008c0006t0010 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1777C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1777 | chr9 | 41892212 | |||||
| chr9:41892235
|
C | T | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(12): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1754G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1754 | chr9 | 41892235 | |||||
| chr9:41892375
|
A | G | 2 | a0003c0003t0008a0018c0024t0008 | 4 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1614T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1614 | chr9 | 41892375 | |||||
| chr9:41892380
|
A | C | 1 | a0008c0006t0010 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1609T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1609 | chr9 | 41892380 | |||||
| chr9:41892474
|
G | A | 1 | a0019c0031t0028 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1515C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1515 | chr9 | 41892474 | |||||
| chr9:41892646
|
C | T | 1 | a0008c0006t0010 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1343G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1343 | chr9 | 41892646 | |||||
| chr9:41892982
|
T | TAAA | 57 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(54): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1006_*1007insTTT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 1006 | chr9 | 41892982 | |||||
| chr9:41893043
|
C | T | 1 | a0026c0025t0019 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 946 | chr9 | 41893043 | |||||
| chr9:41893059
|
A | G | 1 | a0001c0043t0015 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 930 | chr9 | 41893059 | |||||
| chr9:41893352
|
T | C | 1 | a0007c0009t0025 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*637A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 637 | chr9 | 41893352 | |||||
| chr9:41893490
|
T | TA | 57 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(54): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*498dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 498 | chr9 | 41893490 | |||||
| chr9:41893503
|
G | A | 1 | a0019c0031t0028 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 486 | chr9 | 41893503 | |||||
| chr9:41893544
|
A | G | 1 | a0002c0002t0022 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 445 | chr9 | 41893544 | |||||
| chr9:41893616
|
C | T | 18 | a0002c0002t0001a0002c0002t0012a0002c0002t0022others(15): Show | 34 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*373G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 373 | chr9 | 41893616 | |||||
| chr9:41893735
|
C | A | 10 | a0003c0003t0004a0003c0003t0008a0003c0003t0021others(7): Show | 17 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*254G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 254 | chr9 | 41893735 | |||||
| chr9:41893807
|
C | G | 1 | a0002c0002t0022 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 182 | chr9 | 41893807 | |||||
| chr9:41893930
|
A | G | 1 | a0001c0042t0013 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 24/24 | 59 | chr9 | 41893930 | |||||
| chr9:42129147
|
G | C | 1 | a0001c0001t0018 | 1 | NA18947.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 53 | chr9 | 42129147 | |||||
| chr9:42129260
|
C | T | 1 | a0003c0003t0021 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 166 | chr9 | 42129260 | |||||
| chr9:42129306
|
T | C | 1 | a0005c0005t0030 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 212 | chr9 | 42129306 | |||||
| chr9:42129325
|
G | GGACTCGC others(13): Show |
4 | a0004c0004t0005a0026c0025t0019a0027c0026t0020others(1): Show | 8 | HG00280.hp2 HG01175.hp2 HG02109.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-232_-231insAGAAAG others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 232 | chr9 | 42129325 | |||||
| chr9:42129325
|
G | GGACTCGC others(13): Show |
22 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(19): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-232_-231insAGAAAG others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 232 | chr9 | 42129325 | |||||
| chr9:42129329
|
G | GT | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(19): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-236_-235insA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 236 | chr9 | 42129329 | |||||
| chr9:42129330
|
C | CG | 4 | a0004c0004t0005a0026c0025t0019a0027c0026t0020others(1): Show | 8 | HG00280.hp2 HG01175.hp2 HG02109.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-237_-236insC | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 237 | chr9 | 42129330 | |||||
| chr9:42129330
|
C | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(19): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-236G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 236 | chr9 | 42129330 | |||||
| chr9:42129397
|
C | A | 5 | a0001c0001t0003a0001c0001t0031a0009c0008t0009others(2): Show | 16 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-303G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/24 | 303 | chr9 | 42129397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41894242
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3746-132A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894242 | ||||||
| chr9:41894268
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3746-158G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894268 | ||||||
| chr9:41894269
|
G | A | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.3746-159C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894269 | ||||||
| chr9:41894658
|
T | C | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3746-548A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894658 | ||||||
| chr9:41894675
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3746-565G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894675 | ||||||
| chr9:41894717
|
C | T | 11 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.3746-607G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894717 | ||||||
| chr9:41894890
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3746-780G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41894890 | ||||||
| chr9:41895046
|
T | C | 2 | a0004c0004t0005g0029a0004c0004t0005g0030 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3746-936A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895046 | ||||||
| chr9:41895057
|
C | T | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3746-947G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895057 | ||||||
| chr9:41895161
|
C | G | 62 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.3746-1051G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895161 | ||||||
| chr9:41895249
|
A | AT | 43 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(40): Show | 43 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.3746-1140dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895249 | ||||||
| chr9:41895310
|
T | C | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3746-1200A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895310 | ||||||
| chr9:41895345
|
A | G | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0065 | 3 | HG03834.hp2 HG04115.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3746-1235T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895345 | ||||||
| chr9:41895526
|
G | T | 1 | a0009c0008t0009g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3746-1416C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895526 | ||||||
| chr9:41895702
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3746-1592C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895702 | ||||||
| chr9:41895848
|
A | G | 19 | a0001c0001t0003g0099a0003c0003t0004g0075a0003c0003t0004g0081others(16): Show | 19 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.3746-1738T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41895848 | ||||||
| chr9:41896278
|
A | G | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3746-2168T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896278 | ||||||
| chr9:41896366
|
T | C | 7 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(4): Show | 7 | HG02040.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3745+2096A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896366 | ||||||
| chr9:41896485
|
C | A | 102 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.3745+1977G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896485 | ||||||
| chr9:41896487
|
C | A | 102 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.3745+1975G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896487 | ||||||
| chr9:41896488
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3745+1974G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896488 | ||||||
| chr9:41896604
|
C | G | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.3745+1858G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896604 | ||||||
| chr9:41896704
|
C | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3745+1758G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896704 | ||||||
| chr9:41896747
|
C | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3745+1715G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896747 | ||||||
| chr9:41896766
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3745+1696T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896766 | ||||||
| chr9:41896798
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.3745+1664G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896798 | ||||||
| chr9:41896879
|
G | A | 1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3745+1583C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41896879 | ||||||
| chr9:41897048
|
T | TCAAA | 102 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.3745+1410_3745+141 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897048 | ||||||
| chr9:41897091
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3745+1371T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897091 | ||||||
| chr9:41897097
|
G | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.3745+1365C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897097 | ||||||
| chr9:41897413
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3745+1049C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897413 | ||||||
| chr9:41897553
|
C | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3745+909G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897553 | ||||||
| chr9:41897583
|
G | A | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.3745+879C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897583 | ||||||
| chr9:41897644
|
C | T | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3745+818G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897644 | ||||||
| chr9:41897646
|
G | A | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.3745+816C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897646 | ||||||
| chr9:41897695
|
C | T | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3745+767G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897695 | ||||||
| chr9:41897785
|
C | T | 3 | a0005c0005t0006g0076a0005c0005t0030g0092a0023c0028t0006g0084 | 3 | HG01516.hp1 HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3745+677G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897785 | ||||||
| chr9:41897953
|
C | T | 1 | a0002c0002t0012g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3745+509G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897953 | ||||||
| chr9:41897965
|
T | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3745+497A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897965 | ||||||
| chr9:41897966
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3745+496C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41897966 | ||||||
| chr9:41898028
|
A | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3745+434T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41898028 | ||||||
| chr9:41898121
|
A | G | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3745+341T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41898121 | ||||||
| chr9:41898149
|
T | G | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3745+313A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41898149 | ||||||
| chr9:41898368
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3745+94T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41898368 | ||||||
| chr9:41898374
|
T | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3745+88A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41898374 | ||||||
| chr9:41898436
|
C | T | 2 | a0026c0025t0019g0028a0032c0039t0014g0025 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3745+26G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 23/23 | chr9 | 41898436 | ||||||
| chr9:41898582
|
G | A | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3674-49C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 22/23 | chr9 | 41898582 | ||||||
| chr9:41898662
|
G | C | 18 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.3673+107C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 22/23 | chr9 | 41898662 | ||||||
| chr9:41899082
|
ACCCTCGT others(30): Show |
A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3443-120_3443-84de others(38): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899082 | ||||||
| chr9:41899118
|
T | A | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3443-119A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899118 | ||||||
| chr9:41899168
|
T | A | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3443-169A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899168 | ||||||
| chr9:41899484
|
G | C | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3443-485C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899484 | ||||||
| chr9:41899865
|
G | T | 72 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.3443-866C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899865 | ||||||
| chr9:41899889
|
C | A | 63 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.3443-890G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899889 | ||||||
| chr9:41899895
|
C | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3443-896G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41899895 | ||||||
| chr9:41900247
|
T | A | 4 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(1): Show | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.3443-1248A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900247 | ||||||
| chr9:41900268
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3443-1269G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900268 | ||||||
| chr9:41900313
|
C | G | 1 | a0001c0001t0003g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3443-1314G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900313 | ||||||
| chr9:41900480
|
T | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3443-1481A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900480 | ||||||
| chr9:41900495
|
C | G | 3 | a0001c0001t0003g0095a0001c0001t0003g0097a0001c0001t0003g0104 | 3 | HG01952.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.3443-1496G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900495 | ||||||
| chr9:41900591
|
T | G | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3443-1592A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900591 | ||||||
| chr9:41900740
|
C | A | 1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3443-1741G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900740 | ||||||
| chr9:41900741
|
CTTTTTTT others(11): Show |
C | 11 | a0002c0002t0001g0049a0004c0004t0005g0029a0004c0004t0005g0030others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.3443-1760_3443-174 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900741 | ||||||
| chr9:41900741
|
CTTTTTTT others(12): Show |
C | 92 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.3443-1761_3443-174 others(23): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900741 | ||||||
| chr9:41900741
|
CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0003g0100a0002c0002t0001g0040a0005c0005t0006g0076 | 3 | HG01106.hp1 HG01516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3443-1762_3443-174 others(24): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41900741 | ||||||
| chr9:41901057
|
C | T | 63 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.3443-2058G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901057 | ||||||
| chr9:41901287
|
C | CTCCCAGA others(89): Show |
3 | a0001c0001t0002g0018a0001c0001t0017g0012a0001c0001t0031g0098 | 3 | HG00099.hp2 HG00642.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3443-2384_3443-228 others(100): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901287 | ||||||
| chr9:41901446
|
G | A | 63 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.3443-2447C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901446 | ||||||
| chr9:41901597
|
G | T | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3443-2598C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901597 | ||||||
| chr9:41901630
|
G | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3443-2631C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901630 | ||||||
| chr9:41901724
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3443-2725C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901724 | ||||||
| chr9:41901816
|
G | T | 73 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.3443-2817C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901816 | ||||||
| chr9:41901876
|
G | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.3443-2877C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901876 | ||||||
| chr9:41901901
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3443-2902G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901901 | ||||||
| chr9:41901918
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3443-2919C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901918 | ||||||
| chr9:41901935
|
T | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3443-2936A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901935 | ||||||
| chr9:41901951
|
G | A | 62 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.3443-2952C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901951 | ||||||
| chr9:41901955
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3443-2956C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41901955 | ||||||
| chr9:41902027
|
TAAA | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3443-3031_3443-302 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902027 | ||||||
| chr9:41902080
|
C | T | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.3443-3081G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902080 | ||||||
| chr9:41902134
|
A | G | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0032others(6): Show | 9 | HG01175.hp2 HG02083.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.3443-3135T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902134 | ||||||
| chr9:41902149
|
C | T | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3443-3150G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902149 | ||||||
| chr9:41902150
|
T | C | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.3443-3151A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902150 | ||||||
| chr9:41902201
|
CA | C | 8 | a0001c0001t0002g0024a0001c0001t0003g0104a0001c0046t0016g0015others(5): Show | 8 | HG00140.hp2 HG01981.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3443-3203delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902201 | ||||||
| chr9:41902201
|
CAA | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.3443-3204_3443-320 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902201 | ||||||
| chr9:41902215
|
AAAAAAG | A | 7 | a0004c0004t0005g0030a0004c0004t0005g0031a0004c0004t0005g0032others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.3443-3222_3443-321 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902215 | ||||||
| chr9:41902246
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3443-3247A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902246 | ||||||
| chr9:41902282
|
C | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3443-3283G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902282 | ||||||
| chr9:41902423
|
C | T | 2 | a0006c0007t0011g0017a0006c0007t0011g0021 | 2 | HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3443-3424G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902423 | ||||||
| chr9:41902588
|
C | A | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3442+3280G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902588 | ||||||
| chr9:41902646
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+3222T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902646 | ||||||
| chr9:41902658
|
G | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3442+3210C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902658 | ||||||
| chr9:41902672
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+3196G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902672 | ||||||
| chr9:41902696
|
T | A | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3442+3172A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902696 | ||||||
| chr9:41902759
|
C | T | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3442+3109G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902759 | ||||||
| chr9:41902784
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+3084T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902784 | ||||||
| chr9:41902879
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2989T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902879 | ||||||
| chr9:41902890
|
A | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2978T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902890 | ||||||
| chr9:41902896
|
A | G | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3442+2972T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902896 | ||||||
| chr9:41902921
|
G | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.3442+2947C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902921 | ||||||
| chr9:41902930
|
C | G | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3442+2938G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902930 | ||||||
| chr9:41902996
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2872C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41902996 | ||||||
| chr9:41903071
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2797G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903071 | ||||||
| chr9:41903079
|
A | G | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.3442+2789T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903079 | ||||||
| chr9:41903141
|
C | T | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3442+2727G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903141 | ||||||
| chr9:41903154
|
T | C | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3442+2714A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903154 | ||||||
| chr9:41903165
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2703C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903165 | ||||||
| chr9:41903203
|
G | A | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3442+2665C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903203 | ||||||
| chr9:41903378
|
T | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2490A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903378 | ||||||
| chr9:41903397
|
A | AT | 2 | a0009c0008t0009g0105a0009c0008t0009g0106 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3442+2470_3442+247 others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903397 | ||||||
| chr9:41903398
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2470G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903398 | ||||||
| chr9:41903417
|
GCAGA | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2447_3442+245 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903417 | ||||||
| chr9:41903517
|
C | T | 63 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.3442+2351G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903517 | ||||||
| chr9:41903647
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2221A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903647 | ||||||
| chr9:41903672
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2196T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903672 | ||||||
| chr9:41903689
|
C | G | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3442+2179G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903689 | ||||||
| chr9:41903706
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3442+2162G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903706 | ||||||
| chr9:41903723
|
C | T | 11 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.3442+2145G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903723 | ||||||
| chr9:41903819
|
C | CAGAA | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+2045_3442+204 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903819 | ||||||
| chr9:41903902
|
G | T | 1 | a0014c0018t0001g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3442+1966C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903902 | ||||||
| chr9:41903905
|
T | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3442+1963A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903905 | ||||||
| chr9:41903961
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+1907T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41903961 | ||||||
| chr9:41904042
|
G | T | 1 | a0001c0001t0002g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3442+1826C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904042 | ||||||
| chr9:41904199
|
C | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+1669G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904199 | ||||||
| chr9:41904228
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3442+1640C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904228 | ||||||
| chr9:41904275
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3442+1593C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904275 | ||||||
| chr9:41904311
|
GTTTT | G | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.3442+1553_3442+155 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904311 | ||||||
| chr9:41904311
|
GTTTTTT | G | 5 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3442+1551_3442+155 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904311 | ||||||
| chr9:41904311
|
GTTTTTTT | G | 17 | a0002c0002t0001g0040a0002c0002t0001g0049a0002c0002t0001g0052others(14): Show | 17 | HG00642.hp1 HG01934.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.3442+1550_3442+155 others(11): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904311 | ||||||
| chr9:41904311
|
GTTTTTTT others(1): Show |
G | 56 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.3442+1549_3442+155 others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904311 | ||||||
| chr9:41904311
|
GTTTTTTT others(2): Show |
G | 14 | a0001c0001t0002g0006a0001c0001t0003g0093a0001c0001t0003g0095others(11): Show | 14 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.3442+1548_3442+155 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904311 | ||||||
| chr9:41904311
|
GTTTTTTT others(3): Show |
G | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3442+1547_3442+155 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904311 | ||||||
| chr9:41904327
|
T | G | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3442+1541A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904327 | ||||||
| chr9:41904344
|
A | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+1524T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904344 | ||||||
| chr9:41904367
|
C | T | 6 | a0005c0005t0006g0073a0008c0006t0010g0069a0008c0006t0010g0070others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3442+1501G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904367 | ||||||
| chr9:41904474
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3442+1394C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904474 | ||||||
| chr9:41904481
|
G | A | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0065 | 3 | HG03834.hp2 HG04115.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3442+1387C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904481 | ||||||
| chr9:41904532
|
G | A | 2 | a0001c0001t0018g0026a0001c0012t0002g0009 | 2 | HG01943.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.3442+1336C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904532 | ||||||
| chr9:41904612
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+1256C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904612 | ||||||
| chr9:41904619
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3442+1249G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904619 | ||||||
| chr9:41904639
|
A | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3442+1229T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904639 | ||||||
| chr9:41904701
|
C | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+1167G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904701 | ||||||
| chr9:41904719
|
A | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+1149T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904719 | ||||||
| chr9:41904792
|
C | A | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3442+1076G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904792 | ||||||
| chr9:41904845
|
T | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3442+1023A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904845 | ||||||
| chr9:41904870
|
T | G | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.3442+998A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904870 | ||||||
| chr9:41904913
|
G | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3442+955C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904913 | ||||||
| chr9:41904987
|
A | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3442+881T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41904987 | ||||||
| chr9:41905040
|
G | A | 1 | a0012c0022t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3442+828C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905040 | ||||||
| chr9:41905050
|
T | A | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3442+818A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905050 | ||||||
| chr9:41905062
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+806G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905062 | ||||||
| chr9:41905174
|
A | T | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3442+694T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905174 | ||||||
| chr9:41905212
|
GT | G | 11 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.3442+655delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905212 | ||||||
| chr9:41905348
|
A | G | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3442+520T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905348 | ||||||
| chr9:41905359
|
C | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3442+509G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905359 | ||||||
| chr9:41905395
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+473T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905395 | ||||||
| chr9:41905480
|
A | C | 18 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.3442+388T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905480 | ||||||
| chr9:41905557
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3442+311C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905557 | ||||||
| chr9:41905593
|
G | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3442+275C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905593 | ||||||
| chr9:41905693
|
C | T | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3442+175G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905693 | ||||||
| chr9:41905841
|
T | G | 4 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0056others(1): Show | 4 | HG01934.hp2 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3442+27A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | 41905841 | ||||||
| chr9:41906161
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3355-206G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906161 | ||||||
| chr9:41906178
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3355-223G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906178 | ||||||
| chr9:41906187
|
G | T | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3355-232C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906187 | ||||||
| chr9:41906301
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3355-346A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906301 | ||||||
| chr9:41906332
|
A | G | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3355-377T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906332 | ||||||
| chr9:41906349
|
C | T | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3355-394G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906349 | ||||||
| chr9:41906434
|
C | T | 5 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0097others(2): Show | 5 | HG01952.hp2 HG01981.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.3354+420G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906434 | ||||||
| chr9:41906627
|
C | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3354+227G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906627 | ||||||
| chr9:41906634
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3354+220C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906634 | ||||||
| chr9:41906676
|
A | T | 6 | a0005c0005t0006g0073a0008c0006t0010g0069a0008c0006t0010g0070others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3354+178T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906676 | ||||||
| chr9:41906739
|
G | A | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.3354+115C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906739 | ||||||
| chr9:41906777
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3354+77T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906777 | ||||||
| chr9:41906797
|
T | A | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3354+57A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 20/23 | chr9 | 41906797 | ||||||
| chr9:41907077
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.3221-90G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907077 | ||||||
| chr9:41907104
|
A | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-117T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907104 | ||||||
| chr9:41907143
|
A | T | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3221-156T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907143 | ||||||
| chr9:41907155
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-168C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907155 | ||||||
| chr9:41907156
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-169C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907156 | ||||||
| chr9:41907197
|
T | G | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3221-210A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907197 | ||||||
| chr9:41907216
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3221-229C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907216 | ||||||
| chr9:41907339
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-352T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907339 | ||||||
| chr9:41907386
|
C | T | 17 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.3221-399G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907386 | ||||||
| chr9:41907429
|
A | AT | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-443dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907429 | ||||||
| chr9:41907444
|
A | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3221-457T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907444 | ||||||
| chr9:41907489
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-502C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907489 | ||||||
| chr9:41907544
|
T | C | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.3221-557A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907544 | ||||||
| chr9:41907560
|
T | G | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.3221-573A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907560 | ||||||
| chr9:41907591
|
C | T | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3221-604G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907591 | ||||||
| chr9:41907601
|
G | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3221-614C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907601 | ||||||
| chr9:41907618
|
A | AT | 8 | a0001c0043t0015g0013a0002c0002t0001g0041a0002c0002t0001g0045others(5): Show | 8 | HG00558.hp1 HG01255.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.3221-632dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907618 | ||||||
| chr9:41907618
|
A | ATTT | 6 | a0001c0001t0002g0006a0006c0007t0011g0017a0008c0006t0010g0069others(3): Show | 6 | HG01081.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3221-634_3221-632d others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907618 | ||||||
| chr9:41907618
|
A | ATTTT | 17 | a0001c0001t0002g0002a0001c0001t0003g0100a0001c0042t0013g0001others(14): Show | 17 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.3221-635_3221-632d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907618 | ||||||
| chr9:41907618
|
A | ATTTTT | 32 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3221-636_3221-632d others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907618 | ||||||
| chr9:41907618
|
A | ATTTTTT | 18 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0002g0024others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.3221-637_3221-632d others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907618 | ||||||
| chr9:41907661
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3221-674T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907661 | ||||||
| chr9:41907685
|
G | T | 96 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.3221-698C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907685 | ||||||
| chr9:41907817
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3220+740A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907817 | ||||||
| chr9:41907846
|
C | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3220+711G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907846 | ||||||
| chr9:41907909
|
C | A | 3 | a0001c0001t0002g0018a0001c0001t0017g0012a0001c0001t0031g0098 | 3 | HG00099.hp2 HG00642.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3220+648G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41907909 | ||||||
| chr9:41908025
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.3220+532G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41908025 | ||||||
| chr9:41908050
|
G | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3220+507C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41908050 | ||||||
| chr9:41908172
|
A | G | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3220+385T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41908172 | ||||||
| chr9:41908251
|
A | T | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3220+306T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41908251 | ||||||
| chr9:41908445
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.3220+112C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 19/23 | chr9 | 41908445 | ||||||
| chr9:41908923
|
T | A | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2996-142A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41908923 | ||||||
| chr9:41909035
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-254G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909035 | ||||||
| chr9:41909121
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-340A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909121 | ||||||
| chr9:41909163
|
A | T | 62 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.2996-382T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909163 | ||||||
| chr9:41909167
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-386T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909167 | ||||||
| chr9:41909275
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-494G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909275 | ||||||
| chr9:41909290
|
A | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-509T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909290 | ||||||
| chr9:41909326
|
A | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-545T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909326 | ||||||
| chr9:41909352
|
C | T | 1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2996-571G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909352 | ||||||
| chr9:41909358
|
C | A | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2996-577G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909358 | ||||||
| chr9:41909361
|
C | A | 1 | a0003c0011t0004g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2996-580G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909361 | ||||||
| chr9:41909404
|
G | T | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0004g0082others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.2996-623C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909404 | ||||||
| chr9:41909439
|
T | C | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2996-658A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909439 | ||||||
| chr9:41909450
|
G | C | 1 | a0003c0011t0004g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2996-669C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909450 | ||||||
| chr9:41909464
|
G | A | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2996-683C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909464 | ||||||
| chr9:41909478
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-697T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909478 | ||||||
| chr9:41909512
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-731C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909512 | ||||||
| chr9:41909516
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-735C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909516 | ||||||
| chr9:41909518
|
C | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-737G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909518 | ||||||
| chr9:41909566
|
T | C | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2996-785A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909566 | ||||||
| chr9:41909690
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-909T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909690 | ||||||
| chr9:41909745
|
T | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-964A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909745 | ||||||
| chr9:41909812
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1031A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909812 | ||||||
| chr9:41909820
|
C | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1039G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909820 | ||||||
| chr9:41909910
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2996-1129C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909910 | ||||||
| chr9:41909952
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2996-1171G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41909952 | ||||||
| chr9:41910000
|
G | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.2996-1219C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910000 | ||||||
| chr9:41910007
|
T | C | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.2996-1226A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910007 | ||||||
| chr9:41910032
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1251A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910032 | ||||||
| chr9:41910106
|
C | T | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2996-1325G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910106 | ||||||
| chr9:41910109
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1328T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910109 | ||||||
| chr9:41910110
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2996-1329G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910110 | ||||||
| chr9:41910147
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1366A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910147 | ||||||
| chr9:41910201
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1420A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910201 | ||||||
| chr9:41910240
|
G | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1459C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910240 | ||||||
| chr9:41910286
|
C | A | 1 | a0033c0036t0007g0010 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2996-1505G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910286 | ||||||
| chr9:41910328
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2996-1547G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910328 | ||||||
| chr9:41910369
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1588T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910369 | ||||||
| chr9:41910387
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-1606A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910387 | ||||||
| chr9:41910432
|
G | C | 2 | a0002c0002t0001g0052a0002c0002t0001g0053 | 2 | NA18974.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2996-1651C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910432 | ||||||
| chr9:41910436
|
T | A | 1 | a0001c0001t0003g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2996-1655A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910436 | ||||||
| chr9:41910436
|
T | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2996-1655A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910436 | ||||||
| chr9:41910481
|
G | C | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2996-1700C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910481 | ||||||
| chr9:41910513
|
A | G | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2996-1732T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910513 | ||||||
| chr9:41910739
|
T | C | 6 | a0001c0001t0002g0022a0006c0007t0002g0014a0006c0007t0011g0017others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-1958A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910739 | ||||||
| chr9:41910747
|
T | C | 63 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.2996-1966A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910747 | ||||||
| chr9:41910782
|
T | C | 6 | a0001c0001t0002g0022a0006c0007t0002g0014a0006c0007t0011g0017others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-2001A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910782 | ||||||
| chr9:41910844
|
A | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2996-2063T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910844 | ||||||
| chr9:41910889
|
T | A | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2996-2108A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910889 | ||||||
| chr9:41910996
|
A | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-2215T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41910996 | ||||||
| chr9:41911025
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-2244A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911025 | ||||||
| chr9:41911041
|
T | C | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2996-2260A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911041 | ||||||
| chr9:41911185
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-2404A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911185 | ||||||
| chr9:41911193
|
G | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2996-2412C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911193 | ||||||
| chr9:41911194
|
G | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2996-2413C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911194 | ||||||
| chr9:41911230
|
AT | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-2450delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911230 | ||||||
| chr9:41911306
|
CT | C | 22 | a0003c0003t0004g0075a0003c0003t0004g0081a0003c0003t0008g0077others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.2996-2526delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911306 | ||||||
| chr9:41911306
|
CTT | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2996-2527_2996-252 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911306 | ||||||
| chr9:41911488
|
T | A | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2996-2707A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911488 | ||||||
| chr9:41911501
|
G | A | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2996-2720C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911501 | ||||||
| chr9:41911583
|
AGC | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-2804_2996-280 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911583 | ||||||
| chr9:41911773
|
A | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2996-2992T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41911773 | ||||||
| chr9:41912036
|
G | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2996-3255C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912036 | ||||||
| chr9:41912079
|
T | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2996-3298A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912079 | ||||||
| chr9:41912139
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2996-3358C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912139 | ||||||
| chr9:41912158
|
C | T | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2996-3377G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912158 | ||||||
| chr9:41912159
|
G | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2996-3378C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912159 | ||||||
| chr9:41912410
|
C | T | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2996-3629G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912410 | ||||||
| chr9:41912628
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-3847A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912628 | ||||||
| chr9:41912720
|
T | A | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2996-3939A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912720 | ||||||
| chr9:41912871
|
G | A | 3 | a0009c0008t0009g0105a0009c0008t0009g0106a0009c0008t0009g0107 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2996-4090C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912871 | ||||||
| chr9:41912898
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2996-4117T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41912898 | ||||||
| chr9:41913381
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2996-4600G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41913381 | ||||||
| chr9:41913423
|
T | G | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2996-4642A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41913423 | ||||||
| chr9:41913682
|
C | T | 2 | a0006c0007t0011g0017a0006c0007t0011g0021 | 2 | HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2996-4901G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41913682 | ||||||
| chr9:41913833
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-5052G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41913833 | ||||||
| chr9:41913866
|
A | C | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2996-5085T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41913866 | ||||||
| chr9:41913956
|
C | T | 1 | a0004c0004t0005g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2996-5175G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41913956 | ||||||
| chr9:41914000
|
T | A | 6 | a0001c0001t0002g0022a0006c0007t0002g0014a0006c0007t0011g0017others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-5219A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914000 | ||||||
| chr9:41914004
|
A | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2996-5223T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914004 | ||||||
| chr9:41914328
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2996-5547A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914328 | ||||||
| chr9:41914493
|
A | G | 1 | a0002c0002t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2995+5577T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914493 | ||||||
| chr9:41914558
|
G | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2995+5512C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914558 | ||||||
| chr9:41914577
|
A | G | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2995+5493T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914577 | ||||||
| chr9:41914588
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+5482G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914588 | ||||||
| chr9:41914712
|
A | T | 3 | a0005c0005t0006g0076a0022c0030t0006g0085a0023c0028t0006g0084 | 3 | HG01516.hp1 HG01934.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2995+5358T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914712 | ||||||
| chr9:41914878
|
C | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2995+5192G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41914878 | ||||||
| chr9:41915026
|
TA | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2995+5043delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41915026 | ||||||
| chr9:41915414
|
A | G | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2995+4656T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41915414 | ||||||
| chr9:41915564
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2995+4506G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41915564 | ||||||
| chr9:41915710
|
G | GT | 4 | a0001c0001t0003g0096a0001c0001t0031g0098a0004c0004t0005g0029others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.2995+4359dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41915710 | ||||||
| chr9:41915875
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2995+4195C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41915875 | ||||||
| chr9:41916154
|
T | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2995+3916A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916154 | ||||||
| chr9:41916155
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2995+3915G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916155 | ||||||
| chr9:41916269
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2995+3801G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916269 | ||||||
| chr9:41916271
|
C | T | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2995+3799G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916271 | ||||||
| chr9:41916469
|
T | A | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2995+3601A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916469 | ||||||
| chr9:41916476
|
T | C | 1 | a0002c0002t0022g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2995+3594A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916476 | ||||||
| chr9:41916525
|
A | T | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2995+3545T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916525 | ||||||
| chr9:41916620
|
G | A | 2 | a0009c0008t0009g0105a0009c0008t0009g0106 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2995+3450C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916620 | ||||||
| chr9:41916704
|
C | G | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2995+3366G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916704 | ||||||
| chr9:41916783
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+3287G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916783 | ||||||
| chr9:41916817
|
G | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2995+3253C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916817 | ||||||
| chr9:41916877
|
C | A | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2995+3193G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41916877 | ||||||
| chr9:41917108
|
T | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2995+2962A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917108 | ||||||
| chr9:41917236
|
T | C | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2995+2834A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917236 | ||||||
| chr9:41917262
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2995+2808T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917262 | ||||||
| chr9:41917357
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2995+2713A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917357 | ||||||
| chr9:41917442
|
T | A | 1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2995+2628A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917442 | ||||||
| chr9:41917750
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2995+2320C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917750 | ||||||
| chr9:41917813
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2995+2257C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917813 | ||||||
| chr9:41917875
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+2195A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41917875 | ||||||
| chr9:41918076
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(10): Show | 13 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.2995+1994A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918076 | ||||||
| chr9:41918077
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2995+1993G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918077 | ||||||
| chr9:41918078
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+1992C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918078 | ||||||
| chr9:41918179
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2995+1891T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918179 | ||||||
| chr9:41918288
|
A | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+1782T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918288 | ||||||
| chr9:41918472
|
C | A | 3 | a0001c0012t0002g0009a0022c0030t0006g0085a0026c0025t0019g0028 | 3 | HG01943.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2995+1598G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918472 | ||||||
| chr9:41918489
|
A | G | 1 | a0004c0004t0005g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2995+1581T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918489 | ||||||
| chr9:41918586
|
T | C | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2995+1484A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918586 | ||||||
| chr9:41918669
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2995+1401C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918669 | ||||||
| chr9:41918885
|
A | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2995+1185T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918885 | ||||||
| chr9:41918961
|
A | G | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2995+1109T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41918961 | ||||||
| chr9:41919174
|
G | A | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2995+896C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919174 | ||||||
| chr9:41919198
|
G | A | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2995+872C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919198 | ||||||
| chr9:41919357
|
G | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2995+713C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919357 | ||||||
| chr9:41919503
|
A | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2995+567T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919503 | ||||||
| chr9:41919548
|
C | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2995+522G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919548 | ||||||
| chr9:41919553
|
C | T | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2995+517G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919553 | ||||||
| chr9:41919557
|
T | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2995+513A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919557 | ||||||
| chr9:41919588
|
G | T | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2995+482C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919588 | ||||||
| chr9:41919602
|
G | A | 4 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0056others(1): Show | 4 | HG01934.hp2 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2995+468C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919602 | ||||||
| chr9:41919713
|
C | T | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2995+357G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919713 | ||||||
| chr9:41919811
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2995+259G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919811 | ||||||
| chr9:41919875
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2995+195C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 18/23 | chr9 | 41919875 | ||||||
| chr9:41920332
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2756-23T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920332 | ||||||
| chr9:41920507
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2756-198T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920507 | ||||||
| chr9:41920532
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2756-223A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920532 | ||||||
| chr9:41920570
|
G | T | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2756-261C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920570 | ||||||
| chr9:41920579
|
G | A | 1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2756-270C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920579 | ||||||
| chr9:41920793
|
C | A | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2756-484G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920793 | ||||||
| chr9:41920836
|
G | C | 1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2756-527C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920836 | ||||||
| chr9:41920840
|
G | A | 32 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.2756-531C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920840 | ||||||
| chr9:41920841
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2756-532A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920841 | ||||||
| chr9:41920938
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2756-629G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41920938 | ||||||
| chr9:41921010
|
G | T | 1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2756-701C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921010 | ||||||
| chr9:41921037
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2756-728C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921037 | ||||||
| chr9:41921176
|
C | T | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2756-867G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921176 | ||||||
| chr9:41921289
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2756-980C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921289 | ||||||
| chr9:41921442
|
T | G | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2756-1133A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921442 | ||||||
| chr9:41921506
|
G | C | 1 | a0003c0011t0004g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2755+1171C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921506 | ||||||
| chr9:41921544
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2755+1133G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921544 | ||||||
| chr9:41921635
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2755+1042T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921635 | ||||||
| chr9:41921661
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2755+1016T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921661 | ||||||
| chr9:41921784
|
G | A | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2755+893C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921784 | ||||||
| chr9:41921857
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2755+820G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41921857 | ||||||
| chr9:41922133
|
T | C | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2755+544A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922133 | ||||||
| chr9:41922188
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2755+489C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922188 | ||||||
| chr9:41922202
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2755+475C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922202 | ||||||
| chr9:41922242
|
G | A | 2 | a0011c0037t0007g0008a0011c0040t0007g0003 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2755+435C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922242 | ||||||
| chr9:41922290
|
T | C | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.2755+387A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922290 | ||||||
| chr9:41922301
|
T | G | 6 | a0001c0001t0002g0022a0006c0007t0002g0014a0006c0007t0011g0017others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2755+376A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922301 | ||||||
| chr9:41922330
|
G | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2755+347C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922330 | ||||||
| chr9:41922445
|
G | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2755+232C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922445 | ||||||
| chr9:41922476
|
T | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2755+201A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 17/23 | chr9 | 41922476 | ||||||
| chr9:41922978
|
C | T | 6 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2537-83G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41922978 | ||||||
| chr9:41923004
|
G | A | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2537-109C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923004 | ||||||
| chr9:41923042
|
G | A | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2537-147C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923042 | ||||||
| chr9:41923076
|
T | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2537-181A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923076 | ||||||
| chr9:41923209
|
T | A | 14 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(11): Show | 14 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.2537-314A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923209 | ||||||
| chr9:41923272
|
T | C | 2 | a0001c0001t0003g0095a0001c0001t0003g0097 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2537-377A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923272 | ||||||
| chr9:41923502
|
C | T | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2536+421G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923502 | ||||||
| chr9:41923556
|
G | A | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2536+367C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923556 | ||||||
| chr9:41923633
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2536+290C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923633 | ||||||
| chr9:41923633
|
G | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2536+290C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923633 | ||||||
| chr9:41923878
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2536+45G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923878 | ||||||
| chr9:41923894
|
C | T | 2 | a0004c0004t0005g0029a0004c0004t0005g0030 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2536+29G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923894 | ||||||
| chr9:41923914
|
C | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2536+9G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 16/23 | chr9 | 41923914 | ||||||
| chr9:41924246
|
G | A | 9 | a0004c0004t0005g0030a0004c0004t0005g0031a0004c0004t0005g0032others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.2366-153C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924246 | ||||||
| chr9:41924318
|
C | T | 1 | a0004c0004t0005g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2366-225G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924318 | ||||||
| chr9:41924394
|
C | G | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2366-301G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924394 | ||||||
| chr9:41924501
|
T | C | 2 | a0001c0001t0002g0022a0029c0045t0002g0019 | 2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2366-408A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924501 | ||||||
| chr9:41924600
|
A | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2366-507T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924600 | ||||||
| chr9:41924645
|
G | GCA | 4 | a0003c0003t0004g0082a0005c0005t0006g0076a0008c0006t0010g0070others(1): Show | 4 | HG00558.hp2 HG01516.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-554_2366-553d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
G | GCACA | 5 | a0003c0003t0008g0077a0003c0003t0008g0083a0003c0011t0004g0078others(2): Show | 5 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.2366-556_2366-553d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
G | GCACACA | 4 | a0002c0023t0001g0054a0009c0008t0009g0105a0009c0008t0009g0106others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366-558_2366-553d others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
G | GCACACAC others(1): Show |
2 | a0018c0024t0008g0080a0027c0026t0020g0027 | 2 | HG00323.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2366-560_2366-553d others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
G | GCACACAC others(3): Show |
2 | a0003c0003t0004g0081a0003c0003t0008g0086 | 2 | HG03239.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2366-562_2366-553d others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
GCA | G | 6 | a0002c0002t0001g0062a0002c0002t0012g0051a0002c0020t0001g0060others(3): Show | 6 | HG00140.hp2 HG00735.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2366-554_2366-553d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
GCACA | G | 25 | a0002c0002t0001g0044a0002c0002t0001g0047a0002c0002t0001g0048others(22): Show | 25 | HG00323.hp1 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2366-556_2366-553d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
GCACACA | G | 5 | a0001c0001t0002g0004a0002c0002t0022g0068a0011c0040t0007g0003others(2): Show | 5 | HG02486.hp1 HG02572.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2366-558_2366-553d others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
GCACACAC others(1): Show |
G | 7 | a0001c0001t0002g0011a0001c0001t0002g0024a0001c0001t0003g0104others(4): Show | 7 | HG01981.hp1 HG02040.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2366-560_2366-553d others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
GCACACAC others(3): Show |
G | 35 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.2366-562_2366-553d others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924645
|
GCACACAC others(7): Show |
G | 2 | a0001c0012t0002g0009a0026c0025t0019g0028 | 2 | HG01943.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2366-566_2366-553d others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924645 | ||||||
| chr9:41924656
|
C | T | 3 | a0003c0003t0004g0075a0003c0011t0004g0074a0022c0030t0006g0085 | 3 | HG02717.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2366-563G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924656 | ||||||
| chr9:41924658
|
C | T | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2366-565G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924658 | ||||||
| chr9:41924946
|
G | A | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2366-853C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41924946 | ||||||
| chr9:41925291
|
A | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2366-1198T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925291 | ||||||
| chr9:41925331
|
C | T | 2 | a0011c0037t0007g0008a0011c0040t0007g0003 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2366-1238G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925331 | ||||||
| chr9:41925499
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2366-1406T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925499 | ||||||
| chr9:41925594
|
A | AAAAC | 9 | a0001c0001t0002g0022a0001c0046t0016g0015a0006c0007t0002g0014others(6): Show | 9 | HG01175.hp1 HG01255.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.2366-1505_2366-150 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925594 | ||||||
| chr9:41925594
|
AAAAC | A | 3 | a0017c0014t0001g0038a0026c0025t0019g0028a0032c0039t0014g0025 | 3 | HG02486.hp1 HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2366-1505_2366-150 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925594 | ||||||
| chr9:41925666
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2366-1573G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925666 | ||||||
| chr9:41925681
|
G | A | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2366-1588C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925681 | ||||||
| chr9:41925710
|
G | C | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2366-1617C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925710 | ||||||
| chr9:41925786
|
T | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2366-1693A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925786 | ||||||
| chr9:41925977
|
C | A | 34 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(31): Show | 34 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2366-1884G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41925977 | ||||||
| chr9:41926013
|
ATCTC | A | 19 | a0002c0002t0001g0041a0002c0002t0001g0044a0002c0002t0001g0045others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2366-1924_2366-192 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926013 | ||||||
| chr9:41926047
|
C | T | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2366-1954G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926047 | ||||||
| chr9:41926258
|
T | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2366-2165A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926258 | ||||||
| chr9:41926280
|
T | C | 1 | a0003c0003t0004g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2366-2187A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926280 | ||||||
| chr9:41926304
|
C | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2366-2211G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926304 | ||||||
| chr9:41926422
|
GA | G | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.2366-2330delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926422 | ||||||
| chr9:41926427
|
G | T | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2366-2334C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926427 | ||||||
| chr9:41926488
|
G | A | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2366-2395C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926488 | ||||||
| chr9:41926536
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2366-2443T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926536 | ||||||
| chr9:41926574
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366-2481T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926574 | ||||||
| chr9:41926905
|
T | C | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2365+2412A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926905 | ||||||
| chr9:41926917
|
G | C | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2365+2400C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41926917 | ||||||
| chr9:41927197
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2365+2120A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927197 | ||||||
| chr9:41927423
|
A | G | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2365+1894T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927423 | ||||||
| chr9:41927458
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2365+1859C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927458 | ||||||
| chr9:41927473
|
G | GGGAA | 81 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.2365+1840_2365+184 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927473 | ||||||
| chr9:41927473
|
G | GGGAAGGA others(1): Show |
4 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(1): Show | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365+1836_2365+184 others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927473 | ||||||
| chr9:41927933
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2365+1384A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927933 | ||||||
| chr9:41927939
|
A | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2365+1378T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927939 | ||||||
| chr9:41927950
|
C | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2365+1367G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41927950 | ||||||
| chr9:41928016
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2365+1301G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928016 | ||||||
| chr9:41928273
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2365+1044A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928273 | ||||||
| chr9:41928396
|
C | T | 3 | a0003c0003t0008g0077a0003c0003t0008g0083a0018c0024t0008g0080 | 3 | HG00140.hp1 HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.2365+921G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928396 | ||||||
| chr9:41928453
|
T | C | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2365+864A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928453 | ||||||
| chr9:41928458
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2365+859T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928458 | ||||||
| chr9:41928461
|
G | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365+856C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928461 | ||||||
| chr9:41928504
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2365+813G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928504 | ||||||
| chr9:41928642
|
A | T | 1 | a0002c0002t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2365+675T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928642 | ||||||
| chr9:41928767
|
C | T | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2365+550G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928767 | ||||||
| chr9:41928831
|
T | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2365+486A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928831 | ||||||
| chr9:41928880
|
G | C | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2365+437C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928880 | ||||||
| chr9:41928930
|
G | A | 2 | a0001c0001t0002g0004a0001c0043t0015g0013 | 2 | HG00558.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2365+387C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41928930 | ||||||
| chr9:41929078
|
G | A | 2 | a0004c0004t0005g0029a0026c0025t0019g0028 | 2 | HG02622.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2365+239C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41929078 | ||||||
| chr9:41929200
|
G | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2365+117C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41929200 | ||||||
| chr9:41929223
|
A | C | 1 | a0002c0002t0012g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2365+94T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | 41929223 | ||||||
| chr9:41929461
|
G | A | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2238-17C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41929461 | ||||||
| chr9:41929718
|
A | G | 2 | a0011c0037t0007g0008a0011c0040t0007g0003 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2238-274T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41929718 | ||||||
| chr9:41929744
|
AT | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2238-301delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41929744 | ||||||
| chr9:41929748
|
T | A | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2238-304A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41929748 | ||||||
| chr9:41929985
|
T | A | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2238-541A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41929985 | ||||||
| chr9:41930007
|
T | A | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2238-563A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930007 | ||||||
| chr9:41930501
|
A | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.2238-1057T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930501 | ||||||
| chr9:41930562
|
C | CA | 5 | a0002c0002t0001g0044a0002c0002t0001g0052a0002c0002t0001g0053others(2): Show | 5 | HG01071.hp1 HG03942.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2238-1119dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930562 | ||||||
| chr9:41930644
|
T | C | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2238-1200A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930644 | ||||||
| chr9:41930789
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2238-1345G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930789 | ||||||
| chr9:41930824
|
G | A | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2238-1380C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930824 | ||||||
| chr9:41930900
|
A | G | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2238-1456T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41930900 | ||||||
| chr9:41931028
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2238-1584G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41931028 | ||||||
| chr9:41931153
|
T | A | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2238-1709A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41931153 | ||||||
| chr9:41931196
|
T | C | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2238-1752A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41931196 | ||||||
| chr9:41931536
|
C | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2238-2092G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41931536 | ||||||
| chr9:41931593
|
C | T | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.2238-2149G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41931593 | ||||||
| chr9:41931689
|
C | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2238-2245G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41931689 | ||||||
| chr9:41932026
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2238-2582T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932026 | ||||||
| chr9:41932118
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2238-2674C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932118 | ||||||
| chr9:41932210
|
C | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2238-2766G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932210 | ||||||
| chr9:41932390
|
C | A | 1 | a0003c0011t0004g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2238-2946G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932390 | ||||||
| chr9:41932426
|
T | G | 2 | a0011c0037t0007g0008a0011c0040t0007g0003 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2238-2982A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932426 | ||||||
| chr9:41932497
|
C | CAACTTTT others(1): Show |
34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2238-3061_2238-305 others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932497 | ||||||
| chr9:41932520
|
C | CT | 4 | a0001c0046t0016g0015a0005c0005t0006g0073a0008c0006t0010g0071others(1): Show | 4 | HG00323.hp1 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2238-3077dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932520 | ||||||
| chr9:41932559
|
G | A | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2238-3115C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932559 | ||||||
| chr9:41932622
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2238-3178G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932622 | ||||||
| chr9:41932665
|
G | A | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2238-3221C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932665 | ||||||
| chr9:41932686
|
A | G | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2238-3242T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41932686 | ||||||
| chr9:41933063
|
A | G | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2238-3619T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41933063 | ||||||
| chr9:41933337
|
G | C | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0065 | 3 | HG03834.hp2 HG04115.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2238-3893C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41933337 | ||||||
| chr9:41933558
|
G | C | 2 | a0007c0009t0023g0039a0027c0026t0020g0027 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2238-4114C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41933558 | ||||||
| chr9:41933753
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2238-4309G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41933753 | ||||||
| chr9:41933849
|
C | T | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2237+4395G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41933849 | ||||||
| chr9:41933863
|
C | T | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2237+4381G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41933863 | ||||||
| chr9:41934082
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2237+4162C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934082 | ||||||
| chr9:41934100
|
C | CAT | 2 | a0003c0003t0021g0035a0003c0011t0004g0078 | 2 | HG02056.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2237+4142_2237+414 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATAAATA others(11): Show |
1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2237+4143_2237+414 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATAT | 4 | a0003c0003t0004g0075a0003c0011t0004g0074a0022c0030t0006g0085others(1): Show | 4 | HG00099.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2237+4140_2237+414 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(3): Show |
1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2237+4134_2237+414 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(7): Show |
6 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0003g0095others(3): Show | 6 | HG01071.hp2 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2237+4130_2237+414 others(18): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(9): Show |
9 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0099others(6): Show | 9 | HG00280.hp1 HG01516.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2237+4128_2237+414 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(11): Show |
10 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0024others(7): Show | 10 | HG01106.hp1 HG02040.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.2237+4126_2237+414 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(13): Show |
11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0003g0093others(8): Show | 11 | HG00099.hp2 HG01255.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2237+4124_2237+414 others(24): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(15): Show |
9 | a0001c0001t0003g0102a0001c0001t0018g0026a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG02083.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.2237+4122_2237+414 others(26): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934100
|
C | CATATATA others(17): Show |
4 | a0001c0001t0002g0022a0001c0001t0017g0012a0004c0004t0005g0032others(1): Show | 4 | HG00642.hp2 HG01175.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2237+4143_2237+414 others(28): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934100 | ||||||
| chr9:41934112
|
T | TATATATA others(13): Show |
2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2237+4131_2237+413 others(24): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(29): Show |
2 | a0002c0002t0001g0052a0002c0002t0001g0053 | 2 | NA18974.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2237+4131_2237+413 others(40): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(31): Show |
2 | a0002c0002t0001g0041a0002c0002t0024g0061 | 2 | HG02273.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2237+4131_2237+413 others(42): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(37): Show |
1 | a0002c0010t0001g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2237+4131_2237+413 others(48): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(33): Show |
6 | a0002c0002t0001g0050a0002c0002t0001g0059a0002c0002t0012g0051others(3): Show | 6 | HG00140.hp2 HG00323.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.2237+4131_2237+413 others(44): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(37): Show |
1 | a0002c0023t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2237+4131_2237+413 others(48): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(35): Show |
3 | a0002c0002t0001g0045a0002c0002t0001g0056a0002c0002t0001g0062 | 3 | HG00735.hp2 HG01943.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2237+4131_2237+413 others(46): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(37): Show |
2 | a0002c0015t0001g0046a0016c0017t0001g0042 | 2 | HG01081.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2237+4131_2237+413 others(48): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(41): Show |
1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2237+4131_2237+413 others(52): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(39): Show |
1 | a0002c0002t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2237+4131_2237+413 others(50): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(43): Show |
1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2237+4131_2237+413 others(54): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934112
|
T | TATATATA others(45): Show |
1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2237+4131_2237+413 others(56): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934112 | ||||||
| chr9:41934122
|
T | TATATAC | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2237+4121_2237+412 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934122
|
T | TATATATA others(7): Show |
1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2237+4121_2237+412 others(18): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934122
|
T | TATATATA others(17): Show |
1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2237+4121_2237+412 others(28): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934122
|
T | TATATATA others(19): Show |
1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2237+4121_2237+412 others(30): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934122
|
T | TATATATA others(19): Show |
3 | a0007c0016t0001g0036a0017c0014t0001g0038a0026c0025t0019g0028 | 3 | HG02622.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2237+4121_2237+412 others(30): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934122
|
T | TATATATA others(23): Show |
1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2237+4121_2237+412 others(34): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934122
|
T | TATATATA others(23): Show |
1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2237+4121_2237+412 others(34): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934122 | ||||||
| chr9:41934124
|
C | T | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.2237+4120G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934124 | ||||||
| chr9:41934132
|
T | C | 2 | a0027c0026t0020g0027a0032c0039t0014g0025 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2237+4112A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934132 | ||||||
| chr9:41934138
|
T | TAC | 21 | a0002c0002t0001g0041a0002c0002t0001g0044a0002c0002t0001g0045others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.2237+4105_2237+410 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934138 | ||||||
| chr9:41934140
|
T | C | 21 | a0002c0002t0001g0041a0002c0002t0001g0044a0002c0002t0001g0045others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.2237+4104A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934140 | ||||||
| chr9:41934176
|
T | TAC | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2237+4066_2237+406 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934176 | ||||||
| chr9:41934176
|
T | TACACACA others(15): Show |
3 | a0002c0002t0012g0043a0014c0018t0001g0067a0015c0019t0001g0066 | 3 | HG01071.hp1 HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2237+4067_2237+406 others(26): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934176 | ||||||
| chr9:41934188
|
CAT | C | 2 | a0007c0016t0001g0036a0024c0029t0006g0087 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2237+4054_2237+405 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934188 | ||||||
| chr9:41934218
|
CT | C | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.2237+4025delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934218 | ||||||
| chr9:41934362
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2237+3882C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934362 | ||||||
| chr9:41934413
|
G | T | 1 | a0001c0001t0002g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2237+3831C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934413 | ||||||
| chr9:41934415
|
T | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2237+3829A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934415 | ||||||
| chr9:41934512
|
C | T | 33 | a0001c0001t0002g0006a0002c0002t0001g0040a0002c0002t0001g0041others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2237+3732G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934512 | ||||||
| chr9:41934570
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2237+3674C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934570 | ||||||
| chr9:41934624
|
C | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2237+3620G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934624 | ||||||
| chr9:41934904
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2237+3340T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934904 | ||||||
| chr9:41934935
|
A | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2237+3309T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934935 | ||||||
| chr9:41934989
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2237+3255C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41934989 | ||||||
| chr9:41935095
|
A | G | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2237+3149T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41935095 | ||||||
| chr9:41935235
|
A | G | 1 | a0002c0020t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2237+3009T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41935235 | ||||||
| chr9:41935588
|
A | G | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2237+2656T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41935588 | ||||||
| chr9:41935932
|
C | T | 1 | a0001c0012t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2237+2312G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41935932 | ||||||
| chr9:41935959
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2237+2285C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41935959 | ||||||
| chr9:41935991
|
G | T | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2237+2253C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41935991 | ||||||
| chr9:41936160
|
C | T | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2237+2084G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936160 | ||||||
| chr9:41936170
|
G | C | 1 | a0001c0001t0002g0004 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2237+2074C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936170 | ||||||
| chr9:41936192
|
G | A | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2237+2052C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936192 | ||||||
| chr9:41936383
|
T | C | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2237+1861A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936383 | ||||||
| chr9:41936437
|
G | A | 1 | a0004c0004t0005g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2237+1807C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936437 | ||||||
| chr9:41936447
|
G | A | 2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2237+1797C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936447 | ||||||
| chr9:41936479
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+1765C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936479 | ||||||
| chr9:41936480
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2237+1764G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936480 | ||||||
| chr9:41936511
|
T | C | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2237+1733A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936511 | ||||||
| chr9:41936516
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+1728A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936516 | ||||||
| chr9:41936552
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+1692A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936552 | ||||||
| chr9:41936707
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+1537T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936707 | ||||||
| chr9:41936771
|
G | A | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2237+1473C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936771 | ||||||
| chr9:41936781
|
G | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2237+1463C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936781 | ||||||
| chr9:41936904
|
G | C | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2237+1340C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41936904 | ||||||
| chr9:41937019
|
T | C | 2 | a0026c0025t0019g0028a0032c0039t0014g0025 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2237+1225A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937019 | ||||||
| chr9:41937045
|
A | G | 2 | a0004c0004t0005g0034a0008c0006t0010g0069 | 2 | HG02559.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2237+1199T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937045 | ||||||
| chr9:41937087
|
A | T | 2 | a0004c0004t0005g0034a0008c0006t0010g0069 | 2 | HG02559.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2237+1157T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937087 | ||||||
| chr9:41937098
|
A | G | 80 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2237+1146T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937098 | ||||||
| chr9:41937112
|
AATTTATT others(6): Show |
A | 2 | a0004c0004t0005g0034a0008c0006t0010g0069 | 2 | HG02559.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2237+1119_2237+113 others(17): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937112 | ||||||
| chr9:41937114
|
T | TTTA | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2237+1127_2237+112 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937114 | ||||||
| chr9:41937114
|
T | TTTATTA | 7 | a0001c0001t0018g0026a0004c0004t0005g0029a0004c0004t0005g0030others(4): Show | 7 | HG00280.hp2 HG02083.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.2237+1124_2237+112 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937114 | ||||||
| chr9:41937114
|
T | TTTATTAT others(2): Show |
25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2237+1121_2237+112 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937114 | ||||||
| chr9:41937114
|
T | TTTATTAT others(5): Show |
7 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0065others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2237+1118_2237+112 others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937114 | ||||||
| chr9:41937114
|
T | TTTATTAT others(8): Show |
3 | a0002c0002t0001g0059a0002c0002t0001g0063a0015c0019t0001g0066 | 3 | HG01934.hp2 HG02083.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2237+1115_2237+112 others(19): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937114 | ||||||
| chr9:41937114
|
T | TTTATTAT others(11): Show |
2 | a0005c0005t0006g0073a0007c0016t0001g0036 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2237+1112_2237+112 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937114 | ||||||
| chr9:41937197
|
A | G | 2 | a0004c0004t0005g0034a0008c0006t0010g0069 | 2 | HG02559.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2237+1047T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937197 | ||||||
| chr9:41937270
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+974C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937270 | ||||||
| chr9:41937287
|
T | C | 1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2237+957A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937287 | ||||||
| chr9:41937314
|
A | T | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2237+930T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937314 | ||||||
| chr9:41937316
|
G | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2237+928C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937316 | ||||||
| chr9:41937524
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2237+720G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937524 | ||||||
| chr9:41937535
|
TA | T | 6 | a0001c0001t0002g0022a0006c0007t0002g0014a0006c0007t0011g0017others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2237+708delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937535 | ||||||
| chr9:41937665
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2237+579G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937665 | ||||||
| chr9:41937739
|
C | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2237+505G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937739 | ||||||
| chr9:41937789
|
C | G | 2 | a0010c0013t0003g0103a0010c0013t0003g0108 | 2 | HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2237+455G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937789 | ||||||
| chr9:41937841
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+403C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937841 | ||||||
| chr9:41937842
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+402T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937842 | ||||||
| chr9:41937845
|
G | C | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2237+399C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937845 | ||||||
| chr9:41937855
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2237+389C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937855 | ||||||
| chr9:41937953
|
G | A | 11 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2237+291C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41937953 | ||||||
| chr9:41938011
|
C | T | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2237+233G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41938011 | ||||||
| chr9:41938029
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+215A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41938029 | ||||||
| chr9:41938222
|
A | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2237+22T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | 41938222 | ||||||
| chr9:41938422
|
G | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2081-22C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41938422 | ||||||
| chr9:41938447
|
A | G | 10 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(7): Show | 10 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2081-47T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41938447 | ||||||
| chr9:41938625
|
A | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2081-225T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41938625 | ||||||
| chr9:41938993
|
G | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2081-593C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41938993 | ||||||
| chr9:41939039
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2081-639C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939039 | ||||||
| chr9:41939251
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2081-851C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939251 | ||||||
| chr9:41939305
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2081-905G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939305 | ||||||
| chr9:41939353
|
A | G | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2081-953T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939353 | ||||||
| chr9:41939396
|
G | A | 34 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(31): Show | 34 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2081-996C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939396 | ||||||
| chr9:41939478
|
T | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2081-1078A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939478 | ||||||
| chr9:41939510
|
A | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2081-1110T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41939510 | ||||||
| chr9:41940048
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2081-1648G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940048 | ||||||
| chr9:41940083
|
G | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2081-1683C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940083 | ||||||
| chr9:41940128
|
T | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2081-1728A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940128 | ||||||
| chr9:41940327
|
AC | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2081-1928delG | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940327 | ||||||
| chr9:41940434
|
T | C | 1 | a0002c0010t0001g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2081-2034A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940434 | ||||||
| chr9:41940490
|
C | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2081-2090G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940490 | ||||||
| chr9:41940706
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-2306A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940706 | ||||||
| chr9:41940789
|
A | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2081-2389T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940789 | ||||||
| chr9:41940835
|
A | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2081-2435T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940835 | ||||||
| chr9:41940954
|
G | GA | 6 | a0001c0001t0018g0026a0006c0007t0002g0014a0006c0007t0011g0017others(3): Show | 6 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.2081-2555dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41940954 | ||||||
| chr9:41941375
|
C | A | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2081-2975G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41941375 | ||||||
| chr9:41941387
|
A | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2081-2987T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41941387 | ||||||
| chr9:41941483
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2081-3083G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41941483 | ||||||
| chr9:41941565
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2081-3165T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41941565 | ||||||
| chr9:41941719
|
T | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2081-3319A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41941719 | ||||||
| chr9:41942239
|
G | A | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2081-3839C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942239 | ||||||
| chr9:41942330
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-3930C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942330 | ||||||
| chr9:41942357
|
T | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2081-3957A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942357 | ||||||
| chr9:41942440
|
A | C | 4 | a0002c0002t0001g0040a0002c0002t0001g0047a0002c0002t0001g0048others(1): Show | 4 | HG03669.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2081-4040T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942440 | ||||||
| chr9:41942480
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2081-4080C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942480 | ||||||
| chr9:41942484
|
G | T | 1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2081-4084C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942484 | ||||||
| chr9:41942503
|
G | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2081-4103C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942503 | ||||||
| chr9:41942536
|
G | A | 1 | a0008c0006t0010g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2081-4136C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942536 | ||||||
| chr9:41942547
|
C | G | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2081-4147G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942547 | ||||||
| chr9:41942555
|
C | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2081-4155G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942555 | ||||||
| chr9:41942568
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-4168C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942568 | ||||||
| chr9:41942673
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-4273C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942673 | ||||||
| chr9:41942788
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2081-4388G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942788 | ||||||
| chr9:41942816
|
G | A | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2081-4416C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942816 | ||||||
| chr9:41942839
|
A | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2081-4439T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942839 | ||||||
| chr9:41942968
|
G | T | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2081-4568C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41942968 | ||||||
| chr9:41943022
|
T | A | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2081-4622A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943022 | ||||||
| chr9:41943042
|
T | C | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2081-4642A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943042 | ||||||
| chr9:41943127
|
A | G | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2081-4727T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943127 | ||||||
| chr9:41943278
|
T | C | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2081-4878A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943278 | ||||||
| chr9:41943338
|
G | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2081-4938C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943338 | ||||||
| chr9:41943345
|
A | AT | 44 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0018others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2081-4946dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943345 | ||||||
| chr9:41943345
|
A | ATT | 18 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0003g0093others(15): Show | 18 | HG00140.hp2 HG00323.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.2081-4947_2081-494 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943345 | ||||||
| chr9:41943345
|
AT | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2081-4946delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943345 | ||||||
| chr9:41943345
|
ATT | A | 4 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2081-4947_2081-494 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943345 | ||||||
| chr9:41943431
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2081-5031G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943431 | ||||||
| chr9:41943490
|
C | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2081-5090G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943490 | ||||||
| chr9:41943520
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2081-5120A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943520 | ||||||
| chr9:41943568
|
G | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2081-5168C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943568 | ||||||
| chr9:41943595
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2081-5195C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943595 | ||||||
| chr9:41943599
|
G | A | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2081-5199C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943599 | ||||||
| chr9:41943650
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.2081-5250T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943650 | ||||||
| chr9:41943704
|
C | T | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2081-5304G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943704 | ||||||
| chr9:41943866
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2081-5466A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943866 | ||||||
| chr9:41943943
|
A | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2081-5543T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41943943 | ||||||
| chr9:41944105
|
A | G | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2081-5705T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944105 | ||||||
| chr9:41944270
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2081-5870T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944270 | ||||||
| chr9:41944383
|
G | T | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2081-5983C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944383 | ||||||
| chr9:41944394
|
A | C | 2 | a0030c0035t0007g0023a0033c0036t0007g0010 | 2 | HG02083.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2081-5994T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944394 | ||||||
| chr9:41944610
|
G | C | 1 | a0003c0011t0004g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2081-6210C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944610 | ||||||
| chr9:41944630
|
A | G | 1 | a0031c0044t0009g0094 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2081-6230T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944630 | ||||||
| chr9:41944698
|
C | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-6298G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944698 | ||||||
| chr9:41944746
|
A | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-6346T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944746 | ||||||
| chr9:41944879
|
G | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2081-6479C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944879 | ||||||
| chr9:41944962
|
A | C | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2081-6562T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41944962 | ||||||
| chr9:41945199
|
A | T | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-6799T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945199 | ||||||
| chr9:41945294
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2081-6894G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945294 | ||||||
| chr9:41945445
|
G | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2081-7045C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945445 | ||||||
| chr9:41945604
|
C | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2081-7204G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945604 | ||||||
| chr9:41945652
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2081-7252T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945652 | ||||||
| chr9:41945868
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+7315C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945868 | ||||||
| chr9:41945979
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2080+7204T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41945979 | ||||||
| chr9:41946065
|
C | T | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2080+7118G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946065 | ||||||
| chr9:41946085
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+7098T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946085 | ||||||
| chr9:41946090
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2080+7093C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946090 | ||||||
| chr9:41946146
|
A | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2080+7037T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946146 | ||||||
| chr9:41946172
|
T | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+7011A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946172 | ||||||
| chr9:41946268
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+6915C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946268 | ||||||
| chr9:41946465
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2080+6718G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946465 | ||||||
| chr9:41946485
|
A | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+6698T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946485 | ||||||
| chr9:41946528
|
A | G | 75 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2080+6655T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946528 | ||||||
| chr9:41946532
|
GA | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+6650delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946532 | ||||||
| chr9:41946554
|
C | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2080+6629G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946554 | ||||||
| chr9:41946605
|
C | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2080+6578G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946605 | ||||||
| chr9:41946778
|
G | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2080+6405C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946778 | ||||||
| chr9:41946922
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+6261T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946922 | ||||||
| chr9:41946987
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2080+6196G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946987 | ||||||
| chr9:41946995
|
T | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2080+6188A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41946995 | ||||||
| chr9:41947048
|
G | A | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2080+6135C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947048 | ||||||
| chr9:41947086
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2080+6097A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947086 | ||||||
| chr9:41947167
|
T | C | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2080+6016A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947167 | ||||||
| chr9:41947283
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5900T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947283 | ||||||
| chr9:41947311
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2080+5872C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947311 | ||||||
| chr9:41947322
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5861T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947322 | ||||||
| chr9:41947385
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+5798A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947385 | ||||||
| chr9:41947396
|
T | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5787A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947396 | ||||||
| chr9:41947434
|
T | C | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2080+5749A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947434 | ||||||
| chr9:41947492
|
A | G | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2080+5691T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947492 | ||||||
| chr9:41947531
|
T | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2080+5652A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947531 | ||||||
| chr9:41947565
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5618G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947565 | ||||||
| chr9:41947730
|
A | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.2080+5453T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947730 | ||||||
| chr9:41947735
|
C | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2080+5448G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947735 | ||||||
| chr9:41947788
|
C | CAG | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5393_2080+539 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947788 | ||||||
| chr9:41947885
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5298G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41947885 | ||||||
| chr9:41948034
|
G | GA | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2080+5148dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948034 | ||||||
| chr9:41948065
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5118A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948065 | ||||||
| chr9:41948092
|
G | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+5091C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948092 | ||||||
| chr9:41948122
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2080+5061G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948122 | ||||||
| chr9:41948132
|
T | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2080+5051A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948132 | ||||||
| chr9:41948267
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2080+4916A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948267 | ||||||
| chr9:41948368
|
A | AGGCAT | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+4814_2080+481 others(9): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948368 | ||||||
| chr9:41948647
|
G | A | 1 | a0006c0007t0011g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2080+4536C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948647 | ||||||
| chr9:41948650
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+4533T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948650 | ||||||
| chr9:41948701
|
A | C | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2080+4482T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948701 | ||||||
| chr9:41948744
|
G | T | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2080+4439C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948744 | ||||||
| chr9:41948754
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2080+4429T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948754 | ||||||
| chr9:41948826
|
A | T | 1 | a0006c0007t0011g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2080+4357T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948826 | ||||||
| chr9:41948841
|
G | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2080+4342C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948841 | ||||||
| chr9:41948884
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+4299G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948884 | ||||||
| chr9:41948899
|
C | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2080+4284G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948899 | ||||||
| chr9:41948981
|
A | T | 2 | a0004c0004t0005g0029a0004c0004t0005g0030 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2080+4202T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41948981 | ||||||
| chr9:41949001
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2080+4182T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949001 | ||||||
| chr9:41949046
|
T | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+4137A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949046 | ||||||
| chr9:41949206
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2080+3977A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949206 | ||||||
| chr9:41949275
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2080+3908C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949275 | ||||||
| chr9:41949287
|
G | A | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2080+3896C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949287 | ||||||
| chr9:41949484
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+3699G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949484 | ||||||
| chr9:41949495
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+3688G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949495 | ||||||
| chr9:41949564
|
C | T | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2080+3619G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949564 | ||||||
| chr9:41949598
|
A | G | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2080+3585T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949598 | ||||||
| chr9:41949764
|
T | G | 3 | a0006c0007t0011g0017a0006c0007t0011g0021a0006c0041t0002g0020 | 3 | HG02040.hp2 HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2080+3419A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949764 | ||||||
| chr9:41949798
|
G | T | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2080+3385C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949798 | ||||||
| chr9:41949800
|
A | T | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2080+3383T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949800 | ||||||
| chr9:41949932
|
T | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+3251A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949932 | ||||||
| chr9:41949952
|
T | A | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2080+3231A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41949952 | ||||||
| chr9:41950078
|
A | AAC | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+3103_2080+310 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950078 | ||||||
| chr9:41950242
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2080+2941G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950242 | ||||||
| chr9:41950250
|
G | T | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2080+2933C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950250 | ||||||
| chr9:41950316
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2080+2867G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950316 | ||||||
| chr9:41950347
|
G | A | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2080+2836C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950347 | ||||||
| chr9:41950376
|
C | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2807G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950376 | ||||||
| chr9:41950518
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2665G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950518 | ||||||
| chr9:41950525
|
A | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2080+2658T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950525 | ||||||
| chr9:41950532
|
C | T | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2080+2651G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950532 | ||||||
| chr9:41950533
|
G | T | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2080+2650C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950533 | ||||||
| chr9:41950648
|
TA | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2534delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950648 | ||||||
| chr9:41950747
|
C | CT | 34 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(31): Show | 34 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2080+2435dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950747 | ||||||
| chr9:41950747
|
CTTT | C | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.2080+2433_2080+243 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950747 | ||||||
| chr9:41950747
|
CTTTTTTT others(2): Show |
C | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.2080+2427_2080+243 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950747 | ||||||
| chr9:41950747
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0024a0001c0012t0002g0009 | 2 | HG01943.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.2080+2426_2080+243 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950747 | ||||||
| chr9:41950779
|
G | A | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2080+2404C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950779 | ||||||
| chr9:41950803
|
C | G | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2080+2380G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950803 | ||||||
| chr9:41950817
|
G | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2366C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950817 | ||||||
| chr9:41950875
|
G | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2308C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950875 | ||||||
| chr9:41950896
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2287G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950896 | ||||||
| chr9:41950948
|
G | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2080+2235C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950948 | ||||||
| chr9:41950957
|
G | A | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2080+2226C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950957 | ||||||
| chr9:41950967
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2080+2216C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950967 | ||||||
| chr9:41950974
|
C | G | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2080+2209G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950974 | ||||||
| chr9:41950989
|
C | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+2194G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41950989 | ||||||
| chr9:41951000
|
C | T | 1 | a0009c0008t0009g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2080+2183G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951000 | ||||||
| chr9:41951050
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2080+2133T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951050 | ||||||
| chr9:41951117
|
C | T | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2080+2066G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951117 | ||||||
| chr9:41951174
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2080+2009G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951174 | ||||||
| chr9:41951179
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+2004G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951179 | ||||||
| chr9:41951185
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+1998A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951185 | ||||||
| chr9:41951241
|
A | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+1942T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951241 | ||||||
| chr9:41951242
|
T | A | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2080+1941A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951242 | ||||||
| chr9:41951250
|
A | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+1933T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951250 | ||||||
| chr9:41951276
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+1907A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951276 | ||||||
| chr9:41951366
|
A | AT | 27 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2080+1816dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951366 | ||||||
| chr9:41951381
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+1802C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951381 | ||||||
| chr9:41951542
|
A | T | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+1641T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951542 | ||||||
| chr9:41951719
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+1464C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951719 | ||||||
| chr9:41951798
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2080+1385G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951798 | ||||||
| chr9:41951799
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2080+1384C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951799 | ||||||
| chr9:41951895
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+1288C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951895 | ||||||
| chr9:41951937
|
C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2080+1246G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951937 | ||||||
| chr9:41951970
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2080+1213T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41951970 | ||||||
| chr9:41952002
|
G | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2080+1181C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952002 | ||||||
| chr9:41952006
|
G | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2080+1177C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952006 | ||||||
| chr9:41952012
|
C | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2080+1171G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952012 | ||||||
| chr9:41952034
|
G | T | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2080+1149C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952034 | ||||||
| chr9:41952068
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+1115A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952068 | ||||||
| chr9:41952125
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+1058G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952125 | ||||||
| chr9:41952235
|
AAATTT | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+943_2080+947d others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952235 | ||||||
| chr9:41952304
|
G | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2080+879C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952304 | ||||||
| chr9:41952384
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+799C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952384 | ||||||
| chr9:41952403
|
T | C | 2 | a0007c0009t0025g0037a0017c0014t0001g0038 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2080+780A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952403 | ||||||
| chr9:41952408
|
A | T | 1 | a0011c0037t0007g0008 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2080+775T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952408 | ||||||
| chr9:41952428
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+755A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952428 | ||||||
| chr9:41952447
|
A | G | 26 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.2080+736T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952447 | ||||||
| chr9:41952501
|
CG | C | 3 | a0001c0001t0002g0018a0001c0001t0017g0012a0001c0001t0031g0098 | 3 | HG00099.hp2 HG00642.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2080+681delC | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952501 | ||||||
| chr9:41952532
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+651G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952532 | ||||||
| chr9:41952572
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2080+611G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952572 | ||||||
| chr9:41952639
|
C | G | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2080+544G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952639 | ||||||
| chr9:41952806
|
T | C | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2080+377A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952806 | ||||||
| chr9:41952872
|
C | G | 1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2080+311G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952872 | ||||||
| chr9:41952955
|
T | A | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2080+228A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952955 | ||||||
| chr9:41952994
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+189G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41952994 | ||||||
| chr9:41953040
|
G | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2080+143C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41953040 | ||||||
| chr9:41953057
|
C | A | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2080+126G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41953057 | ||||||
| chr9:41953057
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2080+126G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41953057 | ||||||
| chr9:41953143
|
G | T | 2 | a0002c0002t0012g0043a0002c0002t0012g0051 | 2 | HG01071.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2080+40C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | 41953143 | ||||||
| chr9:41953398
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-12G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953398 | ||||||
| chr9:41953430
|
C | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-44G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953430 | ||||||
| chr9:41953430
|
C | T | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1877-44G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953430 | ||||||
| chr9:41953455
|
C | CCTGT | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-70_1877-69ins others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953455 | ||||||
| chr9:41953569
|
A | G | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1877-183T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953569 | ||||||
| chr9:41953602
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-216G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953602 | ||||||
| chr9:41953611
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1877-225C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953611 | ||||||
| chr9:41953619
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-233T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953619 | ||||||
| chr9:41953705
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1877-319T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953705 | ||||||
| chr9:41953801
|
CGAT | C | 2 | a0010c0013t0003g0103a0010c0013t0003g0108 | 2 | HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1877-418_1877-416d others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953801 | ||||||
| chr9:41953803
|
A | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1877-417T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953803 | ||||||
| chr9:41953827
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-441A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953827 | ||||||
| chr9:41953910
|
C | T | 1 | a0009c0008t0009g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1877-524G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41953910 | ||||||
| chr9:41954015
|
G | T | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1877-629C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954015 | ||||||
| chr9:41954016
|
A | T | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1877-630T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954016 | ||||||
| chr9:41954034
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-648C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954034 | ||||||
| chr9:41954039
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-653G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954039 | ||||||
| chr9:41954146
|
G | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-760C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954146 | ||||||
| chr9:41954148
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1877-762A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954148 | ||||||
| chr9:41954169
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-783C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954169 | ||||||
| chr9:41954326
|
A | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-940T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954326 | ||||||
| chr9:41954399
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1013G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954399 | ||||||
| chr9:41954500
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1114G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954500 | ||||||
| chr9:41954643
|
T | C | 1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1877-1257A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954643 | ||||||
| chr9:41954688
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1302G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954688 | ||||||
| chr9:41954716
|
C | A | 2 | a0001c0001t0003g0095a0001c0001t0003g0097 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1877-1330G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954716 | ||||||
| chr9:41954830
|
C | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1444G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954830 | ||||||
| chr9:41954858
|
A | AT | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1473dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954858 | ||||||
| chr9:41954865
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1479C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954865 | ||||||
| chr9:41954933
|
G | A | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1877-1547C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954933 | ||||||
| chr9:41954977
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1877-1591G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41954977 | ||||||
| chr9:41955101
|
G | A | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1877-1715C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955101 | ||||||
| chr9:41955113
|
C | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1727G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955113 | ||||||
| chr9:41955152
|
C | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1766G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955152 | ||||||
| chr9:41955163
|
G | T | 2 | a0007c0009t0023g0039a0007c0016t0001g0036 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1877-1777C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955163 | ||||||
| chr9:41955228
|
C | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1842G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955228 | ||||||
| chr9:41955257
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-1871G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955257 | ||||||
| chr9:41955273
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1877-1887C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955273 | ||||||
| chr9:41955656
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0017g0012 | 2 | HG00642.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1877-2270A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955656 | ||||||
| chr9:41955721
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2335A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955721 | ||||||
| chr9:41955741
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-2355T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955741 | ||||||
| chr9:41955757
|
G | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1877-2371C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955757 | ||||||
| chr9:41955822
|
C | CT | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2437dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955822 | ||||||
| chr9:41955883
|
T | C | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1877-2497A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955883 | ||||||
| chr9:41955947
|
A | C | 89 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1877-2561T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41955947 | ||||||
| chr9:41956027
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2641A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956027 | ||||||
| chr9:41956083
|
A | AT | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2698_1877-269 others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956083 | ||||||
| chr9:41956084
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1877-2698T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956084 | ||||||
| chr9:41956086
|
A | T | 51 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1877-2700T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956086 | ||||||
| chr9:41956097
|
T | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2711A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956097 | ||||||
| chr9:41956168
|
C | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1877-2782G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956168 | ||||||
| chr9:41956203
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2817T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956203 | ||||||
| chr9:41956302
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2916A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956302 | ||||||
| chr9:41956310
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-2924G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956310 | ||||||
| chr9:41956375
|
G | A | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1877-2989C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956375 | ||||||
| chr9:41956387
|
A | AAATAATA others(11): Show |
23 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.1877-3002_1877-300 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956387 | ||||||
| chr9:41956387
|
A | AAATAATA others(14): Show |
5 | a0001c0001t0002g0002a0001c0001t0002g0024a0006c0007t0011g0017others(2): Show | 5 | HG02040.hp2 HG02056.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1877-3002_1877-300 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956387 | ||||||
| chr9:41956387
|
A | AAATAATA others(17): Show |
3 | a0001c0001t0002g0022a0001c0012t0002g0007a0001c0042t0013g0001 | 3 | HG01175.hp1 HG02717.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1877-3002_1877-300 others(28): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956387 | ||||||
| chr9:41956387
|
A | AAATAATA others(20): Show |
3 | a0001c0046t0016g0015a0006c0007t0011g0021a0029c0045t0002g0019 | 3 | HG01255.hp1 HG02486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1877-3002_1877-300 others(31): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956387 | ||||||
| chr9:41956415
|
G | A | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1877-3029C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956415 | ||||||
| chr9:41956482
|
T | C | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1877-3096A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956482 | ||||||
| chr9:41956484
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877-3098G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956484 | ||||||
| chr9:41956492
|
G | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1877-3106C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956492 | ||||||
| chr9:41956702
|
G | GGTTTT | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1877-3321_1877-331 others(9): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956702 | ||||||
| chr9:41956797
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1877-3411T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956797 | ||||||
| chr9:41956815
|
G | T | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1877-3429C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956815 | ||||||
| chr9:41956876
|
T | C | 3 | a0003c0003t0008g0086a0004c0004t0005g0031a0004c0004t0005g0032 | 3 | HG00280.hp2 HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1877-3490A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956876 | ||||||
| chr9:41956877
|
A | C | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1877-3491T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956877 | ||||||
| chr9:41956941
|
G | GACC | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1877-3558_1877-355 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956941 | ||||||
| chr9:41956980
|
A | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1877-3594T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41956980 | ||||||
| chr9:41957270
|
T | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+3503A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957270 | ||||||
| chr9:41957354
|
C | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1876+3419G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957354 | ||||||
| chr9:41957355
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+3418C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957355 | ||||||
| chr9:41957359
|
G | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+3414C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957359 | ||||||
| chr9:41957359
|
G | T | 1 | a0002c0002t0022g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1876+3414C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957359 | ||||||
| chr9:41957438
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+3335A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957438 | ||||||
| chr9:41957771
|
G | T | 2 | a0004c0004t0005g0034a0005c0005t0006g0073 | 2 | HG02572.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1876+3002C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957771 | ||||||
| chr9:41957792
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1876+2981C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957792 | ||||||
| chr9:41957802
|
C | T | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1876+2971G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957802 | ||||||
| chr9:41957908
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+2865G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957908 | ||||||
| chr9:41957917
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+2856G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957917 | ||||||
| chr9:41957921
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1876+2852G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957921 | ||||||
| chr9:41957932
|
G | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1876+2841C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41957932 | ||||||
| chr9:41958005
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1876+2768C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958005 | ||||||
| chr9:41958068
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+2705A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958068 | ||||||
| chr9:41958201
|
A | C | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1876+2572T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958201 | ||||||
| chr9:41958207
|
A | C | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1876+2566T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958207 | ||||||
| chr9:41958399
|
G | T | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1876+2374C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958399 | ||||||
| chr9:41958496
|
G | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+2277C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958496 | ||||||
| chr9:41958826
|
C | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+1947G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958826 | ||||||
| chr9:41958889
|
A | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1876+1884T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958889 | ||||||
| chr9:41958960
|
T | C | 88 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1876+1813A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41958960 | ||||||
| chr9:41959030
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1876+1743C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959030 | ||||||
| chr9:41959251
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1876+1522G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959251 | ||||||
| chr9:41959348
|
T | C | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1876+1425A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959348 | ||||||
| chr9:41959423
|
A | G | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1876+1350T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959423 | ||||||
| chr9:41959424
|
C | T | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1876+1349G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959424 | ||||||
| chr9:41959474
|
C | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+1299G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959474 | ||||||
| chr9:41959983
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+790T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959983 | ||||||
| chr9:41959994
|
T | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+779A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959994 | ||||||
| chr9:41959996
|
C | CT | 9 | a0002c0002t0001g0045a0002c0002t0001g0049a0002c0023t0001g0054others(6): Show | 9 | HG01981.hp2 HG02135.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1876+776dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959996 | ||||||
| chr9:41959996
|
CT | C | 10 | a0002c0002t0001g0052a0002c0002t0001g0056a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+776delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959996 | ||||||
| chr9:41959996
|
CTTTT | C | 33 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1876+773_1876+776d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41959996 | ||||||
| chr9:41960012
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876+761A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41960012 | ||||||
| chr9:41960219
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1876+554G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41960219 | ||||||
| chr9:41960292
|
G | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1876+481C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | 41960292 | ||||||
| chr9:41960959
|
G | T | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1757-67C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41960959 | ||||||
| chr9:41961011
|
T | G | 1 | a0033c0036t0007g0010 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1757-119A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961011 | ||||||
| chr9:41961230
|
T | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1757-338A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961230 | ||||||
| chr9:41961623
|
G | A | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1757-731C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961623 | ||||||
| chr9:41961666
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1757-774G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961666 | ||||||
| chr9:41961734
|
C | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1757-842G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961734 | ||||||
| chr9:41961804
|
C | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1757-912G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961804 | ||||||
| chr9:41961817
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1757-925T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961817 | ||||||
| chr9:41961956
|
T | C | 1 | a0028c0027t0005g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1757-1064A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961956 | ||||||
| chr9:41961963
|
G | A | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1757-1071C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961963 | ||||||
| chr9:41961998
|
G | A | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1757-1106C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41961998 | ||||||
| chr9:41962521
|
A | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1757-1629T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962521 | ||||||
| chr9:41962550
|
T | C | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1757-1658A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962550 | ||||||
| chr9:41962709
|
G | A | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.1757-1817C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962709 | ||||||
| chr9:41962827
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1756+1711G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962827 | ||||||
| chr9:41962829
|
C | T | 2 | a0001c0001t0002g0022a0029c0045t0002g0019 | 2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1756+1709G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962829 | ||||||
| chr9:41962872
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+1666C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962872 | ||||||
| chr9:41962882
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1756+1656C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962882 | ||||||
| chr9:41962913
|
A | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1756+1625T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41962913 | ||||||
| chr9:41963012
|
G | A | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1756+1526C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963012 | ||||||
| chr9:41963016
|
C | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+1522G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963016 | ||||||
| chr9:41963567
|
T | C | 6 | a0004c0004t0005g0034a0011c0037t0007g0008a0011c0040t0007g0003others(3): Show | 6 | HG02083.hp1 NA18949.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1756+971A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963567 | ||||||
| chr9:41963616
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1756+922C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963616 | ||||||
| chr9:41963645
|
G | A | 1 | a0002c0002t0022g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1756+893C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963645 | ||||||
| chr9:41963931
|
A | G | 1 | a0015c0019t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1756+607T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963931 | ||||||
| chr9:41963937
|
T | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1756+601A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963937 | ||||||
| chr9:41963981
|
C | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1756+557G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963981 | ||||||
| chr9:41963996
|
G | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1756+542C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41963996 | ||||||
| chr9:41964275
|
C | T | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1756+263G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41964275 | ||||||
| chr9:41964315
|
C | T | 1 | a0008c0006t0010g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1756+223G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41964315 | ||||||
| chr9:41964346
|
C | T | 1 | a0003c0003t0004g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1756+192G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 11/23 | chr9 | 41964346 | ||||||
| chr9:41964784
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-140C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41964784 | ||||||
| chr9:41964925
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-281C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41964925 | ||||||
| chr9:41965051
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-407G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965051 | ||||||
| chr9:41965118
|
G | A | 33 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1650-474C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965118 | ||||||
| chr9:41965226
|
T | A | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1650-582A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965226 | ||||||
| chr9:41965279
|
C | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1650-635G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965279 | ||||||
| chr9:41965327
|
T | C | 1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1650-683A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965327 | ||||||
| chr9:41965368
|
G | A | 1 | a0003c0003t0008g0083 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1650-724C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965368 | ||||||
| chr9:41965491
|
C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.1650-847G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965491 | ||||||
| chr9:41965563
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1650-919C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965563 | ||||||
| chr9:41965733
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1650-1089C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965733 | ||||||
| chr9:41965735
|
T | C | 11 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1650-1091A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965735 | ||||||
| chr9:41965951
|
G | A | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1650-1307C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41965951 | ||||||
| chr9:41966083
|
T | A | 1 | a0002c0002t0012g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1650-1439A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966083 | ||||||
| chr9:41966095
|
G | C | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1650-1451C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966095 | ||||||
| chr9:41966098
|
C | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1650-1454G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966098 | ||||||
| chr9:41966104
|
C | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1650-1460G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966104 | ||||||
| chr9:41966166
|
T | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1650-1522A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966166 | ||||||
| chr9:41966182
|
C | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-1538G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966182 | ||||||
| chr9:41966428
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1650-1784C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966428 | ||||||
| chr9:41966474
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1650-1830C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966474 | ||||||
| chr9:41966544
|
A | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1650-1900T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966544 | ||||||
| chr9:41966749
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1650-2105G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966749 | ||||||
| chr9:41966836
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1650-2192C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966836 | ||||||
| chr9:41966882
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-2238C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966882 | ||||||
| chr9:41966898
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-2254G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966898 | ||||||
| chr9:41966946
|
G | A | 4 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(1): Show | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1650-2302C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966946 | ||||||
| chr9:41966994
|
C | G | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1650-2350G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41966994 | ||||||
| chr9:41967302
|
A | G | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1650-2658T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967302 | ||||||
| chr9:41967317
|
C | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1650-2673G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967317 | ||||||
| chr9:41967422
|
A | C | 1 | a0006c0007t0011g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1649+2652T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967422 | ||||||
| chr9:41967425
|
T | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1649+2649A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967425 | ||||||
| chr9:41967632
|
G | T | 1 | a0003c0011t0004g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1649+2442C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967632 | ||||||
| chr9:41967778
|
C | T | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1649+2296G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967778 | ||||||
| chr9:41967816
|
A | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649+2258T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967816 | ||||||
| chr9:41967827
|
T | C | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1649+2247A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41967827 | ||||||
| chr9:41968156
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1649+1918T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968156 | ||||||
| chr9:41968318
|
A | C | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1649+1756T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968318 | ||||||
| chr9:41968388
|
C | A | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1649+1686G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968388 | ||||||
| chr9:41968416
|
T | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1649+1658A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968416 | ||||||
| chr9:41968503
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649+1571C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968503 | ||||||
| chr9:41968647
|
G | A | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1649+1427C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968647 | ||||||
| chr9:41968801
|
C | CT | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1649+1272dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968801 | ||||||
| chr9:41968986
|
C | T | 105 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1649+1088G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41968986 | ||||||
| chr9:41969000
|
G | T | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1649+1074C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969000 | ||||||
| chr9:41969080
|
G | A | 2 | a0009c0008t0009g0105a0009c0008t0009g0106 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1649+994C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969080 | ||||||
| chr9:41969108
|
T | C | 1 | a0001c0012t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1649+966A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969108 | ||||||
| chr9:41969267
|
G | C | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1649+807C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969267 | ||||||
| chr9:41969310
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1649+764G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969310 | ||||||
| chr9:41969596
|
C | T | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1649+478G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969596 | ||||||
| chr9:41969710
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1649+364G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969710 | ||||||
| chr9:41969784
|
AT | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1649+289delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969784 | ||||||
| chr9:41969824
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1649+250G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969824 | ||||||
| chr9:41969924
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649+150G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41969924 | ||||||
| chr9:41970010
|
C | G | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1649+64G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41970010 | ||||||
| chr9:41970054
|
T | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1649+20A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 10/23 | chr9 | 41970054 | ||||||
| chr9:41970380
|
G | C | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1478-135C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41970380 | ||||||
| chr9:41970689
|
A | G | 90 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1478-444T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41970689 | ||||||
| chr9:41971135
|
G | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1478-890C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971135 | ||||||
| chr9:41971549
|
C | T | 1 | a0001c0012t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1478-1304G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971549 | ||||||
| chr9:41971598
|
C | T | 28 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1478-1353G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971598 | ||||||
| chr9:41971667
|
C | CA | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1478-1423dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971667 | ||||||
| chr9:41971690
|
G | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1478-1445C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971690 | ||||||
| chr9:41971719
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1478-1474C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971719 | ||||||
| chr9:41971738
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-1493T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971738 | ||||||
| chr9:41971792
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1478-1547G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971792 | ||||||
| chr9:41971817
|
C | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-1572G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971817 | ||||||
| chr9:41971854
|
C | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1478-1609G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41971854 | ||||||
| chr9:41972103
|
T | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1478-1858A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972103 | ||||||
| chr9:41972178
|
A | C | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1478-1933T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972178 | ||||||
| chr9:41972220
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1478-1975G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972220 | ||||||
| chr9:41972320
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-2075T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972320 | ||||||
| chr9:41972495
|
T | C | 1 | a0002c0002t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1478-2250A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972495 | ||||||
| chr9:41972520
|
C | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-2275G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972520 | ||||||
| chr9:41972709
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1478-2464C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972709 | ||||||
| chr9:41972815
|
T | A | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1478-2570A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972815 | ||||||
| chr9:41972936
|
C | CT | 17 | a0001c0046t0016g0015a0003c0003t0004g0081a0003c0003t0004g0082others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.1478-2692dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972936 | ||||||
| chr9:41972936
|
CT | C | 66 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1478-2692delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972936 | ||||||
| chr9:41972945
|
T | G | 3 | a0009c0008t0009g0105a0009c0008t0009g0106a0009c0008t0009g0107 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1478-2700A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972945 | ||||||
| chr9:41972969
|
A | G | 107 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1478-2724T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972969 | ||||||
| chr9:41972983
|
G | A | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1478-2738C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41972983 | ||||||
| chr9:41973033
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1478-2788C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973033 | ||||||
| chr9:41973085
|
G | A | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1478-2840C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973085 | ||||||
| chr9:41973102
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-2857A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973102 | ||||||
| chr9:41973104
|
A | AT | 4 | a0005c0005t0006g0073a0014c0018t0001g0067a0015c0019t0001g0066others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1478-2860dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973104 | ||||||
| chr9:41973122
|
T | G | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1478-2877A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973122 | ||||||
| chr9:41973135
|
G | A | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1478-2890C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973135 | ||||||
| chr9:41973287
|
G | GA | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1478-3043dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973287 | ||||||
| chr9:41973623
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-3378T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973623 | ||||||
| chr9:41973878
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-3633G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973878 | ||||||
| chr9:41973882
|
G | C | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1478-3637C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973882 | ||||||
| chr9:41973926
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478-3681G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41973926 | ||||||
| chr9:41974220
|
G | C | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1478-3975C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974220 | ||||||
| chr9:41974249
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1478-4004A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974249 | ||||||
| chr9:41974348
|
G | GA | 21 | a0001c0001t0002g0024a0003c0003t0004g0081a0003c0003t0004g0082others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1478-4104dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974348 | ||||||
| chr9:41974348
|
G | GAA | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.1478-4105_1478-410 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974348 | ||||||
| chr9:41974603
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-4358G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974603 | ||||||
| chr9:41974630
|
C | T | 4 | a0005c0005t0006g0076a0005c0005t0030g0092a0022c0030t0006g0085others(1): Show | 4 | HG01516.hp1 HG01934.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478-4385G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974630 | ||||||
| chr9:41974992
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1478-4747G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41974992 | ||||||
| chr9:41975076
|
T | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1478-4831A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975076 | ||||||
| chr9:41975088
|
T | G | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1478-4843A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975088 | ||||||
| chr9:41975114
|
T | C | 14 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0002t0001g0047others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1478-4869A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975114 | ||||||
| chr9:41975130
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-4885T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975130 | ||||||
| chr9:41975143
|
T | G | 14 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0002t0001g0047others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1478-4898A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975143 | ||||||
| chr9:41975144
|
C | G | 1 | a0004c0004t0005g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1478-4899G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975144 | ||||||
| chr9:41975149
|
C | T | 14 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0002t0001g0047others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1478-4904G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975149 | ||||||
| chr9:41975194
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-4949G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975194 | ||||||
| chr9:41975228
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1478-4983C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975228 | ||||||
| chr9:41975237
|
C | T | 6 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(3): Show | 6 | HG00323.hp1 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-4992G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975237 | ||||||
| chr9:41975299
|
T | C | 2 | a0003c0003t0021g0035a0007c0009t0023g0039 | 2 | HG02109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1478-5054A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975299 | ||||||
| chr9:41975745
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-5500A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975745 | ||||||
| chr9:41975775
|
G | C | 14 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0002t0001g0047others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1478-5530C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975775 | ||||||
| chr9:41975855
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-5610A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975855 | ||||||
| chr9:41975941
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1478-5696T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975941 | ||||||
| chr9:41975977
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-5732G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41975977 | ||||||
| chr9:41976192
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1478-5947C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976192 | ||||||
| chr9:41976213
|
G | C | 51 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1478-5968C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976213 | ||||||
| chr9:41976259
|
G | A | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1478-6014C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976259 | ||||||
| chr9:41976265
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1478-6020G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976265 | ||||||
| chr9:41976266
|
G | A | 1 | a0033c0036t0007g0010 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1478-6021C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976266 | ||||||
| chr9:41976409
|
C | A | 1 | a0002c0023t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1478-6164G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976409 | ||||||
| chr9:41976513
|
C | A | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1478-6268G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976513 | ||||||
| chr9:41976600
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1478-6355C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976600 | ||||||
| chr9:41976614
|
A | G | 1 | a0001c0001t0017g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1478-6369T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976614 | ||||||
| chr9:41976699
|
G | T | 51 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1478-6454C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976699 | ||||||
| chr9:41976843
|
T | C | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1478-6598A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976843 | ||||||
| chr9:41976952
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1478-6707G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41976952 | ||||||
| chr9:41977092
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-6847C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977092 | ||||||
| chr9:41977371
|
G | A | 1 | a0011c0037t0007g0008 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1478-7126C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977371 | ||||||
| chr9:41977620
|
C | CT | 4 | a0001c0001t0002g0002a0002c0002t0024g0061a0017c0014t0001g0038others(1): Show | 4 | HG02056.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478-7376dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977620 | ||||||
| chr9:41977641
|
G | A | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1478-7396C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977641 | ||||||
| chr9:41977667
|
G | C | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1478-7422C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977667 | ||||||
| chr9:41977678
|
C | T | 4 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(1): Show | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1478-7433G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977678 | ||||||
| chr9:41977765
|
G | A | 1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1478-7520C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977765 | ||||||
| chr9:41977786
|
A | AT | 22 | a0002c0002t0001g0052a0002c0002t0001g0062a0002c0002t0022g0068others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1478-7542dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977786 | ||||||
| chr9:41977786
|
A | ATT | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1478-7543_1478-754 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977786 | ||||||
| chr9:41977786
|
ATT | A | 11 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1478-7543_1478-754 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977786 | ||||||
| chr9:41977786
|
ATTT | A | 27 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0003g0093others(24): Show | 27 | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1478-7544_1478-754 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977786 | ||||||
| chr9:41977786
|
ATTTT | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(10): Show | 13 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1478-7545_1478-754 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977786 | ||||||
| chr9:41977796
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1478-7551A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977796 | ||||||
| chr9:41977833
|
G | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1478-7588C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41977833 | ||||||
| chr9:41978139
|
C | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1478-7894G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978139 | ||||||
| chr9:41978261
|
T | C | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1477+7907A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978261 | ||||||
| chr9:41978270
|
A | T | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1477+7898T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978270 | ||||||
| chr9:41978274
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1477+7894C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978274 | ||||||
| chr9:41978305
|
A | T | 4 | a0001c0001t0003g0099a0009c0008t0009g0105a0009c0008t0009g0106others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+7863T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978305 | ||||||
| chr9:41978427
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1477+7741C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978427 | ||||||
| chr9:41978507
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+7661C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978507 | ||||||
| chr9:41978512
|
G | A | 1 | a0003c0003t0004g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1477+7656C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978512 | ||||||
| chr9:41978583
|
T | A | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1477+7585A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978583 | ||||||
| chr9:41978656
|
G | GGATCCAG others(59): Show |
1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1477+7446_1477+751 others(70): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978656 | ||||||
| chr9:41978663
|
G | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1477+7505C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978663 | ||||||
| chr9:41978901
|
G | A | 1 | a0004c0004t0005g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1477+7267C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41978901 | ||||||
| chr9:41979067
|
C | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+7101G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979067 | ||||||
| chr9:41979079
|
G | T | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1477+7089C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979079 | ||||||
| chr9:41979135
|
C | T | 3 | a0001c0001t0003g0095a0001c0001t0003g0097a0001c0001t0003g0104 | 3 | HG01952.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1477+7033G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979135 | ||||||
| chr9:41979227
|
T | A | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1477+6941A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979227 | ||||||
| chr9:41979255
|
T | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1477+6913A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979255 | ||||||
| chr9:41979639
|
A | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1477+6529T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979639 | ||||||
| chr9:41979653
|
T | TTATATAT others(25): Show |
5 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+6514_1477+651 others(36): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979653 | ||||||
| chr9:41979653
|
T | TTATATAT others(27): Show |
1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1477+6514_1477+651 others(38): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979653 | ||||||
| chr9:41979653
|
T | TTATATAT others(25): Show |
1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1477+6514_1477+651 others(36): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979653 | ||||||
| chr9:41979665
|
A | AT | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1477+6502dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979665 | ||||||
| chr9:41979665
|
A | ATTTTTAA others(24): Show |
1 | a0004c0004t0005g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1477+6502_1477+650 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979665 | ||||||
| chr9:41979665
|
A | T | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1477+6503T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979665 | ||||||
| chr9:41979666
|
T | TTTTTAAA others(24): Show |
7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0032others(4): Show | 7 | HG01175.hp2 HG02083.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+6501_1477+650 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979666 | ||||||
| chr9:41979666
|
T | TTTTTAAA others(26): Show |
4 | a0002c0002t0001g0052a0002c0015t0001g0046a0002c0023t0001g0054others(1): Show | 4 | HG02135.hp2 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+6501_1477+650 others(37): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979666 | ||||||
| chr9:41979666
|
T | TTTTTAAA others(21): Show |
1 | a0030c0035t0007g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1477+6501_1477+650 others(32): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979666 | ||||||
| chr9:41979666
|
T | TTTTTTAA others(24): Show |
2 | a0001c0001t0002g0005a0001c0043t0015g0013 | 2 | HG00558.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1477+6501_1477+650 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979666 | ||||||
| chr9:41979667
|
A | T | 96 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.1477+6501T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979667 | ||||||
| chr9:41979668
|
T | TTTAAAAA others(24): Show |
1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1477+6499_1477+650 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979668 | ||||||
| chr9:41979668
|
T | TTTAAAAA others(26): Show |
22 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(19): Show | 22 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1477+6499_1477+650 others(37): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979668 | ||||||
| chr9:41979668
|
T | TTTTAAAA others(24): Show |
28 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1477+6499_1477+650 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979668 | ||||||
| chr9:41979668
|
T | TTTTAAAA others(26): Show |
1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1477+6499_1477+650 others(37): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979668 | ||||||
| chr9:41979670
|
T | TAAAAAAT others(26): Show |
2 | a0002c0002t0001g0049a0027c0026t0020g0027 | 2 | HG02109.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1477+6497_1477+649 others(37): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979670 | ||||||
| chr9:41979670
|
T | TTAAAAAT others(24): Show |
7 | a0001c0001t0002g0022a0001c0042t0013g0001a0006c0007t0002g0014others(4): Show | 7 | HG01175.hp1 HG02040.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1477+6497_1477+649 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979670 | ||||||
| chr9:41979670
|
T | TTAAAAAT others(26): Show |
2 | a0001c0046t0016g0015a0006c0007t0011g0017 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1477+6497_1477+649 others(37): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979670 | ||||||
| chr9:41979722
|
G | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1477+6446C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979722 | ||||||
| chr9:41979722
|
G | T | 1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1477+6446C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979722 | ||||||
| chr9:41979741
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6427C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979741 | ||||||
| chr9:41979749
|
T | A | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1477+6419A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979749 | ||||||
| chr9:41979762
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+6406C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979762 | ||||||
| chr9:41979795
|
A | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1477+6373T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979795 | ||||||
| chr9:41979835
|
G | A | 3 | a0002c0002t0001g0044a0002c0002t0001g0052a0002c0002t0001g0053 | 3 | NA18974.hp2 NA18998.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1477+6333C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979835 | ||||||
| chr9:41979885
|
G | GAT | 9 | a0005c0005t0006g0073a0005c0005t0006g0076a0005c0005t0030g0092others(6): Show | 9 | HG01516.hp1 HG01934.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+6281_1477+628 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979885 | ||||||
| chr9:41979885
|
G | GATAT | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1477+6279_1477+628 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979885 | ||||||
| chr9:41979885
|
G | GATATATA others(3): Show |
2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1477+6273_1477+628 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979885 | ||||||
| chr9:41979944
|
CT | C | 18 | a0002c0002t0001g0053a0003c0003t0004g0081a0003c0003t0004g0082others(15): Show | 18 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1477+6223delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979944 | ||||||
| chr9:41979944
|
CTT | C | 36 | a0001c0001t0002g0002a0001c0001t0003g0100a0001c0001t0018g0026others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1477+6222_1477+622 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979944 | ||||||
| chr9:41979944
|
CTTT | C | 32 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1477+6221_1477+622 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979944 | ||||||
| chr9:41979944
|
CTTTT | C | 11 | a0001c0001t0002g0024a0001c0042t0013g0001a0004c0004t0005g0029others(8): Show | 11 | HG00280.hp2 HG01516.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1477+6220_1477+622 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979944 | ||||||
| chr9:41979969
|
T | G | 1 | a0030c0035t0007g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1477+6199A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979969 | ||||||
| chr9:41979983
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6185C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41979983 | ||||||
| chr9:41980855
|
A | C | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1477+5313T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41980855 | ||||||
| chr9:41980877
|
C | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1477+5291G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41980877 | ||||||
| chr9:41981341
|
A | T | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1477+4827T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981341 | ||||||
| chr9:41981487
|
C | A | 2 | a0002c0002t0012g0043a0002c0002t0012g0051 | 2 | HG01071.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1477+4681G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981487 | ||||||
| chr9:41981594
|
A | G | 5 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0097others(2): Show | 5 | HG01952.hp2 HG01981.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+4574T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981594 | ||||||
| chr9:41981683
|
T | C | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+4485A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981683 | ||||||
| chr9:41981790
|
C | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1477+4378G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981790 | ||||||
| chr9:41981862
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+4306C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981862 | ||||||
| chr9:41981867
|
A | AC | 51 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1477+4300_1477+430 others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981867 | ||||||
| chr9:41981872
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+4296G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981872 | ||||||
| chr9:41981892
|
C | CAATAAT | 5 | a0005c0005t0006g0091a0008c0006t0010g0070a0008c0006t0010g0071others(2): Show | 5 | HG02083.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+4270_1477+427 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
C | CAATAATA others(2): Show |
13 | a0004c0004t0005g0032a0005c0005t0006g0073a0005c0005t0006g0076others(10): Show | 13 | HG01175.hp2 HG01516.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1477+4267_1477+427 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
C | CAATAATA others(5): Show |
5 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(2): Show | 5 | HG00280.hp2 HG02922.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+4264_1477+427 others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
C | CAATAATA others(8): Show |
11 | a0001c0001t0003g0097a0001c0001t0018g0026a0002c0002t0001g0050others(8): Show | 11 | HG01255.hp1 HG01255.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1477+4261_1477+427 others(19): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
C | CAATAATA others(11): Show |
33 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1477+4258_1477+427 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
C | CAATAATA others(14): Show |
19 | a0001c0001t0002g0004a0001c0001t0002g0018a0002c0002t0001g0044others(16): Show | 19 | HG00323.hp1 HG01071.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1477+4255_1477+427 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
C | CAATAATA others(20): Show |
1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1477+4275_1477+427 others(31): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981892
|
CAAT | C | 3 | a0001c0046t0016g0015a0026c0025t0019g0028a0027c0026t0020g0027 | 3 | HG02109.hp2 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1477+4273_1477+427 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981892 | ||||||
| chr9:41981916
|
T | TAATAATA others(11): Show |
1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1477+4251_1477+425 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981916 | ||||||
| chr9:41981916
|
T | TAATAATA others(14): Show |
1 | a0009c0008t0009g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1477+4251_1477+425 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41981916 | ||||||
| chr9:41982063
|
C | CA | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0018others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1477+4104dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982063 | ||||||
| chr9:41982063
|
C | CAA | 7 | a0001c0001t0002g0005a0001c0001t0003g0101a0004c0004t0005g0032others(4): Show | 7 | HG01175.hp2 HG02040.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1477+4103_1477+410 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982063 | ||||||
| chr9:41982063
|
CA | C | 5 | a0002c0002t0001g0050a0002c0002t0001g0053a0002c0002t0024g0061others(2): Show | 5 | HG01255.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477+4104delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982063 | ||||||
| chr9:41982184
|
C | T | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1477+3984G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982184 | ||||||
| chr9:41982258
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1477+3910C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982258 | ||||||
| chr9:41982350
|
G | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1477+3818C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982350 | ||||||
| chr9:41982365
|
GA | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+3802delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982365 | ||||||
| chr9:41982373
|
A | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1477+3795T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982373 | ||||||
| chr9:41982375
|
C | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+3793G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982375 | ||||||
| chr9:41982382
|
C | T | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1477+3786G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982382 | ||||||
| chr9:41982738
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+3430T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982738 | ||||||
| chr9:41982955
|
C | T | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1477+3213G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41982955 | ||||||
| chr9:41983070
|
G | A | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1477+3098C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983070 | ||||||
| chr9:41983201
|
A | T | 5 | a0005c0005t0006g0076a0005c0005t0006g0091a0005c0005t0030g0092others(2): Show | 5 | HG01516.hp1 HG01934.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+2967T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983201 | ||||||
| chr9:41983249
|
T | C | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1477+2919A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983249 | ||||||
| chr9:41983294
|
A | G | 32 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1477+2874T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983294 | ||||||
| chr9:41983330
|
A | C | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1477+2838T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983330 | ||||||
| chr9:41983457
|
A | AC | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1477+2710_1477+271 others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983457 | ||||||
| chr9:41983666
|
C | T | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1477+2502G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983666 | ||||||
| chr9:41983821
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+2347C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983821 | ||||||
| chr9:41983824
|
C | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1477+2344G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983824 | ||||||
| chr9:41983825
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+2343C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983825 | ||||||
| chr9:41983845
|
C | G | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1477+2323G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983845 | ||||||
| chr9:41983850
|
C | A | 1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1477+2318G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983850 | ||||||
| chr9:41983860
|
T | A | 2 | a0001c0001t0003g0096a0006c0041t0002g0020 | 2 | HG00280.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1477+2308A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983860 | ||||||
| chr9:41983878
|
G | A | 10 | a0003c0003t0004g0081a0003c0003t0004g0082a0003c0003t0008g0077others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.1477+2290C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983878 | ||||||
| chr9:41983886
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1477+2282G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983886 | ||||||
| chr9:41983967
|
G | A | 1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1477+2201C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983967 | ||||||
| chr9:41983967
|
G | T | 1 | a0030c0035t0007g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1477+2201C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983967 | ||||||
| chr9:41983968
|
T | G | 1 | a0030c0035t0007g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1477+2200A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983968 | ||||||
| chr9:41983980
|
T | G | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.1477+2188A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41983980 | ||||||
| chr9:41984005
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+2163G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41984005 | ||||||
| chr9:41984096
|
G | T | 3 | a0002c0002t0022g0068a0009c0008t0009g0105a0009c0008t0009g0106 | 3 | HG00735.hp1 HG02572.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1477+2072C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41984096 | ||||||
| chr9:41984332
|
T | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+1836A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41984332 | ||||||
| chr9:41984874
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+1294C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41984874 | ||||||
| chr9:41984962
|
C | G | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1477+1206G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41984962 | ||||||
| chr9:41985155
|
G | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+1013C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985155 | ||||||
| chr9:41985204
|
A | G | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1477+964T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985204 | ||||||
| chr9:41985218
|
A | G | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1477+950T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985218 | ||||||
| chr9:41985362
|
G | C | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1477+806C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985362 | ||||||
| chr9:41985465
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1477+703G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985465 | ||||||
| chr9:41985599
|
G | T | 1 | a0015c0019t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1477+569C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985599 | ||||||
| chr9:41985629
|
TATG | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1477+536_1477+538d others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985629 | ||||||
| chr9:41985990
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+178C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | 41985990 | ||||||
| chr9:41986602
|
A | T | 1 | a0008c0006t0010g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1334-291T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41986602 | ||||||
| chr9:41986925
|
T | C | 34 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(31): Show | 34 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1334-614A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41986925 | ||||||
| chr9:41987136
|
A | G | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1334-825T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987136 | ||||||
| chr9:41987292
|
T | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1334-981A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987292 | ||||||
| chr9:41987316
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1334-1005G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987316 | ||||||
| chr9:41987368
|
C | T | 84 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1334-1057G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987368 | ||||||
| chr9:41987406
|
T | G | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1334-1095A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987406 | ||||||
| chr9:41987557
|
T | C | 4 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(1): Show | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-1246A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987557 | ||||||
| chr9:41987710
|
T | C | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1334-1399A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41987710 | ||||||
| chr9:41988189
|
T | G | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1334-1878A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988189 | ||||||
| chr9:41988238
|
A | AT | 7 | a0003c0003t0021g0035a0007c0016t0001g0036a0011c0040t0007g0003others(4): Show | 7 | HG02083.hp1 HG02922.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334-1928dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988238 | ||||||
| chr9:41988238
|
A | ATT | 26 | a0002c0002t0001g0041a0002c0002t0001g0044a0002c0002t0001g0050others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1334-1929_1334-192 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988238 | ||||||
| chr9:41988238
|
A | ATTT | 11 | a0002c0002t0001g0045a0002c0002t0001g0047a0002c0002t0001g0048others(8): Show | 11 | HG01175.hp2 HG01934.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1334-1930_1334-192 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988238 | ||||||
| chr9:41988238
|
AT | A | 5 | a0003c0003t0029g0072a0005c0005t0006g0076a0005c0005t0006g0091others(2): Show | 5 | HG01516.hp1 HG01934.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-1928delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988238 | ||||||
| chr9:41988238
|
ATTTT | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0022a0001c0001t0003g0100others(4): Show | 7 | HG01106.hp1 HG01175.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1334-1931_1334-192 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988238 | ||||||
| chr9:41988238
|
ATTTTT | A | 27 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1334-1932_1334-192 others(9): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988238 | ||||||
| chr9:41988269
|
G | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1334-1958C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988269 | ||||||
| chr9:41988289
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1334-1978G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988289 | ||||||
| chr9:41988335
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1334-2024C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988335 | ||||||
| chr9:41988397
|
C | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1334-2086G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988397 | ||||||
| chr9:41988530
|
G | A | 2 | a0001c0042t0013g0001a0024c0029t0006g0087 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-2219C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988530 | ||||||
| chr9:41988799
|
A | C | 2 | a0009c0008t0009g0105a0009c0008t0009g0106 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1334-2488T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988799 | ||||||
| chr9:41988903
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1334-2592G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988903 | ||||||
| chr9:41988919
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1334-2608C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41988919 | ||||||
| chr9:41989214
|
A | C | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1333+2396T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989214 | ||||||
| chr9:41989408
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1333+2202A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989408 | ||||||
| chr9:41989521
|
C | T | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1333+2089G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989521 | ||||||
| chr9:41989531
|
A | G | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1333+2079T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989531 | ||||||
| chr9:41989583
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1333+2027G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989583 | ||||||
| chr9:41989654
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1333+1956T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989654 | ||||||
| chr9:41989700
|
TCAAA | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333+1906_1333+190 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989700 | ||||||
| chr9:41989960
|
G | A | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333+1650C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41989960 | ||||||
| chr9:41990010
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1333+1600A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990010 | ||||||
| chr9:41990100
|
A | G | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1333+1510T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990100 | ||||||
| chr9:41990145
|
T | C | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1333+1465A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990145 | ||||||
| chr9:41990212
|
C | T | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1333+1398G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990212 | ||||||
| chr9:41990297
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+1313C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990297 | ||||||
| chr9:41990313
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+1297C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990313 | ||||||
| chr9:41990560
|
A | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1333+1050T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990560 | ||||||
| chr9:41990582
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1333+1028C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990582 | ||||||
| chr9:41990666
|
C | CT | 32 | a0001c0001t0017g0012a0002c0002t0001g0040a0002c0002t0001g0041others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1333+943dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990666 | ||||||
| chr9:41990701
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+909G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990701 | ||||||
| chr9:41990927
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1333+683C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41990927 | ||||||
| chr9:41991032
|
G | A | 4 | a0001c0001t0003g0100a0001c0001t0003g0102a0010c0013t0003g0103others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333+578C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991032 | ||||||
| chr9:41991114
|
C | T | 11 | a0001c0001t0003g0102a0004c0004t0005g0029a0004c0004t0005g0030others(8): Show | 11 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1333+496G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991114 | ||||||
| chr9:41991134
|
G | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1333+476C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991134 | ||||||
| chr9:41991194
|
A | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1333+416T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991194 | ||||||
| chr9:41991203
|
T | G | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1333+407A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991203 | ||||||
| chr9:41991235
|
A | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1333+375T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991235 | ||||||
| chr9:41991240
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1333+370C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991240 | ||||||
| chr9:41991285
|
G | A | 1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1333+325C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991285 | ||||||
| chr9:41991572
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+38C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 8/23 | chr9 | 41991572 | ||||||
| chr9:41992074
|
T | A | 2 | a0006c0007t0011g0017a0006c0007t0011g0021 | 2 | HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1072-203A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992074 | ||||||
| chr9:41992282
|
A | C | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1072-411T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992282 | ||||||
| chr9:41992364
|
T | G | 1 | a0003c0003t0008g0083 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1072-493A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992364 | ||||||
| chr9:41992393
|
T | C | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1072-522A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992393 | ||||||
| chr9:41992505
|
T | C | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1072-634A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992505 | ||||||
| chr9:41992696
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1072-825C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992696 | ||||||
| chr9:41992828
|
T | C | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1072-957A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992828 | ||||||
| chr9:41992894
|
T | G | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1072-1023A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41992894 | ||||||
| chr9:41993067
|
A | T | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1072-1196T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993067 | ||||||
| chr9:41993156
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1072-1285C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993156 | ||||||
| chr9:41993190
|
C | A | 1 | a0004c0004t0005g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1072-1319G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993190 | ||||||
| chr9:41993247
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1072-1376G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993247 | ||||||
| chr9:41993454
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1072-1583G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993454 | ||||||
| chr9:41993463
|
C | A | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1072-1592G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993463 | ||||||
| chr9:41993727
|
G | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1072-1856C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41993727 | ||||||
| chr9:41994137
|
C | T | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1071+2068G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994137 | ||||||
| chr9:41994204
|
T | C | 2 | a0001c0001t0018g0026a0001c0012t0002g0009 | 2 | HG01943.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1071+2001A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994204 | ||||||
| chr9:41994379
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1071+1826C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994379 | ||||||
| chr9:41994453
|
C | T | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1071+1752G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994453 | ||||||
| chr9:41994578
|
G | T | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1071+1627C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994578 | ||||||
| chr9:41994580
|
G | T | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1071+1625C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994580 | ||||||
| chr9:41994616
|
CT | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1071+1588delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994616 | ||||||
| chr9:41994660
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1071+1545G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994660 | ||||||
| chr9:41994666
|
A | G | 10 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1071+1539T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994666 | ||||||
| chr9:41994734
|
T | C | 3 | a0002c0010t0001g0057a0002c0010t0001g0058a0002c0023t0001g0054 | 3 | HG01952.hp1 HG02135.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1071+1471A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994734 | ||||||
| chr9:41994811
|
T | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1071+1394A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994811 | ||||||
| chr9:41994905
|
A | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1071+1300T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994905 | ||||||
| chr9:41994916
|
T | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1071+1289A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41994916 | ||||||
| chr9:41995078
|
T | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1071+1127A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995078 | ||||||
| chr9:41995343
|
G | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071+862C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995343 | ||||||
| chr9:41995487
|
T | G | 2 | a0003c0003t0021g0035a0016c0017t0001g0042 | 2 | HG01081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1071+718A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995487 | ||||||
| chr9:41995532
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071+673C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995532 | ||||||
| chr9:41995542
|
T | C | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1071+663A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995542 | ||||||
| chr9:41995571
|
T | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071+634A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995571 | ||||||
| chr9:41995579
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071+626G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995579 | ||||||
| chr9:41995588
|
G | A | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1071+617C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995588 | ||||||
| chr9:41995595
|
C | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071+610G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995595 | ||||||
| chr9:41995603
|
C | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071+602G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995603 | ||||||
| chr9:41995679
|
C | G | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1071+526G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995679 | ||||||
| chr9:41995730
|
C | CA | 9 | a0002c0002t0001g0059a0002c0002t0024g0061a0002c0015t0001g0046others(6): Show | 9 | HG02083.hp2 HG02145.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1071+474dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995730 | ||||||
| chr9:41995730
|
C | CAA | 12 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(9): Show | 12 | HG00280.hp2 HG01175.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1071+473_1071+474d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995730 | ||||||
| chr9:41995730
|
CA | C | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1071+474delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995730 | ||||||
| chr9:41995818
|
C | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1071+387G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995818 | ||||||
| chr9:41995910
|
C | T | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1071+295G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995910 | ||||||
| chr9:41995943
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071+262C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41995943 | ||||||
| chr9:41996034
|
C | G | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1071+171G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41996034 | ||||||
| chr9:41996040
|
A | T | 2 | a0007c0009t0023g0039a0027c0026t0020g0027 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1071+165T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41996040 | ||||||
| chr9:41996084
|
A | G | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1071+121T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41996084 | ||||||
| chr9:41996172
|
C | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1071+33G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41996172 | ||||||
| chr9:41996187
|
C | CCGATTAG others(9): Show |
1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071+17_1071+18ins others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41996187 | ||||||
| chr9:41996192
|
T | C | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+13A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | 41996192 | ||||||
| chr9:41996545
|
C | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.928-197G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996545 | ||||||
| chr9:41996557
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.928-209G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996557 | ||||||
| chr9:41996618
|
GTTAAATT others(7): Show |
G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.928-284_928-271del others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996618 | ||||||
| chr9:41996690
|
C | T | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-342G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996690 | ||||||
| chr9:41996755
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.928-407C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996755 | ||||||
| chr9:41996799
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.928-451C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996799 | ||||||
| chr9:41996879
|
A | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.928-531T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996879 | ||||||
| chr9:41996915
|
C | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.928-567G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996915 | ||||||
| chr9:41996930
|
C | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.928-582G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996930 | ||||||
| chr9:41996980
|
A | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+588T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996980 | ||||||
| chr9:41996981
|
A | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+587T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996981 | ||||||
| chr9:41996982
|
G | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+586C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996982 | ||||||
| chr9:41996983
|
G | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+585C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996983 | ||||||
| chr9:41996984
|
T | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+584A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41996984 | ||||||
| chr9:41997316
|
C | T | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.927+252G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41997316 | ||||||
| chr9:41997557
|
T | C | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+11A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | 41997557 | ||||||
| chr9:41997876
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.743-124A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 5/23 | chr9 | 41997876 | ||||||
| chr9:41998027
|
C | A | 3 | a0006c0007t0011g0017a0006c0007t0011g0021a0006c0041t0002g0020 | 3 | HG02040.hp2 HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.743-275G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 5/23 | chr9 | 41998027 | ||||||
| chr9:41998067
|
T | A | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-315A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 5/23 | chr9 | 41998067 | ||||||
| chr9:41998162
|
T | C | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.742+239A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 5/23 | chr9 | 41998162 | ||||||
| chr9:41998205
|
A | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.742+196T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 5/23 | chr9 | 41998205 | ||||||
| chr9:41998877
|
T | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-273A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41998877 | ||||||
| chr9:41998972
|
CTT | C | 2 | a0003c0003t0004g0081a0029c0045t0002g0019 | 2 | HG01255.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.539-370_539-369del others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41998972 | ||||||
| chr9:41999355
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.539-751G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999355 | ||||||
| chr9:41999399
|
G | A | 9 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(6): Show | 9 | HG00140.hp2 HG00323.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.539-795C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999399 | ||||||
| chr9:41999418
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-814C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999418 | ||||||
| chr9:41999421
|
A | T | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-817T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999421 | ||||||
| chr9:41999430
|
C | T | 8 | a0001c0001t0002g0022a0001c0046t0016g0015a0006c0007t0002g0014others(5): Show | 8 | HG01175.hp1 HG01255.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.539-826G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999430 | ||||||
| chr9:41999548
|
T | TAC | 6 | a0001c0001t0017g0012a0003c0003t0008g0077a0003c0003t0008g0083others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-946_539-945dup others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999548 | ||||||
| chr9:41999600
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-996A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999600 | ||||||
| chr9:41999697
|
G | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.539-1093C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999697 | ||||||
| chr9:41999998
|
C | G | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.539-1394G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 41999998 | ||||||
| chr9:42000581
|
T | C | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.539-1977A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000581 | ||||||
| chr9:42000724
|
T | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.539-2120A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000724 | ||||||
| chr9:42000825
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.539-2221T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000825 | ||||||
| chr9:42000832
|
A | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-2228T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000832 | ||||||
| chr9:42000878
|
T | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-2274A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000878 | ||||||
| chr9:42000938
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-2334C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000938 | ||||||
| chr9:42000968
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-2364C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42000968 | ||||||
| chr9:42001266
|
A | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.539-2662T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42001266 | ||||||
| chr9:42001442
|
A | G | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.539-2838T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42001442 | ||||||
| chr9:42001662
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.539-3058T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42001662 | ||||||
| chr9:42001828
|
A | C | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.539-3224T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42001828 | ||||||
| chr9:42001881
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-3277C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42001881 | ||||||
| chr9:42001982
|
C | A | 1 | a0009c0008t0009g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.539-3378G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42001982 | ||||||
| chr9:42002274
|
C | T | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.539-3670G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002274 | ||||||
| chr9:42002344
|
A | G | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.539-3740T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002344 | ||||||
| chr9:42002413
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.539-3809G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002413 | ||||||
| chr9:42002458
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.539-3854T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002458 | ||||||
| chr9:42002493
|
C | T | 2 | a0001c0001t0002g0022a0029c0045t0002g0019 | 2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.539-3889G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002493 | ||||||
| chr9:42002560
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.539-3956A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002560 | ||||||
| chr9:42002816
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.539-4212A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002816 | ||||||
| chr9:42002871
|
C | T | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.539-4267G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002871 | ||||||
| chr9:42002874
|
C | T | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.539-4270G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002874 | ||||||
| chr9:42002879
|
T | A | 1 | a0028c0027t0005g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.539-4275A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002879 | ||||||
| chr9:42002949
|
C | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-4345G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002949 | ||||||
| chr9:42002955
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-4351A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42002955 | ||||||
| chr9:42003050
|
T | C | 1 | a0003c0011t0004g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.539-4446A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003050 | ||||||
| chr9:42003053
|
A | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-4449T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003053 | ||||||
| chr9:42003168
|
C | T | 4 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071others(1): Show | 4 | HG02486.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-4564G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003168 | ||||||
| chr9:42003373
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.539-4769C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003373 | ||||||
| chr9:42003399
|
G | GA | 27 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(24): Show | 27 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.539-4796dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003399 | ||||||
| chr9:42003399
|
GA | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-4796delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003399 | ||||||
| chr9:42003516
|
C | G | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.539-4912G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003516 | ||||||
| chr9:42003572
|
A | C | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.539-4968T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003572 | ||||||
| chr9:42003581
|
C | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-4977G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003581 | ||||||
| chr9:42003634
|
C | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.539-5030G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003634 | ||||||
| chr9:42003695
|
T | C | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.539-5091A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003695 | ||||||
| chr9:42003801
|
A | C | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.539-5197T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003801 | ||||||
| chr9:42003808
|
T | A | 1 | a0008c0006t0010g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.539-5204A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003808 | ||||||
| chr9:42003834
|
G | T | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.539-5230C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003834 | ||||||
| chr9:42003913
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-5309G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003913 | ||||||
| chr9:42003952
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.539-5348G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42003952 | ||||||
| chr9:42004111
|
G | A | 4 | a0003c0003t0008g0077a0003c0003t0008g0083a0003c0003t0008g0086others(1): Show | 4 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-5507C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004111 | ||||||
| chr9:42004212
|
A | T | 1 | a0001c0012t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539-5608T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004212 | ||||||
| chr9:42004278
|
T | A | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.539-5674A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004278 | ||||||
| chr9:42004460
|
A | T | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.539-5856T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004460 | ||||||
| chr9:42004494
|
A | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-5890T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004494 | ||||||
| chr9:42004742
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.539-6138G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004742 | ||||||
| chr9:42004799
|
A | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.539-6195T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004799 | ||||||
| chr9:42004980
|
T | C | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.539-6376A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42004980 | ||||||
| chr9:42005167
|
C | T | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.539-6563G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005167 | ||||||
| chr9:42005293
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.539-6689G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005293 | ||||||
| chr9:42005309
|
G | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-6705C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005309 | ||||||
| chr9:42005341
|
T | C | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.539-6737A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005341 | ||||||
| chr9:42005377
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.539-6773C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005377 | ||||||
| chr9:42005776
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-7172A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005776 | ||||||
| chr9:42005839
|
T | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.539-7235A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005839 | ||||||
| chr9:42005861
|
C | T | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.539-7257G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42005861 | ||||||
| chr9:42006049
|
C | T | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.538+7329G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006049 | ||||||
| chr9:42006079
|
T | C | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.538+7299A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006079 | ||||||
| chr9:42006139
|
T | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538+7239A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006139 | ||||||
| chr9:42006146
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.538+7232G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006146 | ||||||
| chr9:42006325
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.538+7053C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006325 | ||||||
| chr9:42006364
|
A | T | 3 | a0007c0009t0023g0039a0007c0009t0025g0037a0017c0014t0001g0038 | 3 | HG02109.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.538+7014T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006364 | ||||||
| chr9:42006456
|
C | T | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+6922G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006456 | ||||||
| chr9:42006800
|
A | G | 14 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0096others(11): Show | 14 | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.538+6578T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006800 | ||||||
| chr9:42006907
|
A | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538+6471T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006907 | ||||||
| chr9:42006961
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+6417C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42006961 | ||||||
| chr9:42007251
|
G | A | 4 | a0001c0001t0018g0026a0001c0012t0002g0009a0030c0035t0007g0023others(1): Show | 4 | HG01943.hp2 HG02083.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+6127C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007251 | ||||||
| chr9:42007285
|
A | T | 4 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(1): Show | 4 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+6093T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007285 | ||||||
| chr9:42007337
|
G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.538+6041C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007337 | ||||||
| chr9:42007694
|
C | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.538+5684G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007694 | ||||||
| chr9:42007695
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538+5683C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007695 | ||||||
| chr9:42007745
|
G | A | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.538+5633C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007745 | ||||||
| chr9:42007893
|
G | T | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.538+5485C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007893 | ||||||
| chr9:42007973
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.538+5405T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42007973 | ||||||
| chr9:42008030
|
C | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.538+5348G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008030 | ||||||
| chr9:42008085
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.538+5293C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008085 | ||||||
| chr9:42008396
|
T | G | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.538+4982A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008396 | ||||||
| chr9:42008449
|
A | G | 1 | a0003c0003t0008g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.538+4929T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008449 | ||||||
| chr9:42008500
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+4878C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008500 | ||||||
| chr9:42008504
|
G | T | 1 | a0001c0001t0003g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.538+4874C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008504 | ||||||
| chr9:42008620
|
G | T | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538+4758C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008620 | ||||||
| chr9:42008629
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.538+4749C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008629 | ||||||
| chr9:42008806
|
C | T | 4 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071others(1): Show | 4 | HG02486.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+4572G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008806 | ||||||
| chr9:42008811
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538+4567G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42008811 | ||||||
| chr9:42009109
|
A | G | 1 | a0002c0020t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.538+4269T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42009109 | ||||||
| chr9:42009283
|
C | T | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538+4095G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42009283 | ||||||
| chr9:42009379
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+3999C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42009379 | ||||||
| chr9:42009506
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.538+3872G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42009506 | ||||||
| chr9:42009745
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.538+3633G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42009745 | ||||||
| chr9:42009998
|
C | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.538+3380G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42009998 | ||||||
| chr9:42010084
|
C | T | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+3294G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010084 | ||||||
| chr9:42010105
|
G | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.538+3273C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010105 | ||||||
| chr9:42010201
|
G | A | 1 | a0002c0002t0022g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.538+3177C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010201 | ||||||
| chr9:42010391
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.538+2987C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010391 | ||||||
| chr9:42010413
|
G | A | 2 | a0002c0002t0001g0050a0004c0004t0005g0032 | 2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.538+2965C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010413 | ||||||
| chr9:42010545
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.538+2833C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010545 | ||||||
| chr9:42010609
|
G | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.538+2769C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010609 | ||||||
| chr9:42010624
|
C | T | 1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.538+2754G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42010624 | ||||||
| chr9:42011316
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.538+2062C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011316 | ||||||
| chr9:42011442
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.538+1936C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011442 | ||||||
| chr9:42011546
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.538+1832T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011546 | ||||||
| chr9:42011593
|
T | C | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.538+1785A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011593 | ||||||
| chr9:42011616
|
T | TA | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+1761dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011616 | ||||||
| chr9:42011646
|
C | T | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.538+1732G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011646 | ||||||
| chr9:42011674
|
A | C | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.538+1704T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011674 | ||||||
| chr9:42011688
|
G | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.538+1690C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011688 | ||||||
| chr9:42011693
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.538+1685A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011693 | ||||||
| chr9:42011780
|
G | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.538+1598C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011780 | ||||||
| chr9:42011835
|
C | T | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.538+1543G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011835 | ||||||
| chr9:42011875
|
A | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538+1503T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42011875 | ||||||
| chr9:42012043
|
A | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.538+1335T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012043 | ||||||
| chr9:42012157
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.538+1221C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012157 | ||||||
| chr9:42012210
|
C | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.538+1168G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012210 | ||||||
| chr9:42012224
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538+1154T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012224 | ||||||
| chr9:42012251
|
T | G | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.538+1127A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012251 | ||||||
| chr9:42012535
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538+843T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012535 | ||||||
| chr9:42012626
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538+752T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012626 | ||||||
| chr9:42012639
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.538+739A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012639 | ||||||
| chr9:42012757
|
C | T | 1 | a0033c0036t0007g0010 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.538+621G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012757 | ||||||
| chr9:42012874
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.538+504T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012874 | ||||||
| chr9:42012922
|
T | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.538+456A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42012922 | ||||||
| chr9:42013051
|
A | G | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.538+327T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013051 | ||||||
| chr9:42013071
|
A | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.538+307T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013071 | ||||||
| chr9:42013086
|
T | A | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.538+292A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013086 | ||||||
| chr9:42013106
|
A | G | 1 | a0003c0003t0004g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.538+272T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013106 | ||||||
| chr9:42013126
|
G | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+252C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013126 | ||||||
| chr9:42013174
|
A | G | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.538+204T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013174 | ||||||
| chr9:42013198
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538+180A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013198 | ||||||
| chr9:42013226
|
G | A | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538+152C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013226 | ||||||
| chr9:42013231
|
A | C | 30 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.538+147T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4/23 | chr9 | 42013231 | ||||||
| chr9:42013531
|
A | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.391-6T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013531 | ||||||
| chr9:42013559
|
T | C | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.391-34A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013559 | ||||||
| chr9:42013611
|
T | C | 30 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.391-86A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013611 | ||||||
| chr9:42013691
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-166G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013691 | ||||||
| chr9:42013719
|
CG | C | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-195delC | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013719 | ||||||
| chr9:42013720
|
G | A | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-195C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013720 | ||||||
| chr9:42013813
|
C | T | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-288G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013813 | ||||||
| chr9:42013886
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-361C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013886 | ||||||
| chr9:42013908
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-383C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42013908 | ||||||
| chr9:42014034
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-509C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014034 | ||||||
| chr9:42014066
|
G | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-541C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014066 | ||||||
| chr9:42014138
|
C | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-613G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014138 | ||||||
| chr9:42014194
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-669G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014194 | ||||||
| chr9:42014206
|
C | T | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-681G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014206 | ||||||
| chr9:42014210
|
A | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.391-685T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014210 | ||||||
| chr9:42014271
|
C | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.391-746G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014271 | ||||||
| chr9:42014386
|
C | T | 1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.391-861G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014386 | ||||||
| chr9:42014485
|
G | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-960C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014485 | ||||||
| chr9:42014512
|
C | T | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-987G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014512 | ||||||
| chr9:42014516
|
C | T | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.391-991G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014516 | ||||||
| chr9:42014680
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-1155T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014680 | ||||||
| chr9:42014706
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-1181C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014706 | ||||||
| chr9:42014729
|
T | G | 2 | a0006c0007t0011g0017a0006c0007t0011g0021 | 2 | HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.391-1204A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014729 | ||||||
| chr9:42014760
|
C | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-1235G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014760 | ||||||
| chr9:42014790
|
C | CA | 10 | a0002c0002t0001g0049a0002c0002t0024g0061a0006c0007t0002g0014others(7): Show | 10 | HG01255.hp1 HG01934.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.391-1266dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014790 | ||||||
| chr9:42014790
|
CA | C | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.391-1266delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014790 | ||||||
| chr9:42014808
|
A | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.391-1283T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014808 | ||||||
| chr9:42014817
|
C | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-1292G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014817 | ||||||
| chr9:42014986
|
T | A | 1 | a0001c0001t0003g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.391-1461A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42014986 | ||||||
| chr9:42015025
|
C | CT | 33 | a0001c0001t0002g0006a0002c0002t0001g0040a0002c0002t0001g0044others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.391-1501dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015025 | ||||||
| chr9:42015025
|
C | CTT | 12 | a0002c0002t0001g0041a0002c0010t0001g0058a0004c0004t0005g0029others(9): Show | 12 | HG00280.hp2 HG01175.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.391-1502_391-1501d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015025 | ||||||
| chr9:42015025
|
CT | C | 34 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.391-1501delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015025 | ||||||
| chr9:42015117
|
C | T | 2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-1592G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015117 | ||||||
| chr9:42015152
|
G | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.391-1627C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015152 | ||||||
| chr9:42015216
|
G | GA | 3 | a0001c0001t0003g0100a0010c0013t0003g0103a0010c0013t0003g0108 | 3 | HG01106.hp1 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.391-1692dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015216 | ||||||
| chr9:42015255
|
C | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391-1730G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015255 | ||||||
| chr9:42015294
|
T | C | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.391-1769A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015294 | ||||||
| chr9:42015400
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-1875C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015400 | ||||||
| chr9:42015521
|
A | ACT | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-1998_391-1997d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015521 | ||||||
| chr9:42015583
|
T | C | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-2058A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015583 | ||||||
| chr9:42015684
|
G | T | 1 | a0001c0001t0003g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.391-2159C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42015684 | ||||||
| chr9:42016137
|
C | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-2612G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016137 | ||||||
| chr9:42016455
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-2930T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016455 | ||||||
| chr9:42016473
|
G | A | 1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-2948C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016473 | ||||||
| chr9:42016506
|
A | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.391-2981T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016506 | ||||||
| chr9:42016652
|
C | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-3127G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016652 | ||||||
| chr9:42016659
|
A | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-3134T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016659 | ||||||
| chr9:42016890
|
T | A | 3 | a0007c0009t0023g0039a0007c0009t0025g0037a0017c0014t0001g0038 | 3 | HG02109.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.391-3365A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016890 | ||||||
| chr9:42016973
|
T | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-3448A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42016973 | ||||||
| chr9:42017089
|
A | T | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.391-3564T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42017089 | ||||||
| chr9:42017118
|
T | C | 1 | a0018c0024t0008g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.391-3593A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42017118 | ||||||
| chr9:42017197
|
G | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-3672C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42017197 | ||||||
| chr9:42017214
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-3689T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42017214 | ||||||
| chr9:42017604
|
A | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-4079T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42017604 | ||||||
| chr9:42017854
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-4329A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42017854 | ||||||
| chr9:42018114
|
A | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-4589T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018114 | ||||||
| chr9:42018438
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-4913T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018438 | ||||||
| chr9:42018448
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-4923A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018448 | ||||||
| chr9:42018688
|
C | T | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-5163G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018688 | ||||||
| chr9:42018727
|
T | C | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.391-5202A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018727 | ||||||
| chr9:42018734
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-5209G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018734 | ||||||
| chr9:42018824
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-5299C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018824 | ||||||
| chr9:42018881
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-5356G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018881 | ||||||
| chr9:42018996
|
T | A | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.391-5471A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42018996 | ||||||
| chr9:42019013
|
G | C | 35 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.391-5488C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019013 | ||||||
| chr9:42019013
|
G | T | 1 | a0002c0002t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.391-5488C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019013 | ||||||
| chr9:42019288
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-5763C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019288 | ||||||
| chr9:42019468
|
G | A | 4 | a0001c0001t0002g0006a0005c0005t0006g0073a0019c0031t0028g0088others(1): Show | 4 | HG01081.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-5943C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019468 | ||||||
| chr9:42019487
|
T | C | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.391-5962A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019487 | ||||||
| chr9:42019489
|
C | T | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.391-5964G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019489 | ||||||
| chr9:42019503
|
G | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-5978C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019503 | ||||||
| chr9:42019591
|
C | CA | 12 | a0002c0002t0001g0044a0002c0002t0001g0059a0002c0002t0001g0065others(9): Show | 12 | HG00280.hp2 HG01952.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.391-6067dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019591 | ||||||
| chr9:42019591
|
CA | C | 17 | a0001c0001t0002g0024a0001c0042t0013g0001a0002c0002t0001g0052others(14): Show | 17 | HG01255.hp1 HG01516.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.391-6067delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019591 | ||||||
| chr9:42019591
|
CAA | C | 28 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.391-6068_391-6067d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019591 | ||||||
| chr9:42019760
|
C | CA | 10 | a0001c0001t0002g0022a0004c0004t0005g0029a0004c0004t0005g0030others(7): Show | 10 | HG00280.hp2 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-6236dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019760 | ||||||
| chr9:42019760
|
CA | C | 32 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.391-6236delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019760 | ||||||
| chr9:42019806
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-6281C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019806 | ||||||
| chr9:42019940
|
G | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.391-6415C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019940 | ||||||
| chr9:42019999
|
T | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-6474A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42019999 | ||||||
| chr9:42020301
|
T | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-6776A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020301 | ||||||
| chr9:42020329
|
A | C | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.391-6804T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020329 | ||||||
| chr9:42020539
|
T | C | 1 | a0002c0010t0001g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.391-7014A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020539 | ||||||
| chr9:42020568
|
C | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-7043G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020568 | ||||||
| chr9:42020575
|
G | A | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-7050C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020575 | ||||||
| chr9:42020715
|
T | C | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.391-7190A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020715 | ||||||
| chr9:42020726
|
C | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-7201G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020726 | ||||||
| chr9:42020997
|
T | C | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391-7472A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42020997 | ||||||
| chr9:42021022
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-7497T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021022 | ||||||
| chr9:42021163
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-7638C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021163 | ||||||
| chr9:42021348
|
C | A | 1 | a0002c0010t0001g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.391-7823G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021348 | ||||||
| chr9:42021382
|
A | AT | 2 | a0007c0009t0025g0037a0017c0014t0001g0038 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.391-7858dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021382 | ||||||
| chr9:42021538
|
C | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.391-8013G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021538 | ||||||
| chr9:42021543
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.391-8018T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021543 | ||||||
| chr9:42021566
|
A | C | 1 | a0001c0001t0003g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.391-8041T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021566 | ||||||
| chr9:42021866
|
A | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.391-8341T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42021866 | ||||||
| chr9:42022106
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-8581A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022106 | ||||||
| chr9:42022128
|
C | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-8603G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022128 | ||||||
| chr9:42022283
|
T | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-8758A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022283 | ||||||
| chr9:42022345
|
A | G | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-8820T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022345 | ||||||
| chr9:42022346
|
G | A | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-8821C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022346 | ||||||
| chr9:42022385
|
T | C | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.391-8860A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022385 | ||||||
| chr9:42022406
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-8881G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022406 | ||||||
| chr9:42022521
|
G | GT | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-8997dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022521 | ||||||
| chr9:42022640
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-9115G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022640 | ||||||
| chr9:42022820
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-9295T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022820 | ||||||
| chr9:42022882
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-9357A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022882 | ||||||
| chr9:42022951
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-9426G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42022951 | ||||||
| chr9:42023124
|
G | T | 2 | a0008c0006t0010g0069a0008c0006t0010g0070 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.391-9599C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023124 | ||||||
| chr9:42023254
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-9729A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023254 | ||||||
| chr9:42023431
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-9906C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023431 | ||||||
| chr9:42023499
|
C | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.391-9974G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023499 | ||||||
| chr9:42023549
|
T | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.391-10024A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023549 | ||||||
| chr9:42023583
|
G | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-10058C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023583 | ||||||
| chr9:42023670
|
A | T | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.391-10145T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023670 | ||||||
| chr9:42023828
|
T | C | 5 | a0001c0001t0003g0096a0001c0001t0003g0100a0001c0001t0003g0102others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-10303A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023828 | ||||||
| chr9:42023971
|
C | A | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.391-10446G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42023971 | ||||||
| chr9:42024034
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-10509C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024034 | ||||||
| chr9:42024050
|
A | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-10525T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024050 | ||||||
| chr9:42024214
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-10689A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024214 | ||||||
| chr9:42024296
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-10771T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024296 | ||||||
| chr9:42024304
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-10779C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024304 | ||||||
| chr9:42024412
|
G | C | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.391-10887C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024412 | ||||||
| chr9:42024585
|
A | G | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-11060T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024585 | ||||||
| chr9:42024599
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-11074C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024599 | ||||||
| chr9:42024663
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-11138C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024663 | ||||||
| chr9:42024669
|
C | CA | 36 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.391-11145dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024669 | ||||||
| chr9:42024669
|
C | CAA | 5 | a0004c0004t0005g0029a0004c0004t0005g0031a0004c0004t0005g0032others(2): Show | 5 | HG00280.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-11146_391-1114 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024669 | ||||||
| chr9:42024669
|
C | CAAA | 5 | a0006c0007t0002g0014a0006c0007t0011g0017a0006c0007t0011g0021others(2): Show | 5 | HG02040.hp2 HG02145.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-11147_391-1114 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024669 | ||||||
| chr9:42024683
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-11158T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024683 | ||||||
| chr9:42024739
|
G | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-11214C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024739 | ||||||
| chr9:42024769
|
T | G | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.391-11244A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42024769 | ||||||
| chr9:42025040
|
C | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.391-11515G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025040 | ||||||
| chr9:42025200
|
C | T | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-11675G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025200 | ||||||
| chr9:42025201
|
C | T | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-11676G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025201 | ||||||
| chr9:42025217
|
A | C | 1 | a0004c0004t0005g0032 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.391-11692T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025217 | ||||||
| chr9:42025282
|
G | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-11757C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025282 | ||||||
| chr9:42025286
|
G | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-11761C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025286 | ||||||
| chr9:42025344
|
G | A | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.391-11819C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025344 | ||||||
| chr9:42025406
|
C | G | 1 | a0002c0010t0001g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.391-11881G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025406 | ||||||
| chr9:42025442
|
CCTGTTCC others(1): Show |
C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-11925_391-1191 others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025442 | ||||||
| chr9:42025576
|
G | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.391-12051C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025576 | ||||||
| chr9:42025691
|
G | T | 3 | a0007c0009t0023g0039a0007c0009t0025g0037a0017c0014t0001g0038 | 3 | HG02109.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.391-12166C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025691 | ||||||
| chr9:42025719
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-12194A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42025719 | ||||||
| chr9:42026261
|
TC | T | 10 | a0003c0003t0004g0081a0003c0003t0004g0082a0003c0003t0008g0077others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-12737delG | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026261 | ||||||
| chr9:42026319
|
G | A | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391-12794C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026319 | ||||||
| chr9:42026325
|
G | C | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.391-12800C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026325 | ||||||
| chr9:42026360
|
G | A | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.391-12835C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026360 | ||||||
| chr9:42026511
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-12986A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026511 | ||||||
| chr9:42026548
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.391-13023G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026548 | ||||||
| chr9:42026549
|
G | C | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.391-13024C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026549 | ||||||
| chr9:42026595
|
G | GA | 9 | a0002c0002t0001g0045a0002c0002t0001g0049a0002c0002t0022g0068others(6): Show | 9 | HG01981.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-13071dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026595 | ||||||
| chr9:42026595
|
GA | G | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-13071delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026595 | ||||||
| chr9:42026595
|
GAAA | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-13073_391-1307 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026595 | ||||||
| chr9:42026596
|
A | G | 2 | a0007c0009t0025g0037a0017c0014t0001g0038 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.391-13071T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026596 | ||||||
| chr9:42026597
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-13072T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026597 | ||||||
| chr9:42026598
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-13073T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026598 | ||||||
| chr9:42026660
|
C | G | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.391-13135G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026660 | ||||||
| chr9:42026919
|
G | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-13394C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42026919 | ||||||
| chr9:42027373
|
T | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-13848A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027373 | ||||||
| chr9:42027461
|
T | A | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.391-13936A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027461 | ||||||
| chr9:42027516
|
C | T | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.391-13991G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027516 | ||||||
| chr9:42027540
|
G | A | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-14015C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027540 | ||||||
| chr9:42027551
|
T | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-14026A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027551 | ||||||
| chr9:42027743
|
T | G | 2 | a0005c0005t0006g0091a0022c0030t0006g0085 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391-14218A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027743 | ||||||
| chr9:42027751
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-14226C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027751 | ||||||
| chr9:42027818
|
G | A | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.391-14293C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027818 | ||||||
| chr9:42027889
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-14364T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42027889 | ||||||
| chr9:42028318
|
T | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.391-14793A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42028318 | ||||||
| chr9:42028323
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-14798A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42028323 | ||||||
| chr9:42028455
|
T | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-14930A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42028455 | ||||||
| chr9:42028685
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-15160C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42028685 | ||||||
| chr9:42028710
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-15185G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42028710 | ||||||
| chr9:42028744
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-15219C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42028744 | ||||||
| chr9:42029172
|
G | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-15647C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029172 | ||||||
| chr9:42029254
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-15729A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029254 | ||||||
| chr9:42029266
|
A | G | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-15741T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029266 | ||||||
| chr9:42029294
|
A | C | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.391-15769T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029294 | ||||||
| chr9:42029501
|
T | G | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.391-15976A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029501 | ||||||
| chr9:42029532
|
C | CT | 5 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-16008dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029532 | ||||||
| chr9:42029532
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.391-16007G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029532 | ||||||
| chr9:42029571
|
C | A | 3 | a0009c0008t0009g0105a0009c0008t0009g0106a0009c0008t0009g0107 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.391-16046G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029571 | ||||||
| chr9:42029625
|
G | A | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.391-16100C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029625 | ||||||
| chr9:42029913
|
T | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.391-16388A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42029913 | ||||||
| chr9:42030001
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-16476C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030001 | ||||||
| chr9:42030040
|
A | C | 1 | a0002c0002t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.391-16515T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030040 | ||||||
| chr9:42030083
|
G | A | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.391-16558C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030083 | ||||||
| chr9:42030142
|
T | C | 2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-16617A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030142 | ||||||
| chr9:42030143
|
C | CA | 6 | a0002c0002t0001g0059a0002c0010t0001g0057a0002c0010t0001g0058others(3): Show | 6 | HG01952.hp1 HG02083.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-16619dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030143 | ||||||
| chr9:42030210
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-16685G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030210 | ||||||
| chr9:42030452
|
G | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-16927C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030452 | ||||||
| chr9:42030567
|
G | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-17042C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030567 | ||||||
| chr9:42030593
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.391-17068G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030593 | ||||||
| chr9:42030750
|
C | CAG | 2 | a0001c0001t0003g0096a0004c0004t0005g0032 | 2 | HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.391-17227_391-1722 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(3): Show |
1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.391-17235_391-1722 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(5): Show |
4 | a0002c0002t0001g0065a0002c0002t0012g0051a0002c0002t0022g0068others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-17237_391-1722 others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(7): Show |
5 | a0002c0002t0001g0050a0002c0010t0001g0057a0002c0010t0001g0058others(2): Show | 5 | HG01255.hp2 HG01952.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-17239_391-1722 others(18): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(9): Show |
2 | a0002c0002t0001g0040a0008c0006t0010g0071 | 2 | HG03453.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.391-17241_391-1722 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(11): Show |
2 | a0002c0002t0024g0061a0002c0015t0001g0046 | 2 | HG02145.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.391-17243_391-1722 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(13): Show |
6 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049others(3): Show | 6 | HG01081.hp1 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-17245_391-1722 others(24): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(15): Show |
3 | a0002c0002t0001g0062a0002c0002t0012g0043a0002c0020t0001g0060 | 3 | HG00140.hp2 HG00735.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.391-17247_391-1722 others(26): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(17): Show |
4 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0052others(1): Show | 4 | HG01981.hp2 HG02083.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-17249_391-1722 others(28): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
C | CAGAGAGA others(21): Show |
1 | a0012c0022t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391-17253_391-1722 others(32): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
CAG | C | 32 | a0001c0001t0002g0022a0001c0001t0003g0095a0001c0001t0003g0097others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(29): Show |
intron_variant | MODIFIER | c.391-17227_391-1722 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
CAGAG | C | 19 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0018others(16): Show | 19 | HG00558.hp1 HG00642.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.391-17229_391-1722 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
CAGAGAG | C | 4 | a0003c0003t0004g0075a0005c0005t0006g0091a0006c0041t0002g0020others(1): Show | 4 | HG02040.hp2 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-17231_391-1722 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
CAGAGAGA others(1): Show |
C | 3 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0003g0093 | 3 | HG01081.hp2 HG03704.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.391-17233_391-1722 others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
CAGAGAGA others(7): Show |
C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-17239_391-1722 others(18): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030750
|
CAGAGAGA others(11): Show |
C | 1 | a0003c0011t0004g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.391-17243_391-1722 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030750 | ||||||
| chr9:42030764
|
GAGAGAGA others(44): Show |
G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-17290_391-1724 others(55): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030764 | ||||||
| chr9:42030785
|
A | AGAGAGAG others(12): Show |
1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.391-17261_391-1726 others(23): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030785 | ||||||
| chr9:42030786
|
T | G | 3 | a0003c0011t0004g0078a0005c0005t0030g0092a0014c0018t0001g0067 | 3 | HG02056.hp1 HG02559.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.391-17261A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030786 | ||||||
| chr9:42030787
|
G | A | 3 | a0003c0011t0004g0078a0005c0005t0030g0092a0014c0018t0001g0067 | 3 | HG02056.hp1 HG02559.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.391-17262C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030787 | ||||||
| chr9:42030792
|
C | T | 3 | a0003c0011t0004g0078a0005c0005t0030g0092a0014c0018t0001g0067 | 3 | HG02056.hp1 HG02559.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.391-17267G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030792 | ||||||
| chr9:42030792
|
CGA | C | 17 | a0002c0020t0001g0060a0003c0003t0004g0075a0003c0003t0004g0082others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(14): Show |
intron_variant | MODIFIER | c.391-17269_391-1726 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030792 | ||||||
| chr9:42030794
|
A | C | 3 | a0003c0011t0004g0078a0005c0005t0030g0092a0014c0018t0001g0067 | 3 | HG02056.hp1 HG02559.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.391-17269T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030794 | ||||||
| chr9:42030798
|
A | AGAGAGAG others(6): Show |
1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391-17286_391-1727 others(17): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030798 | ||||||
| chr9:42030802
|
A | AGAGAGAG others(2): Show |
4 | a0004c0004t0005g0029a0004c0004t0005g0031a0004c0004t0005g0032others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-17286_391-1727 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030802 | ||||||
| chr9:42030805
|
G | C | 24 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(21): Show | 24 | HG00735.hp2 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.391-17280C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030805 | ||||||
| chr9:42030807
|
G | C | 3 | a0002c0020t0001g0060a0014c0018t0001g0067a0015c0019t0001g0066 | 3 | HG00140.hp2 HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.391-17282C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030807 | ||||||
| chr9:42030808
|
A | AGAG | 4 | a0002c0002t0001g0047a0002c0002t0001g0048a0005c0005t0006g0073others(1): Show | 4 | HG02572.hp2 HG03453.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-17286_391-1728 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030808 | ||||||
| chr9:42030810
|
A | AG | 4 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0023t0001g0054others(1): Show | 4 | HG02135.hp2 HG02622.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-17286dupC | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030810 | ||||||
| chr9:42030811
|
GAGGA | G | 2 | a0003c0003t0004g0081a0032c0039t0014g0025 | 2 | HG02486.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.391-17290_391-1728 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030811 | ||||||
| chr9:42030812
|
A | G | 24 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(21): Show | 24 | HG00735.hp2 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.391-17287T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030812 | ||||||
| chr9:42030813
|
G | A | 24 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(21): Show | 24 | HG00735.hp2 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.391-17288C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GA | 14 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0002t0001g0047others(11): Show | 14 | HG00280.hp2 HG01175.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.391-17289_391-1728 others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GAGAGAGA others(14): Show |
1 | a0001c0001t0003g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.391-17289_391-1728 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGA | 8 | a0001c0001t0002g0004a0001c0001t0003g0093a0001c0001t0003g0095others(5): Show | 8 | HG02040.hp2 HG02273.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-17294_391-1728 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(1): Show |
9 | a0001c0001t0002g0006a0001c0001t0003g0096a0001c0001t0003g0100others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-17296_391-1728 others(12): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(3): Show |
7 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0003g0101others(4): Show | 7 | HG00558.hp1 HG00735.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-17298_391-1728 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(5): Show |
3 | a0006c0007t0011g0017a0006c0007t0011g0021a0011c0040t0007g0003 | 3 | HG02145.hp2 HG03669.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.391-17300_391-1728 others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(7): Show |
4 | a0001c0001t0002g0005a0001c0046t0016g0015a0010c0013t0003g0103others(1): Show | 4 | HG01516.hp2 HG02135.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-17302_391-1728 others(18): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(9): Show |
1 | a0001c0001t0017g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.391-17304_391-1728 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(11): Show |
1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.391-17306_391-1728 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGAGAG others(19): Show |
1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-17314_391-1728 others(30): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030813
|
G | GGAGGAGA others(8): Show |
1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.391-17289_391-1728 others(19): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030813 | ||||||
| chr9:42030909
|
C | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.391-17384G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030909 | ||||||
| chr9:42030915
|
TC | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-17391delG | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030915 | ||||||
| chr9:42030931
|
T | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.391-17406A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030931 | ||||||
| chr9:42030963
|
T | C | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.391-17438A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030963 | ||||||
| chr9:42030985
|
C | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-17460G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42030985 | ||||||
| chr9:42031080
|
G | A | 88 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.391-17555C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031080 | ||||||
| chr9:42031170
|
C | G | 2 | a0005c0005t0006g0091a0022c0030t0006g0085 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391-17645G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031170 | ||||||
| chr9:42031716
|
C | T | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.391-18191G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031716 | ||||||
| chr9:42031754
|
G | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-18229C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031754 | ||||||
| chr9:42031795
|
A | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.391-18270T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031795 | ||||||
| chr9:42031809
|
C | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-18284G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031809 | ||||||
| chr9:42031883
|
T | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-18358A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42031883 | ||||||
| chr9:42032022
|
C | G | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.391-18497G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032022 | ||||||
| chr9:42032022
|
C | T | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.391-18497G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032022 | ||||||
| chr9:42032082
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-18557G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032082 | ||||||
| chr9:42032121
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.391-18596G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032121 | ||||||
| chr9:42032171
|
T | C | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.391-18646A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032171 | ||||||
| chr9:42032561
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-19036C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032561 | ||||||
| chr9:42032607
|
A | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-19082T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032607 | ||||||
| chr9:42032630
|
T | A | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-19105A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032630 | ||||||
| chr9:42032640
|
A | G | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.391-19115T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032640 | ||||||
| chr9:42032767
|
G | A | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.391-19242C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032767 | ||||||
| chr9:42032912
|
G | A | 4 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071others(1): Show | 4 | HG02486.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-19387C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42032912 | ||||||
| chr9:42033069
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-19544C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033069 | ||||||
| chr9:42033074
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-19549A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033074 | ||||||
| chr9:42033274
|
T | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.391-19749A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033274 | ||||||
| chr9:42033470
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.391-19945G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033470 | ||||||
| chr9:42033494
|
C | T | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-19969G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033494 | ||||||
| chr9:42033697
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-20172T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033697 | ||||||
| chr9:42033827
|
G | A | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-20302C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033827 | ||||||
| chr9:42033897
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.391-20372A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42033897 | ||||||
| chr9:42034033
|
G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-20508C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034033 | ||||||
| chr9:42034156
|
C | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.391-20631G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034156 | ||||||
| chr9:42034174
|
G | GTATCTAT others(9): Show |
1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-20650_391-2064 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034174 | ||||||
| chr9:42034178
|
G | C | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-20653C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034178 | ||||||
| chr9:42034182
|
A | C | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-20657T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034182 | ||||||
| chr9:42034186
|
G | C | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-20661C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034186
|
G | GTATCTAT others(9): Show |
6 | a0001c0001t0002g0004a0001c0001t0002g0018a0001c0001t0003g0093others(3): Show | 6 | HG00642.hp2 HG01071.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-20677_391-2066 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034186
|
G | GTATCTAT others(13): Show |
24 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(21): Show | 24 | HG00099.hp2 HG00558.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.391-20681_391-2066 others(24): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034186
|
G | GTATCTAT others(17): Show |
6 | a0001c0001t0002g0006a0001c0001t0003g0095a0001c0001t0003g0100others(3): Show | 6 | HG01081.hp2 HG01106.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-20685_391-2066 others(28): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034186
|
G | GTATCTAT others(21): Show |
2 | a0001c0001t0003g0096a0010c0013t0003g0108 | 2 | HG00280.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.391-20662_391-2066 others(32): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034186
|
G | GTATCTAT others(25): Show |
1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.391-20662_391-2066 others(36): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034186
|
G | GTATCTAT others(29): Show |
1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-20662_391-2066 others(40): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034186 | ||||||
| chr9:42034189
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-20664A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034189 | ||||||
| chr9:42034271
|
C | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-20746G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034271 | ||||||
| chr9:42034317
|
A | G | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.391-20792T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034317 | ||||||
| chr9:42034377
|
C | T | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.391-20852G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034377 | ||||||
| chr9:42034479
|
GC | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-20955delG | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034479 | ||||||
| chr9:42034589
|
C | T | 1 | a0002c0020t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.391-21064G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034589 | ||||||
| chr9:42034725
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-21200G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034725 | ||||||
| chr9:42034743
|
C | T | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.391-21218G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034743 | ||||||
| chr9:42034744
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-21219C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034744 | ||||||
| chr9:42034811
|
C | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-21286G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42034811 | ||||||
| chr9:42035061
|
T | C | 1 | a0009c0008t0009g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.391-21536A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035061 | ||||||
| chr9:42035121
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-21596C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035121 | ||||||
| chr9:42035244
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-21719G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035244 | ||||||
| chr9:42035322
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-21797A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035322 | ||||||
| chr9:42035361
|
C | T | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-21836G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035361 | ||||||
| chr9:42035427
|
G | A | 1 | a0003c0003t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.391-21902C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035427 | ||||||
| chr9:42035594
|
G | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-22069C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035594 | ||||||
| chr9:42035922
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.391-22397T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035922 | ||||||
| chr9:42035967
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-22442C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035967 | ||||||
| chr9:42035977
|
G | A | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.391-22452C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035977 | ||||||
| chr9:42035986
|
T | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-22461A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035986 | ||||||
| chr9:42035988
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-22463C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035988 | ||||||
| chr9:42035992
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.391-22467G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035992 | ||||||
| chr9:42035998
|
C | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-22473G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42035998 | ||||||
| chr9:42036000
|
C | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-22475G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036000 | ||||||
| chr9:42036038
|
G | A | 7 | a0002c0002t0001g0044a0004c0004t0005g0029a0004c0004t0005g0030others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-22513C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036038 | ||||||
| chr9:42036458
|
C | T | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391-22933G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036458 | ||||||
| chr9:42036480
|
G | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.391-22955C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036480 | ||||||
| chr9:42036500
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.391-22975C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036500 | ||||||
| chr9:42036603
|
A | G | 1 | a0004c0004t0005g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.391-23078T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036603 | ||||||
| chr9:42036662
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-23137G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036662 | ||||||
| chr9:42036669
|
G | A | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.391-23144C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036669 | ||||||
| chr9:42036712
|
A | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-23187T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036712 | ||||||
| chr9:42036714
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-23189C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036714 | ||||||
| chr9:42036787
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-23262C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036787 | ||||||
| chr9:42036919
|
G | T | 1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.391-23394C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036919 | ||||||
| chr9:42036981
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-23456C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42036981 | ||||||
| chr9:42037026
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-23501G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037026 | ||||||
| chr9:42037047
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-23522G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037047 | ||||||
| chr9:42037192
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-23667G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037192 | ||||||
| chr9:42037226
|
T | C | 1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391-23701A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037226 | ||||||
| chr9:42037276
|
AAAAAAAG | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-23758_391-2375 others(11): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037276 | ||||||
| chr9:42037378
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.391-23853G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037378 | ||||||
| chr9:42037590
|
A | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-24065T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037590 | ||||||
| chr9:42037627
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-24102T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037627 | ||||||
| chr9:42037692
|
G | T | 88 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.391-24167C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037692 | ||||||
| chr9:42037873
|
T | C | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.391-24348A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037873 | ||||||
| chr9:42037931
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-24406G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037931 | ||||||
| chr9:42037934
|
G | T | 1 | a0002c0002t0012g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.391-24409C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037934 | ||||||
| chr9:42037935
|
G | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-24410C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42037935 | ||||||
| chr9:42038077
|
G | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-24552C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038077 | ||||||
| chr9:42038102
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-24577G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038102 | ||||||
| chr9:42038103
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.391-24578G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038103 | ||||||
| chr9:42038291
|
A | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-24766T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038291 | ||||||
| chr9:42038382
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-24857G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038382 | ||||||
| chr9:42038455
|
T | TA | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-24931dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038455 | ||||||
| chr9:42038469
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-24944C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038469 | ||||||
| chr9:42038488
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-24963T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038488 | ||||||
| chr9:42038809
|
A | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.391-25284T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42038809 | ||||||
| chr9:42039135
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-25610C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039135 | ||||||
| chr9:42039336
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-25811C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039336 | ||||||
| chr9:42039399
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-25874C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039399 | ||||||
| chr9:42039475
|
T | C | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.391-25950A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039475 | ||||||
| chr9:42039705
|
GA | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-26181delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039705 | ||||||
| chr9:42039815
|
G | A | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.391-26290C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039815 | ||||||
| chr9:42039821
|
C | G | 5 | a0001c0001t0003g0096a0001c0001t0003g0100a0001c0001t0003g0102others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-26296G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039821 | ||||||
| chr9:42039855
|
C | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-26330G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039855 | ||||||
| chr9:42039855
|
C | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-26330G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039855 | ||||||
| chr9:42039874
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-26349T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039874 | ||||||
| chr9:42039991
|
T | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-26466A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42039991 | ||||||
| chr9:42040168
|
A | T | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-26643T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040168 | ||||||
| chr9:42040311
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-26786A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040311 | ||||||
| chr9:42040341
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-26816A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040341 | ||||||
| chr9:42040500
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-26975T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040500 | ||||||
| chr9:42040514
|
G | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.391-26989C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040514 | ||||||
| chr9:42040537
|
A | T | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-27012T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040537 | ||||||
| chr9:42040687
|
A | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-27162T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040687 | ||||||
| chr9:42040864
|
G | A | 1 | a0002c0002t0012g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.391-27339C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42040864 | ||||||
| chr9:42041172
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-27647G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041172 | ||||||
| chr9:42041177
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-27652C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041177 | ||||||
| chr9:42041267
|
T | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-27742A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041267 | ||||||
| chr9:42041270
|
T | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-27745A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041270 | ||||||
| chr9:42041313
|
G | A | 1 | a0018c0024t0008g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.391-27788C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041313 | ||||||
| chr9:42041784
|
C | G | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.391-28259G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041784 | ||||||
| chr9:42041799
|
C | T | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391-28274G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041799 | ||||||
| chr9:42041821
|
G | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-28296C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041821 | ||||||
| chr9:42041842
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-28317A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041842 | ||||||
| chr9:42041917
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-28392A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041917 | ||||||
| chr9:42041979
|
A | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-28454T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42041979 | ||||||
| chr9:42042004
|
C | G | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391-28479G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042004 | ||||||
| chr9:42042085
|
G | A | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.391-28560C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042085 | ||||||
| chr9:42042223
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-28698C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042223 | ||||||
| chr9:42042233
|
TA | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-28709delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042233 | ||||||
| chr9:42042547
|
T | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.391-29022A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042547 | ||||||
| chr9:42042624
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-29099T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042624 | ||||||
| chr9:42042707
|
A | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.391-29182T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042707 | ||||||
| chr9:42042741
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-29216G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042741 | ||||||
| chr9:42042742
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-29217C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042742 | ||||||
| chr9:42042865
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391-29340G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042865 | ||||||
| chr9:42042986
|
AATC | A | 2 | a0016c0017t0001g0042a0027c0026t0020g0027 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.391-29464_391-2946 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42042986 | ||||||
| chr9:42043102
|
A | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-29577T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043102 | ||||||
| chr9:42043163
|
T | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.391-29638A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043163 | ||||||
| chr9:42043172
|
C | CT | 40 | a0001c0001t0003g0102a0001c0046t0016g0015a0002c0002t0001g0040others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.391-29648dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043172 | ||||||
| chr9:42043172
|
C | CTT | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.391-29649_391-2964 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043172 | ||||||
| chr9:42043200
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-29675T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043200 | ||||||
| chr9:42043243
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-29718G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043243 | ||||||
| chr9:42043324
|
A | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.391-29799T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043324 | ||||||
| chr9:42043482
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-29957A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043482 | ||||||
| chr9:42043773
|
CACAA | C | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.391-30252_391-3024 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043773 | ||||||
| chr9:42043834
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.391-30309G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043834 | ||||||
| chr9:42043835
|
G | A | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.391-30310C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043835 | ||||||
| chr9:42043861
|
G | A | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.391-30336C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043861 | ||||||
| chr9:42043883
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-30358A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043883 | ||||||
| chr9:42043884
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-30359C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043884 | ||||||
| chr9:42043992
|
C | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.391-30467G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42043992 | ||||||
| chr9:42044081
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.391-30556G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044081 | ||||||
| chr9:42044192
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-30667C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044192 | ||||||
| chr9:42044340
|
G | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391-30815C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044340 | ||||||
| chr9:42044422
|
A | G | 1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.391-30897T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044422 | ||||||
| chr9:42044459
|
T | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-30934A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044459 | ||||||
| chr9:42044518
|
G | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-30993C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044518 | ||||||
| chr9:42044546
|
C | T | 1 | a0008c0006t0010g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.391-31021G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044546 | ||||||
| chr9:42044547
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-31022C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044547 | ||||||
| chr9:42044559
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-31034C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044559 | ||||||
| chr9:42044604
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-31079G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044604 | ||||||
| chr9:42044641
|
G | A | 1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.391-31116C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044641 | ||||||
| chr9:42044653
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-31128C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044653 | ||||||
| chr9:42044821
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-31296T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044821 | ||||||
| chr9:42044914
|
C | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-31389G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044914 | ||||||
| chr9:42044989
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-31464G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42044989 | ||||||
| chr9:42045213
|
C | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+31656G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045213 | ||||||
| chr9:42045214
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+31655G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045214 | ||||||
| chr9:42045235
|
C | T | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.390+31634G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045235 | ||||||
| chr9:42045269
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+31600G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045269 | ||||||
| chr9:42045329
|
T | C | 3 | a0001c0001t0002g0006a0005c0005t0006g0073a0024c0029t0006g0087 | 3 | HG01081.hp2 HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+31540A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045329 | ||||||
| chr9:42045379
|
A | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+31490T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045379 | ||||||
| chr9:42045500
|
A | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.390+31369T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045500 | ||||||
| chr9:42045525
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+31344A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045525 | ||||||
| chr9:42045535
|
C | T | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.390+31334G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045535 | ||||||
| chr9:42045815
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+31054T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045815 | ||||||
| chr9:42045995
|
G | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+30874C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42045995 | ||||||
| chr9:42046037
|
T | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+30832A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046037 | ||||||
| chr9:42046051
|
C | T | 1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.390+30818G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046051 | ||||||
| chr9:42046151
|
C | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.390+30718G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046151 | ||||||
| chr9:42046507
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+30362A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046507 | ||||||
| chr9:42046616
|
A | G | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.390+30253T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046616 | ||||||
| chr9:42046674
|
C | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+30195G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046674 | ||||||
| chr9:42046713
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+30156A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046713 | ||||||
| chr9:42046832
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+30037C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046832 | ||||||
| chr9:42046971
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+29898T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42046971 | ||||||
| chr9:42047004
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+29865C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047004 | ||||||
| chr9:42047025
|
C | T | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.390+29844G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047025 | ||||||
| chr9:42047176
|
C | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.390+29693G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047176 | ||||||
| chr9:42047364
|
G | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+29505C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047364 | ||||||
| chr9:42047369
|
T | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+29500A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047369 | ||||||
| chr9:42047587
|
TTCCC | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+29278_390+2928 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047587 | ||||||
| chr9:42047617
|
A | C | 107 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.390+29252T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047617 | ||||||
| chr9:42047618
|
C | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+29251G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047618 | ||||||
| chr9:42047639
|
A | T | 107 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.390+29230T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047639 | ||||||
| chr9:42047657
|
T | C | 1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.390+29212A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047657 | ||||||
| chr9:42047678
|
C | CCCTT | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+29187_390+2919 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047678 | ||||||
| chr9:42047678
|
CCCTT | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.390+29187_390+2919 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047678 | ||||||
| chr9:42047682
|
T | TCCTC | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+29186_390+2918 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047682 | ||||||
| chr9:42047738
|
C | T | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.390+29131G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047738 | ||||||
| chr9:42047782
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+29087A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047782 | ||||||
| chr9:42047919
|
A | T | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.390+28950T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42047919 | ||||||
| chr9:42048061
|
G | A | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.390+28808C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048061 | ||||||
| chr9:42048141
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.390+28728T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048141 | ||||||
| chr9:42048173
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+28696G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048173 | ||||||
| chr9:42048197
|
A | T | 1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.390+28672T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048197 | ||||||
| chr9:42048230
|
C | G | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.390+28639G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048230 | ||||||
| chr9:42048231
|
G | A | 2 | a0004c0004t0005g0034a0028c0027t0005g0033 | 2 | NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.390+28638C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048231 | ||||||
| chr9:42048741
|
CA | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+28127delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42048741 | ||||||
| chr9:42049247
|
G | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+27622C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049247 | ||||||
| chr9:42049582
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+27287C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049582 | ||||||
| chr9:42049637
|
A | G | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390+27232T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049637 | ||||||
| chr9:42049664
|
T | C | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+27205A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049664 | ||||||
| chr9:42049679
|
G | A | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.390+27190C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049679 | ||||||
| chr9:42049683
|
C | T | 1 | a0002c0010t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.390+27186G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049683 | ||||||
| chr9:42049706
|
T | A | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.390+27163A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049706 | ||||||
| chr9:42049708
|
T | A | 3 | a0005c0005t0006g0076a0005c0005t0030g0092a0023c0028t0006g0084 | 3 | HG01516.hp1 HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.390+27161A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049708 | ||||||
| chr9:42049812
|
T | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+27057A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049812 | ||||||
| chr9:42049886
|
G | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+26983C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049886 | ||||||
| chr9:42049919
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+26950C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049919 | ||||||
| chr9:42049972
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+26897C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42049972 | ||||||
| chr9:42050124
|
A | G | 87 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.390+26745T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050124 | ||||||
| chr9:42050214
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390+26655T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050214 | ||||||
| chr9:42050246
|
A | G | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390+26623T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050246 | ||||||
| chr9:42050459
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.390+26410C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050459 | ||||||
| chr9:42050462
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+26407C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050462 | ||||||
| chr9:42050573
|
C | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+26296G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050573 | ||||||
| chr9:42050585
|
G | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+26284C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050585 | ||||||
| chr9:42050836
|
G | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+26033C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050836 | ||||||
| chr9:42050912
|
C | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+25957G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050912 | ||||||
| chr9:42050962
|
C | T | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+25907G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42050962 | ||||||
| chr9:42051064
|
C | T | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+25805G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051064 | ||||||
| chr9:42051279
|
C | A | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.390+25590G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051279 | ||||||
| chr9:42051316
|
T | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+25553A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051316 | ||||||
| chr9:42051334
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+25535C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051334 | ||||||
| chr9:42051370
|
C | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+25499G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051370 | ||||||
| chr9:42051394
|
C | T | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.390+25475G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051394 | ||||||
| chr9:42051424
|
T | C | 87 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.390+25445A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051424 | ||||||
| chr9:42051567
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+25302C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051567 | ||||||
| chr9:42051652
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+25217A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051652 | ||||||
| chr9:42051717
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+25152A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051717 | ||||||
| chr9:42051840
|
C | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+25029G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051840 | ||||||
| chr9:42051865
|
C | T | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+25004G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051865 | ||||||
| chr9:42051963
|
G | T | 2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+24906C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42051963 | ||||||
| chr9:42052218
|
C | T | 1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.390+24651G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052218 | ||||||
| chr9:42052231
|
A | G | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+24638T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052231 | ||||||
| chr9:42052293
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+24576G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052293 | ||||||
| chr9:42052306
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+24563T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052306 | ||||||
| chr9:42052316
|
C | T | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.390+24553G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052316 | ||||||
| chr9:42052343
|
GC | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+24525delG | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052343 | ||||||
| chr9:42052371
|
G | A | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.390+24498C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052371 | ||||||
| chr9:42052411
|
G | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+24458C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052411 | ||||||
| chr9:42052501
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.390+24368A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052501 | ||||||
| chr9:42052520
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+24349C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052520 | ||||||
| chr9:42052560
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+24309G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052560 | ||||||
| chr9:42052650
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+24219G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052650 | ||||||
| chr9:42052846
|
G | A | 2 | a0001c0001t0003g0095a0001c0001t0003g0097 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.390+24023C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052846 | ||||||
| chr9:42052895
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+23974G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052895 | ||||||
| chr9:42052937
|
G | A | 1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.390+23932C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052937 | ||||||
| chr9:42052944
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.390+23925C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052944 | ||||||
| chr9:42052950
|
G | A | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.390+23919C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42052950 | ||||||
| chr9:42053093
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.390+23776G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053093 | ||||||
| chr9:42053138
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+23731C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053138 | ||||||
| chr9:42053271
|
G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+23598C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053271 | ||||||
| chr9:42053394
|
G | A | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.390+23475C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053394 | ||||||
| chr9:42053724
|
C | G | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+23145G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053724 | ||||||
| chr9:42053815
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+23054G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053815 | ||||||
| chr9:42053898
|
G | A | 1 | a0002c0002t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.390+22971C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053898 | ||||||
| chr9:42053907
|
C | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+22962G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053907 | ||||||
| chr9:42053923
|
C | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+22946G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053923 | ||||||
| chr9:42053941
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+22928G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42053941 | ||||||
| chr9:42054146
|
C | T | 1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.390+22723G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054146 | ||||||
| chr9:42054154
|
A | G | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.390+22715T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054154 | ||||||
| chr9:42054166
|
C | CGT | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+22701_390+2270 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054166 | ||||||
| chr9:42054179
|
G | C | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+22690C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054179 | ||||||
| chr9:42054220
|
C | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+22649G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054220 | ||||||
| chr9:42054259
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+22610T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054259 | ||||||
| chr9:42054268
|
C | T | 87 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.390+22601G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054268 | ||||||
| chr9:42054375
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+22494T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054375 | ||||||
| chr9:42054451
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+22418C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054451 | ||||||
| chr9:42054609
|
G | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+22260C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054609 | ||||||
| chr9:42054688
|
T | A | 1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.390+22181A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054688 | ||||||
| chr9:42054749
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+22120C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054749 | ||||||
| chr9:42054961
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.390+21908G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42054961 | ||||||
| chr9:42055124
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+21745A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055124 | ||||||
| chr9:42055239
|
A | T | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.390+21630T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055239 | ||||||
| chr9:42055291
|
G | GTA | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.390+21576_390+2157 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055291 | ||||||
| chr9:42055291
|
G | GTATA | 4 | a0006c0007t0011g0021a0009c0008t0009g0105a0009c0008t0009g0106others(1): Show | 4 | HG00735.hp1 HG03453.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+21574_390+2157 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055291 | ||||||
| chr9:42055656
|
A | C | 87 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.390+21213T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055656 | ||||||
| chr9:42055656
|
A | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+21213T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055656 | ||||||
| chr9:42055694
|
G | C | 1 | a0001c0001t0017g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.390+21175C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055694 | ||||||
| chr9:42055853
|
C | T | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.390+21016G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055853 | ||||||
| chr9:42055950
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.390+20919T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42055950 | ||||||
| chr9:42056031
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.390+20838C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056031 | ||||||
| chr9:42056048
|
T | C | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+20821A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056048 | ||||||
| chr9:42056067
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+20802C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056067 | ||||||
| chr9:42056076
|
A | T | 1 | a0003c0011t0004g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.390+20793T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056076 | ||||||
| chr9:42056102
|
T | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+20767A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056102 | ||||||
| chr9:42056272
|
T | C | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+20597A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056272 | ||||||
| chr9:42056324
|
A | ATTT | 7 | a0002c0002t0001g0040a0002c0002t0001g0052a0002c0010t0001g0057others(4): Show | 7 | HG01952.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+20542_390+2054 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056324 | ||||||
| chr9:42056326
|
T | TTTA | 2 | a0001c0001t0002g0018a0034c0038t0002g0016 | 2 | HG01071.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.390+20540_390+2054 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056326
|
T | TTTATTA | 2 | a0004c0004t0005g0030a0005c0005t0006g0091 | 2 | HG03486.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.390+20537_390+2054 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056326
|
T | TTTATTAT others(5): Show |
1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+20531_390+2054 others(16): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056326
|
T | TTTTTTA | 4 | a0004c0004t0005g0029a0004c0004t0005g0031a0007c0016t0001g0036others(1): Show | 4 | HG00280.hp2 HG02559.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+20542_390+2054 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056326
|
T | TTTTTTAT others(2): Show |
8 | a0004c0004t0005g0032a0004c0004t0005g0034a0005c0005t0006g0073others(5): Show | 8 | HG01175.hp2 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+20542_390+2054 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056326
|
TTTA | T | 44 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(41): Show |
intron_variant | MODIFIER | c.390+20540_390+2054 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056326
|
TTTATTAT others(2): Show |
T | 2 | a0001c0001t0002g0006a0013c0021t0027g0064 | 2 | HG01081.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.390+20534_390+2054 others(13): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056326 | ||||||
| chr9:42056329
|
A | T | 19 | a0002c0002t0001g0041a0002c0002t0001g0044a0002c0002t0001g0045others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.390+20540T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056329 | ||||||
| chr9:42056332
|
A | T | 3 | a0002c0002t0024g0061a0014c0018t0001g0067a0015c0019t0001g0066 | 3 | HG02559.hp1 HG02738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.390+20537T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056332 | ||||||
| chr9:42056438
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+20431G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056438 | ||||||
| chr9:42056602
|
G | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+20267C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056602 | ||||||
| chr9:42056625
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+20244G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056625 | ||||||
| chr9:42056930
|
A | G | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.390+19939T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056930 | ||||||
| chr9:42056995
|
C | T | 4 | a0001c0012t0002g0007a0001c0012t0002g0009a0007c0009t0023g0039others(1): Show | 4 | HG01943.hp2 HG02109.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+19874G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42056995 | ||||||
| chr9:42057110
|
C | T | 1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.390+19759G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057110 | ||||||
| chr9:42057181
|
C | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.390+19688G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057181 | ||||||
| chr9:42057204
|
CT | C | 91 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.390+19664delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057204 | ||||||
| chr9:42057416
|
T | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+19453A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057416 | ||||||
| chr9:42057483
|
G | A | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+19386C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057483 | ||||||
| chr9:42057540
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+19329A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057540 | ||||||
| chr9:42057546
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+19323T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057546 | ||||||
| chr9:42057663
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+19206A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057663 | ||||||
| chr9:42057761
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+19108T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057761 | ||||||
| chr9:42057769
|
T | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+19100A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057769 | ||||||
| chr9:42057823
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+19046G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057823 | ||||||
| chr9:42057886
|
C | T | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+18983G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42057886 | ||||||
| chr9:42058109
|
A | G | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.390+18760T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058109 | ||||||
| chr9:42058188
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+18681A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058188 | ||||||
| chr9:42058287
|
C | T | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.390+18582G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058287 | ||||||
| chr9:42058302
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+18567T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058302 | ||||||
| chr9:42058332
|
CAGT | C | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+18534_390+1853 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058332 | ||||||
| chr9:42058571
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+18298A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058571 | ||||||
| chr9:42058981
|
T | TCATTGTG others(268): Show |
1 | a0004c0004t0005g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.390+17887_390+1788 others(279): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058981 | ||||||
| chr9:42058981
|
T | TCATTGTG others(270): Show |
4 | a0004c0004t0005g0030a0004c0004t0005g0031a0004c0004t0005g0032others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+17887_390+1788 others(281): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058981 | ||||||
| chr9:42058981
|
T | TCATTGTG others(271): Show |
1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.390+17887_390+1788 others(282): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42058981 | ||||||
| chr9:42059470
|
G | A | 8 | a0003c0003t0004g0081a0004c0004t0005g0029a0004c0004t0005g0030others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+17399C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42059470 | ||||||
| chr9:42059599
|
G | T | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.390+17270C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42059599 | ||||||
| chr9:42059759
|
A | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.390+17110T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42059759 | ||||||
| chr9:42059806
|
T | C | 5 | a0001c0012t0002g0007a0001c0012t0002g0009a0011c0037t0007g0008others(2): Show | 5 | HG01943.hp2 HG02083.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+17063A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42059806 | ||||||
| chr9:42060211
|
A | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.390+16658T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060211 | ||||||
| chr9:42060247
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+16622G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060247 | ||||||
| chr9:42060333
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.390+16536A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060333 | ||||||
| chr9:42060480
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+16389T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060480 | ||||||
| chr9:42060486
|
C | CT | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+16382dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060486 | ||||||
| chr9:42060498
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.390+16371A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060498 | ||||||
| chr9:42060547
|
T | G | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+16322A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060547 | ||||||
| chr9:42060654
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+16215C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060654 | ||||||
| chr9:42060905
|
T | C | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.390+15964A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060905 | ||||||
| chr9:42060973
|
G | A | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.390+15896C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42060973 | ||||||
| chr9:42061083
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+15786G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061083 | ||||||
| chr9:42061118
|
A | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+15751T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061118 | ||||||
| chr9:42061156
|
C | T | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.390+15713G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061156 | ||||||
| chr9:42061163
|
T | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+15706A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061163 | ||||||
| chr9:42061317
|
CT | C | 13 | a0001c0046t0016g0015a0002c0002t0001g0056a0004c0004t0005g0031others(10): Show | 13 | HG00280.hp2 HG01175.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.390+15551delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061317 | ||||||
| chr9:42061317
|
CTT | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.390+15550_390+1555 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061317 | ||||||
| chr9:42061325
|
T | C | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.390+15544A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061325 | ||||||
| chr9:42061326
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.390+15543A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061326 | ||||||
| chr9:42061380
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+15489G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061380 | ||||||
| chr9:42061444
|
A | G | 5 | a0001c0001t0002g0018a0001c0001t0018g0026a0006c0007t0011g0017others(2): Show | 5 | HG01071.hp2 HG02040.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+15425T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061444 | ||||||
| chr9:42061470
|
A | T | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.390+15399T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061470 | ||||||
| chr9:42061506
|
G | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+15363C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061506 | ||||||
| chr9:42061536
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+15333A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061536 | ||||||
| chr9:42061591
|
C | A | 2 | a0001c0001t0002g0022a0029c0045t0002g0019 | 2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.390+15278G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061591 | ||||||
| chr9:42061764
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.390+15105A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061764 | ||||||
| chr9:42061935
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+14934A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42061935 | ||||||
| chr9:42062049
|
C | CT | 40 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.390+14819dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062049 | ||||||
| chr9:42062049
|
C | CTT | 39 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.390+14818_390+1481 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062049 | ||||||
| chr9:42062064
|
C | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.390+14805G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062064 | ||||||
| chr9:42062129
|
C | T | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+14740G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062129 | ||||||
| chr9:42062273
|
T | G | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.390+14596A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062273 | ||||||
| chr9:42062277
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+14592G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062277 | ||||||
| chr9:42062335
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+14534G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062335 | ||||||
| chr9:42062389
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+14480T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062389 | ||||||
| chr9:42062437
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+14432T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062437 | ||||||
| chr9:42062536
|
C | G | 2 | a0004c0004t0005g0034a0028c0027t0005g0033 | 2 | NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.390+14333G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062536 | ||||||
| chr9:42062545
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+14324C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062545 | ||||||
| chr9:42062610
|
G | A | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.390+14259C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062610 | ||||||
| chr9:42062660
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.390+14209A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062660 | ||||||
| chr9:42062732
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+14137A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062732 | ||||||
| chr9:42062739
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+14130T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062739 | ||||||
| chr9:42062799
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+14070G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062799 | ||||||
| chr9:42062875
|
GT | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+13993delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062875 | ||||||
| chr9:42062897
|
C | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+13972G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42062897 | ||||||
| chr9:42063050
|
A | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+13819T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063050 | ||||||
| chr9:42063058
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.390+13811G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063058 | ||||||
| chr9:42063128
|
G | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+13741C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063128 | ||||||
| chr9:42063178
|
C | A | 14 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0096others(11): Show | 14 | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+13691G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063178 | ||||||
| chr9:42063187
|
C | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+13682G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063187 | ||||||
| chr9:42063212
|
G | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+13657C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063212 | ||||||
| chr9:42063626
|
T | C | 1 | a0002c0002t0001g0052 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.390+13243A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063626 | ||||||
| chr9:42063724
|
C | A | 2 | a0026c0025t0019g0028a0032c0039t0014g0025 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.390+13145G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063724 | ||||||
| chr9:42063885
|
C | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.390+12984G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42063885 | ||||||
| chr9:42064031
|
G | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+12838C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064031 | ||||||
| chr9:42064163
|
A | G | 1 | a0008c0006t0010g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390+12706T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064163 | ||||||
| chr9:42064325
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.390+12544A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064325 | ||||||
| chr9:42064390
|
T | C | 88 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.390+12479A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064390 | ||||||
| chr9:42064401
|
A | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+12468T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064401 | ||||||
| chr9:42064436
|
A | G | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+12433T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064436 | ||||||
| chr9:42064581
|
C | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.390+12288G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064581 | ||||||
| chr9:42064751
|
C | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+12118G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064751 | ||||||
| chr9:42064776
|
A | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+12093T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064776 | ||||||
| chr9:42064962
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+11907C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42064962 | ||||||
| chr9:42065133
|
T | A | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.390+11736A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065133 | ||||||
| chr9:42065197
|
A | G | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.390+11672T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065197 | ||||||
| chr9:42065213
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.390+11656A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065213 | ||||||
| chr9:42065252
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.390+11617C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065252 | ||||||
| chr9:42065307
|
T | A | 1 | a0002c0002t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.390+11562A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065307 | ||||||
| chr9:42065457
|
A | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+11412T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065457 | ||||||
| chr9:42065477
|
G | A | 3 | a0005c0005t0006g0076a0005c0005t0030g0092a0023c0028t0006g0084 | 3 | HG01516.hp1 HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.390+11392C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065477 | ||||||
| chr9:42065547
|
G | C | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.390+11322C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065547 | ||||||
| chr9:42065840
|
C | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+11029G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065840 | ||||||
| chr9:42065888
|
C | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+10981G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065888 | ||||||
| chr9:42065888
|
C | G | 1 | a0004c0004t0005g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.390+10981G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065888 | ||||||
| chr9:42065902
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+10967G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065902 | ||||||
| chr9:42065925
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.390+10944G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065925 | ||||||
| chr9:42065956
|
A | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+10913T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065956 | ||||||
| chr9:42065995
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+10874G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42065995 | ||||||
| chr9:42066066
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+10803G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066066 | ||||||
| chr9:42066090
|
C | T | 1 | a0006c0007t0002g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.390+10779G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066090 | ||||||
| chr9:42066125
|
A | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+10744T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066125 | ||||||
| chr9:42066182
|
A | G | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.390+10687T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066182 | ||||||
| chr9:42066222
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+10647A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066222 | ||||||
| chr9:42066246
|
T | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.390+10623A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066246 | ||||||
| chr9:42066255
|
C | A | 1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.390+10614G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066255 | ||||||
| chr9:42066388
|
C | CA | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+10480dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066388 | ||||||
| chr9:42066423
|
C | CT | 34 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.390+10445dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066423 | ||||||
| chr9:42066423
|
C | CTT | 5 | a0002c0002t0001g0065a0002c0002t0024g0061a0005c0005t0030g0092others(2): Show | 5 | HG02559.hp1 HG02738.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+10444_390+1044 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066423 | ||||||
| chr9:42066423
|
CTT | C | 38 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.390+10444_390+1044 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066423 | ||||||
| chr9:42066446
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+10423C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066446 | ||||||
| chr9:42066473
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+10396A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066473 | ||||||
| chr9:42066572
|
G | A | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.390+10297C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066572 | ||||||
| chr9:42066710
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.390+10159G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066710 | ||||||
| chr9:42066864
|
G | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.390+10005C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066864 | ||||||
| chr9:42066897
|
A | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+9972T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42066897 | ||||||
| chr9:42067041
|
G | A | 1 | a0003c0003t0008g0083 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.390+9828C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42067041 | ||||||
| chr9:42067385
|
A | C | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.390+9484T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42067385 | ||||||
| chr9:42067397
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+9472A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42067397 | ||||||
| chr9:42067492
|
C | T | 2 | a0001c0001t0017g0012a0001c0001t0031g0098 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.390+9377G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42067492 | ||||||
| chr9:42067515
|
G | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+9354C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42067515 | ||||||
| chr9:42067986
|
A | G | 1 | a0001c0001t0003g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.390+8883T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42067986 | ||||||
| chr9:42068051
|
C | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+8818G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068051 | ||||||
| chr9:42068338
|
C | T | 3 | a0002c0002t0001g0044a0002c0002t0001g0052a0002c0002t0001g0053 | 3 | NA18974.hp2 NA18998.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.390+8531G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068338 | ||||||
| chr9:42068370
|
AT | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+8498delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068370 | ||||||
| chr9:42068372
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+8497A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068372 | ||||||
| chr9:42068469
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.390+8400G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068469 | ||||||
| chr9:42068504
|
T | G | 4 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071others(1): Show | 4 | HG02486.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+8365A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068504 | ||||||
| chr9:42068918
|
A | T | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+7951T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068918 | ||||||
| chr9:42068986
|
G | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+7883C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42068986 | ||||||
| chr9:42069050
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+7819A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069050 | ||||||
| chr9:42069089
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+7780T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069089 | ||||||
| chr9:42069134
|
T | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+7735A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069134 | ||||||
| chr9:42069150
|
G | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+7719C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069150 | ||||||
| chr9:42069185
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+7684T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069185 | ||||||
| chr9:42069187
|
CAAT | C | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+7679_390+7681d others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069187 | ||||||
| chr9:42069444
|
A | T | 1 | a0008c0006t0010g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.390+7425T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069444 | ||||||
| chr9:42069654
|
A | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+7215T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069654 | ||||||
| chr9:42069762
|
T | C | 1 | a0003c0003t0008g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.390+7107A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069762 | ||||||
| chr9:42069839
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+7030C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42069839 | ||||||
| chr9:42070102
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+6767A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070102 | ||||||
| chr9:42070211
|
TTG | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+6656_390+6657d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070211 | ||||||
| chr9:42070272
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+6597G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070272 | ||||||
| chr9:42070284
|
T | C | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.390+6585A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070284 | ||||||
| chr9:42070363
|
C | A | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.390+6506G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070363 | ||||||
| chr9:42070370
|
C | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+6499G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070370 | ||||||
| chr9:42070387
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+6482C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070387 | ||||||
| chr9:42070421
|
C | T | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.390+6448G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070421 | ||||||
| chr9:42070700
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+6169C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070700 | ||||||
| chr9:42070969
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+5900A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42070969 | ||||||
| chr9:42071235
|
C | T | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390+5634G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071235 | ||||||
| chr9:42071244
|
G | A | 37 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(34): Show | 37 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.390+5625C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071244 | ||||||
| chr9:42071476
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+5393T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071476 | ||||||
| chr9:42071592
|
C | A | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.390+5277G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071592 | ||||||
| chr9:42071638
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.390+5231C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071638 | ||||||
| chr9:42071771
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.390+5098T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071771 | ||||||
| chr9:42071946
|
A | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+4923T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42071946 | ||||||
| chr9:42072072
|
A | T | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+4797T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072072 | ||||||
| chr9:42072092
|
G | T | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.390+4777C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072092 | ||||||
| chr9:42072098
|
T | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+4771A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072098 | ||||||
| chr9:42072317
|
T | C | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.390+4552A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072317 | ||||||
| chr9:42072362
|
T | TAC | 3 | a0007c0009t0023g0039a0007c0009t0025g0037a0017c0014t0001g0038 | 3 | HG02109.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.390+4505_390+4506d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072362 | ||||||
| chr9:42072400
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.390+4469A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072400 | ||||||
| chr9:42072988
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+3881A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42072988 | ||||||
| chr9:42073235
|
T | C | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.390+3634A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073235 | ||||||
| chr9:42073282
|
G | T | 4 | a0003c0003t0008g0077a0003c0003t0008g0083a0003c0003t0008g0086others(1): Show | 4 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+3587C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073282 | ||||||
| chr9:42073427
|
C | A | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.390+3442G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073427 | ||||||
| chr9:42073453
|
A | G | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.390+3416T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073453 | ||||||
| chr9:42073469
|
T | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+3400A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073469 | ||||||
| chr9:42073506
|
CT | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+3362delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073506 | ||||||
| chr9:42073563
|
A | G | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+3306T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073563 | ||||||
| chr9:42073670
|
C | T | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390+3199G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073670 | ||||||
| chr9:42073816
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+3053G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073816 | ||||||
| chr9:42073822
|
A | C | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+3047T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073822 | ||||||
| chr9:42073848
|
C | T | 2 | a0008c0006t0010g0070a0008c0006t0010g0071 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+3021G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073848 | ||||||
| chr9:42073860
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+3009C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073860 | ||||||
| chr9:42073906
|
G | A | 2 | a0005c0005t0006g0091a0022c0030t0006g0085 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.390+2963C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073906 | ||||||
| chr9:42073918
|
G | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+2951C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073918 | ||||||
| chr9:42073952
|
G | T | 84 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.390+2917C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42073952 | ||||||
| chr9:42074084
|
G | T | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+2785C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42074084 | ||||||
| chr9:42074117
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+2752T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42074117 | ||||||
| chr9:42074439
|
G | A | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+2430C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42074439 | ||||||
| chr9:42074463
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.390+2406C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42074463 | ||||||
| chr9:42074857
|
G | C | 1 | a0004c0004t0005g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.390+2012C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42074857 | ||||||
| chr9:42075004
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+1865C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075004 | ||||||
| chr9:42075125
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1744A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075125 | ||||||
| chr9:42075142
|
C | T | 6 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(3): Show | 6 | HG00323.hp1 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1727G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075142 | ||||||
| chr9:42075358
|
A | G | 3 | a0002c0010t0001g0057a0002c0010t0001g0058a0002c0023t0001g0054 | 3 | HG01952.hp1 HG02135.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.390+1511T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075358 | ||||||
| chr9:42075578
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.390+1291T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075578 | ||||||
| chr9:42075836
|
C | CTTA | 28 | a0001c0043t0015g0013a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+1030_390+1032d others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42075836
|
C | CTTATTA | 9 | a0001c0001t0003g0093a0001c0046t0016g0015a0002c0002t0001g0040others(6): Show | 9 | HG01255.hp2 HG02135.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+1027_390+1032d others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42075836
|
C | CTTATTAT others(2): Show |
24 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.390+1024_390+1032d others(11): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42075836
|
C | CTTATTAT others(5): Show |
13 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0003g0095others(10): Show | 13 | HG01516.hp2 HG01952.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.390+1021_390+1032d others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42075836
|
C | CTTATTAT others(8): Show |
6 | a0001c0001t0002g0011a0001c0001t0003g0096a0001c0001t0003g0104others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1018_390+1032d others(17): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42075836
|
C | CTTTA | 5 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0032others(2): Show | 5 | HG01175.hp2 HG03490.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+1032_390+1033i others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42075836
|
CTTA | C | 4 | a0008c0006t0010g0070a0008c0006t0010g0071a0019c0031t0028g0088others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1030_390+1032d others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42075836 | ||||||
| chr9:42076140
|
T | C | 93 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.390+729A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076140 | ||||||
| chr9:42076142
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+727G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076142 | ||||||
| chr9:42076236
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.390+633C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076236 | ||||||
| chr9:42076260
|
C | CA | 40 | a0001c0012t0002g0009a0003c0003t0004g0075a0003c0003t0004g0081others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.390+608dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076260 | ||||||
| chr9:42076260
|
C | CAA | 27 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(24): Show | 27 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.390+607_390+608dup others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076260 | ||||||
| chr9:42076320
|
G | A | 5 | a0001c0001t0003g0096a0001c0001t0003g0100a0001c0001t0003g0102others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+549C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076320 | ||||||
| chr9:42076342
|
T | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.390+527A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076342 | ||||||
| chr9:42076413
|
C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.390+456G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076413 | ||||||
| chr9:42076427
|
T | TA | 7 | a0001c0001t0003g0095a0001c0001t0003g0097a0001c0001t0003g0102others(4): Show | 7 | HG01952.hp2 HG02273.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+441dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076427 | ||||||
| chr9:42076633
|
G | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+236C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076633 | ||||||
| chr9:42076833
|
A | G | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+36T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076833 | ||||||
| chr9:42076844
|
G | C | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+25C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | 42076844 | ||||||
| chr9:42077064
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.197-2A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077064 | ||||||
| chr9:42077184
|
G | GA | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-123dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077184 | ||||||
| chr9:42077441
|
G | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.197-379C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077441 | ||||||
| chr9:42077469
|
C | T | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.197-407G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077469 | ||||||
| chr9:42077608
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-546G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077608 | ||||||
| chr9:42077752
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-690G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077752 | ||||||
| chr9:42077901
|
A | G | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.197-839T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077901 | ||||||
| chr9:42077951
|
C | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-889G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42077951 | ||||||
| chr9:42078242
|
A | G | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.197-1180T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078242 | ||||||
| chr9:42078275
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.197-1213T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078275 | ||||||
| chr9:42078395
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-1333G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078395 | ||||||
| chr9:42078428
|
C | T | 1 | a0004c0004t0005g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.197-1366G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078428 | ||||||
| chr9:42078514
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1452T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078514 | ||||||
| chr9:42078590
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1528A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078590 | ||||||
| chr9:42078676
|
A | G | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.197-1614T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078676 | ||||||
| chr9:42078691
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.197-1629A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078691 | ||||||
| chr9:42078695
|
G | C | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.197-1633C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078695 | ||||||
| chr9:42078895
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1833G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42078895 | ||||||
| chr9:42079050
|
T | C | 25 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.197-1988A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079050 | ||||||
| chr9:42079215
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-2153G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079215 | ||||||
| chr9:42079234
|
G | C | 92 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.197-2172C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079234 | ||||||
| chr9:42079250
|
G | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.197-2188C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079250 | ||||||
| chr9:42079286
|
C | A | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.197-2224G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079286 | ||||||
| chr9:42079389
|
C | G | 2 | a0007c0009t0025g0037a0017c0014t0001g0038 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.197-2327G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079389 | ||||||
| chr9:42079404
|
G | T | 2 | a0005c0005t0030g0092a0027c0026t0020g0027 | 2 | HG02109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.197-2342C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079404 | ||||||
| chr9:42079536
|
G | T | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(44): Show | 47 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.197-2474C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079536 | ||||||
| chr9:42079567
|
C | T | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197-2505G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079567 | ||||||
| chr9:42079582
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-2520G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079582 | ||||||
| chr9:42079678
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-2616G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079678 | ||||||
| chr9:42079703
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-2641C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079703 | ||||||
| chr9:42079811
|
G | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.197-2749C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42079811 | ||||||
| chr9:42080044
|
C | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197-2982G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080044 | ||||||
| chr9:42080196
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-3134G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080196 | ||||||
| chr9:42080271
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-3209G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080271 | ||||||
| chr9:42080297
|
T | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.197-3235A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080297 | ||||||
| chr9:42080447
|
A | G | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.197-3385T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080447 | ||||||
| chr9:42080483
|
G | A | 1 | a0023c0028t0006g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.197-3421C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080483 | ||||||
| chr9:42080511
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.197-3449T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080511 | ||||||
| chr9:42080561
|
G | A | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-3499C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080561 | ||||||
| chr9:42080664
|
T | TC | 85 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.197-3603dupG | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080664 | ||||||
| chr9:42080701
|
A | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.197-3639T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080701 | ||||||
| chr9:42080777
|
G | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-3715C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080777 | ||||||
| chr9:42080888
|
A | C | 35 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-3826T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42080888 | ||||||
| chr9:42081125
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-4063T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081125 | ||||||
| chr9:42081217
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-4155C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081217 | ||||||
| chr9:42081257
|
G | A | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197-4195C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081257 | ||||||
| chr9:42081304
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.197-4242G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081304 | ||||||
| chr9:42081355
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-4293C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081355 | ||||||
| chr9:42081400
|
G | C | 1 | a0003c0003t0004g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.197-4338C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081400 | ||||||
| chr9:42081406
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-4344G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081406 | ||||||
| chr9:42081420
|
A | G | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.197-4358T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081420 | ||||||
| chr9:42081470
|
T | C | 1 | a0002c0002t0012g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.197-4408A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081470 | ||||||
| chr9:42081522
|
T | C | 2 | a0009c0008t0009g0105a0009c0008t0009g0106 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.197-4460A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081522 | ||||||
| chr9:42081550
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-4488C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081550 | ||||||
| chr9:42081979
|
G | T | 1 | a0002c0002t0022g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.197-4917C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42081979 | ||||||
| chr9:42082006
|
T | C | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-4944A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082006 | ||||||
| chr9:42082072
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-5010G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082072 | ||||||
| chr9:42082076
|
C | A | 2 | a0009c0008t0009g0105a0009c0008t0009g0106 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.197-5014G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082076 | ||||||
| chr9:42082410
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-5348C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082410 | ||||||
| chr9:42082450
|
G | A | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.197-5388C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082450 | ||||||
| chr9:42082666
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-5604G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082666 | ||||||
| chr9:42082967
|
G | A | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.197-5905C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42082967 | ||||||
| chr9:42083094
|
A | G | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.197-6032T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42083094 | ||||||
| chr9:42083181
|
C | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197-6119G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42083181 | ||||||
| chr9:42083260
|
T | G | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197-6198A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42083260 | ||||||
| chr9:42083511
|
C | A | 4 | a0001c0001t0003g0099a0009c0008t0009g0105a0009c0008t0009g0106others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-6449G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42083511 | ||||||
| chr9:42083823
|
G | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.197-6761C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42083823 | ||||||
| chr9:42084191
|
C | G | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.197-7129G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084191 | ||||||
| chr9:42084207
|
A | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-7145T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084207 | ||||||
| chr9:42084343
|
G | A | 4 | a0001c0001t0003g0100a0001c0001t0003g0102a0010c0013t0003g0103others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-7281C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084343 | ||||||
| chr9:42084382
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.197-7320A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084382 | ||||||
| chr9:42084879
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-7817G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084879 | ||||||
| chr9:42084892
|
T | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.197-7830A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084892 | ||||||
| chr9:42084939
|
T | C | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.197-7877A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42084939 | ||||||
| chr9:42085045
|
A | T | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.197-7983T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085045 | ||||||
| chr9:42085311
|
G | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-8249C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085311 | ||||||
| chr9:42085314
|
C | G | 3 | a0002c0010t0001g0057a0002c0010t0001g0058a0002c0023t0001g0054 | 3 | HG01952.hp1 HG02135.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.197-8252G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085314 | ||||||
| chr9:42085453
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-8391C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085453 | ||||||
| chr9:42085539
|
T | C | 1 | a0014c0018t0001g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.197-8477A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085539 | ||||||
| chr9:42085622
|
T | C | 1 | a0002c0002t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.197-8560A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085622 | ||||||
| chr9:42085691
|
G | A | 1 | a0015c0019t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.197-8629C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085691 | ||||||
| chr9:42085784
|
T | C | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.197-8722A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085784 | ||||||
| chr9:42085790
|
G | A | 1 | a0016c0017t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.197-8728C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085790 | ||||||
| chr9:42085922
|
A | G | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.197-8860T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085922 | ||||||
| chr9:42085954
|
T | C | 1 | a0004c0004t0005g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.197-8892A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42085954 | ||||||
| chr9:42086119
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.197-9057G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086119 | ||||||
| chr9:42086136
|
G | A | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.197-9074C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086136 | ||||||
| chr9:42086245
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-9183G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086245 | ||||||
| chr9:42086301
|
T | C | 9 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0049others(6): Show | 9 | HG00140.hp2 HG00323.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-9239A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086301 | ||||||
| chr9:42086304
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.197-9242C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086304 | ||||||
| chr9:42086379
|
A | AAT | 4 | a0002c0002t0001g0044a0002c0002t0012g0051a0005c0005t0006g0076others(1): Show | 4 | HG01516.hp1 HG01934.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-9319_197-9318d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086379 | ||||||
| chr9:42086447
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-9385A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086447 | ||||||
| chr9:42086466
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-9404G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086466 | ||||||
| chr9:42086634
|
T | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.197-9572A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086634 | ||||||
| chr9:42086641
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.197-9579G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086641 | ||||||
| chr9:42086745
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-9683A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086745 | ||||||
| chr9:42086804
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-9742T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086804 | ||||||
| chr9:42086868
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-9806A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42086868 | ||||||
| chr9:42087037
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-9975C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087037 | ||||||
| chr9:42087063
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-10001A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087063 | ||||||
| chr9:42087089
|
C | A | 3 | a0007c0009t0023g0039a0007c0009t0025g0037a0017c0014t0001g0038 | 3 | HG02109.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.197-10027G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087089 | ||||||
| chr9:42087089
|
C | T | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-10027G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087089 | ||||||
| chr9:42087116
|
T | C | 8 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0018g0026others(5): Show | 8 | HG00099.hp2 HG01071.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-10054A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087116 | ||||||
| chr9:42087259
|
T | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.197-10197A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087259 | ||||||
| chr9:42087260
|
A | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-10198T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087260 | ||||||
| chr9:42087277
|
T | G | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.197-10215A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087277 | ||||||
| chr9:42087385
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-10323C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087385 | ||||||
| chr9:42087462
|
G | A | 94 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.197-10400C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087462 | ||||||
| chr9:42087708
|
G | A | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.197-10646C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42087708 | ||||||
| chr9:42088041
|
C | A | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.197-10979G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088041 | ||||||
| chr9:42088155
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-11093C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088155 | ||||||
| chr9:42088192
|
C | G | 27 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(24): Show | 27 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.197-11130G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088192 | ||||||
| chr9:42088220
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-11158A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088220 | ||||||
| chr9:42088281
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-11219G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088281 | ||||||
| chr9:42088519
|
CGTAA | C | 9 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-11461_197-1145 others(8): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088519 | ||||||
| chr9:42088603
|
T | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-11541A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088603 | ||||||
| chr9:42088835
|
G | A | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.197-11773C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088835 | ||||||
| chr9:42088870
|
T | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-11808A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088870 | ||||||
| chr9:42088946
|
G | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.197-11884C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42088946 | ||||||
| chr9:42089033
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-11971T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089033 | ||||||
| chr9:42089075
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-12013C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089075 | ||||||
| chr9:42089092
|
C | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-12030G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089092 | ||||||
| chr9:42089105
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.197-12043A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089105 | ||||||
| chr9:42089132
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-12070C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089132 | ||||||
| chr9:42089145
|
G | GAAAGGGA others(9): Show |
42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-12084_197-1208 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089145 | ||||||
| chr9:42089151
|
G | GAGA | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-12090_197-1208 others(7): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089151 | ||||||
| chr9:42089154
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-12092T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089154 | ||||||
| chr9:42089167
|
G | A | 1 | a0014c0018t0001g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.197-12105C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089167 | ||||||
| chr9:42089234
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.197-12172C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089234 | ||||||
| chr9:42089351
|
A | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.197-12289T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089351 | ||||||
| chr9:42089368
|
T | C | 3 | a0003c0003t0008g0077a0003c0003t0008g0083a0018c0024t0008g0080 | 3 | HG00140.hp1 HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.197-12306A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089368 | ||||||
| chr9:42089520
|
T | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-12458A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089520 | ||||||
| chr9:42089767
|
G | A | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.197-12705C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089767 | ||||||
| chr9:42089943
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-12881A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42089943 | ||||||
| chr9:42090093
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-13031T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090093 | ||||||
| chr9:42090100
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-13038G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090100 | ||||||
| chr9:42090164
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-13102G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090164 | ||||||
| chr9:42090176
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.197-13114C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090176 | ||||||
| chr9:42090229
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.197-13167A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090229 | ||||||
| chr9:42090613
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.197-13551C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090613 | ||||||
| chr9:42090675
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.197-13613G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090675 | ||||||
| chr9:42090675
|
CTA | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.197-13615_197-1361 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090675 | ||||||
| chr9:42090738
|
C | CAT | 89 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.197-13678_197-1367 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090738 | ||||||
| chr9:42090783
|
C | CATATGTG others(19): Show |
1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197-13722_197-1372 others(30): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(29): Show |
2 | a0001c0001t0003g0093a0001c0001t0031g0098 | 2 | HG00099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.197-13722_197-1372 others(40): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(31): Show |
1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.197-13722_197-1372 others(42): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(33): Show |
6 | a0001c0001t0003g0095a0001c0001t0003g0101a0001c0001t0003g0102others(3): Show | 6 | HG01255.hp1 HG02040.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-13722_197-1372 others(44): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(35): Show |
10 | a0001c0001t0002g0011a0001c0001t0003g0097a0001c0001t0003g0100others(7): Show | 10 | HG00642.hp2 HG01106.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-13722_197-1372 others(46): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(37): Show |
12 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(9): Show | 12 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-13722_197-1372 others(48): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(39): Show |
7 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0003g0099others(4): Show | 7 | HG01175.hp1 HG01516.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-13722_197-1372 others(50): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(45): Show |
1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.197-13722_197-1372 others(56): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(23): Show |
1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-13722_197-1372 others(34): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(27): Show |
1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-13722_197-1372 others(38): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(39): Show |
1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.197-13722_197-1372 others(50): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(25): Show |
6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-13722_197-1372 others(36): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090783
|
C | CATATGTG others(33): Show |
1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-13722_197-1372 others(44): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090783 | ||||||
| chr9:42090789
|
T | C | 5 | a0001c0001t0002g0018a0001c0001t0018g0026a0006c0007t0011g0017others(2): Show | 5 | HG01071.hp2 HG02040.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-13727A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090789 | ||||||
| chr9:42090791
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.197-13729A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090791 | ||||||
| chr9:42090810
|
C | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-13748G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090810 | ||||||
| chr9:42090840
|
T | TAC | 5 | a0005c0005t0006g0076a0008c0006t0010g0069a0008c0006t0010g0070others(2): Show | 5 | HG01516.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-13780_197-1377 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090840 | ||||||
| chr9:42090840
|
TAC | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.197-13780_197-1377 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090840 | ||||||
| chr9:42090840
|
TACACAC | T | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+13783_197-1377 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090840 | ||||||
| chr9:42090932
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+13697C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090932 | ||||||
| chr9:42090961
|
A | AAT | 7 | a0007c0016t0001g0036a0008c0006t0010g0069a0008c0006t0010g0070others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+13666_196+1366 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090961 | ||||||
| chr9:42090971
|
T | TAC | 5 | a0004c0004t0005g0029a0004c0004t0005g0031a0004c0004t0005g0032others(2): Show | 5 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+13657_196+1365 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090971 | ||||||
| chr9:42090973
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+13656A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090973 | ||||||
| chr9:42090973
|
T | TATACAC | 2 | a0005c0005t0006g0073a0019c0031t0028g0088 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.196+13655_196+1365 others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090973 | ||||||
| chr9:42090973
|
TAC | T | 16 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0022others(13): Show | 16 | HG00642.hp2 HG01071.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+13654_196+1365 others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090973 | ||||||
| chr9:42090975
|
C | T | 65 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.196+13654G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090975 | ||||||
| chr9:42090977
|
C | T | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.196+13652G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090977 | ||||||
| chr9:42090979
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+13650G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090979 | ||||||
| chr9:42090981
|
C | T | 7 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0018g0026others(4): Show | 7 | HG01071.hp2 HG02040.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+13648G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090981 | ||||||
| chr9:42090983
|
C | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.196+13646G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42090983 | ||||||
| chr9:42091021
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+13608G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091021 | ||||||
| chr9:42091063
|
T | A | 1 | a0002c0010t0001g0058 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.196+13566A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091063 | ||||||
| chr9:42091095
|
T | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+13534A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091095 | ||||||
| chr9:42091460
|
C | T | 3 | a0001c0001t0002g0018a0006c0007t0011g0017a0006c0007t0011g0021 | 3 | HG01071.hp2 HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.196+13169G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091460 | ||||||
| chr9:42091503
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.196+13126G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091503 | ||||||
| chr9:42091671
|
T | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+12958A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091671 | ||||||
| chr9:42091736
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196+12893G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091736 | ||||||
| chr9:42091868
|
A | T | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.196+12761T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091868 | ||||||
| chr9:42091880
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+12749T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42091880 | ||||||
| chr9:42092221
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+12408C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092221 | ||||||
| chr9:42092290
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+12339C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092290 | ||||||
| chr9:42092575
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+12054G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092575 | ||||||
| chr9:42092577
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+12052T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092577 | ||||||
| chr9:42092745
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+11884C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092745 | ||||||
| chr9:42092828
|
G | A | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.196+11801C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092828 | ||||||
| chr9:42092881
|
T | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+11748A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42092881 | ||||||
| chr9:42093065
|
T | A | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196+11564A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093065 | ||||||
| chr9:42093068
|
C | T | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196+11561G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093068 | ||||||
| chr9:42093074
|
C | T | 1 | a0001c0001t0003g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.196+11555G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093074 | ||||||
| chr9:42093085
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+11544T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093085 | ||||||
| chr9:42093217
|
A | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+11412T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093217 | ||||||
| chr9:42093218
|
C | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+11411G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093218 | ||||||
| chr9:42093277
|
G | A | 1 | a0029c0045t0002g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196+11352C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093277 | ||||||
| chr9:42093302
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+11327C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093302 | ||||||
| chr9:42093355
|
C | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+11274G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093355 | ||||||
| chr9:42093371
|
T | TA | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+11257dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093371 | ||||||
| chr9:42093372
|
A | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196+11257T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093372 | ||||||
| chr9:42093380
|
A | AG | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+11248_196+1124 others(5): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093380 | ||||||
| chr9:42093385
|
T | C | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196+11244A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093385 | ||||||
| chr9:42093480
|
G | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+11149C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093480 | ||||||
| chr9:42093537
|
A | G | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+11092T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093537 | ||||||
| chr9:42093741
|
T | C | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.196+10888A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093741 | ||||||
| chr9:42093764
|
A | T | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.196+10865T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093764 | ||||||
| chr9:42093878
|
C | G | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.196+10751G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42093878 | ||||||
| chr9:42094023
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+10606A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094023 | ||||||
| chr9:42094060
|
G | T | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.196+10569C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094060 | ||||||
| chr9:42094108
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.196+10521A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094108 | ||||||
| chr9:42094154
|
A | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+10475T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094154 | ||||||
| chr9:42094197
|
C | T | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196+10432G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094197 | ||||||
| chr9:42094347
|
TA | T | 5 | a0006c0007t0011g0021a0007c0009t0023g0039a0007c0009t0025g0037others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+10281delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094347 | ||||||
| chr9:42094369
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+10260G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094369 | ||||||
| chr9:42094417
|
A | C | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.196+10212T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094417 | ||||||
| chr9:42094417
|
A | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+10212T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094417 | ||||||
| chr9:42094582
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+10047C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094582 | ||||||
| chr9:42094613
|
G | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+10016C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094613 | ||||||
| chr9:42094633
|
G | A | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196+9996C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094633 | ||||||
| chr9:42094715
|
CAAGG | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+9910_196+9913d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094715 | ||||||
| chr9:42094744
|
A | AAGGG | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+9881_196+9884d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42094744 | ||||||
| chr9:42095043
|
TTC | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+9584_196+9585d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095043 | ||||||
| chr9:42095181
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9448A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095181 | ||||||
| chr9:42095193
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.196+9436C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095193 | ||||||
| chr9:42095193
|
G | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9436C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095193 | ||||||
| chr9:42095209
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9420A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095209 | ||||||
| chr9:42095222
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9407A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095222 | ||||||
| chr9:42095370
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9259G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095370 | ||||||
| chr9:42095526
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9103A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095526 | ||||||
| chr9:42095602
|
A | G | 1 | a0001c0001t0003g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.196+9027T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095602 | ||||||
| chr9:42095729
|
G | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+8900C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095729 | ||||||
| chr9:42095755
|
C | T | 2 | a0001c0001t0017g0012a0001c0001t0031g0098 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.196+8874G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095755 | ||||||
| chr9:42095928
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+8701C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095928 | ||||||
| chr9:42095930
|
C | T | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+8699G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095930 | ||||||
| chr9:42095973
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.196+8656G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42095973 | ||||||
| chr9:42096088
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+8541C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096088 | ||||||
| chr9:42096119
|
C | T | 2 | a0002c0002t0001g0065a0013c0021t0027g0064 | 2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.196+8510G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096119 | ||||||
| chr9:42096145
|
T | C | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+8484A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096145 | ||||||
| chr9:42096162
|
C | T | 1 | a0003c0011t0004g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.196+8467G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096162 | ||||||
| chr9:42096164
|
G | A | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.196+8465C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096164 | ||||||
| chr9:42096185
|
C | A | 1 | a0022c0030t0006g0085 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.196+8444G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096185 | ||||||
| chr9:42096244
|
C | T | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.196+8385G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096244 | ||||||
| chr9:42096258
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+8371G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096258 | ||||||
| chr9:42096259
|
G | A | 29 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.196+8370C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096259 | ||||||
| chr9:42096502
|
G | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+8127C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096502 | ||||||
| chr9:42096706
|
T | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+7923A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096706 | ||||||
| chr9:42096780
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+7849G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096780 | ||||||
| chr9:42096999
|
G | A | 4 | a0003c0003t0008g0077a0003c0003t0008g0083a0003c0003t0008g0086others(1): Show | 4 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+7630C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42096999 | ||||||
| chr9:42097097
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+7532G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097097 | ||||||
| chr9:42097290
|
C | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+7339G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097290 | ||||||
| chr9:42097291
|
C | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+7338G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097291 | ||||||
| chr9:42097332
|
G | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.196+7297C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097332 | ||||||
| chr9:42097582
|
T | C | 1 | a0001c0012t0002g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.196+7047A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097582 | ||||||
| chr9:42097936
|
G | A | 1 | a0001c0001t0017g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.196+6693C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097936 | ||||||
| chr9:42097998
|
G | A | 33 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+6631C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42097998 | ||||||
| chr9:42098022
|
T | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+6607A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098022 | ||||||
| chr9:42098031
|
C | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.196+6598G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098031 | ||||||
| chr9:42098161
|
G | A | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.196+6468C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098161 | ||||||
| chr9:42098234
|
T | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+6395A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098234 | ||||||
| chr9:42098339
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+6290G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098339 | ||||||
| chr9:42098353
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+6276G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098353 | ||||||
| chr9:42098417
|
CA | C | 42 | a0001c0001t0003g0102a0002c0002t0001g0040a0002c0002t0001g0041others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.196+6211delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098417 | ||||||
| chr9:42098417
|
CAA | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.196+6210_196+6211d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098417 | ||||||
| chr9:42098439
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+6190G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098439 | ||||||
| chr9:42098444
|
A | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+6185T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098444 | ||||||
| chr9:42098538
|
A | G | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.196+6091T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098538 | ||||||
| chr9:42098570
|
G | A | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196+6059C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098570 | ||||||
| chr9:42098582
|
C | CA | 83 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.196+6046dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098582 | ||||||
| chr9:42098582
|
C | CAA | 4 | a0006c0007t0011g0017a0008c0006t0010g0070a0009c0008t0009g0106others(1): Show | 4 | HG00735.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+6045_196+6046d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098582 | ||||||
| chr9:42098599
|
C | A | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.196+6030G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098599 | ||||||
| chr9:42098606
|
C | CA | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+6022dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098606 | ||||||
| chr9:42098648
|
A | AC | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+5980_196+5981i others(3): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098648 | ||||||
| chr9:42098810
|
T | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+5819A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098810 | ||||||
| chr9:42098855
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+5774C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098855 | ||||||
| chr9:42098937
|
A | G | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196+5692T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098937 | ||||||
| chr9:42098975
|
C | T | 7 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0018g0026others(4): Show | 7 | HG01071.hp2 HG01175.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+5654G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098975 | ||||||
| chr9:42098982
|
G | A | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.196+5647C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42098982 | ||||||
| chr9:42099026
|
T | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+5603A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099026 | ||||||
| chr9:42099117
|
G | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+5512C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099117 | ||||||
| chr9:42099208
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+5421A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099208 | ||||||
| chr9:42099359
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+5270G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099359 | ||||||
| chr9:42099416
|
C | T | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.196+5213G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099416 | ||||||
| chr9:42099627
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+5002T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099627 | ||||||
| chr9:42099803
|
C | T | 51 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.196+4826G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099803 | ||||||
| chr9:42099830
|
T | C | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196+4799A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099830 | ||||||
| chr9:42099863
|
C | T | 94 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.196+4766G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099863 | ||||||
| chr9:42099955
|
G | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+4674C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42099955 | ||||||
| chr9:42100096
|
G | A | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.196+4533C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100096 | ||||||
| chr9:42100117
|
C | A | 4 | a0003c0003t0008g0077a0003c0003t0008g0083a0003c0003t0008g0086others(1): Show | 4 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+4512G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100117 | ||||||
| chr9:42100118
|
C | A | 4 | a0003c0003t0008g0077a0003c0003t0008g0083a0003c0003t0008g0086others(1): Show | 4 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+4511G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100118 | ||||||
| chr9:42100177
|
C | T | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196+4452G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100177 | ||||||
| chr9:42100179
|
C | A | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.196+4450G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100179 | ||||||
| chr9:42100239
|
C | CAT | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+4389_196+4390i others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100239 | ||||||
| chr9:42100316
|
T | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+4313A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100316 | ||||||
| chr9:42100394
|
T | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.196+4235A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100394 | ||||||
| chr9:42100584
|
T | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+4045A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100584 | ||||||
| chr9:42100658
|
C | A | 1 | a0006c0041t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.196+3971G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100658 | ||||||
| chr9:42100796
|
T | G | 1 | a0011c0040t0007g0003 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.196+3833A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42100796 | ||||||
| chr9:42101196
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+3433C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101196 | ||||||
| chr9:42101219
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+3410T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101219 | ||||||
| chr9:42101225
|
C | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+3404G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101225 | ||||||
| chr9:42101361
|
C | A | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196+3268G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101361 | ||||||
| chr9:42101822
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.196+2807C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101822 | ||||||
| chr9:42101840
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+2789G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101840 | ||||||
| chr9:42101925
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+2704G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101925 | ||||||
| chr9:42101962
|
A | C | 88 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.196+2667T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101962 | ||||||
| chr9:42101980
|
T | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+2649A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101980 | ||||||
| chr9:42101988
|
C | A | 1 | a0033c0036t0007g0010 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.196+2641G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101988 | ||||||
| chr9:42101988
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+2641G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42101988 | ||||||
| chr9:42102056
|
G | GATAA | 7 | a0003c0003t0004g0082a0003c0011t0004g0078a0006c0007t0002g0014others(4): Show | 7 | HG00558.hp2 HG01255.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+2569_196+2572d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102056 | ||||||
| chr9:42102056
|
GATAAATA others(1): Show |
G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+2565_196+2572d others(10): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102056 | ||||||
| chr9:42102056
|
GATAAATA others(5): Show |
G | 28 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.196+2561_196+2572d others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102056 | ||||||
| chr9:42102100
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+2529A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102100 | ||||||
| chr9:42102333
|
G | A | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.196+2296C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102333 | ||||||
| chr9:42102387
|
C | T | 1 | a0002c0002t0001g0047 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+2242G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102387 | ||||||
| chr9:42102536
|
T | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.196+2093A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102536 | ||||||
| chr9:42102616
|
C | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+2013G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102616 | ||||||
| chr9:42102797
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.196+1832G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102797 | ||||||
| chr9:42102851
|
C | T | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+1778G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102851 | ||||||
| chr9:42102881
|
T | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+1748A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102881 | ||||||
| chr9:42102915
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196+1714A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102915 | ||||||
| chr9:42102962
|
A | G | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+1667T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42102962 | ||||||
| chr9:42103232
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+1397G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103232 | ||||||
| chr9:42103418
|
T | TA | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.196+1210dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103418 | ||||||
| chr9:42103418
|
T | TAA | 16 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0018g0026others(13): Show | 16 | HG00735.hp1 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.196+1209_196+1210d others(4): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103418 | ||||||
| chr9:42103418
|
T | TAAAA | 5 | a0004c0004t0005g0029a0004c0004t0005g0031a0004c0004t0005g0032others(2): Show | 5 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+1207_196+1210d others(6): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103418 | ||||||
| chr9:42103462
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+1167C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103462 | ||||||
| chr9:42103521
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+1108T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103521 | ||||||
| chr9:42103559
|
T | TA | 8 | a0002c0010t0001g0058a0003c0003t0008g0083a0005c0005t0006g0091others(5): Show | 8 | HG00642.hp1 HG02622.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+1069dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103559 | ||||||
| chr9:42103559
|
TA | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.196+1069delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103559 | ||||||
| chr9:42103649
|
T | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+980A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103649 | ||||||
| chr9:42103698
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.196+931C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103698 | ||||||
| chr9:42103727
|
T | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.196+902A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103727 | ||||||
| chr9:42103734
|
C | CA | 9 | a0002c0002t0001g0065a0004c0004t0005g0029a0004c0004t0005g0030others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+894dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103734 | ||||||
| chr9:42103956
|
T | C | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196+673A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42103956 | ||||||
| chr9:42104295
|
TA | T | 84 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.196+333delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42104295 | ||||||
| chr9:42104297
|
A | G | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196+332T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42104297 | ||||||
| chr9:42104359
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+270C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | 42104359 | ||||||
| chr9:42104962
|
G | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-223C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42104962 | ||||||
| chr9:42104974
|
T | A | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.86-235A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42104974 | ||||||
| chr9:42105209
|
A | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-470T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105209 | ||||||
| chr9:42105266
|
G | A | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.86-527C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105266 | ||||||
| chr9:42105450
|
C | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-711G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105450 | ||||||
| chr9:42105465
|
T | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.86-726A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105465 | ||||||
| chr9:42105472
|
C | A | 2 | a0014c0018t0001g0067a0015c0019t0001g0066 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.86-733G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105472 | ||||||
| chr9:42105575
|
C | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-836G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105575 | ||||||
| chr9:42105584
|
C | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-845G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105584 | ||||||
| chr9:42105590
|
G | T | 1 | a0009c0008t0009g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.86-851C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105590 | ||||||
| chr9:42105609
|
A | G | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.86-870T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105609 | ||||||
| chr9:42105627
|
C | T | 1 | a0001c0043t0015g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.86-888G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105627 | ||||||
| chr9:42105714
|
A | T | 1 | a0001c0001t0031g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.86-975T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105714 | ||||||
| chr9:42105720
|
A | T | 1 | a0006c0007t0011g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.86-981T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105720 | ||||||
| chr9:42105760
|
G | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-1021C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105760 | ||||||
| chr9:42105963
|
T | A | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.86-1224A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42105963 | ||||||
| chr9:42106072
|
C | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-1333G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106072 | ||||||
| chr9:42106157
|
A | G | 9 | a0003c0003t0004g0081a0003c0003t0004g0082a0003c0003t0008g0077others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-1418T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106157 | ||||||
| chr9:42106169
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.86-1430T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106169 | ||||||
| chr9:42106311
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-1572G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106311 | ||||||
| chr9:42106375
|
AT | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-1637delA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106375 | ||||||
| chr9:42106668
|
C | T | 1 | a0015c0019t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.86-1929G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106668 | ||||||
| chr9:42106685
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.86-1946C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106685 | ||||||
| chr9:42106795
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-2056C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106795 | ||||||
| chr9:42106976
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.86-2237A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42106976 | ||||||
| chr9:42107017
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-2278G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107017 | ||||||
| chr9:42107022
|
A | G | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.86-2283T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107022 | ||||||
| chr9:42107029
|
C | A | 1 | a0010c0013t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.86-2290G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107029 | ||||||
| chr9:42107101
|
G | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-2362C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107101 | ||||||
| chr9:42107156
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.86-2417G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107156 | ||||||
| chr9:42107173
|
A | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-2434T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107173 | ||||||
| chr9:42107264
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-2525G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107264 | ||||||
| chr9:42107305
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-2566A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107305 | ||||||
| chr9:42107362
|
C | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.86-2623G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107362 | ||||||
| chr9:42107364
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-2625C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107364 | ||||||
| chr9:42107656
|
C | T | 2 | a0007c0009t0025g0037a0017c0014t0001g0038 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.86-2917G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107656 | ||||||
| chr9:42107803
|
G | A | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.86-3064C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107803 | ||||||
| chr9:42107933
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-3194G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107933 | ||||||
| chr9:42107944
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-3205A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107944 | ||||||
| chr9:42107959
|
A | G | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.86-3220T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107959 | ||||||
| chr9:42107974
|
TA | T | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.86-3236delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42107974 | ||||||
| chr9:42108270
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-3531G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108270 | ||||||
| chr9:42108309
|
G | A | 7 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0018g0026others(4): Show | 7 | HG01071.hp2 HG01175.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-3570C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108309 | ||||||
| chr9:42108523
|
G | C | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-3784C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108523 | ||||||
| chr9:42108552
|
G | C | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.86-3813C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108552 | ||||||
| chr9:42108683
|
C | T | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.86-3944G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108683 | ||||||
| chr9:42108693
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-3954A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108693 | ||||||
| chr9:42108761
|
G | C | 1 | a0001c0001t0002g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.86-4022C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108761 | ||||||
| chr9:42108770
|
C | G | 4 | a0002c0002t0001g0065a0002c0002t0012g0043a0002c0002t0012g0051others(1): Show | 4 | HG01071.hp1 HG03942.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-4031G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108770 | ||||||
| chr9:42108864
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-4125C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108864 | ||||||
| chr9:42108967
|
A | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-4228T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42108967 | ||||||
| chr9:42109330
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-4591T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109330 | ||||||
| chr9:42109356
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-4617G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109356 | ||||||
| chr9:42109357
|
G | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-4618C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109357 | ||||||
| chr9:42109442
|
G | GA | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-4704dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109442 | ||||||
| chr9:42109454
|
G | T | 1 | a0031c0044t0009g0094 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.86-4715C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109454 | ||||||
| chr9:42109568
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.86-4829C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109568 | ||||||
| chr9:42109585
|
C | T | 1 | a0002c0023t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.86-4846G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109585 | ||||||
| chr9:42109596
|
T | C | 1 | a0014c0018t0001g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86-4857A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109596 | ||||||
| chr9:42109599
|
G | A | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.86-4860C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109599 | ||||||
| chr9:42109956
|
C | T | 5 | a0001c0001t0002g0018a0001c0001t0018g0026a0006c0007t0011g0017others(2): Show | 5 | HG01071.hp2 HG02040.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-5217G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42109956 | ||||||
| chr9:42110057
|
C | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-5318G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110057 | ||||||
| chr9:42110137
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.86-5398C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110137 | ||||||
| chr9:42110156
|
C | CTG | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-5418_86-5417ins others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110156 | ||||||
| chr9:42110220
|
T | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-5481A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110220 | ||||||
| chr9:42110319
|
G | A | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.86-5580C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110319 | ||||||
| chr9:42110441
|
C | T | 7 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0018g0026others(4): Show | 7 | HG01071.hp2 HG01175.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-5702G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110441 | ||||||
| chr9:42110447
|
A | C | 1 | a0028c0027t0005g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.86-5708T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110447 | ||||||
| chr9:42110531
|
TA | T | 43 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(40): Show | 43 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.86-5793delT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110531 | ||||||
| chr9:42110685
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-5946C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110685 | ||||||
| chr9:42110702
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-5963A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110702 | ||||||
| chr9:42110736
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.86-5997G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110736 | ||||||
| chr9:42110766
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.86-6027C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110766 | ||||||
| chr9:42110910
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-6171A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42110910 | ||||||
| chr9:42111122
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-6383A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111122 | ||||||
| chr9:42111236
|
C | T | 1 | a0015c0019t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.86-6497G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111236 | ||||||
| chr9:42111333
|
T | C | 1 | a0002c0015t0001g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.86-6594A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111333 | ||||||
| chr9:42111461
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-6722C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111461 | ||||||
| chr9:42111485
|
C | T | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.86-6746G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111485 | ||||||
| chr9:42111537
|
G | T | 7 | a0002c0002t0001g0044a0002c0002t0001g0052a0002c0002t0001g0053others(4): Show | 7 | HG01071.hp1 HG03942.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-6798C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111537 | ||||||
| chr9:42111770
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-7031C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111770 | ||||||
| chr9:42111831
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-7092C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111831 | ||||||
| chr9:42111831
|
G | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-7092C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42111831 | ||||||
| chr9:42112189
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-7450G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112189 | ||||||
| chr9:42112238
|
C | T | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.86-7499G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112238 | ||||||
| chr9:42112494
|
A | G | 1 | a0024c0029t0006g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.86-7755T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112494 | ||||||
| chr9:42112586
|
T | C | 5 | a0001c0001t0002g0018a0001c0001t0018g0026a0006c0007t0011g0017others(2): Show | 5 | HG01071.hp2 HG02040.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-7847A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112586 | ||||||
| chr9:42112644
|
C | T | 1 | a0008c0006t0010g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.86-7905G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112644 | ||||||
| chr9:42112868
|
G | GT | 5 | a0001c0001t0002g0006a0002c0002t0001g0049a0002c0002t0022g0068others(2): Show | 5 | HG01081.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-8130dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112868 | ||||||
| chr9:42112868
|
G | GTT | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.86-8131_86-8130dup others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112868 | ||||||
| chr9:42112868
|
G | GTTT | 7 | a0001c0046t0016g0015a0004c0004t0005g0029a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-8132_86-8130dup others(3): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112868 | ||||||
| chr9:42112893
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-8154C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112893 | ||||||
| chr9:42112946
|
G | T | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.86-8207C>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112946 | ||||||
| chr9:42112967
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-8228T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112967 | ||||||
| chr9:42112971
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-8232T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112971 | ||||||
| chr9:42112991
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-8252C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42112991 | ||||||
| chr9:42113051
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.86-8312C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113051 | ||||||
| chr9:42113087
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.86-8348G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113087 | ||||||
| chr9:42113228
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-8489C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113228 | ||||||
| chr9:42113236
|
C | G | 2 | a0005c0005t0006g0091a0022c0030t0006g0085 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.86-8497G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113236 | ||||||
| chr9:42113540
|
T | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-8801A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113540 | ||||||
| chr9:42113626
|
C | T | 1 | a0002c0020t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.86-8887G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113626 | ||||||
| chr9:42113790
|
G | A | 9 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0024others(6): Show | 9 | HG01943.hp2 HG02056.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-9051C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113790 | ||||||
| chr9:42113816
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.86-9077C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113816 | ||||||
| chr9:42113879
|
T | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.86-9140A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113879 | ||||||
| chr9:42113958
|
T | TA | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-9220dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42113958 | ||||||
| chr9:42114130
|
G | A | 1 | a0021c0032t0004g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.86-9391C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114130 | ||||||
| chr9:42114145
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-9406A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114145 | ||||||
| chr9:42114213
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-9474T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114213 | ||||||
| chr9:42114286
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-9547G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114286 | ||||||
| chr9:42114349
|
C | T | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.86-9610G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114349 | ||||||
| chr9:42114357
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-9618C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114357 | ||||||
| chr9:42114400
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.86-9661C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114400 | ||||||
| chr9:42114507
|
T | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.86-9768A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114507 | ||||||
| chr9:42114536
|
C | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-9797G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114536 | ||||||
| chr9:42114629
|
A | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-9890T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114629 | ||||||
| chr9:42114777
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-10038C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114777 | ||||||
| chr9:42114865
|
C | T | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-10126G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114865 | ||||||
| chr9:42114887
|
T | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.86-10148A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114887 | ||||||
| chr9:42114922
|
C | T | 2 | a0001c0001t0002g0022a0029c0045t0002g0019 | 2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.86-10183G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42114922 | ||||||
| chr9:42115027
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.86-10288G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115027 | ||||||
| chr9:42115162
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.86-10423A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115162 | ||||||
| chr9:42115213
|
C | T | 1 | a0005c0005t0030g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.86-10474G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115213 | ||||||
| chr9:42115311
|
C | T | 29 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-10572G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115311 | ||||||
| chr9:42115374
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-10635G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115374 | ||||||
| chr9:42115433
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-10694G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115433 | ||||||
| chr9:42115438
|
G | A | 2 | a0005c0005t0006g0073a0024c0029t0006g0087 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.86-10699C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115438 | ||||||
| chr9:42115563
|
C | T | 1 | a0002c0002t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.86-10824G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115563 | ||||||
| chr9:42115578
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-10839A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115578 | ||||||
| chr9:42115583
|
G | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-10844C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115583 | ||||||
| chr9:42115604
|
T | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-10865A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115604 | ||||||
| chr9:42115610
|
C | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-10871G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115610 | ||||||
| chr9:42115718
|
C | T | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-10979G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115718 | ||||||
| chr9:42115737
|
T | C | 4 | a0007c0009t0023g0039a0007c0009t0025g0037a0007c0016t0001g0036others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-10998A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115737 | ||||||
| chr9:42115801
|
C | T | 2 | a0002c0002t0001g0040a0002c0020t0001g0060 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.86-11062G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115801 | ||||||
| chr9:42115802
|
A | G | 88 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.86-11063T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115802 | ||||||
| chr9:42115842
|
C | T | 3 | a0001c0001t0003g0095a0001c0001t0003g0097a0001c0001t0003g0104 | 3 | HG01952.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.86-11103G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115842 | ||||||
| chr9:42115922
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-11183C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115922 | ||||||
| chr9:42115984
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.86-11245G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42115984 | ||||||
| chr9:42116008
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-11269G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116008 | ||||||
| chr9:42116035
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-11296C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116035 | ||||||
| chr9:42116040
|
T | C | 8 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-11301A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116040 | ||||||
| chr9:42116076
|
C | G | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.86-11337G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116076 | ||||||
| chr9:42116096
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-11357C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116096 | ||||||
| chr9:42116317
|
C | T | 29 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-11578G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116317 | ||||||
| chr9:42116321
|
T | G | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.86-11582A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116321 | ||||||
| chr9:42116655
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-11916A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116655 | ||||||
| chr9:42116710
|
T | C | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-11971A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116710 | ||||||
| chr9:42116720
|
C | T | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-11981G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116720 | ||||||
| chr9:42116759
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.86-12020C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116759 | ||||||
| chr9:42116829
|
G | A | 2 | a0005c0005t0006g0076a0023c0028t0006g0084 | 2 | HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.86-12090C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116829 | ||||||
| chr9:42116857
|
A | G | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.86-12118T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116857 | ||||||
| chr9:42116858
|
A | C | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.86-12119T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42116858 | ||||||
| chr9:42117074
|
T | C | 1 | a0001c0001t0017g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.85+11936A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117074 | ||||||
| chr9:42117081
|
T | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+11929A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117081 | ||||||
| chr9:42117115
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+11895T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117115 | ||||||
| chr9:42117175
|
C | A | 1 | a0034c0038t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.85+11835G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117175 | ||||||
| chr9:42117217
|
T | C | 1 | a0006c0007t0011g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.85+11793A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117217 | ||||||
| chr9:42117382
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.85+11628A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117382 | ||||||
| chr9:42117387
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+11623C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117387 | ||||||
| chr9:42117400
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+11610G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117400 | ||||||
| chr9:42117788
|
A | T | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+11222T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117788 | ||||||
| chr9:42117853
|
C | T | 1 | a0006c0007t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.85+11157G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117853 | ||||||
| chr9:42117876
|
C | T | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85+11134G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117876 | ||||||
| chr9:42117979
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+11031T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42117979 | ||||||
| chr9:42118042
|
A | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+10968T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118042 | ||||||
| chr9:42118107
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+10903T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118107 | ||||||
| chr9:42118139
|
C | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.85+10871G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118139 | ||||||
| chr9:42118162
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+10848G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118162 | ||||||
| chr9:42118174
|
T | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+10836A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118174 | ||||||
| chr9:42118375
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.85+10635G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118375 | ||||||
| chr9:42118530
|
A | C | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85+10480T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118530 | ||||||
| chr9:42118672
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+10338A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118672 | ||||||
| chr9:42118830
|
T | TCAAAATC others(24): Show |
17 | a0002c0002t0001g0041a0002c0002t0001g0047a0002c0002t0001g0048others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.85+10149_85+10179d others(33): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
T | TCAAAATC others(55): Show |
5 | a0002c0002t0001g0040a0002c0002t0001g0059a0002c0002t0022g0068others(2): Show | 5 | HG02083.hp2 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+10118_85+10179d others(64): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
T | TCAAAATC others(86): Show |
1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.85+10087_85+10179d others(95): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(24): Show |
T | 8 | a0002c0002t0001g0063a0003c0011t0004g0078a0005c0005t0006g0073others(5): Show | 8 | HG01934.hp2 HG02056.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+10149_85+10179d others(33): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(55): Show |
T | 4 | a0014c0018t0001g0067a0015c0019t0001g0066a0017c0014t0001g0038others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+10118_85+10179d others(64): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(86): Show |
T | 9 | a0001c0001t0002g0024a0001c0001t0003g0104a0001c0043t0015g0013others(6): Show | 9 | HG00558.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.85+10087_85+10179d others(95): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(117): Show |
T | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.85+10056_85+10179d others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(148): Show |
T | 3 | a0001c0001t0003g0096a0001c0042t0013g0001a0034c0038t0002g0016 | 3 | HG00280.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.85+10025_85+10179d others(2): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(210): Show |
T | 5 | a0004c0004t0005g0030a0004c0004t0005g0031a0004c0004t0005g0032others(2): Show | 5 | HG00280.hp2 HG01175.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+9963_85+10179de others(1): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118830
|
TCAAAATC others(241): Show |
T | 2 | a0004c0004t0005g0029a0011c0040t0007g0003 | 2 | HG03490.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.85+9932_85+10179de others(1): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118830 | ||||||
| chr9:42118898
|
T | A | 1 | a0007c0009t0025g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.85+10112A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118898 | ||||||
| chr9:42118929
|
T | A | 1 | a0017c0014t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85+10081A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118929 | ||||||
| chr9:42118960
|
T | A | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+10050A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118960 | ||||||
| chr9:42118972
|
A | G | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.85+10038T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118972 | ||||||
| chr9:42118991
|
T | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85+10019A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42118991 | ||||||
| chr9:42119003
|
A | G | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.85+10007T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119003 | ||||||
| chr9:42119110
|
C | G | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85+9900G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119110 | ||||||
| chr9:42119199
|
A | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+9811T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119199 | ||||||
| chr9:42119200
|
G | A | 7 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(4): Show | 7 | HG00280.hp2 HG01175.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+9810C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119200 | ||||||
| chr9:42119442
|
C | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+9568G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119442 | ||||||
| chr9:42119514
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+9496T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119514 | ||||||
| chr9:42119528
|
C | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.85+9482G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119528 | ||||||
| chr9:42119550
|
G | A | 1 | a0003c0003t0004g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.85+9460C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119550 | ||||||
| chr9:42119554
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+9456C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119554 | ||||||
| chr9:42119613
|
C | T | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+9397G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119613 | ||||||
| chr9:42119894
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.85+9116G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42119894 | ||||||
| chr9:42120032
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+8978T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120032 | ||||||
| chr9:42120324
|
C | T | 1 | a0001c0046t0016g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85+8686G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120324 | ||||||
| chr9:42120358
|
C | G | 1 | a0031c0044t0009g0094 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.85+8652G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120358 | ||||||
| chr9:42120416
|
A | C | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85+8594T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120416 | ||||||
| chr9:42120416
|
A | G | 2 | a0003c0003t0021g0035a0016c0017t0001g0042 | 2 | HG01081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.85+8594T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120416 | ||||||
| chr9:42120603
|
A | C | 1 | a0013c0021t0027g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.85+8407T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120603 | ||||||
| chr9:42120715
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+8295A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120715 | ||||||
| chr9:42120743
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+8267C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120743 | ||||||
| chr9:42120754
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.85+8256A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120754 | ||||||
| chr9:42120902
|
C | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.85+8108G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120902 | ||||||
| chr9:42120936
|
C | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.85+8074G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42120936 | ||||||
| chr9:42121071
|
G | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+7939C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121071 | ||||||
| chr9:42121145
|
T | A | 1 | a0002c0020t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.85+7865A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121145 | ||||||
| chr9:42121191
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+7819G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121191 | ||||||
| chr9:42121309
|
C | T | 3 | a0009c0008t0009g0105a0009c0008t0009g0106a0009c0008t0009g0107 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.85+7701G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121309 | ||||||
| chr9:42121427
|
T | A | 1 | a0007c0009t0023g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85+7583A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121427 | ||||||
| chr9:42121557
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+7453C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121557 | ||||||
| chr9:42121568
|
T | C | 1 | a0001c0001t0018g0026 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.85+7442A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121568 | ||||||
| chr9:42121747
|
C | T | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.85+7263G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121747 | ||||||
| chr9:42121961
|
C | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.85+7049G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42121961 | ||||||
| chr9:42122104
|
T | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.85+6906A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122104 | ||||||
| chr9:42122313
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+6697T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122313 | ||||||
| chr9:42122490
|
A | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+6520T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122490 | ||||||
| chr9:42122509
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+6501C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122509 | ||||||
| chr9:42122567
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+6443T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122567 | ||||||
| chr9:42122667
|
G | A | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+6343C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122667 | ||||||
| chr9:42122758
|
A | G | 29 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.85+6252T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42122758 | ||||||
| chr9:42123060
|
A | G | 1 | a0007c0016t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+5950T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42123060 | ||||||
| chr9:42123274
|
G | A | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+5736C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42123274 | ||||||
| chr9:42123287
|
A | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+5723T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42123287 | ||||||
| chr9:42123804
|
A | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+5206T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42123804 | ||||||
| chr9:42123818
|
G | A | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.85+5192C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42123818 | ||||||
| chr9:42123943
|
C | G | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+5067G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42123943 | ||||||
| chr9:42124015
|
A | T | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.85+4995T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124015 | ||||||
| chr9:42124034
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.85+4976C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124034 | ||||||
| chr9:42124249
|
G | A | 1 | a0030c0035t0007g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85+4761C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124249 | ||||||
| chr9:42124481
|
T | A | 1 | a0002c0002t0024g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.85+4529A>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124481 | ||||||
| chr9:42124549
|
G | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.85+4461C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124549 | ||||||
| chr9:42124635
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+4375C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124635 | ||||||
| chr9:42124722
|
C | T | 2 | a0004c0004t0005g0031a0004c0004t0005g0032 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.85+4288G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124722 | ||||||
| chr9:42124762
|
A | T | 1 | a0003c0003t0021g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.85+4248T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42124762 | ||||||
| chr9:42125081
|
A | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+3929T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125081 | ||||||
| chr9:42125109
|
C | T | 1 | a0027c0026t0020g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+3901G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125109 | ||||||
| chr9:42125185
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.85+3825C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125185 | ||||||
| chr9:42125412
|
C | G | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85+3598G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125412 | ||||||
| chr9:42125453
|
G | A | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.85+3557C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125453 | ||||||
| chr9:42125602
|
A | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.85+3408T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125602 | ||||||
| chr9:42125631
|
G | GA | 3 | a0009c0008t0009g0105a0009c0008t0009g0106a0009c0008t0009g0107 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.85+3378dupT | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125631 | ||||||
| chr9:42125665
|
G | GT | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+3344dupA | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125665 | ||||||
| chr9:42125672
|
T | G | 1 | a0002c0002t0001g0062 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+3338A>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125672 | ||||||
| chr9:42125706
|
C | T | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.85+3304G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125706 | ||||||
| chr9:42125867
|
C | T | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+3143G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125867 | ||||||
| chr9:42125896
|
C | G | 86 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+3114G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125896 | ||||||
| chr9:42125907
|
C | T | 3 | a0004c0004t0005g0029a0004c0004t0005g0030a0027c0026t0020g0027 | 3 | HG02109.hp2 HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.85+3103G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125907 | ||||||
| chr9:42125914
|
A | G | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+3096T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42125914 | ||||||
| chr9:42126004
|
C | T | 1 | a0003c0003t0008g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.85+3006G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126004 | ||||||
| chr9:42126013
|
C | G | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85+2997G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126013 | ||||||
| chr9:42126413
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+2597G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126413 | ||||||
| chr9:42126550
|
G | A | 1 | a0010c0013t0003g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.85+2460C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126550 | ||||||
| chr9:42126594
|
C | T | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85+2416G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126594 | ||||||
| chr9:42126603
|
C | T | 1 | a0005c0005t0006g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85+2407G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126603 | ||||||
| chr9:42126624
|
C | T | 2 | a0003c0003t0004g0075a0003c0011t0004g0074 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.85+2386G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126624 | ||||||
| chr9:42126697
|
G | A | 3 | a0005c0005t0006g0073a0019c0031t0028g0088a0024c0029t0006g0087 | 3 | HG02572.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.85+2313C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126697 | ||||||
| chr9:42126698
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+2312A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126698 | ||||||
| chr9:42126772
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+2238C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126772 | ||||||
| chr9:42126850
|
A | G | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+2160T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42126850 | ||||||
| chr9:42127013
|
C | T | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.85+1997G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127013 | ||||||
| chr9:42127049
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.85+1961T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127049 | ||||||
| chr9:42127086
|
T | C | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+1924A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127086 | ||||||
| chr9:42127147
|
T | C | 1 | a0019c0031t0028g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+1863A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127147 | ||||||
| chr9:42127185
|
T | C | 28 | a0002c0002t0001g0041a0002c0002t0001g0044a0002c0002t0001g0045others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.85+1825A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127185 | ||||||
| chr9:42127262
|
C | T | 1 | a0001c0042t0013g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.85+1748G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127262 | ||||||
| chr9:42127305
|
C | A | 1 | a0002c0002t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85+1705G>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127305 | ||||||
| chr9:42127320
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.85+1690G>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127320 | ||||||
| chr9:42127425
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.85+1585C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127425 | ||||||
| chr9:42127597
|
G | A | 1 | a0026c0025t0019g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+1413C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127597 | ||||||
| chr9:42127854
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.85+1156T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42127854 | ||||||
| chr9:42128023
|
A | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.85+987T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128023 | ||||||
| chr9:42128098
|
T | C | 1 | a0032c0039t0014g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.85+912A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128098 | ||||||
| chr9:42128372
|
T | C | 1 | a0025c0034t0004g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.85+638A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128372 | ||||||
| chr9:42128405
|
T | C | 2 | a0002c0002t0001g0065a0013c0021t0027g0064 | 2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.85+605A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128405 | ||||||
| chr9:42128602
|
C | G | 36 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.85+408G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128602 | ||||||
| chr9:42128621
|
T | C | 1 | a0005c0005t0006g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.85+389A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128621 | ||||||
| chr9:42128787
|
A | T | 1 | a0005c0005t0006g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85+223T>A | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128787 | ||||||
| chr9:42128800
|
A | C | 26 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+210T>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128800 | ||||||
| chr9:42128830
|
G | C | 6 | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+180C>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128830 | ||||||
| chr9:42128850
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.85+160T>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128850 | ||||||
| chr9:42128875
|
T | C | 29 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.85+135A>G | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128875 | ||||||
| chr9:42128979
|
G | A | 3 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.85+31C>T | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128979 | ||||||
| chr9:42128993
|
C | G | 1 | a0003c0003t0029g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.85+17G>C | CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 1/23 | chr9 | 42128993 |