| geneid | 23114 |
|---|---|
| ensemblid | ENSG00000163531.17 |
| hgncid | 29866 |
| symbol | NFASC |
| name | neurofascin |
| refseq_nuc | NM_001005388.3 |
| refseq_prot | NP_001005388.2 |
| ensembl_nuc | ENST00000339876.11 |
| ensembl_prot | ENSP00000344786.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 204828652 |
| end | 205022822 |
| strand | + |
| ver | v1.2 |
| region | chr1:204828652-205022822 |
| region5000 | chr1:204823652-205027822 |
| regionname0 | NFASC_chr1_204828652_205022822 |
| regionname5000 | NFASC_chr1_204823652_205027822 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1240 | 145 | 49 | 45 | 33 | 4 | 12 | 22 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002 | 0/0 | 1240 | 50 | 5 | 10 | 30 | 0 | 5 | 21 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003 | 0/0 | 1240 | 15 | 15 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004 | 0/0 | 1240 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0005 | 0/0 | 1240 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0006 | 0/0 | 1240 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0007 | 0/0 | 1240 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0008 | 0/0 | 1240 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0009 | 0/0 | 1240 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0010 | 0/0 | 1240 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0011 | 0/0 | 1240 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0012 | 0/0 | 1240 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0013 | 0/0 | 1240 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| 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 | 3723 | 46 | 7 | 13 | 19 | 1 | 6 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0002 | 1/0 | 3723 | 37 | 20 | 8 | 7 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0003 | 0/0 | 3723 | 30 | 1 | 6 | 20 | 0 | 3 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0004 | 0/1 | 3723 | 23 | 5 | 8 | 7 | 2 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0005 | 0/0 | 3723 | 9 | 6 | 2 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0006 | 0/0 | 3723 | 6 | 1 | 0 | 5 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0007 | 0/0 | 3723 | 4 | 0 | 0 | 2 | 0 | 2 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0008 | 0/0 | 3723 | 4 | 2 | 0 | 2 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0009 | 0/0 | 3723 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0010 | 0/0 | 3723 | 4 | 3 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0011 | 0/0 | 3723 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0012 | 0/0 | 3723 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0013 | 0/0 | 3723 | 3 | 0 | 2 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0014 | 0/0 | 3723 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0015 | 0/0 | 3723 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0016 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0017 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0018 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0019 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0020 | 0/0 | 3723 | 2 | 1 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0021 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0022 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0023 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0024 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0025 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0026 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0027 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0028 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0029 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0030 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0031 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0032 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0033 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0034 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0035 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0036 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0037 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0038 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0039 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0040 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0041 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0042 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0043 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0044 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0045 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0046 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0047 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0048 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0049 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| c0050 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| 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 | 6622 | 85 | 3 | 36 | 33 | 3 | 9 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0002 | 0/0 | 6626 | 24 | 6 | 3 | 11 | 0 | 4 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0003 | 0/0 | 6622 | 10 | 10 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0004 | 0/0 | 6619 | 9 | 9 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0005 | 0/0 | 6622 | 8 | 7 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0006 | 0/0 | 6630 | 7 | 0 | 1 | 5 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0007 | 0/0 | 6626 | 6 | 5 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0008 | 1/0 | 6614 | 6 | 3 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0009 | 0/0 | 6626 | 4 | 0 | 4 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0010 | 0/0 | 6623 | 4 | 2 | 1 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0011 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0012 | 0/0 | 6626 | 3 | 0 | 0 | 3 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0013 | 0/0 | 6622 | 3 | 0 | 0 | 3 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0014 | 0/0 | 6614 | 3 | 1 | 1 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0015 | 0/0 | 6622 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0016 | 0/0 | 6618 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0017 | 0/0 | 6626 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0018 | 0/0 | 6618 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0019 | 0/0 | 6630 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0020 | 0/0 | 6618 | 2 | 1 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0021 | 0/0 | 6626 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0022 | 0/0 | 6622 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0023 | 0/0 | 6622 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0024 | 0/0 | 6634 | 2 | 1 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0025 | 0/0 | 6622 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0026 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0027 | 0/0 | 6619 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0028 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0029 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0030 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0031 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0032 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0033 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0034 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0035 | 0/0 | 6626 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0036 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0037 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0038 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0039 | 0/0 | 6622 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0040 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0041 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0042 | 0/0 | 6622 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0043 | 0/0 | 6626 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0044 | 0/0 | 6627 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0045 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0046 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0047 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0048 | 0/0 | 6614 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0049 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0050 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0051 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0052 | 0/0 | 6626 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| t0053 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| 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 | 3723 | 46 | 7 | 13 | 19 | 1 | 6 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002 | 1/0 | 3723 | 37 | 20 | 8 | 7 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004 | 0/1 | 3723 | 23 | 5 | 8 | 7 | 2 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005 | 0/0 | 3723 | 9 | 6 | 2 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0010 | 0/0 | 3723 | 4 | 3 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0012 | 0/0 | 3723 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0014 | 0/0 | 3723 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0015 | 0/0 | 3723 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0017 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0021 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0022 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0026 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0027 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0030 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0032 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0035 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0036 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0038 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0039 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0041 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0042 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0043 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003 | 0/0 | 3723 | 30 | 1 | 6 | 20 | 0 | 3 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0006 | 0/0 | 3723 | 6 | 1 | 0 | 5 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0007 | 0/0 | 3723 | 4 | 0 | 0 | 2 | 0 | 2 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0008 | 0/0 | 3723 | 4 | 2 | 0 | 2 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0013 | 0/0 | 3723 | 3 | 0 | 2 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0028 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0033 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0040 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0009 | 0/0 | 3723 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0016 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0018 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0019 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0023 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0024 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0029 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0049 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0011 | 0/0 | 3723 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0020 | 0/0 | 3723 | 2 | 1 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0005c0046 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0005c0047 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0006c0048 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0007c0045 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0008c0025 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0009c0031 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0010c0034 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0011c0037 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0012c0044 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0013c0050 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10344 | 22 | 0 | 8 | 10 | 1 | 3 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0002 | 0/0 | 10348 | 3 | 0 | 0 | 1 | 0 | 2 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0004 | 0/0 | 10341 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0005 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0006 | 0/0 | 10352 | 3 | 0 | 0 | 3 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0007 | 0/0 | 10348 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0009 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0010 | 0/0 | 10345 | 2 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0012 | 0/0 | 10348 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0015 | 0/0 | 10344 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0023 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0033 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0040 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0043 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0051 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0001t0052 | 0/0 | 10348 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0001 | 0/0 | 10344 | 7 | 0 | 2 | 5 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0002 | 0/0 | 10348 | 10 | 6 | 2 | 1 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0004 | 0/0 | 10341 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0006 | 0/0 | 10352 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0008 | 1/0 | 10336 | 5 | 2 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0009 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0011 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0019 | 0/0 | 10352 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0020 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0025 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0028 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0045 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0002t0050 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0001 | 0/1 | 10344 | 16 | 2 | 8 | 3 | 2 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0002 | 0/0 | 10348 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0005 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0038 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0041 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0004t0047 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005t0001 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005t0005 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005t0006 | 0/0 | 10352 | 2 | 0 | 1 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005t0007 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005t0022 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0005t0034 | 0/0 | 10348 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0010t0004 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0010t0005 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0010t0024 | 0/0 | 10356 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0010t0030 | 0/0 | 10348 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0012t0001 | 0/0 | 10344 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0014t0001 | 0/0 | 10344 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0015t0005 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0015t0029 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0015t0049 | 0/0 | 10356 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0017t0001 | 0/0 | 10344 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0021t0001 | 0/0 | 10344 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0022t0001 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0022t0048 | 0/0 | 10336 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0026t0002 | 0/0 | 10348 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0027t0014 | 0/0 | 10336 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0030t0001 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0032t0001 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0035t0036 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0036t0044 | 0/0 | 10349 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0038t0014 | 0/0 | 10336 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0039t0032 | 0/0 | 10356 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0041t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0042t0001 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0001c0043t0027 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0001 | 0/0 | 10344 | 14 | 0 | 3 | 10 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0002 | 0/0 | 10348 | 5 | 0 | 1 | 4 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0006 | 0/0 | 10352 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0009 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0010 | 0/0 | 10345 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0012 | 0/0 | 10348 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0013 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0021 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0035 | 0/0 | 10348 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0037 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0039 | 0/0 | 10344 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0042 | 0/0 | 10344 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0003t0046 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0006t0001 | 0/0 | 10344 | 3 | 0 | 0 | 3 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0006t0002 | 0/0 | 10348 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0006t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0007t0001 | 0/0 | 10344 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0007t0016 | 0/0 | 10340 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0008t0002 | 0/0 | 10348 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0008t0011 | 0/0 | 10352 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0008t0012 | 0/0 | 10348 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0013t0001 | 0/0 | 10344 | 3 | 0 | 2 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0028t0014 | 0/0 | 10336 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0033t0001 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0002c0040t0004 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0009t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0009t0007 | 0/0 | 10348 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0009t0008 | 0/0 | 10336 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0016t0026 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0016t0053 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0018t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0018t0018 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0019t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0019t0005 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0023t0007 | 0/0 | 10348 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0023t0018 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0024t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0029t0031 | 0/0 | 10348 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0003c0049t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0011t0005 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0011t0010 | 0/0 | 10345 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0011t0017 | 0/0 | 10348 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0020t0003 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0004c0020t0024 | 0/0 | 10356 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0005c0046t0001 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0005c0047t0021 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0006c0048t0025 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0007c0045t0013 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0008c0025t0015 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0009c0031t0001 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0010c0034t0009 | 0/0 | 10348 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0011c0037t0004 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0012c0044t0013 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| a0013c0050t0020 | 0/0 | 10340 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | copy fasta | chr1 | 204823652 | 205027822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0009g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0015g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0015g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0023g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0023g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0033g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0040g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0043g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0051g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0001t0052g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0008g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0008g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0008g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0009g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0020g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0028g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0045g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0002t0050g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0038g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0041g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0004t0047g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0007g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0022g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0022g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0005t0034g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0010t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0010t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0010t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0010t0030g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0012t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0012t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0012t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0014t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0014t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0015t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0015t0029g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0015t0049g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0017t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0017t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0021t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0021t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0022t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0022t0048g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0026t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0027t0014g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0030t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0032t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0035t0036g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0036t0044g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0038t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0039t0032g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0041t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0042t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0001c0043t0027g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0021g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0035g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0037g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0039g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0042g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0003t0046g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0006t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0006t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0006t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0006t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0007t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0007t0016g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0008t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0008t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0008t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0008t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0013t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0013t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0013t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0028t0014g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0033t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0002c0040t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0009t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0009t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0009t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0009t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0016t0026g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0016t0053g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0018t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0018t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0019t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0019t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0023t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0023t0018g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0024t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0029t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0003c0049t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0004c0011t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0004c0011t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0004c0011t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0004c0011t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0004c0020t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0004c0020t0024g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0005c0046t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0005c0047t0021g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0006c0048t0025g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0007c0045t0013g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0008c0025t0015g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0009c0031t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0010c0034t0009g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0011c0037t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0012c0044t0013g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| a0013c0050t0020g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0161 | EUR | FIN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00423 | hp1 | a0001 | c0001 | t0052 | g0085 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00423 | hp2 | a0001 | c0001 | t0012 | g0063 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0049 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00558 | hp1 | a0002 | c0006 | t0002 | g0021 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00639 | hp1 | a0002 | c0028 | t0014 | g0183 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00639 | hp2 | a0002 | c0013 | t0001 | g0167 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00673 | hp1 | a0001 | c0004 | t0038 | g0096 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00673 | hp2 | a0002 | c0008 | t0012 | g0026 | EAS | CHS | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00735 | hp1 | a0001 | c0012 | t0001 | g0056 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0181 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00738 | hp1 | a0008 | c0025 | t0015 | g0155 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00741 | hp1 | a0005 | c0047 | t0021 | g0077 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG00741 | hp2 | a0001 | c0021 | t0001 | g0198 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01069 | hp1 | a0001 | c0002 | t0008 | g0106 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01069 | hp2 | a0001 | c0017 | t0001 | g0173 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01071 | hp1 | a0001 | c0002 | t0008 | g0105 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01074 | hp2 | a0001 | c0022 | t0048 | g0150 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0174 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0127 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01109 | hp2 | a0001 | c0002 | t0045 | g0098 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01167 | hp1 | a0001 | c0012 | t0001 | g0054 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0176 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01168 | hp1 | a0001 | c0001 | t0015 | g0093 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01168 | hp2 | a0002 | c0003 | t0002 | g0213 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01169 | hp1 | a0001 | c0012 | t0001 | g0055 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01169 | hp2 | a0001 | c0001 | t0015 | g0212 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01175 | hp2 | a0009 | c0031 | t0001 | g0209 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01192 | hp1 | a0004 | c0020 | t0024 | g0020 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01192 | hp2 | a0001 | c0042 | t0001 | g0072 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01243 | hp1 | a0001 | c0005 | t0007 | g0066 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01255 | hp1 | a0001 | c0032 | t0001 | g0196 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01256 | hp1 | a0001 | c0002 | t0009 | g0193 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01257 | hp1 | a0001 | c0022 | t0001 | g0092 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01257 | hp2 | a0010 | c0034 | t0009 | g0214 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01261 | hp1 | a0001 | c0017 | t0001 | g0199 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0094 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01346 | hp2 | a0001 | c0005 | t0006 | g0152 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01358 | hp1 | a0001 | c0030 | t0001 | g0030 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01358 | hp2 | a0002 | c0033 | t0001 | g0169 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01496 | hp1 | a0001 | c0010 | t0005 | g0175 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01496 | hp2 | a0002 | c0013 | t0001 | g0211 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01928 | hp1 | a0002 | c0003 | t0009 | g0051 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0029 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01978 | hp1 | a0001 | c0004 | t0001 | g0091 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01978 | hp2 | a0001 | c0035 | t0036 | g0208 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02004 | hp1 | a0001 | c0004 | t0001 | g0083 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02004 | hp2 | a0002 | c0003 | t0021 | g0159 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0129 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0166 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02055 | hp1 | a0003 | c0016 | t0026 | g0141 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02055 | hp2 | a0003 | c0016 | t0053 | g0041 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02129 | hp1 | a0002 | c0003 | t0002 | g0050 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02145 | hp1 | a0001 | c0002 | t0019 | g0008 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02257 | hp1 | a0001 | c0002 | t0019 | g0090 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02257 | hp2 | a0003 | c0019 | t0005 | g0007 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02258 | hp1 | a0003 | c0009 | t0007 | g0138 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02258 | hp2 | a0001 | c0004 | t0005 | g0153 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02280 | hp1 | a0003 | c0009 | t0007 | g0165 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0046 | AMR | PEL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02451 | hp1 | a0001 | c0005 | t0005 | g0131 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02451 | hp2 | a0001 | c0002 | t0025 | g0042 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02523 | hp2 | a0001 | c0004 | t0002 | g0204 | EAS | KHV | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02572 | hp2 | a0004 | c0011 | t0017 | g0019 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0147 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02602 | hp2 | a0001 | c0026 | t0002 | g0178 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0185 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02622 | hp1 | a0003 | c0023 | t0018 | g0188 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02622 | hp2 | a0002 | c0008 | t0011 | g0102 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02630 | hp2 | a0001 | c0010 | t0004 | g0194 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02717 | hp1 | a0001 | c0015 | t0005 | g0114 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02717 | hp2 | a0004 | c0011 | t0017 | g0018 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02886 | hp1 | a0004 | c0011 | t0005 | g0103 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02886 | hp2 | a0001 | c0004 | t0003 | g0203 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02897 | hp1 | a0001 | c0010 | t0024 | g0151 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02897 | hp2 | a0001 | c0005 | t0034 | g0135 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02922 | hp1 | a0001 | c0039 | t0032 | g0006 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02922 | hp2 | a0001 | c0002 | t0011 | g0144 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02965 | hp1 | a0002 | c0003 | t0010 | g0088 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02965 | hp2 | a0001 | c0005 | t0005 | g0061 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02976 | hp2 | a0003 | c0009 | t0003 | g0187 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03017 | hp1 | a0001 | c0014 | t0001 | g0200 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03017 | hp2 | a0001 | c0027 | t0014 | g0184 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03041 | hp1 | a0001 | c0002 | t0020 | g0100 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03041 | hp2 | a0001 | c0015 | t0029 | g0101 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0191 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03098 | hp2 | a0001 | c0004 | t0041 | g0065 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03130 | hp1 | a0001 | c0001 | t0023 | g0156 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03139 | hp1 | a0002 | c0006 | t0003 | g0128 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03139 | hp2 | a0006 | c0048 | t0025 | g0040 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03195 | hp1 | a0001 | c0002 | t0028 | g0104 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03195 | hp2 | a0004 | c0011 | t0010 | g0014 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03209 | hp2 | a0002 | c0008 | t0011 | g0126 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03225 | hp1 | a0001 | c0015 | t0049 | g0119 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03225 | hp2 | a0004 | c0020 | t0003 | g0197 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0073 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03239 | hp2 | a0013 | c0050 | t0020 | g0177 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0107 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03486 | hp2 | a0003 | c0018 | t0003 | g0136 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03491 | hp1 | a0001 | c0014 | t0001 | g0002 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03491 | hp2 | a0002 | c0007 | t0001 | g0047 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03492 | hp1 | a0002 | c0007 | t0001 | g0080 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03492 | hp2 | a0001 | c0014 | t0001 | g0002 | SAS | PJL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03516 | hp1 | a0001 | c0010 | t0030 | g0217 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0062 | AFR | ESN | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03540 | hp1 | a0003 | c0018 | t0018 | g0145 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03540 | hp2 | a0003 | c0023 | t0007 | g0108 | AFR | GWD | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0109 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03579 | hp2 | a0003 | c0019 | t0003 | g0116 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03831 | hp1 | a0002 | c0003 | t0042 | g0182 | SAS | BEB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18522 | hp1 | a0001 | c0005 | t0022 | g0134 | AFR | YRI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | YRI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18612 | hp1 | a0002 | c0003 | t0035 | g0207 | EAS | CHB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18612 | hp2 | a0002 | c0006 | t0001 | g0037 | EAS | CHB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18906 | hp1 | a0001 | c0005 | t0022 | g0089 | AFR | YRI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18906 | hp2 | a0003 | c0009 | t0008 | g0190 | AFR | YRI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18950 | hp1 | a0002 | c0003 | t0037 | g0068 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0095 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18951 | hp2 | a0002 | c0013 | t0001 | g0022 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18962 | hp1 | a0002 | c0003 | t0006 | g0221 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18969 | hp1 | a0001 | c0001 | t0040 | g0113 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18970 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18974 | hp1 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0076 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18982 | hp1 | a0001 | c0004 | t0001 | g0112 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18982 | hp2 | a0002 | c0003 | t0012 | g0222 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18986 | hp1 | a0001 | c0001 | t0033 | g0038 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0223 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18990 | hp2 | a0002 | c0006 | t0001 | g0070 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19002 | hp1 | a0002 | c0003 | t0046 | g0016 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19002 | hp2 | a0002 | c0007 | t0016 | g0074 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19003 | hp1 | a0002 | c0003 | t0013 | g0132 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19005 | hp1 | a0002 | c0006 | t0002 | g0035 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19007 | hp1 | a0002 | c0007 | t0016 | g0075 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19007 | hp2 | a0012 | c0044 | t0013 | g0010 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19009 | hp2 | a0001 | c0002 | t0006 | g0195 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19010 | hp1 | a0007 | c0045 | t0013 | g0015 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19010 | hp2 | a0002 | c0006 | t0001 | g0017 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19011 | hp2 | a0002 | c0008 | t0002 | g0123 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19030 | hp1 | a0001 | c0043 | t0027 | g0224 | AFR | LWK | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | LWK | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | LWK | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19043 | hp2 | a0001 | c0002 | t0008 | g0143 | AFR | LWK | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19054 | hp1 | a0001 | c0004 | t0047 | g0031 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19060 | hp2 | a0001 | c0001 | t0051 | g0036 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0032 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19091 | hp1 | a0005 | c0046 | t0001 | g0034 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19240 | hp1 | a0002 | c0040 | t0004 | g0052 | AFR | YRI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | YRI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA20129 | hp1 | a0001 | c0002 | t0008 | g0137 | AFR | ASW | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA20129 | hp2 | a0003 | c0024 | t0003 | g0115 | AFR | ASW | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0142 | EUR | TSI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA20805 | hp2 | a0001 | c0005 | t0006 | g0172 | EUR | TSI | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA20905 | hp1 | a0002 | c0003 | t0039 | g0218 | SAS | GIH | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0171 | SAS | GIH | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01123 | hp1 | a0001 | c0021 | t0001 | g0170 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG01123 | hp2 | a0001 | c0001 | t0043 | g0028 | AMR | CLM | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02109 | hp2 | a0003 | c0029 | t0031 | g0005 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0157 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG02559 | hp2 | a0001 | c0036 | t0044 | g0220 | AFR | ACB | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03471 | hp1 | a0001 | c0002 | t0050 | g0099 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG03471 | hp2 | a0011 | c0037 | t0004 | g0110 | AFR | MSL | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG06807 | hp1 | a0003 | c0049 | t0003 | g0186 | AFR | USA | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | USA | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA21309 | hp1 | a0001 | c0041 | t0003 | g0118 | AFR | LWK | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| NA21309 | hp2 | a0001 | c0038 | t0014 | g0078 | AFR | LWK | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0206 | REF | REF | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0008 | g0154 | REF | REF | NFASC_chr1_204823652_205027822 | NFASC | chr1 | 204823652 | 205027822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204944337
|
C | T | 1 | a0013 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.22C>T | p.Pro8Ser | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/30 | 352/10336 | 22/3723 | 8/1240 | chr1 | 204944337 | ||
| chr1:204952014
|
C | T | 1 | a0006 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.113C>T | p.Thr38Met | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/30 | 443/10336 | 113/3723 | 38/1240 | chr1 | 204952014 | ||
| chr1:204954892
|
C | T | 2 | a0005a0007 | 3 | HG00741.hp1 NA19010.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.476C>T | p.Thr159Met | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/30 | 806/10336 | 476/3723 | 159/1240 | chr1 | 204954892 | ||
| chr1:204968878
|
C | T | 1 | a0012 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.899C>T | p.Ala300Val | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/30 | 1229/10336 | 899/3723 | 300/1240 | chr1 | 204968878 | ||
| chr1:204975289
|
G | A | 1 | a0008 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1577G>A | p.Arg526Gln | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/30 | 1907/10336 | 1577/3723 | 526/1240 | chr1 | 204975289 | ||
| chr1:204981868
|
G | A | 1 | a0009 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2318G>A | p.Arg773Gln | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/30 | 2648/10336 | 2318/3723 | 773/1240 | chr1 | 204981868 | ||
| chr1:204997172
|
C | T | 1 | a0011 | 1 | HG03471.hp2 | missense_variant&splice_region_variant | MODERATE | c.2785C>T | p.Pro929Ser | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/30 | 3115/10336 | 2785/3723 | 929/1240 | chr1 | 204997172 | ||
| chr1:204997274
|
A | G | 2 | a0003a0004 | 21 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
missense_variant | MODERATE | c.2887A>G | p.Ile963Val | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/30 | 3217/10336 | 2887/3723 | 963/1240 | chr1 | 204997274 | ||
| chr1:204997300
|
C | G | 6 | a0002a0004a0005others(3): Show | 61 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(58): Show |
missense_variant | MODERATE | c.2913C>G | p.Ile971Met | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/30 | 3243/10336 | 2913/3723 | 971/1240 | chr1 | 204997300 | ||
| chr1:204997316
|
G | A | 1 | a0010 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.2929G>A | p.Val977Ile | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/30 | 3259/10336 | 2929/3723 | 977/1240 | chr1 | 204997316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204944381
|
C | T | 1 | a0003c0049 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.66C>T | p.Gly22Gly | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/30 | 396/10336 | 66/3723 | 22/1240 | chr1 | 204944381 | ||
| chr1:204954911
|
G | A | 2 | a0003c0016a0003c0024 | 3 | HG02055.hp1 HG02055.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.495G>A | p.Pro165Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/30 | 825/10336 | 495/3723 | 165/1240 | chr1 | 204954911 | ||
| chr1:204970635
|
C | T | 3 | a0001c0015a0003c0023a0004c0011 | 9 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.1023C>T | p.Asp341Asp | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/30 | 1353/10336 | 1023/3723 | 341/1240 | chr1 | 204970635 | ||
| chr1:204973400
|
C | T | 1 | a0001c0043 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1260C>T | p.Asn420Asn | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/30 | 1590/10336 | 1260/3723 | 420/1240 | chr1 | 204973400 | ||
| chr1:204974234
|
C | T | 1 | a0001c0042 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1335C>T | p.Tyr445Tyr | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 13/30 | 1665/10336 | 1335/3723 | 445/1240 | chr1 | 204974234 | ||
| chr1:204974774
|
C | T | 3 | a0001c0010a0001c0041a0001c0043 | 6 | HG01496.hp1 HG02630.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.1509C>T | p.Ala503Ala | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/30 | 1839/10336 | 1509/3723 | 503/1240 | chr1 | 204974774 | ||
| chr1:204974819
|
C | A | 13 | a0001c0001a0001c0012a0001c0026others(10): Show | 92 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.1554C>A | p.Val518Val | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/30 | 1884/10336 | 1554/3723 | 518/1240 | chr1 | 204974819 | ||
| chr1:204976693
|
C | T | 1 | a0001c0030 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1729C>T | p.Leu577Leu | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/30 | 2059/10336 | 1729/3723 | 577/1240 | chr1 | 204976693 | ||
| chr1:204976743
|
C | T | 1 | a0001c0012 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.1779C>T | p.Val593Val | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/30 | 2109/10336 | 1779/3723 | 593/1240 | chr1 | 204976743 | ||
| chr1:204979531
|
A | G | 13 | a0001c0005a0001c0014a0001c0021others(10): Show | 28 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(25): Show |
synonymous_variant | LOW | c.2148A>G | p.Pro716Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 19/30 | 2478/10336 | 2148/3723 | 716/1240 | chr1 | 204979531 | ||
| chr1:204980374
|
C | T | 1 | a0003c0016 | 2 | HG02055.hp1 HG02055.hp2 |
synonymous_variant | LOW | c.2181C>T | p.Pro727Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/30 | 2511/10336 | 2181/3723 | 727/1240 | chr1 | 204980374 | ||
| chr1:204982010
|
C | T | 2 | a0001c0022a0005c0047 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
synonymous_variant | LOW | c.2460C>T | p.Ser820Ser | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/30 | 2790/10336 | 2460/3723 | 820/1240 | chr1 | 204982010 | ||
| chr1:204988640
|
G | C | 2 | a0001c0032a0002c0033 | 2 | HG01255.hp1 HG01358.hp2 |
synonymous_variant | LOW | c.2601G>C | p.Gly867Gly | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/30 | 2931/10336 | 2601/3723 | 867/1240 | chr1 | 204988640 | ||
| chr1:204997225
|
C | T | 1 | a0001c0036 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2838C>T | p.Thr946Thr | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/30 | 3168/10336 | 2838/3723 | 946/1240 | chr1 | 204997225 | ||
| chr1:205001174
|
T | C | 11 | a0001c0004a0001c0021a0001c0026others(8): Show | 44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
synonymous_variant | LOW | c.3024T>C | p.Pro1008Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/30 | 3354/10336 | 3024/3723 | 1008/1240 | chr1 | 205001174 | ||
| chr1:205002666
|
C | T | 1 | a0001c0039 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.3207C>T | p.Pro1069Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/30 | 3537/10336 | 3207/3723 | 1069/1240 | chr1 | 205002666 | ||
| chr1:205009576
|
G | A | 5 | a0001c0014a0001c0017a0001c0035others(2): Show | 10 | HG00639.hp2 HG01069.hp2 HG01192.hp2 others(7): Show |
synonymous_variant | LOW | c.3309G>A | p.Ala1103Ala | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/30 | 3639/10336 | 3309/3723 | 1103/1240 | chr1 | 205009576 | ||
| chr1:205016506
|
G | A | 3 | a0001c0027a0001c0038a0002c0028 | 3 | HG00639.hp1 HG03017.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.3690G>A | p.Thr1230Thr | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4020/10336 | 3690/3723 | 1230/1240 | chr1 | 205016506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204828763
|
C | G | 3 | a0001c0002t0025a0003c0016t0053a0006c0048t0025 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-219C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/30 | 115553 | chr1 | 204828763 | |||||
| chr1:204944230
|
G | T | 2 | a0001c0001t0051a0001c0001t0052 | 2 | HG00423.hp1 NA19060.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/30 | chr1 | 204944230 | ||||||
| chr1:205016541
|
G | A | 1 | a0002c0007t0016 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2 | chr1 | 205016541 | |||||
| chr1:205016766
|
G | A | 12 | a0001c0001t0004a0001c0002t0004a0001c0002t0028others(9): Show | 18 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 227 | chr1 | 205016766 | |||||
| chr1:205017129
|
G | A | 1 | a0003c0029t0031 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 590 | chr1 | 205017129 | |||||
| chr1:205017231
|
C | T | 26 | a0001c0001t0005a0001c0001t0015a0001c0002t0003others(23): Show | 30 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*692C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 692 | chr1 | 205017231 | |||||
| chr1:205017322
|
A | G | 3 | a0001c0010t0024a0001c0015t0049a0004c0020t0024 | 3 | HG01192.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 783 | chr1 | 205017322 | |||||
| chr1:205017458
|
T | C | 115 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(112): Show | 216 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*919T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 919 | chr1 | 205017458 | |||||
| chr1:205017516
|
A | G | 2 | a0001c0001t0015a0008c0025t0015 | 3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*977A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 977 | chr1 | 205017516 | |||||
| chr1:205017674
|
T | C | 2 | a0001c0002t0011a0002c0008t0011 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1135T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1135 | chr1 | 205017674 | |||||
| chr1:205017991
|
G | A | 22 | a0001c0001t0005a0001c0001t0015a0001c0002t0003others(19): Show | 24 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1452G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1452 | chr1 | 205017991 | |||||
| chr1:205018001
|
G | C | 1 | a0001c0039t0032 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1462 | chr1 | 205018001 | |||||
| chr1:205018093
|
C | T | 1 | a0001c0015t0049 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1554C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1554 | chr1 | 205018093 | |||||
| chr1:205018260
|
A | G | 1 | a0001c0002t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1721 | chr1 | 205018260 | |||||
| chr1:205018282
|
G | A | 1 | a0001c0001t0033 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1743 | chr1 | 205018282 | |||||
| chr1:205018366
|
C | T | 1 | a0001c0004t0047 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1827C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1827 | chr1 | 205018366 | |||||
| chr1:205018501
|
T | G | 24 | a0001c0001t0005a0001c0001t0015a0001c0002t0003others(21): Show | 27 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1962T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1962 | chr1 | 205018501 | |||||
| chr1:205018522
|
C | G | 1 | a0002c0003t0046 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 1983 | chr1 | 205018522 | |||||
| chr1:205018825
|
C | T | 49 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(46): Show | 62 | HG00738.hp1 HG00741.hp1 HG01109.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2286C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2286 | chr1 | 205018825 | |||||
| chr1:205018844
|
G | A | 1 | a0002c0003t0035 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2305G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2305 | chr1 | 205018844 | |||||
| chr1:205018905
|
T | C | 1 | a0001c0001t0033 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2366 | chr1 | 205018905 | |||||
| chr1:205019055
|
C | A | 56 | a0001c0001t0001a0001c0001t0010a0001c0001t0012others(53): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2516C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2516 | chr1 | 205019055 | |||||
| chr1:205019407
|
T | C | 44 | a0001c0001t0001a0001c0001t0012a0001c0001t0033others(41): Show | 112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2868T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2868 | chr1 | 205019407 | |||||
| chr1:205019475
|
C | CCATT | 12 | a0001c0001t0004a0001c0002t0004a0001c0002t0020others(9): Show | 17 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2959_*2962dupTTCA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(1): Show |
57 | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(54): Show | 125 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2955_*2962dupTTCA others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(5): Show |
33 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(30): Show | 56 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2951_*2962dupTTCA others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(9): Show |
8 | a0001c0001t0006a0001c0002t0006a0001c0002t0011others(5): Show | 13 | HG01346.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2947_*2962dupTTCA others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(13): Show |
4 | a0001c0010t0024a0001c0015t0049a0001c0039t0032others(1): Show | 4 | HG01192.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2943_*2962dupTTCA others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019555
|
C | T | 1 | a0002c0003t0042 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3016C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3016 | chr1 | 205019555 | |||||
| chr1:205019854
|
T | C | 6 | a0001c0001t0010a0001c0036t0044a0002c0003t0010others(3): Show | 7 | HG00741.hp1 HG01109.hp1 HG02004.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3315T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3315 | chr1 | 205019854 | |||||
| chr1:205019899
|
G | A | 4 | a0001c0022t0048a0001c0027t0014a0001c0038t0014others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3360G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3360 | chr1 | 205019899 | |||||
| chr1:205020031
|
T | C | 1 | a0002c0007t0016 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3492T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3492 | chr1 | 205020031 | |||||
| chr1:205020035
|
T | G | 44 | a0001c0001t0001a0001c0001t0012a0001c0001t0033others(41): Show | 112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*3496T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3496 | chr1 | 205020035 | |||||
| chr1:205020290
|
G | T | 4 | a0001c0001t0009a0001c0002t0009a0002c0003t0009others(1): Show | 4 | HG01256.hp1 HG01257.hp2 HG01928.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3751G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3751 | chr1 | 205020290 | |||||
| chr1:205020407
|
T | G | 1 | a0002c0007t0016 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3868T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3868 | chr1 | 205020407 | |||||
| chr1:205020482
|
C | T | 2 | a0001c0001t0023a0003c0016t0053 | 3 | HG02055.hp2 HG03130.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3943C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3943 | chr1 | 205020482 | |||||
| chr1:205020488
|
AGAG | A | 4 | a0001c0001t0010a0001c0036t0044a0002c0003t0010others(1): Show | 5 | HG01109.hp1 HG02559.hp2 HG02602.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3953_*3955delGAG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3953 | INFO_REALIGN_3_PRIME | chr1 | 205020488 | ||||
| chr1:205020490
|
A | G | 1 | a0001c0001t0043 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3951A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 3951 | chr1 | 205020490 | |||||
| chr1:205020601
|
C | T | 3 | a0001c0001t0023a0001c0005t0022a0003c0016t0053 | 5 | HG02055.hp2 HG03130.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4062C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4062 | chr1 | 205020601 | |||||
| chr1:205020622
|
C | T | 1 | a0001c0002t0050 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4083C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4083 | chr1 | 205020622 | |||||
| chr1:205020783
|
C | A | 7 | a0001c0001t0010a0001c0036t0044a0002c0003t0010others(4): Show | 9 | HG00741.hp1 HG01109.hp1 HG02004.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4244C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4244 | chr1 | 205020783 | |||||
| chr1:205020951
|
G | T | 1 | a0001c0004t0041 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4412G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4412 | chr1 | 205020951 | |||||
| chr1:205020968
|
C | T | 2 | a0001c0015t0029a0004c0011t0017 | 3 | HG02572.hp2 HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4429C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4429 | chr1 | 205020968 | |||||
| chr1:205020984
|
T | A | 1 | a0003c0016t0026 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4445T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4445 | chr1 | 205020984 | |||||
| chr1:205021032
|
TAGAG | T | 4 | a0001c0001t0023a0001c0002t0045a0001c0005t0022others(1): Show | 6 | HG01109.hp2 HG02055.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4496_*4499delAGAG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4496 | INFO_REALIGN_3_PRIME | chr1 | 205021032 | ||||
| chr1:205021057
|
A | G | 36 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(33): Show | 44 | HG00738.hp1 HG01109.hp2 HG01168.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4518A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4518 | chr1 | 205021057 | |||||
| chr1:205021337
|
A | G | 1 | a0001c0043t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4798A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 4798 | chr1 | 205021337 | |||||
| chr1:205021578
|
A | G | 1 | a0001c0001t0040 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5039A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5039 | chr1 | 205021578 | |||||
| chr1:205021704
|
G | C | 1 | a0001c0036t0044 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5165G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5165 | chr1 | 205021704 | |||||
| chr1:205021732
|
G | C | 116 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(113): Show | 217 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*5193G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5193 | chr1 | 205021732 | |||||
| chr1:205021907
|
G | A | 8 | a0001c0001t0004a0001c0002t0004a0001c0002t0028others(5): Show | 12 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5368G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5368 | chr1 | 205021907 | |||||
| chr1:205021983
|
G | A | 1 | a0002c0007t0016 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5444G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5444 | chr1 | 205021983 | |||||
| chr1:205021991
|
C | T | 1 | a0001c0001t0040 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5452C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5452 | chr1 | 205021991 | |||||
| chr1:205022132
|
T | C | 30 | a0001c0001t0004a0001c0001t0005a0001c0001t0015others(27): Show | 36 | HG00738.hp1 HG01109.hp2 HG01168.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5593T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5593 | chr1 | 205022132 | |||||
| chr1:205022252
|
C | T | 10 | a0001c0001t0005a0001c0002t0025a0001c0002t0050others(7): Show | 11 | HG01496.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5713C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5713 | chr1 | 205022252 | |||||
| chr1:205022404
|
C | A | 1 | a0002c0007t0016 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5865C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5865 | chr1 | 205022404 | |||||
| chr1:205022435
|
G | A | 1 | a0002c0007t0016 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5896G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5896 | chr1 | 205022435 | |||||
| chr1:205022468
|
C | G | 61 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(58): Show | 89 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*5929C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5929 | chr1 | 205022468 | |||||
| chr1:205022487
|
C | T | 1 | a0002c0003t0037 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5948C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 5948 | chr1 | 205022487 | |||||
| chr1:205022642
|
C | T | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(20): Show | 43 | HG00544.hp2 HG00558.hp1 HG01106.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*6103C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 6103 | chr1 | 205022642 | |||||
| chr1:205022713
|
G | A | 1 | a0001c0035t0036 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6174G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 6174 | chr1 | 205022713 | |||||
| chr1:205022759
|
T | TA | 8 | a0001c0001t0004a0001c0002t0004a0001c0002t0028others(5): Show | 12 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6227dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 30/30 | 6228 | INFO_REALIGN_3_PRIME | chr1 | 205022759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204828864
|
G | C | 127 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(124): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-200+82G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204828864 | ||||||
| chr1:204828941
|
G | A | 1 | a0001c0001t0006g0003 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-200+159G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204828941 | ||||||
| chr1:204828979
|
G | A | 127 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(124): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-200+197G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204828979 | ||||||
| chr1:204829213
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+431T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204829213 | ||||||
| chr1:204829602
|
T | C | 40 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(37): Show | 40 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.-200+820T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204829602 | ||||||
| chr1:204829615
|
A | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-200+833A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204829615 | ||||||
| chr1:204829806
|
T | G | 147 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(144): Show | 147 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.-200+1024T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204829806 | ||||||
| chr1:204829991
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-200+1209G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204829991 | ||||||
| chr1:204830006
|
G | GGT | 35 | a0001c0001t0001g0025a0001c0001t0001g0097a0001c0001t0006g0003others(32): Show | 35 | HG00558.hp1 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-200+1263_-200+126 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
G | GGTGT | 35 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0081others(32): Show | 35 | HG00423.hp1 HG00423.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-200+1261_-200+126 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
G | GGTGTGT | 13 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0058others(10): Show | 13 | HG00558.hp2 HG00735.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-200+1259_-200+126 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
G | GGTGTGTG others(1): Show |
8 | a0001c0001t0001g0048a0001c0001t0007g0130a0001c0005t0005g0131others(5): Show | 8 | HG00544.hp2 HG01928.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+1257_-200+126 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
G | GGTGTGTG others(3): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0004t0001g0046others(1): Show | 4 | HG01981.hp2 HG02293.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+1255_-200+126 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
G | GGTGTGTG others(5): Show |
2 | a0002c0003t0001g0043a0012c0044t0013g0010 | 2 | NA19007.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-200+1253_-200+126 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
G | GTGTGTGT others(8): Show |
1 | a0001c0002t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-200+1224_-200+122 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830006 | ||||||
| chr1:204830006
|
G | T | 4 | a0001c0002t0003g0009a0001c0002t0025g0042a0003c0016t0053g0041others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+1224G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830006 | ||||||
| chr1:204830006
|
GGT | G | 12 | a0001c0001t0001g0039a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.-200+1263_-200+126 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
GGTGT | G | 81 | a0001c0001t0001g0149a0001c0001t0001g0201a0001c0001t0001g0202others(78): Show | 83 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.-200+1261_-200+126 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830006
|
GGTGTGTG others(3): Show |
G | 1 | a0002c0003t0001g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-200+1255_-200+126 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830006 | |||||
| chr1:204830215
|
G | A | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+1433G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830215 | ||||||
| chr1:204830528
|
C | T | 4 | a0001c0001t0010g0127a0002c0006t0003g0128a0002c0008t0011g0126others(1): Show | 4 | HG01109.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+1746C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830528 | ||||||
| chr1:204830578
|
TTGTGTGT others(11): Show |
T | 1 | a0002c0003t0001g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-200+1846_-200+186 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830578 | |||||
| chr1:204830652
|
G | C | 1 | a0002c0003t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-200+1870G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830652 | ||||||
| chr1:204830657
|
T | TAG | 97 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(94): Show | 97 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-200+1895_-200+189 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830657 | |||||
| chr1:204830657
|
T | TAGAGAGA others(3): Show |
3 | a0001c0002t0020g0100a0001c0002t0045g0098a0001c0002t0050g0099 | 3 | HG01109.hp2 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-200+1887_-200+189 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830657 | |||||
| chr1:204830657
|
TAGAGAGA others(3): Show |
T | 28 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-200+1887_-200+189 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204830657 | |||||
| chr1:204830685
|
C | T | 2 | a0002c0003t0001g0223a0002c0003t0012g0222 | 2 | NA18982.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-200+1903C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830685 | ||||||
| chr1:204830688
|
G | A | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+1906G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830688 | ||||||
| chr1:204830755
|
C | A | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+1973C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830755 | ||||||
| chr1:204830761
|
G | A | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+1979G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830761 | ||||||
| chr1:204830785
|
G | A | 1 | a0001c0002t0019g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-200+2003G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830785 | ||||||
| chr1:204830801
|
A | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(25): Show | 28 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-200+2019A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830801 | ||||||
| chr1:204830831
|
G | C | 3 | a0001c0012t0001g0054a0001c0012t0001g0055a0001c0012t0001g0056 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-200+2049G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830831 | ||||||
| chr1:204830877
|
A | G | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+2095A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830877 | ||||||
| chr1:204830878
|
C | T | 3 | a0001c0002t0020g0100a0001c0002t0045g0098a0001c0002t0050g0099 | 3 | HG01109.hp2 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-200+2096C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830878 | ||||||
| chr1:204830989
|
C | T | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+2207C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204830989 | ||||||
| chr1:204831010
|
G | C | 2 | a0001c0002t0002g0140a0001c0002t0008g0143 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-200+2228G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831010 | ||||||
| chr1:204831088
|
C | T | 1 | a0002c0003t0006g0221 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-200+2306C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831088 | ||||||
| chr1:204831355
|
C | T | 11 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0002t0002g0148others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-200+2573C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831355 | ||||||
| chr1:204831397
|
T | C | 8 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0002t0002g0140others(5): Show | 8 | HG02602.hp1 HG02922.hp2 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+2615T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831397 | ||||||
| chr1:204831590
|
A | C | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+2808A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831590 | ||||||
| chr1:204831595
|
C | A | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+2813C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831595 | ||||||
| chr1:204831794
|
C | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(34): Show | 37 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.-200+3012C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831794 | ||||||
| chr1:204831859
|
C | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-200+3077C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204831859 | ||||||
| chr1:204832143
|
GAACACCT others(8): Show |
G | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+3364_-200+337 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204832143 | |||||
| chr1:204832159
|
A | T | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+3377A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832159 | ||||||
| chr1:204832346
|
G | T | 3 | a0001c0005t0001g0062a0001c0005t0005g0061a0002c0040t0004g0052 | 3 | HG02965.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-200+3564G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832346 | ||||||
| chr1:204832380
|
G | A | 220 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(217): Show | 222 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.-200+3598G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832380 | ||||||
| chr1:204832425
|
CTGCAAGG others(17): Show |
C | 2 | a0001c0002t0002g0140a0001c0002t0008g0143 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-200+3644_-200+366 others(28): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832425 | ||||||
| chr1:204832490
|
G | T | 1 | a0001c0002t0002g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-200+3708G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832490 | ||||||
| chr1:204832850
|
G | A | 1 | a0003c0009t0007g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-200+4068G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832850 | ||||||
| chr1:204832866
|
G | A | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+4084G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204832866 | ||||||
| chr1:204833234
|
A | G | 128 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-200+4452A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833234 | ||||||
| chr1:204833265
|
CA | C | 8 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0002t0002g0140others(5): Show | 8 | HG02602.hp1 HG02922.hp2 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+4486delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204833265 | |||||
| chr1:204833340
|
T | C | 1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-200+4558T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833340 | ||||||
| chr1:204833418
|
C | T | 2 | a0001c0005t0022g0089a0002c0003t0010g0088 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-200+4636C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833418 | ||||||
| chr1:204833429
|
T | C | 1 | a0001c0001t0012g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-200+4647T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833429 | ||||||
| chr1:204833513
|
A | C | 1 | a0002c0003t0039g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-200+4731A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833513 | ||||||
| chr1:204833680
|
T | G | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+4898T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833680 | ||||||
| chr1:204833752
|
G | T | 5 | a0001c0015t0005g0114a0004c0011t0010g0014a0004c0011t0017g0018others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-200+4970G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833752 | ||||||
| chr1:204833887
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+5105T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833887 | ||||||
| chr1:204833947
|
A | G | 62 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(59): Show | 62 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-200+5165A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204833947 | ||||||
| chr1:204834174
|
C | A | 1 | a0003c0009t0007g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-200+5392C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834174 | ||||||
| chr1:204834211
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-200+5429G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834211 | ||||||
| chr1:204834250
|
C | T | 2 | a0002c0003t0002g0124a0002c0003t0002g0125 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-200+5468C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834250 | ||||||
| chr1:204834519
|
C | T | 6 | a0001c0001t0002g0120a0001c0001t0006g0121a0001c0002t0001g0122others(3): Show | 6 | HG00544.hp1 NA18955.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-200+5737C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834519 | ||||||
| chr1:204834538
|
C | T | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+5756C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834538 | ||||||
| chr1:204834606
|
G | A | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+5824G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834606 | ||||||
| chr1:204834844
|
G | A | 1 | a0002c0006t0002g0021 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-200+6062G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834844 | ||||||
| chr1:204834903
|
C | A | 6 | a0001c0001t0002g0120a0001c0001t0006g0121a0001c0002t0001g0122others(3): Show | 6 | HG00544.hp1 NA18955.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-200+6121C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204834903 | ||||||
| chr1:204835013
|
C | G | 127 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(124): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-200+6231C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835013 | ||||||
| chr1:204835076
|
G | C | 2 | a0001c0001t0023g0156a0001c0002t0004g0157 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-200+6294G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835076 | ||||||
| chr1:204835213
|
C | CT | 12 | a0001c0001t0001g0149a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-200+6456dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204835213 | |||||
| chr1:204835213
|
CT | C | 15 | a0001c0002t0002g0140a0001c0002t0008g0143a0001c0004t0001g0087others(12): Show | 15 | HG01074.hp2 HG01175.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-200+6456delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204835213 | |||||
| chr1:204835213
|
CTT | C | 59 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0058others(56): Show | 59 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-200+6455_-200+645 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204835213 | |||||
| chr1:204835213
|
CTTT | C | 37 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(34): Show | 37 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.-200+6454_-200+645 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204835213 | |||||
| chr1:204835213
|
CTTTT | C | 9 | a0001c0001t0004g0117a0001c0001t0010g0127a0001c0015t0049g0119others(6): Show | 9 | HG01109.hp1 HG02615.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-200+6453_-200+645 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204835213 | |||||
| chr1:204835213
|
CTTTTT | C | 17 | a0001c0001t0002g0120a0001c0001t0006g0121a0001c0001t0023g0109others(14): Show | 17 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-200+6452_-200+645 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204835213 | |||||
| chr1:204835241
|
G | A | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+6459G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835241 | ||||||
| chr1:204835362
|
A | G | 127 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(124): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-200+6580A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835362 | ||||||
| chr1:204835421
|
G | A | 3 | a0001c0002t0008g0137a0001c0004t0001g0139a0003c0009t0007g0138 | 3 | HG02258.hp1 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-200+6639G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835421 | ||||||
| chr1:204835605
|
A | G | 26 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(23): Show | 26 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-200+6823A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835605 | ||||||
| chr1:204835705
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0052g0085 | 2 | HG00423.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-200+6923C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835705 | ||||||
| chr1:204835752
|
C | T | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+6970C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835752 | ||||||
| chr1:204835776
|
T | G | 1 | a0002c0003t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-200+6994T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835776 | ||||||
| chr1:204835801
|
C | T | 1 | a0010c0034t0009g0214 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-200+7019C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835801 | ||||||
| chr1:204835815
|
G | A | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+7033G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835815 | ||||||
| chr1:204835845
|
A | G | 2 | a0001c0002t0002g0140a0001c0002t0008g0143 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-200+7063A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204835845 | ||||||
| chr1:204836167
|
C | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-200+7385C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204836167 | ||||||
| chr1:204836428
|
G | T | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+7646G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204836428 | ||||||
| chr1:204836468
|
C | T | 29 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(26): Show | 29 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-200+7686C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204836468 | ||||||
| chr1:204836616
|
A | G | 2 | a0001c0001t0015g0212a0002c0003t0002g0213 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-200+7834A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204836616 | ||||||
| chr1:204836775
|
C | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+7993C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204836775 | ||||||
| chr1:204836948
|
C | A | 1 | a0001c0022t0048g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-200+8166C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204836948 | ||||||
| chr1:204837047
|
T | A | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-200+8265T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837047 | ||||||
| chr1:204837102
|
G | A | 1 | a0002c0003t0037g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-200+8320G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837102 | ||||||
| chr1:204837316
|
G | T | 1 | a0003c0018t0018g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-200+8534G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837316 | ||||||
| chr1:204837351
|
G | T | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+8569G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837351 | ||||||
| chr1:204837353
|
C | A | 1 | a0002c0013t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-200+8571C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837353 | ||||||
| chr1:204837385
|
A | G | 1 | a0002c0007t0001g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-200+8603A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837385 | ||||||
| chr1:204837456
|
T | A | 3 | a0001c0005t0001g0062a0001c0005t0005g0061a0002c0040t0004g0052 | 3 | HG02965.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-200+8674T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837456 | ||||||
| chr1:204837460
|
G | A | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+8678G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837460 | ||||||
| chr1:204837477
|
A | C | 8 | a0001c0001t0051g0036a0001c0004t0002g0032a0001c0004t0047g0031others(5): Show | 8 | HG00558.hp1 NA18612.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-200+8695A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837477 | ||||||
| chr1:204837565
|
A | G | 1 | a0002c0013t0001g0211 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-200+8783A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837565 | ||||||
| chr1:204837695
|
T | G | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+8913T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837695 | ||||||
| chr1:204837737
|
G | A | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+8955G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837737 | ||||||
| chr1:204837773
|
GATTCTGC others(19): Show |
G | 29 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(26): Show | 29 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-200+8992_-200+901 others(30): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837773 | ||||||
| chr1:204837800
|
G | T | 29 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(26): Show | 29 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-200+9018G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837800 | ||||||
| chr1:204837999
|
C | T | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+9217C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204837999 | ||||||
| chr1:204838090
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0002g0210 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-200+9308A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838090 | ||||||
| chr1:204838123
|
C | G | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+9341C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838123 | ||||||
| chr1:204838297
|
A | G | 26 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(23): Show | 26 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-200+9515A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838297 | ||||||
| chr1:204838359
|
TTAGAG | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+9580_-200+958 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204838359 | |||||
| chr1:204838372
|
G | A | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+9590G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838372 | ||||||
| chr1:204838390
|
A | G | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-200+9608A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838390 | ||||||
| chr1:204838524
|
A | G | 4 | a0001c0001t0010g0127a0002c0006t0003g0128a0002c0008t0011g0126others(1): Show | 4 | HG01109.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+9742A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838524 | ||||||
| chr1:204838588
|
G | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(35): Show | 38 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.-200+9806G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838588 | ||||||
| chr1:204838595
|
G | A | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+9813G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838595 | ||||||
| chr1:204838646
|
T | A | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+9864T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838646 | ||||||
| chr1:204838809
|
C | A | 3 | a0001c0005t0001g0062a0001c0005t0005g0061a0002c0040t0004g0052 | 3 | HG02965.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-200+10027C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204838809 | ||||||
| chr1:204839006
|
C | T | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+10224C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839006 | ||||||
| chr1:204839042
|
T | G | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+10260T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839042 | ||||||
| chr1:204839126
|
C | T | 2 | a0001c0001t0023g0156a0001c0002t0004g0157 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-200+10344C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839126 | ||||||
| chr1:204839270
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+10488G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839270 | ||||||
| chr1:204839367
|
AAACACAC others(6): Show |
A | 1 | a0001c0002t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-200+10587_-200+10 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839367 | |||||
| chr1:204839368
|
A | AAC | 6 | a0001c0001t0005g0133a0001c0001t0006g0168a0001c0004t0001g0161others(3): Show | 7 | HG00323.hp1 HG00738.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.-200+10635_-200+10 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
A | AACACACA others(7): Show |
1 | a0001c0001t0007g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-200+10623_-200+10 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AAC | A | 35 | a0001c0001t0001g0044a0001c0001t0001g0111a0001c0001t0002g0146others(32): Show | 35 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-200+10635_-200+10 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACAC | A | 17 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0007g0160others(14): Show | 18 | HG00741.hp2 HG01071.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.-200+10633_-200+10 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACAC | A | 13 | a0001c0001t0001g0067a0001c0001t0001g0149a0001c0001t0010g0147others(10): Show | 13 | HG00639.hp2 HG01109.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.-200+10631_-200+10 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(1): Show |
A | 3 | a0001c0002t0050g0099a0001c0004t0001g0142a0001c0004t0005g0153 | 3 | HG02258.hp2 HG03471.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-200+10629_-200+10 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(3): Show |
A | 2 | a0001c0035t0036g0208a0004c0011t0010g0014 | 2 | HG01978.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-200+10627_-200+10 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(5): Show |
A | 6 | a0001c0004t0047g0031a0002c0003t0001g0011a0002c0003t0046g0016others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-200+10625_-200+10 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(7): Show |
A | 26 | a0001c0001t0001g0053a0001c0001t0002g0120a0001c0001t0004g0117others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-200+10623_-200+10 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(9): Show |
A | 30 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0048others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-200+10621_-200+10 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(11): Show |
A | 9 | a0001c0001t0001g0039a0001c0001t0033g0038a0001c0001t0051g0036others(6): Show | 9 | HG02965.hp1 HG02965.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-200+10619_-200+10 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(13): Show |
A | 43 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.-200+10617_-200+10 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839368
|
AACACACA others(15): Show |
A | 2 | a0001c0015t0049g0119a0011c0037t0004g0110 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-200+10615_-200+10 others(28): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204839368 | |||||
| chr1:204839449
|
C | T | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+10667C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839449 | ||||||
| chr1:204839528
|
G | A | 1 | a0001c0002t0002g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-200+10746G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839528 | ||||||
| chr1:204839600
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+10818T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839600 | ||||||
| chr1:204839996
|
T | C | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+11214T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204839996 | ||||||
| chr1:204840015
|
T | C | 119 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(116): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-200+11233T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840015 | ||||||
| chr1:204840196
|
C | T | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+11414C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840196 | ||||||
| chr1:204840197
|
A | G | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+11415A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840197 | ||||||
| chr1:204840448
|
G | C | 13 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0002t0001g0057others(10): Show | 13 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-200+11666G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840448 | ||||||
| chr1:204840546
|
T | A | 54 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(51): Show | 54 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-200+11764T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840546 | ||||||
| chr1:204840735
|
G | T | 2 | a0001c0001t0007g0160a0001c0002t0002g0216 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-200+11953G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840735 | ||||||
| chr1:204840779
|
G | C | 1 | a0002c0033t0001g0169 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-200+11997G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840779 | ||||||
| chr1:204840845
|
A | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0097others(1): Show | 4 | HG01081.hp1 HG01255.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+12063A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204840845 | ||||||
| chr1:204841033
|
G | A | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+12251G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204841033 | ||||||
| chr1:204841064
|
G | A | 1 | a0001c0041t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-200+12282G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204841064 | ||||||
| chr1:204841067
|
C | G | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+12285C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204841067 | ||||||
| chr1:204841071
|
C | T | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+12289C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204841071 | ||||||
| chr1:204841322
|
C | T | 1 | a0001c0002t0009g0193 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-200+12540C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204841322 | ||||||
| chr1:204841508
|
A | G | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+12726A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204841508 | ||||||
| chr1:204842000
|
T | A | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+13218T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842000 | ||||||
| chr1:204842320
|
A | G | 1 | a0002c0003t0006g0221 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-200+13538A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842320 | ||||||
| chr1:204842364
|
G | C | 2 | a0001c0001t0001g0086a0001c0001t0052g0085 | 2 | HG00423.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-200+13582G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842364 | ||||||
| chr1:204842374
|
T | C | 2 | a0001c0001t0001g0086a0001c0001t0052g0085 | 2 | HG00423.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-200+13592T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842374 | ||||||
| chr1:204842488
|
CTT | C | 81 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(78): Show | 81 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-200+13708_-200+13 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204842488 | |||||
| chr1:204842567
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-200+13785C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842567 | ||||||
| chr1:204842806
|
C | T | 2 | a0001c0002t0019g0008a0001c0039t0032g0006 | 2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-200+14024C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842806 | ||||||
| chr1:204842990
|
G | C | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+14208G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204842990 | ||||||
| chr1:204843186
|
G | A | 19 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(16): Show | 19 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-200+14404G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843186 | ||||||
| chr1:204843348
|
A | G | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+14566A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843348 | ||||||
| chr1:204843400
|
C | T | 1 | a0001c0004t0001g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-200+14618C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843400 | ||||||
| chr1:204843570
|
C | T | 87 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(84): Show | 87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-200+14788C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843570 | ||||||
| chr1:204843587
|
T | TCTTC | 12 | a0001c0001t0001g0053a0001c0001t0006g0168a0001c0001t0009g0029others(9): Show | 12 | HG01123.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-200+14844_-200+14 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843587 | |||||
| chr1:204843587
|
T | TCTTCCTT others(1): Show |
2 | a0001c0001t0007g0130a0001c0010t0024g0151 | 2 | HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-200+14840_-200+14 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843587 | |||||
| chr1:204843587
|
TCTTCCTT others(1): Show |
T | 5 | a0002c0003t0012g0222a0004c0011t0010g0014a0004c0011t0017g0018others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-200+14840_-200+14 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843587 | |||||
| chr1:204843587
|
TCTTCCTT others(5): Show |
T | 6 | a0001c0002t0025g0042a0001c0005t0001g0062a0001c0005t0005g0061others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-200+14836_-200+14 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843587 | |||||
| chr1:204843587
|
TCTTCCTT others(17): Show |
T | 23 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(20): Show | 23 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-200+14824_-200+14 others(30): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843587 | |||||
| chr1:204843594
|
TC | T | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+14814delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843594 | |||||
| chr1:204843598
|
TCCTTCCT others(33): Show |
T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+14820_-200+14 others(46): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843598 | |||||
| chr1:204843601
|
T | C | 1 | a0002c0003t0001g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-200+14819T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843601 | ||||||
| chr1:204843610
|
TCCTTCCT others(17): Show |
T | 3 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0004t0001g0142 | 3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-200+14832_-200+14 others(30): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843610 | |||||
| chr1:204843614
|
TCCTTCCT others(9): Show |
T | 45 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(42): Show | 45 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-200+14836_-200+14 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843614 | |||||
| chr1:204843614
|
TCCTTCCT others(17): Show |
T | 2 | a0001c0015t0049g0119a0011c0037t0004g0110 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-200+14836_-200+14 others(30): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843614 | |||||
| chr1:204843618
|
TCCTTCCT others(5): Show |
T | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-200+14840_-200+14 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843618 | |||||
| chr1:204843622
|
TCCTTCCT others(1): Show |
T | 8 | a0001c0002t0002g0140a0001c0004t0002g0204a0001c0010t0004g0194others(5): Show | 8 | HG01257.hp1 HG01257.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-200+14844_-200+14 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843622 | |||||
| chr1:204843626
|
T | C | 26 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(23): Show | 26 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-200+14844T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843626 | ||||||
| chr1:204843626
|
T | TCCTC | 21 | a0001c0001t0001g0044a0001c0001t0001g0111a0001c0001t0001g0162others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-200+14872_-200+14 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843626 | |||||
| chr1:204843626
|
T | TCCTTCCT others(5): Show |
1 | a0002c0013t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-200+14847_-200+14 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843626 | |||||
| chr1:204843626
|
TCCTC | T | 51 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0048others(48): Show | 52 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-200+14872_-200+14 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843626 | |||||
| chr1:204843628
|
C | CT | 4 | a0001c0002t0004g0004a0001c0002t0019g0008a0001c0039t0032g0006others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+14847dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843628 | |||||
| chr1:204843630
|
C | T | 29 | a0001c0001t0001g0053a0001c0001t0001g0163a0001c0001t0002g0210others(26): Show | 30 | HG00558.hp1 HG00673.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-200+14848C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843630 | ||||||
| chr1:204843632
|
C | T | 4 | a0001c0002t0004g0004a0001c0002t0019g0008a0001c0039t0032g0006others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+14850C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843632 | ||||||
| chr1:204843638
|
C | G | 2 | a0001c0001t0001g0081a0001c0001t0040g0113 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-200+14856C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843638 | ||||||
| chr1:204843658
|
T | C | 10 | a0001c0002t0004g0004a0001c0002t0019g0008a0001c0002t0025g0042others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-200+14876T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843658 | ||||||
| chr1:204843662
|
TCCTC | T | 50 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(47): Show | 50 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-200+14888_-200+14 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843662 | |||||
| chr1:204843666
|
C | T | 10 | a0001c0002t0004g0004a0001c0002t0019g0008a0001c0002t0025g0042others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-200+14884C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843666 | ||||||
| chr1:204843686
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+14904T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843686 | ||||||
| chr1:204843687
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+14905T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843687 | ||||||
| chr1:204843708
|
CTCTT | C | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+14930_-200+14 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204843708 | |||||
| chr1:204843777
|
G | A | 1 | a0002c0003t0006g0221 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-200+14995G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843777 | ||||||
| chr1:204843922
|
C | T | 42 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(39): Show | 42 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-200+15140C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204843922 | ||||||
| chr1:204844052
|
C | T | 12 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0015t0005g0114others(9): Show | 12 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-200+15270C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844052 | ||||||
| chr1:204844325
|
A | G | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+15543A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844325 | ||||||
| chr1:204844444
|
A | G | 1 | a0001c0002t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-200+15662A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844444 | ||||||
| chr1:204844504
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+15722T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844504 | ||||||
| chr1:204844602
|
T | C | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+15820T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844602 | ||||||
| chr1:204844603
|
G | A | 1 | a0001c0041t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-200+15821G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844603 | ||||||
| chr1:204844606
|
C | T | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+15824C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844606 | ||||||
| chr1:204844772
|
G | A | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+15990G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844772 | ||||||
| chr1:204844794
|
C | T | 90 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(87): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-200+16012C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844794 | ||||||
| chr1:204844846
|
T | G | 1 | a0004c0020t0003g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-200+16064T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844846 | ||||||
| chr1:204844924
|
C | T | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+16142C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844924 | ||||||
| chr1:204844981
|
A | G | 1 | a0001c0010t0004g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-200+16199A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204844981 | ||||||
| chr1:204845147
|
A | G | 1 | a0013c0050t0020g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-200+16365A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845147 | ||||||
| chr1:204845204
|
G | A | 1 | a0001c0021t0001g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-200+16422G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845204 | ||||||
| chr1:204845295
|
C | CA | 100 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0058others(97): Show | 101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-200+16527dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204845295 | |||||
| chr1:204845295
|
C | CAAAAA | 24 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0006g0121others(21): Show | 24 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+16523_-200+16 others(11): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204845295 | |||||
| chr1:204845295
|
C | CAAAAAA | 5 | a0001c0001t0010g0127a0001c0002t0003g0009a0002c0008t0011g0126others(2): Show | 5 | HG01109.hp1 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-200+16522_-200+16 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204845295 | |||||
| chr1:204845318
|
C | T | 1 | a0001c0001t0023g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-200+16536C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845318 | ||||||
| chr1:204845462
|
A | T | 33 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-200+16680A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845462 | ||||||
| chr1:204845470
|
A | G | 2 | a0001c0014t0001g0002a0001c0014t0001g0200 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-200+16688A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845470 | ||||||
| chr1:204845492
|
C | G | 33 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-200+16710C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845492 | ||||||
| chr1:204845613
|
A | G | 33 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-200+16831A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845613 | ||||||
| chr1:204845765
|
A | G | 33 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-200+16983A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845765 | ||||||
| chr1:204845845
|
C | T | 2 | a0003c0023t0007g0108a0003c0029t0031g0005 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-200+17063C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845845 | ||||||
| chr1:204845894
|
T | C | 27 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-200+17112T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845894 | ||||||
| chr1:204845910
|
A | T | 33 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-200+17128A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204845910 | ||||||
| chr1:204846036
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-200+17254G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846036 | ||||||
| chr1:204846086
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+17304G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846086 | ||||||
| chr1:204846200
|
C | CA | 78 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(75): Show | 78 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-200+17431dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846200 | |||||
| chr1:204846200
|
C | CAA | 6 | a0001c0001t0004g0117a0001c0002t0025g0042a0001c0015t0049g0119others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-200+17430_-200+17 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846200 | |||||
| chr1:204846218
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+17436G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846218 | ||||||
| chr1:204846310
|
A | G | 3 | a0001c0004t0001g0206a0001c0032t0001g0196a0002c0013t0001g0167 | 3 | HG00639.hp2 HG01255.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-200+17528A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846310 | ||||||
| chr1:204846450
|
G | A | 87 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(84): Show | 87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-200+17668G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846450 | ||||||
| chr1:204846484
|
T | C | 87 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(84): Show | 87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-200+17702T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846484 | ||||||
| chr1:204846550
|
C | G | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-200+17768C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846550 | ||||||
| chr1:204846601
|
G | T | 87 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(84): Show | 87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-200+17819G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846601 | ||||||
| chr1:204846733
|
C | G | 1 | a0001c0001t0004g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-200+17951C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846733 | ||||||
| chr1:204846929
|
A | G | 1 | a0001c0015t0049g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-200+18147A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846929 | ||||||
| chr1:204846952
|
C | CGTGTGTG others(5): Show |
6 | a0001c0001t0001g0081a0001c0001t0040g0113a0001c0015t0005g0114others(3): Show | 6 | HG02132.hp2 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+18180_-200+18 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846952 | |||||
| chr1:204846952
|
C | CGTGTGTG others(7): Show |
1 | a0001c0041t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-200+18180_-200+18 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846952 | |||||
| chr1:204846952
|
C | CGTGTGTG others(9): Show |
2 | a0001c0002t0001g0122a0002c0008t0011g0126 | 2 | HG00544.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-200+18180_-200+18 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846952 | |||||
| chr1:204846952
|
C | CGTGTGTG others(11): Show |
16 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(13): Show | 16 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-200+18180_-200+18 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846952 | |||||
| chr1:204846952
|
C | CGTGTGTG others(13): Show |
1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+18180_-200+18 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846952 | |||||
| chr1:204846953
|
G | GTGTGTGT others(3): Show |
45 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0082others(42): Show | 45 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-200+18180_-200+18 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846953 | |||||
| chr1:204846955
|
G | GTGTGTGT others(1): Show |
9 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-200+18180_-200+18 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846955 | |||||
| chr1:204846963
|
G | C | 6 | a0001c0001t0001g0079a0001c0001t0023g0109a0001c0015t0029g0101others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-200+18181G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204846963 | ||||||
| chr1:204846974
|
T | TGTGTGTG others(10): Show |
1 | a0001c0001t0023g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-200+18197_-200+18 others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846974 | |||||
| chr1:204846974
|
T | TGTGTGTG others(12): Show |
4 | a0001c0015t0029g0101a0002c0008t0011g0102a0003c0023t0007g0108others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+18197_-200+18 others(25): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204846974 | |||||
| chr1:204847294
|
T | C | 3 | a0001c0001t0010g0127a0002c0008t0011g0126a0003c0024t0003g0115 | 3 | HG01109.hp1 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-200+18512T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204847294 | ||||||
| chr1:204847545
|
C | T | 86 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-200+18763C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204847545 | ||||||
| chr1:204847574
|
C | T | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0002c0006t0003g0128others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+18792C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204847574 | ||||||
| chr1:204847633
|
A | G | 1 | a0002c0006t0001g0070 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-200+18851A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204847633 | ||||||
| chr1:204848066
|
C | T | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+19284C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848066 | ||||||
| chr1:204848292
|
G | A | 4 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+19510G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848292 | ||||||
| chr1:204848324
|
C | T | 3 | a0001c0002t0025g0042a0003c0016t0053g0041a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-200+19542C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848324 | ||||||
| chr1:204848736
|
G | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+19954G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848736 | ||||||
| chr1:204848780
|
C | T | 1 | a0004c0011t0017g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-200+19998C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848780 | ||||||
| chr1:204848853
|
C | A | 1 | a0003c0018t0018g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-200+20071C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848853 | ||||||
| chr1:204848922
|
A | G | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+20140A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848922 | ||||||
| chr1:204848968
|
A | G | 2 | a0001c0004t0005g0153a0001c0010t0024g0151 | 2 | HG02258.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-200+20186A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204848968 | ||||||
| chr1:204849371
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0033g0038 | 3 | NA18955.hp1 NA18986.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-200+20589C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204849371 | ||||||
| chr1:204849431
|
G | T | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+20649G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204849431 | ||||||
| chr1:204849895
|
C | A | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+21113C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204849895 | ||||||
| chr1:204849935
|
A | G | 86 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-200+21153A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204849935 | ||||||
| chr1:204850016
|
G | A | 3 | a0001c0015t0029g0101a0002c0008t0011g0102a0003c0023t0007g0108 | 3 | HG02622.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-200+21234G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850016 | ||||||
| chr1:204850121
|
A | G | 1 | a0002c0003t0037g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-200+21339A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850121 | ||||||
| chr1:204850221
|
C | T | 2 | a0001c0005t0022g0089a0002c0003t0010g0088 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-200+21439C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850221 | ||||||
| chr1:204850633
|
T | C | 86 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-200+21851T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850633 | ||||||
| chr1:204850789
|
C | A | 74 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(71): Show | 74 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-200+22007C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850789 | ||||||
| chr1:204850829
|
T | C | 86 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-200+22047T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850829 | ||||||
| chr1:204850911
|
A | C | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+22129A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204850911 | ||||||
| chr1:204851298
|
T | C | 1 | a0002c0003t0039g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-200+22516T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851298 | ||||||
| chr1:204851326
|
CT | C | 88 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(85): Show | 88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-200+22560delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204851326 | |||||
| chr1:204851418
|
C | T | 74 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(71): Show | 74 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-200+22636C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851418 | ||||||
| chr1:204851574
|
C | T | 3 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0004t0001g0142 | 3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-200+22792C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851574 | ||||||
| chr1:204851596
|
G | A | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+22814G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851596 | ||||||
| chr1:204851631
|
T | C | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0002c0006t0003g0128others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+22849T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851631 | ||||||
| chr1:204851746
|
A | G | 1 | a0002c0008t0002g0123 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-200+22964A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851746 | ||||||
| chr1:204851960
|
T | G | 1 | a0002c0006t0001g0017 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-200+23178T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204851960 | ||||||
| chr1:204852036
|
G | A | 80 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-200+23254G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852036 | ||||||
| chr1:204852085
|
T | C | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+23303T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852085 | ||||||
| chr1:204852115
|
A | G | 2 | a0001c0001t0023g0156a0001c0002t0004g0157 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-200+23333A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852115 | ||||||
| chr1:204852162
|
G | C | 4 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+23380G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852162 | ||||||
| chr1:204852168
|
G | A | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+23386G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852168 | ||||||
| chr1:204852263
|
C | G | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-200+23481C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852263 | ||||||
| chr1:204852342
|
T | C | 25 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-200+23560T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852342 | ||||||
| chr1:204852360
|
C | T | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+23578C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852360 | ||||||
| chr1:204852424
|
T | C | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+23642T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852424 | ||||||
| chr1:204852455
|
G | A | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-200+23673G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852455 | ||||||
| chr1:204852559
|
A | G | 86 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-200+23777A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852559 | ||||||
| chr1:204852672
|
A | G | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+23890A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852672 | ||||||
| chr1:204852993
|
A | G | 4 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+24211A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204852993 | ||||||
| chr1:204853351
|
T | G | 1 | a0001c0001t0052g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-200+24569T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204853351 | ||||||
| chr1:204853799
|
C | G | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+25017C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204853799 | ||||||
| chr1:204853907
|
G | A | 4 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+25125G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204853907 | ||||||
| chr1:204853908
|
G | A | 1 | a0002c0007t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-200+25126G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204853908 | ||||||
| chr1:204853969
|
C | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+25187C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204853969 | ||||||
| chr1:204854033
|
A | G | 113 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(110): Show | 113 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.-200+25251A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854033 | ||||||
| chr1:204854129
|
C | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+25347C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854129 | ||||||
| chr1:204854133
|
A | G | 5 | a0001c0001t0023g0109a0001c0015t0029g0101a0002c0008t0011g0102others(2): Show | 5 | HG02622.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-200+25351A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854133 | ||||||
| chr1:204854140
|
A | G | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-200+25358A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854140 | ||||||
| chr1:204854309
|
G | A | 2 | a0001c0004t0002g0204a0002c0003t0001g0166 | 2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-200+25527G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854309 | ||||||
| chr1:204854365
|
C | T | 1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-200+25583C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854365 | ||||||
| chr1:204854535
|
G | A | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+25753G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854535 | ||||||
| chr1:204854795
|
C | G | 2 | a0001c0002t0004g0004a0003c0029t0031g0005 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-200+26013C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854795 | ||||||
| chr1:204854825
|
C | T | 1 | a0001c0002t0019g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-200+26043C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854825 | ||||||
| chr1:204854833
|
G | C | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+26051G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204854833 | ||||||
| chr1:204855419
|
CAAT | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+26642_-200+26 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204855419 | |||||
| chr1:204855471
|
G | A | 26 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(23): Show | 26 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-200+26689G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855471 | ||||||
| chr1:204855482
|
G | A | 1 | a0001c0041t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-200+26700G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855482 | ||||||
| chr1:204855527
|
G | T | 77 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(74): Show | 77 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-200+26745G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855527 | ||||||
| chr1:204855584
|
G | A | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+26802G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855584 | ||||||
| chr1:204855636
|
G | A | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+26854G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855636 | ||||||
| chr1:204855666
|
G | A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-200+26884G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855666 | ||||||
| chr1:204855910
|
G | A | 85 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(82): Show | 85 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-200+27128G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855910 | ||||||
| chr1:204855957
|
A | G | 1 | a0001c0002t0019g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-200+27175A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204855957 | ||||||
| chr1:204856010
|
C | T | 4 | a0001c0001t0010g0127a0002c0008t0011g0126a0003c0024t0003g0115others(1): Show | 4 | HG01109.hp1 HG01175.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+27228C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856010 | ||||||
| chr1:204856074
|
C | T | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-200+27292C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856074 | ||||||
| chr1:204856142
|
T | G | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+27360T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856142 | ||||||
| chr1:204856158
|
C | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(80): Show | 83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+27376C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856158 | ||||||
| chr1:204856182
|
G | A | 1 | a0001c0032t0001g0196 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-200+27400G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856182 | ||||||
| chr1:204856254
|
A | G | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+27472A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856254 | ||||||
| chr1:204856382
|
G | GGT | 32 | a0001c0001t0005g0133a0001c0001t0006g0121a0001c0001t0012g0063others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-200+27636_-200+27 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGT | 74 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(71): Show | 74 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-200+27634_-200+27 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGTGT | 37 | a0001c0001t0001g0058a0001c0001t0001g0163a0001c0001t0001g0215others(34): Show | 37 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-200+27632_-200+27 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGTGTG others(1): Show |
30 | a0001c0001t0001g0111a0001c0001t0001g0149a0001c0001t0001g0162others(27): Show | 32 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-200+27630_-200+27 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGTGTG others(3): Show |
19 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0004g0117others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-200+27628_-200+27 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGTGTG others(5): Show |
7 | a0001c0002t0002g0158a0001c0004t0001g0181a0001c0005t0001g0062others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-200+27626_-200+27 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGTGTG others(7): Show |
1 | a0002c0003t0012g0222 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-200+27624_-200+27 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856382
|
G | GGTGTGTG others(9): Show |
2 | a0001c0015t0005g0114a0002c0003t0001g0223 | 2 | HG02717.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-200+27622_-200+27 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856382 | |||||
| chr1:204856413
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-200+27631G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856413 | ||||||
| chr1:204856418
|
T | TGTGA | 3 | a0001c0002t0004g0004a0001c0002t0019g0008a0001c0039t0032g0006 | 3 | HG02109.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-200+27637_-200+27 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856418 | |||||
| chr1:204856418
|
T | TGTGTGTG others(1): Show |
3 | a0001c0002t0003g0009a0003c0019t0005g0007a0003c0029t0031g0005 | 3 | HG02109.hp2 HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-200+27637_-200+27 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204856418 | |||||
| chr1:204856434
|
C | T | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-200+27652C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856434 | ||||||
| chr1:204856478
|
T | A | 1 | a0001c0005t0006g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-200+27696T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856478 | ||||||
| chr1:204856666
|
A | C | 39 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.-200+27884A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856666 | ||||||
| chr1:204856680
|
C | G | 39 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.-200+27898C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856680 | ||||||
| chr1:204856717
|
G | A | 1 | a0001c0002t0002g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-200+27935G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856717 | ||||||
| chr1:204856738
|
C | G | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+27956C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856738 | ||||||
| chr1:204856839
|
G | A | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+28057G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856839 | ||||||
| chr1:204856846
|
A | G | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+28064A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856846 | ||||||
| chr1:204856986
|
A | G | 80 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-200+28204A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204856986 | ||||||
| chr1:204857020
|
G | T | 1 | a0001c0010t0005g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-200+28238G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857020 | ||||||
| chr1:204857089
|
G | A | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+28307G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857089 | ||||||
| chr1:204857162
|
A | G | 2 | a0001c0027t0014g0184a0002c0003t0001g0171 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-200+28380A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857162 | ||||||
| chr1:204857200
|
A | G | 80 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-200+28418A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857200 | ||||||
| chr1:204857336
|
T | C | 80 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-200+28554T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857336 | ||||||
| chr1:204857347
|
C | T | 1 | a0001c0035t0036g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-200+28565C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857347 | ||||||
| chr1:204857475
|
CT | C | 80 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-200+28694delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857475 | ||||||
| chr1:204857552
|
G | A | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+28770G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857552 | ||||||
| chr1:204857606
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0111a0001c0002t0002g0069others(5): Show | 8 | HG01168.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+28824C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857606 | ||||||
| chr1:204857756
|
C | A | 80 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-200+28974C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857756 | ||||||
| chr1:204857916
|
C | CTTTT | 18 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(15): Show | 18 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-200+29136_-200+29 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204857916 | |||||
| chr1:204857916
|
C | CTTTTT | 57 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(54): Show | 57 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-200+29136_-200+29 others(11): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204857916 | |||||
| chr1:204857916
|
C | CTTTTTT | 5 | a0001c0001t0010g0127a0002c0008t0011g0126a0003c0024t0003g0115others(2): Show | 5 | HG01109.hp1 HG01175.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-200+29136_-200+29 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204857916 | |||||
| chr1:204857919
|
C | T | 82 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0079others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-200+29137C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857919 | ||||||
| chr1:204857919
|
CT | C | 6 | a0001c0001t0001g0012a0001c0001t0015g0093a0001c0017t0001g0173others(3): Show | 6 | HG01069.hp2 HG01168.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+29154delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204857919 | |||||
| chr1:204857980
|
C | T | 3 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0004t0001g0142 | 3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-200+29198C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857980 | ||||||
| chr1:204857996
|
T | C | 1 | a0010c0034t0009g0214 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-200+29214T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204857996 | ||||||
| chr1:204858198
|
G | A | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-200+29416G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858198 | ||||||
| chr1:204858393
|
G | T | 4 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+29611G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858393 | ||||||
| chr1:204858409
|
C | A | 38 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(35): Show | 38 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-200+29627C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858409 | ||||||
| chr1:204858479
|
G | T | 1 | a0001c0010t0030g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-200+29697G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858479 | ||||||
| chr1:204858517
|
A | G | 88 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(85): Show | 88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-200+29735A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858517 | ||||||
| chr1:204858529
|
T | C | 79 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(76): Show | 79 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-200+29747T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858529 | ||||||
| chr1:204858653
|
C | T | 10 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-200+29871C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858653 | ||||||
| chr1:204858807
|
G | A | 38 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-200+30025G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858807 | ||||||
| chr1:204858822
|
A | T | 6 | a0001c0004t0001g0161a0001c0004t0001g0176a0001c0021t0001g0170others(3): Show | 6 | HG00323.hp1 HG00639.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+30040A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858822 | ||||||
| chr1:204858905
|
G | A | 4 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-200+30123G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858905 | ||||||
| chr1:204858913
|
C | G | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-200+30131C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204858913 | ||||||
| chr1:204858978
|
C | CTTTTTT | 9 | a0001c0001t0004g0064a0001c0002t0004g0004a0001c0002t0019g0008others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-200+30208_-200+30 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204858978 | |||||
| chr1:204858978
|
CT | C | 37 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(34): Show | 37 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-200+30213delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204858978 | |||||
| chr1:204859175
|
G | A | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-200+30393G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204859175 | ||||||
| chr1:204859290
|
A | C | 10 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-200+30508A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204859290 | ||||||
| chr1:204859326
|
C | G | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+30544C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204859326 | ||||||
| chr1:204859697
|
T | C | 2 | a0002c0003t0042g0182a0002c0028t0014g0183 | 2 | HG00639.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-200+30915T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204859697 | ||||||
| chr1:204860106
|
G | A | 69 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(66): Show | 69 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-200+31324G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860106 | ||||||
| chr1:204860136
|
C | T | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+31354C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860136 | ||||||
| chr1:204860163
|
G | A | 2 | a0001c0002t0011g0144a0001c0043t0027g0224 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-200+31381G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860163 | ||||||
| chr1:204860171
|
A | G | 1 | a0002c0007t0001g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-200+31389A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860171 | ||||||
| chr1:204860613
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+31831G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860613 | ||||||
| chr1:204860628
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0033g0038 | 3 | NA18955.hp1 NA18986.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-200+31846A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860628 | ||||||
| chr1:204860770
|
T | C | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+31988T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860770 | ||||||
| chr1:204860860
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-200+32078T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860860 | ||||||
| chr1:204860943
|
A | G | 81 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(78): Show | 81 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-200+32161A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204860943 | ||||||
| chr1:204860993
|
G | GT | 85 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(82): Show | 85 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-200+32220dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204860993 | |||||
| chr1:204861078
|
C | CT | 38 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0202others(35): Show | 39 | HG00673.hp2 HG00738.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-200+32323dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204861078 | |||||
| chr1:204861078
|
C | CTT | 6 | a0001c0001t0002g0146a0001c0002t0002g0219a0001c0002t0004g0004others(3): Show | 6 | HG01358.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+32322_-200+32 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204861078 | |||||
| chr1:204861078
|
CT | C | 65 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(62): Show | 65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-200+32323delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204861078 | |||||
| chr1:204861078
|
CTT | C | 7 | a0001c0001t0001g0086a0001c0001t0004g0064a0001c0002t0002g0073others(4): Show | 7 | HG01243.hp1 HG01346.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-200+32322_-200+32 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204861078 | |||||
| chr1:204861078
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+32314_-200+32 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204861078 | |||||
| chr1:204861078
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-200+32311_-200+32 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204861078 | |||||
| chr1:204861122
|
T | C | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-200+32340T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861122 | ||||||
| chr1:204861192
|
A | G | 81 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(78): Show | 81 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-200+32410A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861192 | ||||||
| chr1:204861224
|
G | A | 2 | a0001c0001t0007g0160a0001c0002t0002g0216 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-200+32442G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861224 | ||||||
| chr1:204861251
|
G | A | 26 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(23): Show | 26 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-200+32469G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861251 | ||||||
| chr1:204861503
|
T | A | 73 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-200+32721T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861503 | ||||||
| chr1:204861650
|
C | T | 2 | a0001c0041t0003g0118a0003c0019t0003g0116 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-200+32868C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861650 | ||||||
| chr1:204861768
|
C | T | 1 | a0002c0003t0001g0001 | 2 | HG00738.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-200+32986C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861768 | ||||||
| chr1:204861778
|
C | T | 3 | a0001c0002t0020g0100a0001c0002t0045g0098a0001c0002t0050g0099 | 3 | HG01109.hp2 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-200+32996C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861778 | ||||||
| chr1:204861924
|
G | A | 30 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-200+33142G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861924 | ||||||
| chr1:204861937
|
T | C | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+33155T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204861937 | ||||||
| chr1:204862242
|
C | T | 36 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0004g0117others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-200+33460C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204862242 | ||||||
| chr1:204862581
|
A | C | 3 | a0001c0001t0015g0093a0001c0001t0015g0212a0001c0002t0009g0193 | 3 | HG01168.hp1 HG01169.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-200+33799A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204862581 | ||||||
| chr1:204862971
|
G | A | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-200+34189G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204862971 | ||||||
| chr1:204863172
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-200+34390G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863172 | ||||||
| chr1:204863179
|
G | A | 8 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+34397G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863179 | ||||||
| chr1:204863232
|
A | G | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+34450A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863232 | ||||||
| chr1:204863263
|
C | T | 2 | a0001c0002t0001g0057a0002c0003t0002g0049 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.-200+34481C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863263 | ||||||
| chr1:204863447
|
C | G | 6 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+34665C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863447 | ||||||
| chr1:204863467
|
A | T | 1 | a0001c0002t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-200+34685A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863467 | ||||||
| chr1:204863717
|
C | T | 4 | a0001c0001t0010g0127a0002c0008t0011g0126a0003c0024t0003g0115others(1): Show | 4 | HG01109.hp1 HG01175.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+34935C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863717 | ||||||
| chr1:204863726
|
G | A | 48 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(45): Show | 48 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-200+34944G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863726 | ||||||
| chr1:204863740
|
C | T | 1 | a0001c0005t0007g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-200+34958C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863740 | ||||||
| chr1:204863804
|
C | T | 2 | a0001c0002t0002g0073a0002c0007t0001g0080 | 2 | HG03239.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-200+35022C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863804 | ||||||
| chr1:204863847
|
CA | C | 53 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(50): Show | 53 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-200+35081delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204863847 | |||||
| chr1:204863916
|
G | A | 2 | a0002c0003t0042g0182a0002c0028t0014g0183 | 2 | HG00639.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-200+35134G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863916 | ||||||
| chr1:204863934
|
AAGAG | A | 38 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(35): Show | 38 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-200+35160_-200+35 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204863934 | |||||
| chr1:204863944
|
G | A | 3 | a0001c0001t0015g0093a0001c0001t0015g0212a0001c0002t0009g0193 | 3 | HG01168.hp1 HG01169.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-200+35162G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204863944 | ||||||
| chr1:204863950
|
GAGAA | G | 2 | a0001c0004t0001g0112a0001c0005t0001g0062 | 2 | HG03516.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-200+35180_-200+35 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204863950 | |||||
| chr1:204864072
|
C | T | 3 | a0001c0001t0007g0160a0001c0002t0002g0216a0002c0003t0010g0088 | 3 | HG02630.hp1 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-200+35290C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864072 | ||||||
| chr1:204864077
|
C | T | 70 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(67): Show | 70 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-200+35295C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864077 | ||||||
| chr1:204864281
|
T | C | 6 | a0001c0001t0001g0053a0001c0001t0009g0029a0001c0001t0043g0028others(3): Show | 6 | HG00673.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-200+35499T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864281 | ||||||
| chr1:204864318
|
G | A | 65 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(62): Show | 65 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-200+35536G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864318 | ||||||
| chr1:204864502
|
A | G | 83 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(80): Show | 83 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-200+35720A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864502 | ||||||
| chr1:204864723
|
C | G | 16 | a0001c0001t0001g0163a0001c0001t0002g0146a0001c0001t0002g0210others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-200+35941C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864723 | ||||||
| chr1:204864903
|
T | G | 55 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(52): Show | 55 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-200+36121T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204864903 | ||||||
| chr1:204865017
|
G | C | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+36235G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204865017 | ||||||
| chr1:204865081
|
T | C | 221 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(218): Show | 223 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.-200+36299T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204865081 | ||||||
| chr1:204865082
|
G | A | 2 | a0002c0003t0001g0001a0002c0003t0006g0221 | 3 | HG00738.hp2 HG01074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-200+36300G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204865082 | ||||||
| chr1:204865152
|
T | G | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+36370T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204865152 | ||||||
| chr1:204865154
|
C | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+36372C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204865154 | ||||||
| chr1:204865371
|
A | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-200+36589A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204865371 | ||||||
| chr1:204865724
|
ATTC | A | 3 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0004t0001g0142 | 3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-200+36952_-200+36 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204865724 | |||||
| chr1:204866107
|
C | T | 1 | a0001c0002t0002g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-200+37325C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866107 | ||||||
| chr1:204866191
|
C | G | 1 | a0001c0015t0049g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-200+37409C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866191 | ||||||
| chr1:204866214
|
A | G | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+37432A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866214 | ||||||
| chr1:204866260
|
T | C | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-200+37478T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866260 | ||||||
| chr1:204866281
|
C | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-200+37499C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866281 | ||||||
| chr1:204866400
|
G | A | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+37618G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866400 | ||||||
| chr1:204866403
|
C | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+37621C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866403 | ||||||
| chr1:204866571
|
T | A | 1 | a0010c0034t0009g0214 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-200+37789T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204866571 | ||||||
| chr1:204867249
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+38467G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867249 | ||||||
| chr1:204867309
|
A | G | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+38527A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867309 | ||||||
| chr1:204867409
|
C | CCA | 44 | a0001c0001t0001g0163a0001c0001t0001g0201a0001c0001t0002g0210others(41): Show | 45 | HG00423.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.-200+38657_-200+38 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867409
|
C | CCACA | 4 | a0001c0001t0004g0117a0001c0002t0011g0144a0002c0040t0004g0052others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+38655_-200+38 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867409
|
C | CCACACA | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+38653_-200+38 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867409
|
CCA | C | 92 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(89): Show | 93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-200+38657_-200+38 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867409
|
CCACA | C | 14 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-200+38655_-200+38 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867409
|
CCACACA | C | 25 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0084others(22): Show | 25 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-200+38653_-200+38 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867409
|
CCACACAC others(1): Show |
C | 24 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0009g0029others(21): Show | 24 | HG00423.hp1 HG00741.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-200+38651_-200+38 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204867409 | |||||
| chr1:204867524
|
A | G | 42 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(39): Show | 42 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.-200+38742A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867524 | ||||||
| chr1:204867567
|
TCAGATAG others(6): Show |
T | 1 | a0002c0006t0002g0035 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-200+38786_-200+38 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867567 | ||||||
| chr1:204867645
|
A | G | 2 | a0001c0004t0002g0204a0002c0003t0001g0166 | 2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-200+38863A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867645 | ||||||
| chr1:204867732
|
C | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+38950C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867732 | ||||||
| chr1:204867733
|
G | A | 41 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(38): Show | 41 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.-200+38951G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867733 | ||||||
| chr1:204867805
|
A | T | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+39023A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204867805 | ||||||
| chr1:204868150
|
C | T | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+39368C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868150 | ||||||
| chr1:204868156
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-200+39374G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868156 | ||||||
| chr1:204868191
|
C | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(27): Show | 30 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-200+39409C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868191 | ||||||
| chr1:204868219
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-200+39437G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868219 | ||||||
| chr1:204868376
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-200+39594C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868376 | ||||||
| chr1:204868576
|
C | T | 1 | a0001c0001t0023g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-200+39794C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868576 | ||||||
| chr1:204868615
|
C | G | 29 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(26): Show | 29 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-200+39833C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868615 | ||||||
| chr1:204868634
|
T | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-200+39852T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868634 | ||||||
| chr1:204868693
|
T | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-200+39911T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204868693 | ||||||
| chr1:204869186
|
G | A | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+40404G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204869186 | ||||||
| chr1:204869461
|
C | A | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+40679C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204869461 | ||||||
| chr1:204869582
|
A | C | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+40800A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204869582 | ||||||
| chr1:204869619
|
C | A | 1 | a0003c0019t0005g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-200+40837C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204869619 | ||||||
| chr1:204869672
|
C | T | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-200+40890C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204869672 | ||||||
| chr1:204869865
|
T | A | 2 | a0001c0001t0004g0117a0002c0040t0004g0052 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-200+41083T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204869865 | ||||||
| chr1:204870011
|
A | G | 4 | a0001c0015t0029g0101a0002c0008t0011g0102a0003c0023t0007g0108others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+41229A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870011 | ||||||
| chr1:204870014
|
C | T | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-200+41232C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870014 | ||||||
| chr1:204870026
|
T | G | 161 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(158): Show | 162 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-200+41244T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870026 | ||||||
| chr1:204870195
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-200+41413C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870195 | ||||||
| chr1:204870553
|
G | A | 1 | a0002c0013t0001g0211 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-200+41771G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870553 | ||||||
| chr1:204870824
|
T | C | 1 | a0001c0035t0036g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-200+42042T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870824 | ||||||
| chr1:204870831
|
G | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-200+42049G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870831 | ||||||
| chr1:204870976
|
C | A | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-200+42194C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204870976 | ||||||
| chr1:204871352
|
G | A | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+42570G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204871352 | ||||||
| chr1:204871357
|
C | T | 2 | a0001c0004t0001g0174a0001c0010t0005g0175 | 2 | HG01106.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-200+42575C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204871357 | ||||||
| chr1:204871508
|
T | C | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-200+42726T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204871508 | ||||||
| chr1:204872067
|
C | T | 4 | a0001c0001t0006g0003a0001c0004t0001g0013a0002c0003t0001g0024others(1): Show | 4 | HG01243.hp2 NA18951.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+43285C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872067 | ||||||
| chr1:204872153
|
C | G | 27 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-200+43371C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872153 | ||||||
| chr1:204872185
|
A | G | 1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-200+43403A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872185 | ||||||
| chr1:204872252
|
T | A | 1 | a0003c0016t0026g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-200+43470T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872252 | ||||||
| chr1:204872441
|
C | T | 1 | a0002c0003t0037g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-200+43659C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872441 | ||||||
| chr1:204872661
|
G | T | 1 | a0001c0005t0034g0135 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-200+43879G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872661 | ||||||
| chr1:204872662
|
C | T | 1 | a0001c0005t0034g0135 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-200+43880C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872662 | ||||||
| chr1:204872974
|
G | A | 27 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-200+44192G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204872974 | ||||||
| chr1:204873009
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-200+44227G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873009 | ||||||
| chr1:204873052
|
A | G | 105 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(102): Show | 105 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-200+44270A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873052 | ||||||
| chr1:204873118
|
G | A | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-200+44336G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873118 | ||||||
| chr1:204873156
|
GGC | G | 162 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(159): Show | 163 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.-200+44375_-200+44 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873156 | ||||||
| chr1:204873160
|
C | T | 162 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(159): Show | 163 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.-200+44378C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873160 | ||||||
| chr1:204873161
|
CTTGCA | C | 162 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(159): Show | 163 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.-200+44382_-200+44 others(11): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204873161 | |||||
| chr1:204873286
|
C | T | 1 | a0002c0007t0001g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-200+44504C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873286 | ||||||
| chr1:204873341
|
C | A | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+44559C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873341 | ||||||
| chr1:204873426
|
C | T | 1 | a0001c0035t0036g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-200+44644C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873426 | ||||||
| chr1:204873512
|
G | A | 1 | a0002c0003t0037g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-200+44730G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873512 | ||||||
| chr1:204873641
|
G | A | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-200+44859G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873641 | ||||||
| chr1:204873658
|
G | A | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-200+44876G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873658 | ||||||
| chr1:204873676
|
TC | T | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-200+44896delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204873676 | |||||
| chr1:204873687
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-200+44905G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873687 | ||||||
| chr1:204873955
|
G | A | 43 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-200+45173G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204873955 | ||||||
| chr1:204874064
|
A | C | 27 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-200+45282A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874064 | ||||||
| chr1:204874116
|
GCT | G | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-200+45341_-200+45 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204874116 | |||||
| chr1:204874156
|
G | A | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-200+45374G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874156 | ||||||
| chr1:204874181
|
G | C | 102 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(99): Show | 102 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.-200+45399G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874181 | ||||||
| chr1:204874251
|
A | G | 2 | a0001c0002t0019g0008a0001c0039t0032g0006 | 2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-200+45469A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874251 | ||||||
| chr1:204874266
|
C | G | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-200+45484C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874266 | ||||||
| chr1:204874531
|
G | A | 7 | a0001c0001t0001g0045a0001c0004t0001g0046a0001c0004t0001g0087others(4): Show | 7 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-200+45749G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874531 | ||||||
| chr1:204874562
|
C | T | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-200+45780C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874562 | ||||||
| chr1:204874564
|
C | T | 2 | a0001c0004t0001g0174a0001c0010t0005g0175 | 2 | HG01106.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-200+45782C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874564 | ||||||
| chr1:204874573
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-200+45791A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874573 | ||||||
| chr1:204874771
|
C | T | 2 | a0001c0002t0002g0158a0001c0002t0006g0195 | 2 | NA18954.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-199-45861C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874771 | ||||||
| chr1:204874777
|
T | C | 1 | a0005c0047t0021g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-199-45855T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874777 | ||||||
| chr1:204874836
|
T | A | 13 | a0001c0001t0004g0064a0001c0002t0002g0148a0001c0002t0002g0189others(10): Show | 13 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-199-45796T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204874836 | ||||||
| chr1:204875073
|
T | TTTG | 36 | a0001c0001t0002g0120a0001c0001t0005g0133a0001c0001t0006g0121others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-199-45523_-199-45 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
T | TTTGTTG | 16 | a0001c0001t0002g0146a0001c0001t0007g0160a0001c0001t0010g0147others(13): Show | 17 | HG00738.hp2 HG01074.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-199-45526_-199-45 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
T | TTTGTTGT others(2): Show |
8 | a0001c0001t0001g0163a0001c0001t0002g0210a0001c0001t0004g0117others(5): Show | 8 | HG01175.hp2 HG01978.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-199-45529_-199-45 others(15): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTG | T | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-199-45523_-199-45 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTGTTG | T | 17 | a0001c0001t0004g0064a0001c0001t0051g0036a0001c0002t0001g0023others(14): Show | 17 | HG01243.hp1 HG02132.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-199-45526_-199-45 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTGTTGT others(5): Show |
T | 1 | a0001c0005t0005g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-199-45532_-199-45 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875140
|
G | T | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-45492G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875140 | ||||||
| chr1:204875499
|
C | T | 1 | a0002c0007t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-199-45133C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875499 | ||||||
| chr1:204875522
|
T | G | 1 | a0001c0042t0001g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-199-45110T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875522 | ||||||
| chr1:204875665
|
C | A | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-44967C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875665 | ||||||
| chr1:204875665
|
CT | C | 43 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-199-44964delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204875665 | |||||
| chr1:204875719
|
G | A | 1 | a0001c0017t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-199-44913G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875719 | ||||||
| chr1:204875831
|
A | G | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-199-44801A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875831 | ||||||
| chr1:204875846
|
G | A | 1 | a0002c0003t0039g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-199-44786G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875846 | ||||||
| chr1:204875937
|
A | G | 56 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(53): Show | 56 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-199-44695A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875937 | ||||||
| chr1:204875981
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-199-44651A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204875981 | ||||||
| chr1:204876033
|
G | T | 2 | a0001c0004t0001g0071a0002c0003t0039g0218 | 2 | HG06807.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-199-44599G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876033 | ||||||
| chr1:204876219
|
T | C | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-44413T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876219 | ||||||
| chr1:204876573
|
A | G | 5 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-44059A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876573 | ||||||
| chr1:204876631
|
A | G | 1 | a0001c0002t0002g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-199-44001A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876631 | ||||||
| chr1:204876664
|
G | A | 71 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(68): Show | 71 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-199-43968G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876664 | ||||||
| chr1:204876724
|
A | G | 3 | a0001c0002t0019g0008a0001c0039t0032g0006a0003c0016t0026g0141 | 3 | HG02055.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-199-43908A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876724 | ||||||
| chr1:204876903
|
C | T | 3 | a0001c0002t0002g0140a0001c0015t0049g0119a0003c0019t0003g0116 | 3 | HG03225.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-199-43729C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876903 | ||||||
| chr1:204876917
|
C | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-43715C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876917 | ||||||
| chr1:204876960
|
G | A | 1 | a0002c0006t0001g0017 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-199-43672G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876960 | ||||||
| chr1:204876991
|
A | T | 1 | a0001c0001t0009g0029 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-199-43641A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876991 | ||||||
| chr1:204876994
|
A | ATG | 1 | a0001c0014t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-199-43636_-199-43 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876994 | |||||
| chr1:204876994
|
ATGTATAT others(67): Show |
A | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-199-43636_-199-43 others(80): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876994 | |||||
| chr1:204876996
|
G | A | 83 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(80): Show | 83 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-199-43636G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204876996 | ||||||
| chr1:204876996
|
G | GTA | 11 | a0001c0001t0001g0044a0001c0001t0002g0120a0001c0002t0001g0057others(8): Show | 11 | HG00558.hp2 HG00741.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.-199-43605_-199-43 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
G | GTATA | 5 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199-43607_-199-43 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTA | G | 28 | a0001c0001t0001g0111a0001c0001t0001g0162a0001c0001t0006g0168others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.-199-43605_-199-43 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTATA | G | 12 | a0001c0001t0002g0146a0001c0001t0005g0133a0001c0001t0007g0160others(9): Show | 12 | HG02559.hp1 HG02602.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-199-43607_-199-43 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTATATA | G | 13 | a0001c0001t0007g0130a0001c0002t0002g0140a0001c0002t0008g0137others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-199-43609_-199-43 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTATATAT others(1): Show |
G | 5 | a0001c0001t0001g0163a0001c0001t0002g0210a0001c0015t0049g0119others(2): Show | 6 | HG00738.hp2 HG01074.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199-43611_-199-43 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204877000
|
A | G | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-43632A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877000 | ||||||
| chr1:204877002
|
A | G | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-43630A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877002 | ||||||
| chr1:204877015
|
TATATATA others(59): Show |
T | 1 | a0005c0047t0021g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-199-43616_-199-43 others(72): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877015 | ||||||
| chr1:204877016
|
ATATATAT others(45): Show |
A | 6 | a0001c0001t0001g0012a0001c0001t0001g0086a0001c0001t0033g0038others(3): Show | 6 | HG01346.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199-43597_-199-43 others(58): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877016 | |||||
| chr1:204877018
|
ATATATAT others(43): Show |
A | 4 | a0001c0002t0004g0004a0001c0012t0001g0054a0001c0012t0001g0055others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(56): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877018 | |||||
| chr1:204877020
|
ATATATAT others(10): Show |
A | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-199-43603_-199-43 others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877020 | |||||
| chr1:204877020
|
ATATATAT others(41): Show |
A | 3 | a0001c0004t0001g0112a0002c0007t0001g0047a0002c0007t0001g0080 | 3 | HG03491.hp2 HG03492.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(54): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877020 | |||||
| chr1:204877021
|
TATATATA others(53): Show |
T | 11 | a0001c0001t0001g0053a0001c0001t0006g0003a0001c0002t0001g0027others(8): Show | 11 | HG00558.hp1 HG00673.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-199-43610_-199-43 others(66): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877021 | ||||||
| chr1:204877022
|
ATATATAA others(31): Show |
A | 4 | a0001c0001t0001g0045a0001c0001t0001g0097a0001c0004t0001g0087others(1): Show | 4 | HG01175.hp1 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(44): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877022 | |||||
| chr1:204877022
|
ATATATAA others(39): Show |
A | 2 | a0001c0001t0043g0028a0002c0003t0037g0068 | 2 | HG01123.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(52): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877022 | |||||
| chr1:204877023
|
TATATAAT others(51): Show |
T | 20 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0040g0113others(17): Show | 20 | HG01192.hp1 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-199-43608_-199-43 others(64): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877023 | ||||||
| chr1:204877024
|
ATATAATA others(6): Show |
A | 2 | a0001c0005t0022g0089a0001c0015t0005g0114 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(26): Show |
A | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-199-43607_-199-43 others(39): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877024 | ||||||
| chr1:204877024
|
ATATAATA others(28): Show |
A | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-199-43606_-199-43 others(41): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(29): Show |
A | 5 | a0001c0001t0001g0082a0001c0001t0052g0085a0001c0002t0002g0073others(2): Show | 5 | HG00423.hp1 HG01081.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(42): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(37): Show |
A | 3 | a0001c0004t0001g0046a0002c0003t0002g0049a0002c0006t0001g0070 | 3 | HG00544.hp2 HG02293.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(50): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(57): Show |
A | 2 | a0001c0004t0041g0065a0001c0005t0007g0066 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-43607_-199-43 others(70): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877024 | ||||||
| chr1:204877025
|
TATAATAT others(49): Show |
T | 9 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0058others(6): Show | 9 | HG02572.hp2 HG02717.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-199-43606_-199-43 others(62): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877025 | ||||||
| chr1:204877026
|
ATAATATA others(4): Show |
A | 1 | a0001c0005t0005g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-199-43603_-199-43 others(17): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877026 | |||||
| chr1:204877026
|
ATAATATA others(26): Show |
A | 6 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-199-43604_-199-43 others(39): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877026 | |||||
| chr1:204877026
|
ATAATATA others(35): Show |
A | 6 | a0001c0001t0001g0079a0001c0001t0009g0029a0001c0002t0001g0060others(3): Show | 6 | HG01192.hp2 HG01358.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(48): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877026 | |||||
| chr1:204877026
|
ATAATATA others(49): Show |
A | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-199-43605_-199-43 others(62): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877026 | ||||||
| chr1:204877027
|
T | A | 3 | a0001c0004t0003g0203a0004c0020t0003g0197a0011c0037t0004g0110 | 3 | HG02886.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-199-43605T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877027 | ||||||
| chr1:204877027
|
TA | T | 3 | a0001c0010t0024g0151a0001c0038t0014g0078a0002c0028t0014g0183 | 3 | HG00639.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-199-43603delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877027 | |||||
| chr1:204877028
|
AATATATA others(24): Show |
A | 1 | a0003c0049t0003g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-199-43603_-199-43 others(37): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877028 | ||||||
| chr1:204877028
|
AATATATA others(25): Show |
A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(38): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877028 | ||||||
| chr1:204877028
|
AATATATA others(33): Show |
A | 6 | a0001c0001t0001g0084a0001c0004t0001g0076a0001c0004t0001g0083others(3): Show | 6 | HG00673.hp1 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-199-43603_-199-43 others(46): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877028 | ||||||
| chr1:204877029
|
A | T | 1 | a0001c0002t0008g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-199-43603A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877029 | ||||||
| chr1:204877030
|
T | A | 1 | a0001c0002t0008g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-199-43602T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877030 | ||||||
| chr1:204877030
|
T | TA | 2 | a0001c0001t0004g0117a0002c0040t0004g0052 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-199-43601dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877030 | |||||
| chr1:204877037
|
T | A | 6 | a0001c0001t0004g0117a0001c0002t0008g0143a0001c0010t0024g0151others(3): Show | 6 | HG02615.hp2 HG02897.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199-43595T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877037 | ||||||
| chr1:204877037
|
TTA | T | 4 | a0001c0001t0005g0133a0001c0002t0002g0069a0001c0002t0009g0193others(1): Show | 4 | HG01256.hp1 HG01256.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-199-43584_-199-43 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877037 | |||||
| chr1:204877039
|
A | T | 3 | a0001c0001t0004g0117a0001c0002t0008g0143a0002c0040t0004g0052 | 3 | HG02615.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-199-43593A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877039 | ||||||
| chr1:204877045
|
ATATAATA others(30): Show |
A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-199-43586_-199-43 others(43): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877045 | ||||||
| chr1:204877050
|
ATATATTT others(3): Show |
A | 3 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0043t0027g0224 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-199-43576_-199-43 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877050 | |||||
| chr1:204877052
|
ATATTTAT others(1): Show |
A | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-43576_-199-43 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877052 | |||||
| chr1:204877059
|
T | A | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-199-43573T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877059 | ||||||
| chr1:204877060
|
T | A | 2 | a0001c0001t0004g0064a0001c0010t0024g0151 | 2 | HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-199-43572T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877060 | ||||||
| chr1:204877068
|
T | A | 11 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0097others(8): Show | 11 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-43564T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877068 | ||||||
| chr1:204877068
|
T | TTATATAT others(18): Show |
1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-199-43558_-199-43 others(31): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877068 | |||||
| chr1:204877068
|
T | TTATATAT others(20): Show |
2 | a0003c0024t0003g0115a0009c0031t0001g0209 | 2 | HG01175.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-199-43560_-199-43 others(33): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877068 | |||||
| chr1:204877068
|
TTA | T | 7 | a0001c0001t0023g0109a0001c0002t0008g0143a0001c0005t0022g0089others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-199-43553_-199-43 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204877068 | |||||
| chr1:204877081
|
A | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0045a0001c0001t0001g0079others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-199-43551A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877081 | ||||||
| chr1:204877087
|
T | A | 2 | a0001c0001t0001g0067a0001c0002t0002g0073 | 2 | HG03239.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-199-43545T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877087 | ||||||
| chr1:204877090
|
T | A | 2 | a0001c0004t0041g0065a0001c0005t0007g0066 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-43542T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877090 | ||||||
| chr1:204877091
|
T | A | 44 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(41): Show | 44 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-199-43541T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877091 | ||||||
| chr1:204877108
|
A | T | 1 | a0001c0001t0009g0029 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-199-43524A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877108 | ||||||
| chr1:204877147
|
A | G | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-199-43485A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877147 | ||||||
| chr1:204877200
|
C | A | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-43432C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877200 | ||||||
| chr1:204877268
|
C | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-43364C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877268 | ||||||
| chr1:204877290
|
G | A | 1 | a0004c0020t0003g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-199-43342G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877290 | ||||||
| chr1:204877336
|
A | G | 84 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(81): Show | 84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-199-43296A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877336 | ||||||
| chr1:204877347
|
G | A | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-43285G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877347 | ||||||
| chr1:204877354
|
G | A | 1 | a0001c0005t0007g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-199-43278G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877354 | ||||||
| chr1:204877481
|
G | A | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-43151G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877481 | ||||||
| chr1:204877644
|
C | T | 29 | a0001c0001t0001g0163a0001c0001t0002g0146a0001c0001t0002g0210others(26): Show | 30 | HG00738.hp2 HG01074.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-199-42988C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877644 | ||||||
| chr1:204877755
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-199-42877C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877755 | ||||||
| chr1:204877756
|
G | A | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-42876G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877756 | ||||||
| chr1:204877946
|
A | G | 1 | a0002c0003t0035g0207 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-199-42686A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877946 | ||||||
| chr1:204877973
|
G | A | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-42659G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204877973 | ||||||
| chr1:204878014
|
C | T | 1 | a0005c0046t0001g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-199-42618C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878014 | ||||||
| chr1:204878143
|
T | G | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-42489T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878143 | ||||||
| chr1:204878366
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-42266G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878366 | ||||||
| chr1:204878442
|
T | C | 2 | a0002c0003t0002g0124a0002c0003t0002g0125 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-199-42190T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878442 | ||||||
| chr1:204878540
|
C | T | 3 | a0002c0008t0011g0126a0003c0024t0003g0115a0009c0031t0001g0209 | 3 | HG01175.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-199-42092C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878540 | ||||||
| chr1:204878601
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-42031A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878601 | ||||||
| chr1:204878660
|
T | G | 17 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(14): Show | 17 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-199-41972T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878660 | ||||||
| chr1:204878683
|
C | T | 3 | a0003c0016t0053g0041a0003c0019t0005g0007a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-199-41949C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878683 | ||||||
| chr1:204878691
|
G | A | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-199-41941G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878691 | ||||||
| chr1:204878771
|
G | A | 2 | a0001c0001t0023g0156a0001c0002t0004g0157 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-199-41861G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878771 | ||||||
| chr1:204878787
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-41845G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878787 | ||||||
| chr1:204878947
|
G | C | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-199-41685G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204878947 | ||||||
| chr1:204879003
|
C | G | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-41629C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879003 | ||||||
| chr1:204879059
|
C | G | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-199-41573C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879059 | ||||||
| chr1:204879190
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-41442A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879190 | ||||||
| chr1:204879233
|
T | C | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-41399T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879233 | ||||||
| chr1:204879264
|
A | G | 25 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(22): Show | 25 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.-199-41368A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879264 | ||||||
| chr1:204879266
|
T | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-41366T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879266 | ||||||
| chr1:204879317
|
TTG | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-41311_-199-41 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204879317 | |||||
| chr1:204879907
|
C | A | 51 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0111others(48): Show | 52 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-199-40725C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879907 | ||||||
| chr1:204879942
|
G | T | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-40690G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879942 | ||||||
| chr1:204879958
|
G | A | 1 | a0003c0018t0018g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-199-40674G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879958 | ||||||
| chr1:204879972
|
C | T | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-40660C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204879972 | ||||||
| chr1:204880028
|
G | T | 41 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(38): Show | 41 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.-199-40604G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880028 | ||||||
| chr1:204880148
|
G | T | 3 | a0003c0016t0053g0041a0003c0019t0005g0007a0006c0048t0025g0040 | 3 | HG02055.hp2 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-199-40484G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880148 | ||||||
| chr1:204880197
|
G | T | 2 | a0001c0004t0003g0203a0004c0020t0003g0197 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-199-40435G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880197 | ||||||
| chr1:204880203
|
C | T | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-199-40429C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880203 | ||||||
| chr1:204880222
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-40410G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880222 | ||||||
| chr1:204880323
|
A | AT | 4 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-199-40301dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204880323 | |||||
| chr1:204880358
|
T | G | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-40274T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880358 | ||||||
| chr1:204880465
|
C | T | 7 | a0001c0001t0004g0064a0001c0002t0008g0143a0001c0004t0041g0065others(4): Show | 7 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-199-40167C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880465 | ||||||
| chr1:204880505
|
G | A | 1 | a0001c0002t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-199-40127G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880505 | ||||||
| chr1:204880507
|
C | T | 1 | a0001c0021t0001g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-199-40125C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880507 | ||||||
| chr1:204880522
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-40110A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880522 | ||||||
| chr1:204880599
|
G | A | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-199-40033G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880599 | ||||||
| chr1:204880613
|
A | G | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-40019A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880613 | ||||||
| chr1:204880791
|
C | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-199-39841C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880791 | ||||||
| chr1:204880818
|
C | T | 5 | a0001c0001t0051g0036a0001c0004t0002g0032a0002c0006t0001g0037others(2): Show | 5 | HG00558.hp1 NA18612.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-39814C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880818 | ||||||
| chr1:204880819
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-199-39813G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204880819 | ||||||
| chr1:204881144
|
A | G | 1 | a0004c0020t0024g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-199-39488A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204881144 | ||||||
| chr1:204881349
|
G | T | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-39283G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204881349 | ||||||
| chr1:204881374
|
C | T | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-199-39258C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204881374 | ||||||
| chr1:204881568
|
G | A | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-39064G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204881568 | ||||||
| chr1:204881589
|
C | T | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-199-39043C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204881589 | ||||||
| chr1:204881608
|
C | T | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-39024C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204881608 | ||||||
| chr1:204882104
|
C | T | 5 | a0001c0001t0023g0109a0001c0015t0029g0101a0002c0008t0011g0102others(2): Show | 5 | HG02622.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199-38528C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882104 | ||||||
| chr1:204882242
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-38390T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882242 | ||||||
| chr1:204882427
|
T | TC | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-38198dupC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204882427 | |||||
| chr1:204882433
|
C | G | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-38199C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882433 | ||||||
| chr1:204882501
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0040g0113a0002c0003t0001g0059 | 3 | HG02132.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-199-38131T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882501 | ||||||
| chr1:204882554
|
A | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-38078A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882554 | ||||||
| chr1:204882602
|
C | G | 5 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-38030C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882602 | ||||||
| chr1:204882679
|
G | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0033g0038 | 3 | NA18955.hp1 NA18986.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-199-37953G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882679 | ||||||
| chr1:204882811
|
T | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-37821T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882811 | ||||||
| chr1:204882815
|
G | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-37817G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882815 | ||||||
| chr1:204882893
|
G | A | 1 | a0001c0004t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-199-37739G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882893 | ||||||
| chr1:204882907
|
C | T | 1 | a0003c0018t0018g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-199-37725C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882907 | ||||||
| chr1:204882962
|
C | T | 23 | a0001c0001t0002g0120a0001c0001t0006g0121a0001c0001t0012g0063others(20): Show | 23 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.-199-37670C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204882962 | ||||||
| chr1:204883161
|
C | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-37471C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883161 | ||||||
| chr1:204883165
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-199-37467C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883165 | ||||||
| chr1:204883211
|
C | T | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-199-37421C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883211 | ||||||
| chr1:204883244
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-199-37388G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883244 | ||||||
| chr1:204883356
|
G | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-37276G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883356 | ||||||
| chr1:204883371
|
C | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-37261C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883371 | ||||||
| chr1:204883464
|
C | G | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-37168C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883464 | ||||||
| chr1:204883498
|
A | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-37134A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883498 | ||||||
| chr1:204883569
|
G | C | 2 | a0001c0001t0004g0117a0002c0040t0004g0052 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-199-37063G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883569 | ||||||
| chr1:204883636
|
C | G | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-199-36996C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883636 | ||||||
| chr1:204883715
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-36917T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883715 | ||||||
| chr1:204883765
|
G | A | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-199-36867G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883765 | ||||||
| chr1:204883811
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-199-36821A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883811 | ||||||
| chr1:204883813
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-199-36819G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883813 | ||||||
| chr1:204883924
|
C | T | 1 | a0001c0002t0002g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-199-36708C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204883924 | ||||||
| chr1:204884055
|
T | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-36577T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884055 | ||||||
| chr1:204884135
|
G | A | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-36497G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884135 | ||||||
| chr1:204884210
|
A | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-36422A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884210 | ||||||
| chr1:204884255
|
C | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(42): Show | 45 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-199-36377C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884255 | ||||||
| chr1:204884353
|
A | G | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-36279A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884353 | ||||||
| chr1:204884384
|
G | A | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-199-36248G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884384 | ||||||
| chr1:204884425
|
C | T | 8 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-36207C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884425 | ||||||
| chr1:204884876
|
G | A | 2 | a0001c0004t0001g0206a0002c0013t0001g0167 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-199-35756G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884876 | ||||||
| chr1:204884932
|
A | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-35700A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204884932 | ||||||
| chr1:204885143
|
A | C | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-35489A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204885143 | ||||||
| chr1:204885230
|
T | A | 2 | a0001c0001t0001g0163a0001c0001t0002g0210 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-199-35402T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204885230 | ||||||
| chr1:204885278
|
A | C | 2 | a0001c0014t0001g0002a0001c0014t0001g0200 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-199-35354A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204885278 | ||||||
| chr1:204885389
|
TG | T | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 42 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-199-35235delG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204885389 | |||||
| chr1:204885390
|
G | T | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-35242G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204885390 | ||||||
| chr1:204885391
|
G | C | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-199-35241G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204885391 | ||||||
| chr1:204885994
|
C | T | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-199-34638C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204885994 | ||||||
| chr1:204886001
|
G | A | 1 | a0001c0041t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-199-34631G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204886001 | ||||||
| chr1:204886311
|
A | T | 12 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(9): Show | 12 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-199-34321A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204886311 | ||||||
| chr1:204886543
|
A | C | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-199-34089A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204886543 | ||||||
| chr1:204886770
|
G | A | 1 | a0001c0004t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-199-33862G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204886770 | ||||||
| chr1:204886838
|
G | A | 59 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(56): Show | 59 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.-199-33794G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204886838 | ||||||
| chr1:204886911
|
C | T | 104 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(101): Show | 104 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-199-33721C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204886911 | ||||||
| chr1:204887206
|
G | T | 2 | a0001c0004t0002g0032a0002c0006t0002g0021 | 2 | HG00558.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-199-33426G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204887206 | ||||||
| chr1:204887586
|
C | CT | 36 | a0001c0001t0001g0044a0001c0001t0001g0149a0001c0001t0001g0215others(33): Show | 37 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-199-33016dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
C | CTT | 17 | a0001c0001t0001g0045a0001c0001t0001g0111a0001c0001t0007g0160others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.-199-33017_-199-33 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
C | CTTT | 24 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0097others(21): Show | 24 | HG00423.hp1 HG00673.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-199-33018_-199-33 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
C | CTTTT | 10 | a0001c0001t0001g0084a0001c0001t0009g0029a0001c0002t0001g0060others(7): Show | 10 | HG00735.hp1 HG00741.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-199-33019_-199-33 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CT | C | 20 | a0001c0001t0015g0212a0001c0002t0002g0148a0001c0002t0002g0189others(17): Show | 20 | HG01169.hp2 HG01192.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.-199-33016delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CTTTTTTT others(4): Show |
C | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-199-33026_-199-33 others(17): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CTTTTTTT others(7): Show |
C | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-199-33029_-199-33 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887629
|
T | C | 81 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(78): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-199-33003T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204887629 | ||||||
| chr1:204887830
|
C | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-32802C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204887830 | ||||||
| chr1:204887845
|
G | A | 4 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0010t0024g0151others(1): Show | 4 | HG02897.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-32787G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204887845 | ||||||
| chr1:204888016
|
G | T | 7 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-199-32616G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888016 | ||||||
| chr1:204888031
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-199-32601C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888031 | ||||||
| chr1:204888322
|
C | T | 1 | a0001c0002t0002g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-199-32310C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888322 | ||||||
| chr1:204888505
|
A | C | 6 | a0001c0001t0001g0111a0001c0002t0009g0193a0001c0004t0001g0091others(3): Show | 6 | HG01168.hp2 HG01256.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-199-32127A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888505 | ||||||
| chr1:204888569
|
C | T | 3 | a0001c0001t0015g0093a0001c0001t0015g0212a0001c0002t0002g0069 | 3 | HG01168.hp1 HG01169.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-199-32063C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888569 | ||||||
| chr1:204888869
|
G | A | 12 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0002t0008g0137others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-199-31763G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888869 | ||||||
| chr1:204888881
|
T | A | 1 | a0012c0044t0013g0010 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-199-31751T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204888881 | ||||||
| chr1:204889197
|
T | C | 12 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0002t0008g0137others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-199-31435T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204889197 | ||||||
| chr1:204889258
|
A | G | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-31374A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204889258 | ||||||
| chr1:204889690
|
A | C | 2 | a0001c0027t0014g0184a0002c0003t0001g0171 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-199-30942A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204889690 | ||||||
| chr1:204889710
|
A | G | 1 | a0012c0044t0013g0010 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-199-30922A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204889710 | ||||||
| chr1:204889740
|
A | G | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-199-30892A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204889740 | ||||||
| chr1:204889947
|
G | A | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-30685G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204889947 | ||||||
| chr1:204890138
|
T | A | 1 | a0001c0004t0001g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-199-30494T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890138 | ||||||
| chr1:204890380
|
G | A | 3 | a0001c0002t0002g0140a0001c0015t0049g0119a0003c0019t0003g0116 | 3 | HG03225.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-199-30252G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890380 | ||||||
| chr1:204890385
|
C | T | 1 | a0002c0007t0001g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-199-30247C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890385 | ||||||
| chr1:204890486
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-199-30146G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890486 | ||||||
| chr1:204890565
|
CT | C | 60 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0079others(57): Show | 60 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-199-30055delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204890565 | |||||
| chr1:204890621
|
A | G | 145 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(142): Show | 145 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.-199-30011A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890621 | ||||||
| chr1:204890669
|
C | A | 3 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0004t0001g0142 | 3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-199-29963C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890669 | ||||||
| chr1:204890694
|
C | T | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-29938C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890694 | ||||||
| chr1:204890780
|
G | A | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-29852G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204890780 | ||||||
| chr1:204891104
|
C | T | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-29528C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891104 | ||||||
| chr1:204891119
|
G | A | 1 | a0002c0003t0001g0001 | 2 | HG00738.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-199-29513G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891119 | ||||||
| chr1:204891194
|
G | A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-199-29438G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891194 | ||||||
| chr1:204891397
|
G | T | 1 | a0002c0003t0001g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-199-29235G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891397 | ||||||
| chr1:204891593
|
C | T | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-199-29039C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891593 | ||||||
| chr1:204891594
|
G | T | 1 | a0001c0010t0024g0151 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-199-29038G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891594 | ||||||
| chr1:204891697
|
A | G | 1 | a0001c0002t0004g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-199-28935A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891697 | ||||||
| chr1:204891840
|
G | A | 108 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(105): Show | 108 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-199-28792G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891840 | ||||||
| chr1:204891851
|
A | T | 1 | a0002c0003t0021g0159 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-199-28781A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891851 | ||||||
| chr1:204891955
|
C | T | 108 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(105): Show | 108 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-199-28677C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891955 | ||||||
| chr1:204891963
|
A | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-28669A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204891963 | ||||||
| chr1:204892106
|
G | A | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-199-28526G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892106 | ||||||
| chr1:204892134
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-28498A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892134 | ||||||
| chr1:204892192
|
A | G | 2 | a0001c0001t0015g0093a0001c0001t0015g0212 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-199-28440A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892192 | ||||||
| chr1:204892243
|
C | T | 108 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(105): Show | 108 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-199-28389C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892243 | ||||||
| chr1:204892256
|
C | T | 108 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(105): Show | 108 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-199-28376C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892256 | ||||||
| chr1:204892399
|
G | C | 1 | a0001c0002t0002g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-199-28233G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892399 | ||||||
| chr1:204892691
|
A | G | 43 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-199-27941A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204892691 | ||||||
| chr1:204893516
|
A | C | 47 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(44): Show | 47 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-199-27116A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204893516 | ||||||
| chr1:204893598
|
G | A | 2 | a0001c0004t0002g0032a0002c0006t0002g0021 | 2 | HG00558.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-199-27034G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204893598 | ||||||
| chr1:204893645
|
G | A | 11 | a0001c0002t0003g0009a0001c0002t0004g0004a0001c0002t0019g0008others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-26987G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204893645 | ||||||
| chr1:204893690
|
G | A | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-26942G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204893690 | ||||||
| chr1:204893993
|
A | G | 108 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(105): Show | 108 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-199-26639A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204893993 | ||||||
| chr1:204894001
|
C | A | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-199-26631C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204894001 | ||||||
| chr1:204894076
|
A | C | 51 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(48): Show | 51 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-199-26556A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204894076 | ||||||
| chr1:204894178
|
T | A | 118 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(115): Show | 118 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-199-26454T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204894178 | ||||||
| chr1:204895024
|
A | G | 118 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(115): Show | 118 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-199-25608A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204895024 | ||||||
| chr1:204895593
|
G | A | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-199-25039G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204895593 | ||||||
| chr1:204895952
|
A | G | 5 | a0001c0001t0001g0163a0001c0001t0002g0210a0001c0004t0001g0071others(2): Show | 6 | HG00738.hp2 HG01074.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-199-24680A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204895952 | ||||||
| chr1:204896044
|
G | A | 3 | a0001c0005t0005g0061a0001c0010t0024g0151a0001c0043t0027g0224 | 3 | HG02897.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-199-24588G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896044 | ||||||
| chr1:204896083
|
T | G | 1 | a0001c0010t0024g0151 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-199-24549T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896083 | ||||||
| chr1:204896156
|
A | C | 92 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(89): Show | 92 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-199-24476A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896156 | ||||||
| chr1:204896314
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-199-24318G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896314 | ||||||
| chr1:204896420
|
C | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(28): Show | 31 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199-24212C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896420 | ||||||
| chr1:204896530
|
T | A | 39 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-199-24102T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896530 | ||||||
| chr1:204896776
|
C | T | 14 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(11): Show | 14 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-199-23856C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896776 | ||||||
| chr1:204896923
|
G | A | 3 | a0001c0005t0005g0061a0001c0010t0024g0151a0001c0043t0027g0224 | 3 | HG02897.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-199-23709G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204896923 | ||||||
| chr1:204897237
|
T | C | 161 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(158): Show | 162 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-199-23395T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897237 | ||||||
| chr1:204897275
|
A | C | 3 | a0001c0005t0005g0061a0001c0010t0024g0151a0001c0043t0027g0224 | 3 | HG02897.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-199-23357A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897275 | ||||||
| chr1:204897296
|
C | T | 2 | a0001c0002t0008g0143a0001c0005t0022g0089 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-199-23336C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897296 | ||||||
| chr1:204897355
|
A | C | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-199-23277A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897355 | ||||||
| chr1:204897578
|
C | CT | 5 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-23040dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204897578 | |||||
| chr1:204897578
|
CT | C | 21 | a0001c0001t0002g0120a0001c0001t0004g0117a0001c0001t0006g0121others(18): Show | 21 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-199-23040delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204897578 | |||||
| chr1:204897640
|
C | T | 18 | a0001c0001t0002g0120a0001c0001t0006g0121a0001c0001t0012g0063others(15): Show | 18 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.-199-22992C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897640 | ||||||
| chr1:204897749
|
T | G | 3 | a0001c0001t0005g0133a0001c0001t0023g0109a0001c0021t0001g0170 | 3 | HG01123.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-199-22883T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897749 | ||||||
| chr1:204897751
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-199-22881G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897751 | ||||||
| chr1:204897791
|
A | C | 1 | a0003c0018t0018g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-199-22841A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204897791 | ||||||
| chr1:204898145
|
A | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-199-22487A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204898145 | ||||||
| chr1:204898301
|
G | A | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-22331G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204898301 | ||||||
| chr1:204898309
|
T | C | 1 | a0001c0002t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-199-22323T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204898309 | ||||||
| chr1:204898509
|
TATC | T | 3 | a0001c0001t0007g0160a0001c0002t0002g0216a0002c0003t0010g0088 | 3 | HG02630.hp1 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-199-22120_-199-22 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204898509 | |||||
| chr1:204898553
|
G | C | 1 | a0005c0047t0021g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-199-22079G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204898553 | ||||||
| chr1:204898957
|
G | C | 2 | a0001c0015t0005g0114a0002c0006t0003g0128 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-199-21675G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204898957 | ||||||
| chr1:204899164
|
G | A | 2 | a0001c0001t0006g0121a0001c0001t0012g0063 | 2 | HG00423.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-199-21468G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899164 | ||||||
| chr1:204899369
|
G | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(45): Show | 48 | HG00558.hp1 HG00673.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-199-21263G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899369 | ||||||
| chr1:204899420
|
A | AG | 143 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(140): Show | 144 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.-199-21211dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204899420 | |||||
| chr1:204899439
|
C | T | 5 | a0001c0002t0002g0219a0001c0002t0025g0042a0001c0002t0045g0098others(2): Show | 5 | HG01109.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-21193C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899439 | ||||||
| chr1:204899449
|
C | T | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-199-21183C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899449 | ||||||
| chr1:204899709
|
T | C | 49 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(46): Show | 50 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-199-20923T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899709 | ||||||
| chr1:204899757
|
C | T | 8 | a0001c0001t0001g0058a0001c0001t0051g0036a0001c0004t0002g0032others(5): Show | 8 | HG00558.hp1 NA18612.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-199-20875C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899757 | ||||||
| chr1:204899960
|
C | T | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-199-20672C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899960 | ||||||
| chr1:204899976
|
G | A | 1 | a0002c0003t0002g0213 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-199-20656G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204899976 | ||||||
| chr1:204900009
|
A | G | 1 | a0001c0005t0034g0135 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-199-20623A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204900009 | ||||||
| chr1:204900067
|
T | A | 111 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(108): Show | 112 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-199-20565T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204900067 | ||||||
| chr1:204900176
|
A | G | 3 | a0001c0002t0008g0137a0003c0009t0007g0138a0003c0009t0007g0165 | 3 | HG02258.hp1 HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-199-20456A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204900176 | ||||||
| chr1:204900326
|
T | G | 14 | a0001c0001t0004g0064a0001c0002t0003g0009a0001c0002t0004g0004others(11): Show | 14 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-199-20306T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204900326 | ||||||
| chr1:204900431
|
A | G | 42 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0082others(39): Show | 43 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-199-20201A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204900431 | ||||||
| chr1:204900879
|
G | A | 10 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0002t0008g0137others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-199-19753G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204900879 | ||||||
| chr1:204901529
|
A | G | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-199-19103A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204901529 | ||||||
| chr1:204901860
|
G | A | 29 | a0001c0001t0002g0146a0001c0001t0007g0160a0001c0001t0010g0147others(26): Show | 30 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.-199-18772G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204901860 | ||||||
| chr1:204901930
|
C | G | 82 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0082others(79): Show | 84 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.-199-18702C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204901930 | ||||||
| chr1:204902018
|
C | T | 110 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0082others(107): Show | 112 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(109): Show |
intron_variant | MODIFIER | c.-199-18614C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902018 | ||||||
| chr1:204902122
|
C | T | 39 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0149others(36): Show | 39 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.-199-18510C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902122 | ||||||
| chr1:204902123
|
G | A | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-18509G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902123 | ||||||
| chr1:204902130
|
C | T | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-18502C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902130 | ||||||
| chr1:204902366
|
C | T | 1 | a0002c0006t0001g0070 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-199-18266C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902366 | ||||||
| chr1:204902542
|
T | C | 1 | a0001c0002t0002g0073 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-199-18090T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902542 | ||||||
| chr1:204902648
|
T | C | 4 | a0001c0001t0005g0133a0001c0002t0011g0144a0001c0005t0005g0131others(1): Show | 4 | HG02451.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-17984T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902648 | ||||||
| chr1:204902676
|
A | C | 11 | a0001c0001t0004g0117a0001c0001t0010g0127a0001c0002t0002g0140others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-17956A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902676 | ||||||
| chr1:204902681
|
G | A | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-17951G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902681 | ||||||
| chr1:204902702
|
T | C | 221 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(218): Show | 223 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.-199-17930T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902702 | ||||||
| chr1:204902853
|
G | A | 45 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0082others(42): Show | 47 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-199-17779G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902853 | ||||||
| chr1:204902900
|
G | A | 2 | a0001c0004t0003g0203a0004c0020t0003g0197 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-199-17732G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902900 | ||||||
| chr1:204902940
|
A | G | 18 | a0001c0001t0004g0117a0001c0001t0005g0133a0001c0001t0010g0127others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-199-17692A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902940 | ||||||
| chr1:204902960
|
A | C | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-199-17672A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204902960 | ||||||
| chr1:204903329
|
G | A | 1 | a0001c0001t0012g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-199-17303G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903329 | ||||||
| chr1:204903359
|
C | T | 5 | a0001c0002t0002g0192a0001c0004t0001g0161a0001c0035t0036g0208others(2): Show | 5 | HG00323.hp1 HG01106.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199-17273C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903359 | ||||||
| chr1:204903504
|
G | T | 3 | a0001c0001t0023g0156a0001c0002t0004g0157a0001c0010t0030g0217 | 3 | HG02559.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-199-17128G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903504 | ||||||
| chr1:204903529
|
A | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-199-17103A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903529 | ||||||
| chr1:204903714
|
G | A | 19 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0202others(16): Show | 19 | HG00544.hp1 HG00738.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-199-16918G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903714 | ||||||
| chr1:204903894
|
A | G | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-199-16738A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903894 | ||||||
| chr1:204903906
|
G | C | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-16726G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204903906 | ||||||
| chr1:204904345
|
G | A | 1 | a0002c0003t0039g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-199-16287G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204904345 | ||||||
| chr1:204904565
|
A | C | 4 | a0001c0001t0001g0084a0001c0001t0009g0029a0001c0001t0043g0028others(1): Show | 4 | HG01123.hp2 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-199-16067A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204904565 | ||||||
| chr1:204904630
|
C | A | 1 | a0002c0003t0002g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-199-16002C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204904630 | ||||||
| chr1:204904819
|
T | C | 16 | a0001c0001t0007g0130a0001c0001t0010g0127a0001c0002t0001g0180others(13): Show | 16 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-199-15813T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204904819 | ||||||
| chr1:204904883
|
TC | T | 133 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(130): Show | 133 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-199-15747delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204904883 | |||||
| chr1:204905072
|
G | T | 1 | a0001c0002t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-199-15560G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905072 | ||||||
| chr1:204905132
|
T | A | 14 | a0001c0004t0001g0139a0001c0005t0005g0131a0001c0005t0034g0135others(11): Show | 14 | HG01192.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-199-15500T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905132 | ||||||
| chr1:204905164
|
A | C | 3 | a0001c0002t0001g0060a0001c0004t0001g0076a0002c0003t0013g0132 | 3 | HG02135.hp2 NA18974.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-199-15468A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905164 | ||||||
| chr1:204905183
|
C | G | 44 | a0001c0001t0001g0111a0001c0001t0006g0003a0001c0001t0012g0063others(41): Show | 44 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-199-15449C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905183 | ||||||
| chr1:204905189
|
A | G | 1 | a0004c0011t0010g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-199-15443A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905189 | ||||||
| chr1:204905331
|
G | T | 49 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 49 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-199-15301G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905331 | ||||||
| chr1:204905370
|
G | GT | 5 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199-15250dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204905370 | |||||
| chr1:204905370
|
GT | G | 55 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0202others(52): Show | 55 | HG00323.hp1 HG00558.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-199-15250delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204905370 | |||||
| chr1:204905420
|
G | A | 1 | a0002c0007t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-199-15212G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905420 | ||||||
| chr1:204905443
|
C | T | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-15189C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905443 | ||||||
| chr1:204905466
|
G | A | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-199-15166G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905466 | ||||||
| chr1:204905477
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 49 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-199-15155T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905477 | ||||||
| chr1:204905728
|
G | A | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-14904G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204905728 | ||||||
| chr1:204906048
|
G | A | 1 | a0001c0010t0030g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-199-14584G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906048 | ||||||
| chr1:204906132
|
G | A | 2 | a0001c0002t0002g0192a0001c0035t0036g0208 | 2 | HG01106.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-199-14500G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906132 | ||||||
| chr1:204906202
|
A | T | 16 | a0001c0001t0007g0130a0001c0001t0010g0127a0001c0002t0001g0180others(13): Show | 16 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-199-14430A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906202 | ||||||
| chr1:204906272
|
C | A | 2 | a0001c0004t0003g0203a0004c0020t0003g0197 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-199-14360C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906272 | ||||||
| chr1:204906443
|
G | A | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-199-14189G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906443 | ||||||
| chr1:204906517
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-199-14115G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906517 | ||||||
| chr1:204906687
|
A | AT | 5 | a0001c0005t0005g0061a0001c0005t0022g0089a0001c0043t0027g0224others(2): Show | 5 | HG02622.hp2 HG02965.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-13932dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204906687 | |||||
| chr1:204906687
|
AT | A | 80 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0111others(77): Show | 82 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-199-13932delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204906687 | |||||
| chr1:204906736
|
G | A | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-199-13896G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906736 | ||||||
| chr1:204906750
|
TCGGCTCA others(18): Show |
T | 5 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-13881_-199-13 others(31): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906750 | ||||||
| chr1:204906751
|
CGGCTCAC others(18): Show |
C | 82 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0081others(79): Show | 82 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-199-13874_-199-13 others(31): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204906751 | |||||
| chr1:204906776
|
G | T | 5 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-13856G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906776 | ||||||
| chr1:204906779
|
C | T | 53 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(50): Show | 53 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.-199-13853C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906779 | ||||||
| chr1:204906805
|
CCCCGAGT others(17): Show |
C | 1 | a0001c0002t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-199-13822_-199-13 others(30): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204906805 | |||||
| chr1:204906839
|
C | A | 2 | a0001c0001t0001g0048a0011c0037t0004g0110 | 2 | HG02129.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-199-13793C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906839 | ||||||
| chr1:204906840
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-199-13792T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906840 | ||||||
| chr1:204906844
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-199-13788C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906844 | ||||||
| chr1:204906877
|
G | T | 9 | a0001c0001t0023g0156a0001c0002t0002g0148a0001c0002t0002g0189others(6): Show | 9 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-199-13755G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906877 | ||||||
| chr1:204906882
|
A | G | 12 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0002t0019g0090others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-199-13750A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906882 | ||||||
| chr1:204906885
|
A | G | 7 | a0001c0001t0001g0086a0001c0001t0004g0064a0001c0004t0041g0065others(4): Show | 7 | HG01243.hp1 HG01346.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-199-13747A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906885 | ||||||
| chr1:204906904
|
G | C | 39 | a0001c0001t0001g0067a0001c0001t0001g0202a0001c0001t0002g0120others(36): Show | 39 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-199-13728G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906904 | ||||||
| chr1:204906904
|
G | T | 83 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(80): Show | 83 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-199-13728G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906904 | ||||||
| chr1:204906905
|
C | G | 122 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(119): Show | 122 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-199-13727C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906905 | ||||||
| chr1:204906930
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-199-13702G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906930 | ||||||
| chr1:204906934
|
T | C | 2 | a0001c0002t0001g0023a0002c0003t0001g0171 | 2 | HG02132.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-199-13698T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906934 | ||||||
| chr1:204906935
|
G | A | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-199-13697G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204906935 | ||||||
| chr1:204907296
|
A | G | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-13336A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204907296 | ||||||
| chr1:204907308
|
GTTGT | G | 27 | a0001c0001t0006g0003a0001c0001t0012g0063a0001c0001t0015g0093others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-199-13317_-199-13 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204907308 | |||||
| chr1:204907521
|
G | A | 2 | a0003c0019t0005g0007a0003c0024t0003g0115 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-199-13111G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204907521 | ||||||
| chr1:204907570
|
G | T | 1 | a0001c0001t0051g0036 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-199-13062G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204907570 | ||||||
| chr1:204907693
|
C | T | 1 | a0002c0006t0002g0035 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-199-12939C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204907693 | ||||||
| chr1:204907838
|
T | G | 24 | a0001c0001t0004g0064a0001c0001t0007g0130a0001c0001t0010g0127others(21): Show | 24 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-199-12794T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204907838 | ||||||
| chr1:204907941
|
T | C | 95 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(92): Show | 95 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-199-12691T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204907941 | ||||||
| chr1:204907944
|
A | ATG | 23 | a0001c0001t0004g0064a0001c0002t0002g0148a0001c0002t0002g0189others(20): Show | 23 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-199-12666_-199-12 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204907944 | |||||
| chr1:204907944
|
A | ATGTG | 3 | a0001c0001t0023g0156a0001c0002t0045g0098a0001c0010t0030g0217 | 3 | HG01109.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-199-12668_-199-12 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204907944 | |||||
| chr1:204907944
|
ATG | A | 93 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(90): Show | 93 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.-199-12666_-199-12 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204907944 | |||||
| chr1:204908014
|
T | C | 190 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(187): Show | 192 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-199-12618T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908014 | ||||||
| chr1:204908068
|
A | G | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-12564A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908068 | ||||||
| chr1:204908212
|
G | A | 1 | a0001c0002t0019g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-199-12420G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908212 | ||||||
| chr1:204908262
|
A | T | 2 | a0001c0001t0023g0156a0001c0010t0030g0217 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-199-12370A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908262 | ||||||
| chr1:204908297
|
A | G | 2 | a0001c0001t0015g0093a0001c0001t0015g0212 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-199-12335A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908297 | ||||||
| chr1:204908350
|
C | T | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-199-12282C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908350 | ||||||
| chr1:204908524
|
G | A | 195 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(192): Show | 197 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.-199-12108G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908524 | ||||||
| chr1:204908542
|
T | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-199-12090T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908542 | ||||||
| chr1:204908808
|
T | G | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-199-11824T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908808 | ||||||
| chr1:204908901
|
C | A | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-11731C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908901 | ||||||
| chr1:204908917
|
A | G | 21 | a0001c0001t0004g0064a0001c0001t0007g0130a0001c0002t0001g0180others(18): Show | 21 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-199-11715A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204908917 | ||||||
| chr1:204909399
|
A | G | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-11233A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909399 | ||||||
| chr1:204909474
|
GAAAGTTC others(3): Show |
G | 4 | a0001c0004t0001g0139a0001c0043t0027g0224a0003c0019t0005g0007others(1): Show | 4 | HG02257.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-199-11156_-199-11 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204909474 | |||||
| chr1:204909485
|
A | G | 1 | a0002c0007t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-199-11147A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909485 | ||||||
| chr1:204909576
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-11056A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909576 | ||||||
| chr1:204909592
|
G | A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-199-11040G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909592 | ||||||
| chr1:204909660
|
A | G | 4 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-10972A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909660 | ||||||
| chr1:204909763
|
T | A | 5 | a0001c0001t0005g0133a0001c0002t0008g0137a0001c0002t0011g0144others(2): Show | 5 | HG02451.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-10869T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909763 | ||||||
| chr1:204909809
|
A | G | 4 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-10823A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909809 | ||||||
| chr1:204909893
|
T | C | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-10739T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909893 | ||||||
| chr1:204909961
|
A | G | 75 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(72): Show | 75 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.-199-10671A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204909961 | ||||||
| chr1:204910027
|
A | G | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-199-10605A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910027 | ||||||
| chr1:204910046
|
A | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-199-10586A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910046 | ||||||
| chr1:204910155
|
G | GTA | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-10467_-199-10 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204910155 | |||||
| chr1:204910381
|
G | C | 3 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106 | 3 | HG01069.hp1 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-199-10251G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910381 | ||||||
| chr1:204910425
|
T | G | 1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-199-10207T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910425 | ||||||
| chr1:204910516
|
A | ATCT | 105 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-199-10114_-199-10 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204910516 | |||||
| chr1:204910621
|
A | G | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-199-10011A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910621 | ||||||
| chr1:204910695
|
A | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-9937A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910695 | ||||||
| chr1:204910824
|
A | AT | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-9799dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204910824 | |||||
| chr1:204910906
|
G | C | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-9726G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910906 | ||||||
| chr1:204910947
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-9685A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204910947 | ||||||
| chr1:204911079
|
C | T | 4 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-9553C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204911079 | ||||||
| chr1:204911260
|
T | C | 21 | a0001c0001t0004g0064a0001c0001t0007g0130a0001c0002t0001g0180others(18): Show | 21 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-199-9372T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204911260 | ||||||
| chr1:204911376
|
G | A | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-199-9256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204911376 | ||||||
| chr1:204911408
|
A | C | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-9224A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204911408 | ||||||
| chr1:204911582
|
G | A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-199-9050G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204911582 | ||||||
| chr1:204912077
|
A | G | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-8555A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912077 | ||||||
| chr1:204912079
|
G | A | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-8553G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912079 | ||||||
| chr1:204912139
|
T | C | 12 | a0001c0001t0023g0156a0001c0002t0002g0148a0001c0002t0002g0189others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-199-8493T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912139 | ||||||
| chr1:204912210
|
C | T | 101 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-199-8422C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912210 | ||||||
| chr1:204912214
|
G | A | 12 | a0001c0001t0023g0156a0001c0002t0002g0148a0001c0002t0002g0189others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-199-8418G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912214 | ||||||
| chr1:204912274
|
A | G | 4 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-8358A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912274 | ||||||
| chr1:204912285
|
T | G | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-8347T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912285 | ||||||
| chr1:204912471
|
T | C | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-8161T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912471 | ||||||
| chr1:204912480
|
T | C | 3 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-199-8152T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912480 | ||||||
| chr1:204912523
|
G | A | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-8109G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912523 | ||||||
| chr1:204912566
|
G | A | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-199-8066G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912566 | ||||||
| chr1:204912571
|
C | G | 21 | a0001c0001t0004g0064a0001c0001t0007g0130a0001c0002t0001g0180others(18): Show | 21 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-199-8061C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912571 | ||||||
| chr1:204912865
|
A | AT | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-7767_-199-776 others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912865 | ||||||
| chr1:204912867
|
AT | A | 3 | a0001c0043t0027g0224a0003c0019t0005g0007a0003c0024t0003g0115 | 3 | HG02257.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-199-7764delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912867 | ||||||
| chr1:204912880
|
T | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(64): Show | 67 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-199-7752T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912880 | ||||||
| chr1:204912884
|
T | C | 21 | a0001c0001t0004g0064a0001c0001t0007g0130a0001c0002t0001g0180others(18): Show | 21 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-199-7748T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912884 | ||||||
| chr1:204912889
|
G | A | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-7743G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912889 | ||||||
| chr1:204912905
|
A | G | 1 | a0001c0005t0001g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-199-7727A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204912905 | ||||||
| chr1:204913042
|
A | T | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-199-7590A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913042 | ||||||
| chr1:204913100
|
A | C | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-7532A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913100 | ||||||
| chr1:204913104
|
A | G | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-7528A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913104 | ||||||
| chr1:204913148
|
T | TAAC | 97 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-199-7482_-199-748 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204913148 | |||||
| chr1:204913164
|
C | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-7468C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913164 | ||||||
| chr1:204913382
|
G | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-199-7250G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913382 | ||||||
| chr1:204913405
|
A | G | 96 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-199-7227A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913405 | ||||||
| chr1:204913450
|
A | G | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-199-7182A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913450 | ||||||
| chr1:204913761
|
T | C | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-6871T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913761 | ||||||
| chr1:204913823
|
A | G | 105 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-199-6809A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204913823 | ||||||
| chr1:204914051
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0010g0147 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-199-6581A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914051 | ||||||
| chr1:204914098
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-199-6534C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914098 | ||||||
| chr1:204914264
|
T | C | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-199-6368T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914264 | ||||||
| chr1:204914283
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-6349A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914283 | ||||||
| chr1:204914320
|
G | A | 4 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-6312G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914320 | ||||||
| chr1:204914467
|
A | G | 1 | a0001c0002t0001g0205 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-199-6165A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914467 | ||||||
| chr1:204914730
|
C | T | 2 | a0001c0002t0019g0008a0001c0039t0032g0006 | 2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-199-5902C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914730 | ||||||
| chr1:204914753
|
G | A | 1 | a0013c0050t0020g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-199-5879G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914753 | ||||||
| chr1:204914825
|
T | A | 144 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(141): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-199-5807T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914825 | ||||||
| chr1:204914835
|
G | C | 1 | a0001c0017t0001g0173 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-199-5797G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914835 | ||||||
| chr1:204914903
|
G | A | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-199-5729G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914903 | ||||||
| chr1:204914976
|
A | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(71): Show | 74 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-199-5656A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204914976 | ||||||
| chr1:204915049
|
A | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(71): Show | 74 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-199-5583A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915049 | ||||||
| chr1:204915097
|
G | A | 1 | a0002c0008t0002g0123 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-199-5535G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915097 | ||||||
| chr1:204915163
|
C | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-5469C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915163 | ||||||
| chr1:204915216
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-199-5416G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915216 | ||||||
| chr1:204915225
|
G | A | 1 | a0002c0008t0002g0123 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-199-5407G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915225 | ||||||
| chr1:204915271
|
ACT | A | 2 | a0001c0005t0005g0131a0001c0005t0034g0135 | 2 | HG02451.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-199-5358_-199-535 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204915271 | |||||
| chr1:204915297
|
A | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-5335A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915297 | ||||||
| chr1:204915302
|
A | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-5330A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915302 | ||||||
| chr1:204915471
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-5161A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915471 | ||||||
| chr1:204915516
|
C | T | 5 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199-5116C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915516 | ||||||
| chr1:204915581
|
G | A | 38 | a0001c0001t0001g0082a0001c0001t0005g0133a0001c0002t0001g0023others(35): Show | 40 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-199-5051G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915581 | ||||||
| chr1:204915693
|
T | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-4939T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915693 | ||||||
| chr1:204915708
|
T | A | 106 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-199-4924T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915708 | ||||||
| chr1:204915722
|
G | T | 3 | a0001c0015t0005g0114a0002c0008t0011g0126a0009c0031t0001g0209 | 3 | HG01175.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-199-4910G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915722 | ||||||
| chr1:204915743
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-4889G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915743 | ||||||
| chr1:204915909
|
T | C | 12 | a0001c0001t0023g0156a0001c0002t0002g0148a0001c0002t0002g0189others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-199-4723T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915909 | ||||||
| chr1:204915976
|
A | T | 2 | a0002c0003t0002g0124a0002c0003t0002g0125 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-199-4656A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204915976 | ||||||
| chr1:204916006
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-4626G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916006 | ||||||
| chr1:204916045
|
T | C | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-199-4587T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916045 | ||||||
| chr1:204916082
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-4550G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916082 | ||||||
| chr1:204916237
|
T | C | 2 | a0001c0001t0005g0133a0001c0002t0011g0144 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-199-4395T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916237 | ||||||
| chr1:204916355
|
G | A | 2 | a0001c0001t0007g0160a0001c0002t0002g0216 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-199-4277G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916355 | ||||||
| chr1:204916356
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-4276G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916356 | ||||||
| chr1:204916405
|
A | G | 1 | a0001c0002t0001g0027 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-199-4227A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916405 | ||||||
| chr1:204916523
|
C | T | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-199-4109C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916523 | ||||||
| chr1:204916722
|
G | GTTTGTTT | 191 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(188): Show | 193 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.-199-3899_-199-389 others(11): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204916722 | |||||
| chr1:204916830
|
T | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-199-3802T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916830 | ||||||
| chr1:204916853
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0052g0085 | 2 | HG00423.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-199-3779G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204916853 | ||||||
| chr1:204917114
|
G | T | 2 | a0003c0019t0005g0007a0003c0024t0003g0115 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-199-3518G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204917114 | ||||||
| chr1:204917285
|
A | G | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-3347A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204917285 | ||||||
| chr1:204917441
|
A | T | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-199-3191A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204917441 | ||||||
| chr1:204917728
|
C | T | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-2904C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204917728 | ||||||
| chr1:204917933
|
A | G | 2 | a0001c0001t0007g0160a0001c0002t0002g0216 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-199-2699A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204917933 | ||||||
| chr1:204917944
|
A | C | 6 | a0001c0005t0005g0061a0001c0005t0022g0089a0001c0015t0049g0119others(3): Show | 6 | HG02622.hp2 HG02965.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199-2688A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204917944 | ||||||
| chr1:204918044
|
G | A | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-199-2588G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204918044 | ||||||
| chr1:204918474
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-199-2158G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204918474 | ||||||
| chr1:204918551
|
A | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(71): Show | 74 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-199-2081A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204918551 | ||||||
| chr1:204918584
|
C | CT | 94 | a0001c0001t0001g0082a0001c0001t0004g0064a0001c0001t0005g0133others(91): Show | 96 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-199-2029dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204918584 | |||||
| chr1:204918584
|
CT | C | 7 | a0001c0001t0001g0162a0001c0001t0040g0113a0001c0002t0019g0008others(4): Show | 7 | HG00323.hp2 HG02004.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-199-2029delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204918584 | |||||
| chr1:204918765
|
T | C | 1 | a0001c0004t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-199-1867T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204918765 | ||||||
| chr1:204918805
|
C | T | 6 | a0001c0005t0005g0061a0001c0005t0022g0089a0001c0015t0049g0119others(3): Show | 6 | HG02622.hp2 HG02965.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199-1827C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204918805 | ||||||
| chr1:204918840
|
C | T | 1 | a0001c0002t0050g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-199-1792C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204918840 | ||||||
| chr1:204919216
|
G | T | 38 | a0001c0001t0001g0082a0001c0001t0005g0133a0001c0002t0001g0023others(35): Show | 40 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-199-1416G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204919216 | ||||||
| chr1:204919408
|
G | A | 59 | a0001c0001t0001g0082a0001c0001t0004g0064a0001c0001t0005g0133others(56): Show | 61 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-199-1224G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204919408 | ||||||
| chr1:204919520
|
A | G | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-199-1112A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204919520 | ||||||
| chr1:204919524
|
A | C | 4 | a0001c0001t0001g0084a0001c0001t0009g0029a0001c0001t0043g0028others(1): Show | 4 | HG01123.hp2 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-199-1108A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204919524 | ||||||
| chr1:204919626
|
G | T | 39 | a0001c0001t0001g0082a0001c0001t0005g0133a0001c0002t0001g0023others(36): Show | 41 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-199-1006G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204919626 | ||||||
| chr1:204920003
|
A | T | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-199-629A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204920003 | ||||||
| chr1:204920205
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-199-427G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204920205 | ||||||
| chr1:204920404
|
C | T | 59 | a0001c0001t0001g0082a0001c0001t0004g0064a0001c0001t0005g0133others(56): Show | 61 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-199-228C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204920404 | ||||||
| chr1:204920427
|
C | CT | 47 | a0001c0001t0001g0202a0001c0001t0006g0003a0001c0001t0010g0127others(44): Show | 47 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-199-185dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204920427 | |||||
| chr1:204920427
|
CT | C | 7 | a0001c0001t0004g0064a0001c0002t0045g0098a0001c0004t0041g0065others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-199-185delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204920427 | |||||
| chr1:204920427
|
CTT | C | 16 | a0001c0002t0001g0180a0001c0002t0002g0069a0001c0002t0002g0192others(13): Show | 16 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-199-186_-199-185d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204920427 | |||||
| chr1:204920447
|
T | C | 2 | a0001c0010t0024g0151a0003c0016t0053g0041 | 2 | HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-199-185T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204920447 | ||||||
| chr1:204920447
|
T | TC | 72 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(69): Show | 72 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-199-184dupC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204920447 | |||||
| chr1:204920458
|
GCTTTGAA others(3): Show |
G | 1 | a0001c0002t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-199-165_-199-156d others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 204920458 | |||||
| chr1:204920608
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0040g0113 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-199-24C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | chr1 | 204920608 | ||||||
| chr1:204920781
|
G | A | 5 | a0001c0001t0001g0202a0002c0003t0039g0218a0002c0003t0042g0182others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+41G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204920781 | ||||||
| chr1:204920793
|
G | T | 1 | a0002c0003t0009g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-91+53G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204920793 | ||||||
| chr1:204920843
|
C | G | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-91+103C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204920843 | ||||||
| chr1:204920960
|
G | A | 1 | a0001c0002t0019g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-91+220G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204920960 | ||||||
| chr1:204921226
|
C | G | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+486C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921226 | ||||||
| chr1:204921512
|
G | A | 4 | a0001c0004t0001g0139a0001c0043t0027g0224a0003c0019t0005g0007others(1): Show | 4 | HG02257.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+772G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921512 | ||||||
| chr1:204921522
|
T | G | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+782T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921522 | ||||||
| chr1:204921603
|
A | G | 77 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(74): Show | 77 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-91+863A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921603 | ||||||
| chr1:204921664
|
G | A | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+924G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921664 | ||||||
| chr1:204921670
|
C | A | 2 | a0003c0019t0005g0007a0003c0024t0003g0115 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-91+930C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921670 | ||||||
| chr1:204921843
|
T | C | 1 | a0001c0004t0001g0087 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-91+1103T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921843 | ||||||
| chr1:204921950
|
G | A | 3 | a0001c0004t0002g0204a0002c0003t0001g0059a0002c0003t0001g0166 | 3 | HG02015.hp2 HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-91+1210G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204921950 | ||||||
| chr1:204922030
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-91+1290G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922030 | ||||||
| chr1:204922107
|
C | T | 31 | a0001c0001t0001g0082a0001c0002t0001g0057a0001c0002t0001g0205others(28): Show | 32 | HG00558.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-91+1367C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922107 | ||||||
| chr1:204922182
|
G | A | 2 | a0002c0006t0001g0037a0002c0006t0002g0035 | 2 | NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-91+1442G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922182 | ||||||
| chr1:204922320
|
C | G | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-91+1580C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922320 | ||||||
| chr1:204922419
|
A | G | 191 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(188): Show | 193 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.-91+1679A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922419 | ||||||
| chr1:204922429
|
C | G | 2 | a0003c0019t0005g0007a0003c0024t0003g0115 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-91+1689C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922429 | ||||||
| chr1:204922649
|
G | C | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+1909G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922649 | ||||||
| chr1:204922829
|
A | G | 2 | a0001c0005t0005g0131a0001c0005t0034g0135 | 2 | HG02451.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-91+2089A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922829 | ||||||
| chr1:204922987
|
C | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-91+2247C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204922987 | ||||||
| chr1:204923201
|
C | T | 139 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(136): Show | 141 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-91+2461C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923201 | ||||||
| chr1:204923322
|
G | T | 7 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+2582G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923322 | ||||||
| chr1:204923375
|
C | T | 3 | a0001c0002t0001g0023a0001c0004t0001g0071a0002c0003t0001g0001 | 4 | HG00738.hp2 HG01074.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+2635C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923375 | ||||||
| chr1:204923434
|
C | T | 1 | a0002c0003t0046g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-91+2694C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923434 | ||||||
| chr1:204923518
|
T | A | 6 | a0001c0004t0001g0139a0001c0015t0049g0119a0001c0043t0027g0224others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-91+2778T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923518 | ||||||
| chr1:204923575
|
C | T | 4 | a0001c0004t0003g0203a0001c0005t0001g0062a0003c0029t0031g0005others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+2835C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923575 | ||||||
| chr1:204923713
|
G | A | 3 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102 | 3 | HG02622.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-91+2973G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923713 | ||||||
| chr1:204923715
|
C | A | 5 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+2975C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923715 | ||||||
| chr1:204923928
|
C | T | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-91+3188C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204923928 | ||||||
| chr1:204924078
|
C | G | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-91+3338C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924078 | ||||||
| chr1:204924186
|
C | T | 1 | a0002c0003t0021g0159 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-91+3446C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924186 | ||||||
| chr1:204924274
|
A | T | 1 | a0002c0006t0001g0037 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-91+3534A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924274 | ||||||
| chr1:204924395
|
A | C | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-91+3655A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924395 | ||||||
| chr1:204924524
|
G | C | 2 | a0001c0005t0005g0131a0001c0005t0034g0135 | 2 | HG02451.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-91+3784G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924524 | ||||||
| chr1:204924576
|
G | A | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-91+3836G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924576 | ||||||
| chr1:204924757
|
A | C | 35 | a0001c0001t0006g0003a0001c0001t0010g0127a0001c0001t0012g0063others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-91+4017A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204924757 | ||||||
| chr1:204925056
|
A | G | 4 | a0001c0001t0006g0003a0002c0003t0001g0024a0002c0003t0001g0129others(1): Show | 4 | HG02015.hp1 NA18990.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+4316A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925056 | ||||||
| chr1:204925066
|
G | T | 16 | a0001c0001t0007g0160a0001c0002t0002g0216a0001c0002t0020g0100others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-91+4326G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925066 | ||||||
| chr1:204925184
|
G | A | 5 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+4444G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925184 | ||||||
| chr1:204925271
|
A | G | 2 | a0003c0019t0005g0007a0003c0024t0003g0115 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-91+4531A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925271 | ||||||
| chr1:204925371
|
C | T | 1 | a0002c0003t0002g0049 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-91+4631C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925371 | ||||||
| chr1:204925388
|
A | C | 17 | a0001c0001t0007g0160a0001c0002t0002g0216a0001c0002t0020g0100others(14): Show | 17 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-91+4648A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925388 | ||||||
| chr1:204925442
|
C | T | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-91+4702C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925442 | ||||||
| chr1:204925500
|
T | C | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+4760T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204925500 | ||||||
| chr1:204926036
|
A | C | 1 | a0001c0005t0005g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-91+5296A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926036 | ||||||
| chr1:204926088
|
G | A | 41 | a0001c0001t0001g0082a0001c0001t0001g0163a0001c0001t0005g0133others(38): Show | 43 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-91+5348G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926088 | ||||||
| chr1:204926380
|
G | GTA | 37 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(34): Show | 37 | HG00423.hp1 HG01168.hp2 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.-91+5666_-91+5667d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
G | GTATA | 14 | a0001c0001t0001g0086a0001c0001t0002g0146a0001c0001t0040g0113others(11): Show | 14 | HG00544.hp1 HG00673.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-91+5664_-91+5667d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
G | GTATATA | 11 | a0001c0001t0006g0003a0001c0001t0006g0168a0001c0002t0002g0191others(8): Show | 11 | HG00558.hp1 HG02886.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+5662_-91+5667d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
G | GTATATAT others(13): Show |
1 | a0001c0002t0002g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-91+5648_-91+5667d others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
GTA | G | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+5666_-91+5667d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926394
|
ATATATAT others(15): Show |
A | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-91+5656_-91+5677d others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926394 | |||||
| chr1:204926396
|
ATATATAT others(9): Show |
A | 1 | a0001c0015t0029g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-91+5658_-91+5673d others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926396
|
ATATATAT others(13): Show |
A | 10 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+5658_-91+5677d others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926396
|
ATATATAT others(14): Show |
A | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-91+5658_-91+5678d others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926396
|
ATATATAT others(15): Show |
A | 5 | a0001c0001t0004g0064a0001c0004t0041g0065a0001c0005t0007g0066others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+5658_-91+5679d others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926398
|
ATATATAT others(14): Show |
A | 33 | a0001c0001t0001g0082a0001c0001t0001g0163a0001c0001t0005g0133others(30): Show | 35 | HG00738.hp2 HG00741.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-91+5660_-91+5680d others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926398 | |||||
| chr1:204926398
|
ATATATAT others(15): Show |
A | 14 | a0001c0001t0007g0130a0001c0002t0001g0180a0001c0002t0002g0069others(11): Show | 14 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.-91+5660_-91+5681d others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926398 | |||||
| chr1:204926400
|
ATATATAT others(12): Show |
A | 10 | a0001c0002t0001g0057a0001c0004t0001g0179a0001c0022t0048g0150others(7): Show | 10 | HG00558.hp2 HG00741.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-91+5662_-91+5680d others(21): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926400 | |||||
| chr1:204926400
|
ATATATAT others(14): Show |
A | 1 | a0001c0002t0011g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-91+5662_-91+5682d others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926400 | |||||
| chr1:204926400
|
ATATATAT others(15): Show |
A | 1 | a0001c0042t0001g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-91+5662_-91+5683d others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926400 | |||||
| chr1:204926404
|
A | T | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-91+5664A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926404 | ||||||
| chr1:204926406
|
A | ATATATAT others(12): Show |
1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(21): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(22): Show |
1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(31): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(27): Show |
1 | a0004c0011t0005g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(36): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(23): Show |
1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(32): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(24): Show |
1 | a0003c0023t0018g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(33): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(25): Show |
1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(34): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(7): Show |
1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(7): Show |
1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATT | 8 | a0001c0001t0001g0111a0001c0001t0012g0063a0001c0001t0023g0156others(5): Show | 8 | HG00423.hp2 HG01169.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+5692_-91+5693d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATTT | 6 | a0001c0001t0001g0097a0001c0004t0001g0046a0001c0004t0002g0204others(3): Show | 6 | HG00735.hp1 HG01167.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+5691_-91+5693d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | T | 8 | a0001c0004t0001g0206a0001c0005t0005g0131a0001c0039t0032g0006others(5): Show | 8 | HG00639.hp2 HG01192.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+5666A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926406 | ||||||
| chr1:204926407
|
T | TA | 7 | a0001c0001t0001g0053a0001c0001t0033g0038a0001c0004t0001g0112others(4): Show | 7 | HG01358.hp2 HG03239.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+5667_-91+5668i others(3): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATA | 9 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(6): Show | 9 | HG01071.hp2 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-91+5667_-91+5668i others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATA | 5 | a0001c0001t0001g0162a0001c0001t0001g0215a0001c0001t0002g0120others(2): Show | 5 | HG00323.hp2 HG03491.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+5667_-91+5668i others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATATA others(6): Show |
1 | a0002c0003t0010g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(15): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATATA others(8): Show |
1 | a0003c0023t0007g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-91+5667_-91+5668i others(17): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926407 | ||||||
| chr1:204926408
|
T | A | 41 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0084others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-91+5668T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926408 | ||||||
| chr1:204926409
|
T | A | 20 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0079others(17): Show | 20 | HG01123.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-91+5669T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926409 | ||||||
| chr1:204926410
|
T | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0015g0093others(9): Show | 12 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-91+5670T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926410 | ||||||
| chr1:204926411
|
T | A | 1 | a0003c0023t0007g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-91+5671T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926411 | ||||||
| chr1:204926412
|
T | A | 1 | a0001c0001t0052g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-91+5672T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926412 | ||||||
| chr1:204926616
|
G | C | 2 | a0001c0010t0024g0151a0002c0040t0004g0052 | 2 | HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-91+5876G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926616 | ||||||
| chr1:204926768
|
T | G | 8 | a0001c0004t0001g0139a0001c0004t0005g0153a0001c0015t0029g0101others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+6028T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926768 | ||||||
| chr1:204926793
|
G | A | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-91+6053G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926793 | ||||||
| chr1:204926943
|
C | G | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-91+6203C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926943 | ||||||
| chr1:204926967
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-91+6227C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204926967 | ||||||
| chr1:204927053
|
T | C | 5 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+6313T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927053 | ||||||
| chr1:204927191
|
C | T | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+6451C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927191 | ||||||
| chr1:204927196
|
A | G | 4 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+6456A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927196 | ||||||
| chr1:204927308
|
A | G | 1 | a0002c0003t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-91+6568A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927308 | ||||||
| chr1:204927362
|
C | G | 1 | a0001c0001t0002g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-91+6622C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927362 | ||||||
| chr1:204927486
|
G | C | 5 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+6746G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927486 | ||||||
| chr1:204927711
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-91+6971C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927711 | ||||||
| chr1:204927737
|
A | G | 1 | a0001c0001t0010g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-91+6997A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927737 | ||||||
| chr1:204927810
|
G | A | 16 | a0001c0001t0007g0160a0001c0002t0002g0216a0001c0002t0020g0100others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-91+7070G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204927810 | ||||||
| chr1:204928001
|
G | C | 3 | a0001c0004t0005g0153a0001c0015t0049g0119a0003c0019t0003g0116 | 3 | HG02258.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-91+7261G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204928001 | ||||||
| chr1:204928206
|
G | A | 5 | a0004c0011t0010g0014a0004c0011t0017g0018a0004c0011t0017g0019others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+7466G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204928206 | ||||||
| chr1:204928444
|
G | C | 66 | a0001c0001t0001g0082a0001c0001t0001g0163a0001c0001t0004g0064others(63): Show | 68 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.-91+7704G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204928444 | ||||||
| chr1:204928518
|
G | A | 2 | a0001c0005t0005g0131a0001c0005t0034g0135 | 2 | HG02451.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-91+7778G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204928518 | ||||||
| chr1:204928620
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-91+7880G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204928620 | ||||||
| chr1:204928902
|
G | A | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+8162G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204928902 | ||||||
| chr1:204929002
|
A | G | 2 | a0001c0017t0001g0199a0001c0021t0001g0170 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-91+8262A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204929002 | ||||||
| chr1:204929129
|
G | T | 2 | a0002c0008t0011g0126a0009c0031t0001g0209 | 2 | HG01175.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-91+8389G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204929129 | ||||||
| chr1:204929919
|
G | A | 2 | a0001c0005t0005g0131a0001c0005t0034g0135 | 2 | HG02451.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-91+9179G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204929919 | ||||||
| chr1:204929956
|
C | T | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-91+9216C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204929956 | ||||||
| chr1:204930016
|
A | G | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-91+9276A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930016 | ||||||
| chr1:204930018
|
G | A | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-91+9278G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930018 | ||||||
| chr1:204930187
|
T | C | 1 | a0001c0004t0001g0046 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-91+9447T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930187 | ||||||
| chr1:204930308
|
C | T | 1 | a0007c0045t0013g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+9568C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930308 | ||||||
| chr1:204930513
|
G | A | 1 | a0001c0005t0034g0135 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-91+9773G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930513 | ||||||
| chr1:204930650
|
G | A | 7 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-91+9910G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930650 | ||||||
| chr1:204930757
|
A | C | 2 | a0001c0001t0001g0081a0001c0001t0040g0113 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-91+10017A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930757 | ||||||
| chr1:204930789
|
C | T | 18 | a0001c0001t0001g0163a0001c0001t0010g0127a0001c0001t0012g0063others(15): Show | 18 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.-91+10049C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930789 | ||||||
| chr1:204930829
|
A | G | 2 | a0001c0002t0019g0008a0003c0024t0003g0115 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-91+10089A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204930829 | ||||||
| chr1:204931085
|
A | G | 12 | a0001c0002t0011g0144a0001c0002t0045g0098a0001c0005t0001g0062others(9): Show | 12 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-91+10345A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204931085 | ||||||
| chr1:204931218
|
G | T | 1 | a0002c0003t0002g0050 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-91+10478G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204931218 | ||||||
| chr1:204931374
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-91+10634C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204931374 | ||||||
| chr1:204931655
|
C | T | 1 | a0002c0003t0001g0166 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-91+10915C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204931655 | ||||||
| chr1:204931882
|
A | G | 2 | a0001c0001t0015g0093a0001c0001t0015g0212 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-91+11142A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204931882 | ||||||
| chr1:204931927
|
A | G | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-91+11187A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204931927 | ||||||
| chr1:204932060
|
T | C | 3 | a0001c0015t0005g0114a0001c0043t0027g0224a0002c0008t0011g0126 | 3 | HG02717.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-91+11320T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932060 | ||||||
| chr1:204932113
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-91+11373G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932113 | ||||||
| chr1:204932154
|
C | T | 2 | a0001c0001t0023g0109a0003c0018t0003g0136 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-91+11414C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932154 | ||||||
| chr1:204932280
|
A | G | 27 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(24): Show | 27 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-91+11540A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932280 | ||||||
| chr1:204932489
|
T | A | 4 | a0001c0015t0005g0114a0002c0008t0011g0126a0005c0046t0001g0034others(1): Show | 4 | HG02717.hp1 HG03209.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-11737T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932489 | ||||||
| chr1:204932519
|
A | T | 1 | a0001c0010t0005g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-90-11707A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932519 | ||||||
| chr1:204932564
|
G | C | 1 | a0001c0002t0019g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-90-11662G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204932564 | ||||||
| chr1:204933196
|
G | A | 3 | a0001c0004t0003g0203a0001c0004t0005g0153a0004c0020t0003g0197 | 3 | HG02258.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-90-11030G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204933196 | ||||||
| chr1:204933233
|
C | G | 2 | a0001c0015t0005g0114a0002c0008t0011g0126 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-90-10993C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204933233 | ||||||
| chr1:204933298
|
G | C | 29 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(26): Show | 29 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-90-10928G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204933298 | ||||||
| chr1:204933473
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(59): Show | 62 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90-10753A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204933473 | ||||||
| chr1:204933789
|
T | A | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-90-10437T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204933789 | ||||||
| chr1:204934069
|
C | T | 4 | a0001c0001t0002g0146a0001c0001t0010g0147a0002c0003t0001g0001others(1): Show | 5 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-10157C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934069 | ||||||
| chr1:204934132
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-90-10094C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934132 | ||||||
| chr1:204934137
|
C | CA | 38 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0111others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-90-10072dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204934137 | |||||
| chr1:204934137
|
C | CAA | 66 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0146others(63): Show | 68 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-90-10073_-90-1007 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204934137 | |||||
| chr1:204934294
|
G | T | 21 | a0001c0002t0001g0023a0001c0002t0004g0107a0001c0002t0008g0105others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-90-9932G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934294 | ||||||
| chr1:204934487
|
G | A | 1 | a0001c0022t0048g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-90-9739G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934487 | ||||||
| chr1:204934695
|
A | G | 155 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(152): Show | 157 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.-90-9531A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934695 | ||||||
| chr1:204934715
|
C | G | 2 | a0001c0015t0005g0114a0002c0008t0011g0126 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-90-9511C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934715 | ||||||
| chr1:204934746
|
C | T | 71 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(68): Show | 73 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-90-9480C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934746 | ||||||
| chr1:204934757
|
G | T | 1 | a0003c0024t0003g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-90-9469G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934757 | ||||||
| chr1:204934830
|
T | C | 25 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(22): Show | 25 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-90-9396T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934830 | ||||||
| chr1:204934947
|
T | C | 3 | a0001c0015t0005g0114a0002c0008t0011g0126a0003c0024t0003g0115 | 3 | HG02717.hp1 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-9279T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204934947 | ||||||
| chr1:204935208
|
A | G | 4 | a0001c0002t0011g0144a0001c0005t0005g0061a0001c0005t0022g0089others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-9018A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935208 | ||||||
| chr1:204935253
|
G | A | 1 | a0003c0009t0003g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-90-8973G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935253 | ||||||
| chr1:204935399
|
T | C | 48 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0005g0133others(45): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90-8827T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935399 | ||||||
| chr1:204935489
|
C | T | 6 | a0001c0002t0001g0060a0001c0004t0002g0204a0001c0004t0038g0096others(3): Show | 6 | HG00673.hp1 HG00673.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-8737C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935489 | ||||||
| chr1:204935575
|
T | C | 11 | a0001c0002t0001g0023a0001c0004t0003g0203a0001c0004t0005g0153others(8): Show | 11 | HG01192.hp1 HG02132.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90-8651T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935575 | ||||||
| chr1:204935707
|
G | A | 65 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0005g0133others(62): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-90-8519G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935707 | ||||||
| chr1:204935877
|
G | A | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-8349G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935877 | ||||||
| chr1:204935892
|
T | A | 74 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0146others(71): Show | 76 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-90-8334T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204935892 | ||||||
| chr1:204936036
|
G | A | 4 | a0001c0001t0006g0003a0002c0003t0001g0024a0002c0003t0035g0207others(1): Show | 4 | NA18612.hp1 NA18990.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-8190G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936036 | ||||||
| chr1:204936063
|
G | C | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-90-8163G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936063 | ||||||
| chr1:204936141
|
G | A | 1 | a0001c0001t0012g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-90-8085G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936141 | ||||||
| chr1:204936180
|
TTCCC | T | 14 | a0001c0002t0008g0137a0001c0002t0011g0144a0001c0002t0025g0042others(11): Show | 14 | HG01175.hp2 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-90-8043_-90-8040d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936180 | |||||
| chr1:204936183
|
C | T | 183 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(180): Show | 185 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-90-8043C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936183 | ||||||
| chr1:204936192
|
C | T | 124 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(121): Show | 124 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-90-8034C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936192 | ||||||
| chr1:204936196
|
TTC | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0162a0001c0001t0015g0093others(2): Show | 5 | HG00323.hp2 HG01168.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-8028_-90-8027d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936196 | |||||
| chr1:204936197
|
TC | T | 113 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0044others(110): Show | 113 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-90-8028delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936197 | ||||||
| chr1:204936198
|
C | CTT | 3 | a0001c0002t0009g0193a0001c0004t0001g0083a0003c0024t0003g0115 | 3 | HG01256.hp1 HG02004.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-8024_-90-8023d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936198 | |||||
| chr1:204936198
|
C | CTTT | 40 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0005g0133others(37): Show | 42 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-90-8025_-90-8023d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936198 | |||||
| chr1:204936198
|
C | CTTTT | 5 | a0001c0002t0001g0122a0001c0002t0002g0191a0001c0002t0045g0098others(2): Show | 5 | HG00544.hp1 HG01109.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-8026_-90-8023d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936198 | |||||
| chr1:204936198
|
C | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0058a0001c0001t0043g0028others(3): Show | 6 | HG01123.hp2 HG02015.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-8028C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936198 | ||||||
| chr1:204936201
|
TTTC | T | 12 | a0001c0002t0008g0137a0001c0002t0011g0144a0001c0002t0050g0099others(9): Show | 12 | HG01175.hp2 HG01496.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90-8022_-90-8020d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936201 | |||||
| chr1:204936202
|
TTC | T | 8 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0049g0119others(5): Show | 8 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-8022_-90-8021d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936202 | |||||
| chr1:204936203
|
TC | T | 4 | a0001c0002t0001g0023a0001c0039t0032g0006a0005c0046t0001g0034others(1): Show | 4 | HG02132.hp1 HG02922.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-8022delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936203 | ||||||
| chr1:204936204
|
C | T | 172 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(169): Show | 174 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-90-8022C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936204 | ||||||
| chr1:204936204
|
CT | C | 5 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-8007delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936204 | |||||
| chr1:204936258
|
G | A | 2 | a0001c0001t0023g0109a0003c0018t0003g0136 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-7968G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936258 | ||||||
| chr1:204936327
|
G | A | 23 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(20): Show | 23 | HG01175.hp2 HG01192.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-90-7899G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936327 | ||||||
| chr1:204936342
|
C | T | 1 | a0001c0004t0001g0083 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-90-7884C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936342 | ||||||
| chr1:204936391
|
G | A | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-90-7835G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936391 | ||||||
| chr1:204936418
|
C | T | 50 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(47): Show | 50 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90-7808C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936418 | ||||||
| chr1:204936689
|
C | T | 2 | a0001c0005t0001g0062a0006c0048t0025g0040 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-90-7537C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936689 | ||||||
| chr1:204936716
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-7510T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936716 | ||||||
| chr1:204936780
|
A | G | 42 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(39): Show | 42 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-90-7446A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936780 | ||||||
| chr1:204936792
|
G | A | 42 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(39): Show | 42 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-90-7434G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936792 | ||||||
| chr1:204936866
|
ACT | A | 3 | a0001c0038t0014g0078a0003c0019t0005g0007a0009c0031t0001g0209 | 3 | HG01175.hp2 HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-90-7351_-90-7350d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204936866 | |||||
| chr1:204936868
|
T | G | 2 | a0004c0011t0017g0018a0004c0011t0017g0019 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-90-7358T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936868 | ||||||
| chr1:204936906
|
C | T | 156 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(153): Show | 158 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.-90-7320C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936906 | ||||||
| chr1:204936925
|
A | G | 41 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-90-7301A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204936925 | ||||||
| chr1:204937047
|
T | TA | 41 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0005g0133others(38): Show | 43 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-90-7178dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204937047 | |||||
| chr1:204937071
|
G | T | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-7155G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937071 | ||||||
| chr1:204937106
|
G | A | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-7120G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937106 | ||||||
| chr1:204937153
|
T | TAAA | 48 | a0001c0002t0001g0023a0001c0002t0004g0107a0001c0002t0008g0105others(45): Show | 48 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-90-7064_-90-7062d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204937153 | |||||
| chr1:204937170
|
C | G | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-7056C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937170 | ||||||
| chr1:204937208
|
T | A | 1 | a0001c0001t0002g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-90-7018T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937208 | ||||||
| chr1:204937268
|
C | A | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6958C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937268 | ||||||
| chr1:204937371
|
T | C | 42 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(39): Show | 42 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-90-6855T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937371 | ||||||
| chr1:204937385
|
A | G | 39 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(36): Show | 39 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-90-6841A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937385 | ||||||
| chr1:204937466
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6760T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937466 | ||||||
| chr1:204937472
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6754T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937472 | ||||||
| chr1:204937486
|
C | T | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6740C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937486 | ||||||
| chr1:204937501
|
G | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6725G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937501 | ||||||
| chr1:204937604
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6622T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937604 | ||||||
| chr1:204937688
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6538T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937688 | ||||||
| chr1:204937700
|
G | A | 2 | a0001c0001t0001g0084a0001c0030t0001g0030 | 2 | HG01358.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-90-6526G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937700 | ||||||
| chr1:204937759
|
C | T | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-90-6467C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937759 | ||||||
| chr1:204937794
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6432T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937794 | ||||||
| chr1:204937811
|
G | T | 28 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(25): Show | 28 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-90-6415G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937811 | ||||||
| chr1:204937818
|
A | G | 14 | a0001c0002t0008g0137a0001c0002t0011g0144a0001c0002t0025g0042others(11): Show | 14 | HG01175.hp2 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-90-6408A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937818 | ||||||
| chr1:204937826
|
A | G | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-90-6400A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937826 | ||||||
| chr1:204937869
|
A | G | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6357A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937869 | ||||||
| chr1:204937915
|
A | G | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6311A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937915 | ||||||
| chr1:204937946
|
C | G | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-6280C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204937946 | ||||||
| chr1:204938173
|
G | A | 3 | a0001c0004t0003g0203a0001c0004t0005g0153a0004c0020t0003g0197 | 3 | HG02258.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-90-6053G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938173 | ||||||
| chr1:204938185
|
C | G | 51 | a0001c0002t0001g0023a0001c0002t0004g0107a0001c0002t0008g0105others(48): Show | 51 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-90-6041C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938185 | ||||||
| chr1:204938263
|
G | A | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-5963G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938263 | ||||||
| chr1:204938466
|
A | G | 1 | a0002c0028t0014g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90-5760A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938466 | ||||||
| chr1:204938533
|
C | G | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-5693C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938533 | ||||||
| chr1:204938554
|
A | G | 42 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(39): Show | 42 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-90-5672A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938554 | ||||||
| chr1:204938561
|
A | T | 25 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(22): Show | 25 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-90-5665A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938561 | ||||||
| chr1:204938655
|
C | A | 9 | a0001c0002t0001g0023a0001c0004t0003g0203a0001c0004t0005g0153others(6): Show | 9 | HG01192.hp1 HG02132.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-90-5571C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938655 | ||||||
| chr1:204938656
|
A | G | 100 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0146others(97): Show | 102 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.-90-5570A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938656 | ||||||
| chr1:204938688
|
G | A | 3 | a0001c0005t0005g0131a0001c0005t0034g0135a0002c0003t0010g0088 | 3 | HG02451.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-90-5538G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938688 | ||||||
| chr1:204938837
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-90-5389A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938837 | ||||||
| chr1:204938844
|
T | A | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-5382T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938844 | ||||||
| chr1:204938862
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-5364T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204938862 | ||||||
| chr1:204939033
|
G | GATGT | 16 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(13): Show | 16 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-90-5190_-90-5189i others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939033 | |||||
| chr1:204939037
|
G | T | 40 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(37): Show | 40 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-90-5189G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939037 | ||||||
| chr1:204939038
|
A | ATG | 25 | a0001c0001t0001g0045a0001c0001t0001g0163a0001c0001t0004g0117others(22): Show | 25 | HG01069.hp2 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-90-5140_-90-5139d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGGATG | 3 | a0001c0001t0002g0146a0001c0001t0010g0147a0002c0003t0001g0001 | 4 | HG00738.hp2 HG01074.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-5186_-90-5185i others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGGATGT others(1): Show |
2 | a0001c0002t0045g0098a0001c0027t0014g0184 | 2 | HG01109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-90-5186_-90-5185i others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATG | 14 | a0001c0001t0005g0133a0001c0002t0001g0057a0001c0004t0001g0091others(11): Show | 14 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(1): Show |
21 | a0001c0001t0001g0082a0001c0002t0001g0205a0001c0002t0006g0195others(18): Show | 21 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(3): Show |
10 | a0001c0002t0001g0122a0001c0002t0002g0073a0001c0002t0009g0193others(7): Show | 11 | HG00544.hp1 HG00741.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(7): Show |
1 | a0001c0004t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-90-5185_-90-5184i others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTG | 27 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(24): Show | 27 | HG00544.hp2 HG00735.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-90-5142_-90-5139d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTG | 18 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0201others(15): Show | 18 | HG01071.hp2 HG01358.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90-5144_-90-5139d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(1): Show |
12 | a0001c0001t0001g0053a0001c0001t0001g0079a0001c0001t0001g0149others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-90-5146_-90-5139d others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(3): Show |
4 | a0001c0002t0003g0009a0001c0002t0008g0143a0002c0003t0001g0164others(1): Show | 4 | HG03139.hp2 NA18974.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-5148_-90-5139d others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(5): Show |
1 | a0001c0015t0049g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-90-5150_-90-5139d others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0162a0001c0005t0001g0062 | 2 | HG00323.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-90-5152_-90-5139d others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
ATG | A | 14 | a0001c0001t0002g0120a0001c0001t0004g0064a0001c0001t0007g0130others(11): Show | 14 | HG01261.hp1 HG02109.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.-90-5140_-90-5139d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
ATGTG | A | 7 | a0001c0004t0041g0065a0001c0005t0007g0066a0001c0039t0032g0006others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90-5142_-90-5139d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939040
|
G | A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90-5186G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939040 | ||||||
| chr1:204939040
|
G | GTA | 5 | a0001c0002t0008g0137a0001c0002t0020g0100a0001c0002t0025g0042others(2): Show | 5 | HG02451.hp2 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204939040 | |||||
| chr1:204939042
|
G | A | 8 | a0001c0002t0011g0144a0001c0002t0028g0104a0001c0005t0005g0061others(5): Show | 8 | HG01175.hp2 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-5184G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939042 | ||||||
| chr1:204939044
|
G | A | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90-5182G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939044 | ||||||
| chr1:204939288
|
A | G | 42 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(39): Show | 42 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-90-4938A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939288 | ||||||
| chr1:204939507
|
T | C | 1 | a0003c0018t0018g0145 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-90-4719T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939507 | ||||||
| chr1:204939741
|
G | A | 10 | a0001c0002t0001g0023a0001c0004t0003g0203a0001c0004t0005g0153others(7): Show | 10 | HG01192.hp1 HG02132.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90-4485G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939741 | ||||||
| chr1:204939832
|
T | C | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-4394T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939832 | ||||||
| chr1:204939930
|
T | C | 52 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-90-4296T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204939930 | ||||||
| chr1:204940028
|
G | C | 2 | a0002c0003t0001g0129a0002c0003t0037g0068 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-90-4198G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940028 | ||||||
| chr1:204940139
|
A | G | 7 | a0001c0001t0023g0156a0001c0002t0002g0148a0001c0002t0002g0189others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90-4087A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940139 | ||||||
| chr1:204940180
|
C | T | 1 | a0001c0010t0005g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-90-4046C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940180 | ||||||
| chr1:204940218
|
C | T | 47 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0005g0133others(44): Show | 49 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-90-4008C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940218 | ||||||
| chr1:204940435
|
A | G | 2 | a0003c0016t0026g0141a0003c0016t0053g0041 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-90-3791A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940435 | ||||||
| chr1:204940580
|
G | A | 41 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-90-3646G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940580 | ||||||
| chr1:204940588
|
CCTT | C | 41 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-90-3635_-90-3633d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204940588 | |||||
| chr1:204940601
|
C | T | 41 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-90-3625C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940601 | ||||||
| chr1:204940642
|
A | T | 1 | a0001c0002t0002g0073 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-90-3584A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940642 | ||||||
| chr1:204940643
|
G | A | 59 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0001g0023others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.-90-3583G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940643 | ||||||
| chr1:204940644
|
T | C | 39 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(36): Show | 39 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-90-3582T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940644 | ||||||
| chr1:204940688
|
A | G | 7 | a0001c0001t0023g0156a0001c0002t0002g0148a0001c0002t0002g0189others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90-3538A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940688 | ||||||
| chr1:204940898
|
G | A | 1 | a0001c0004t0038g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-90-3328G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940898 | ||||||
| chr1:204940924
|
T | G | 2 | a0001c0002t0002g0069a0001c0002t0002g0192 | 2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-90-3302T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204940924 | ||||||
| chr1:204941228
|
T | A | 103 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0146others(100): Show | 105 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-90-2998T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941228 | ||||||
| chr1:204941233
|
T | A | 28 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(25): Show | 28 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-90-2993T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941233 | ||||||
| chr1:204941263
|
T | G | 1 | a0002c0003t0001g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-90-2963T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941263 | ||||||
| chr1:204941384
|
T | C | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-2842T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941384 | ||||||
| chr1:204941448
|
A | G | 64 | a0001c0001t0001g0202a0001c0001t0004g0064a0001c0001t0023g0156others(61): Show | 64 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.-90-2778A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941448 | ||||||
| chr1:204941473
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-90-2753A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941473 | ||||||
| chr1:204941560
|
T | C | 64 | a0001c0001t0001g0202a0001c0001t0004g0064a0001c0001t0023g0156others(61): Show | 64 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.-90-2666T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941560 | ||||||
| chr1:204941688
|
G | T | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-90-2538G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941688 | ||||||
| chr1:204941779
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-90-2447A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204941779 | ||||||
| chr1:204942025
|
T | C | 1 | a0001c0005t0001g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-90-2201T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942025 | ||||||
| chr1:204942096
|
G | A | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-2130G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942096 | ||||||
| chr1:204942203
|
G | C | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-90-2023G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942203 | ||||||
| chr1:204942378
|
A | C | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-90-1848A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942378 | ||||||
| chr1:204942660
|
GA | G | 37 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0010g0147others(34): Show | 39 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-90-1562delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr1 | 204942660 | |||||
| chr1:204942671
|
C | G | 98 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(95): Show | 100 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-90-1555C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942671 | ||||||
| chr1:204942813
|
C | A | 2 | a0001c0002t0002g0140a0001c0002t0002g0219 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-90-1413C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942813 | ||||||
| chr1:204942838
|
G | A | 2 | a0001c0022t0001g0092a0005c0047t0021g0077 | 2 | HG00741.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-90-1388G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942838 | ||||||
| chr1:204942849
|
T | C | 7 | a0001c0002t0008g0137a0001c0002t0011g0144a0001c0002t0025g0042others(4): Show | 7 | HG02451.hp2 HG02622.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90-1377T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942849 | ||||||
| chr1:204942966
|
C | T | 93 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(90): Show | 95 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-90-1260C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942966 | ||||||
| chr1:204942972
|
C | T | 52 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-90-1254C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204942972 | ||||||
| chr1:204943278
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-90-948G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943278 | ||||||
| chr1:204943439
|
C | T | 154 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(151): Show | 156 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.-90-787C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943439 | ||||||
| chr1:204943637
|
A | C | 52 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-90-589A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943637 | ||||||
| chr1:204943691
|
C | T | 6 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0050g0099others(3): Show | 6 | HG02451.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-535C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943691 | ||||||
| chr1:204943700
|
C | G | 46 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(43): Show | 48 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-90-526C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943700 | ||||||
| chr1:204943715
|
G | A | 52 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-90-511G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943715 | ||||||
| chr1:204943973
|
G | T | 41 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(38): Show | 43 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-90-253G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204943973 | ||||||
| chr1:204944143
|
C | G | 75 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(72): Show | 75 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.-90-83C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 2/29 | chr1 | 204944143 | ||||||
| chr1:204944460
|
T | G | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+54T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204944460 | ||||||
| chr1:204944508
|
T | G | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+102T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204944508 | ||||||
| chr1:204944524
|
A | G | 154 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(151): Show | 156 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.91+118A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204944524 | ||||||
| chr1:204944624
|
G | C | 73 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0146others(70): Show | 75 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.91+218G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204944624 | ||||||
| chr1:204944666
|
G | A | 3 | a0001c0005t0005g0131a0001c0005t0034g0135a0002c0003t0010g0088 | 3 | HG02451.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.91+260G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204944666 | ||||||
| chr1:204944754
|
C | T | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91+348C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204944754 | ||||||
| chr1:204945037
|
T | G | 4 | a0001c0001t0004g0064a0001c0002t0045g0098a0001c0004t0041g0065others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+631T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945037 | ||||||
| chr1:204945074
|
C | CA | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.91+669dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 204945074 | |||||
| chr1:204945391
|
T | C | 2 | a0002c0003t0001g0129a0002c0003t0037g0068 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.91+985T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945391 | ||||||
| chr1:204945514
|
GCTGCCC | G | 65 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(62): Show | 65 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.91+1116_91+1121del others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 204945514 | |||||
| chr1:204945565
|
T | G | 1 | a0001c0017t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+1159T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945565 | ||||||
| chr1:204945638
|
C | T | 1 | a0001c0005t0006g0152 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.91+1232C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945638 | ||||||
| chr1:204945690
|
C | T | 3 | a0001c0010t0005g0175a0001c0038t0014g0078a0009c0031t0001g0209 | 3 | HG01175.hp2 HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.91+1284C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945690 | ||||||
| chr1:204945916
|
C | T | 1 | a0001c0002t0020g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.91+1510C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945916 | ||||||
| chr1:204945964
|
G | A | 7 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+1558G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204945964 | ||||||
| chr1:204946265
|
A | G | 148 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(145): Show | 150 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.91+1859A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946265 | ||||||
| chr1:204946365
|
G | A | 7 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+1959G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946365 | ||||||
| chr1:204946513
|
A | G | 2 | a0001c0001t0007g0160a0001c0002t0002g0216 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.91+2107A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946513 | ||||||
| chr1:204946530
|
C | A | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.91+2124C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946530 | ||||||
| chr1:204946620
|
T | A | 1 | a0004c0011t0017g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+2214T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946620 | ||||||
| chr1:204946629
|
G | A | 26 | a0001c0001t0001g0202a0001c0002t0004g0107a0001c0002t0008g0105others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.91+2223G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946629 | ||||||
| chr1:204946717
|
A | G | 4 | a0001c0001t0004g0064a0001c0002t0045g0098a0001c0004t0041g0065others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+2311A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946717 | ||||||
| chr1:204946776
|
A | G | 148 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(145): Show | 150 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.91+2370A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946776 | ||||||
| chr1:204946792
|
T | C | 155 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(152): Show | 157 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.91+2386T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946792 | ||||||
| chr1:204946811
|
T | C | 53 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(50): Show | 53 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.91+2405T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946811 | ||||||
| chr1:204946813
|
C | T | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91+2407C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946813 | ||||||
| chr1:204946823
|
C | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91+2417C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204946823 | ||||||
| chr1:204947010
|
G | C | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+2604G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947010 | ||||||
| chr1:204947111
|
G | A | 7 | a0001c0002t0008g0137a0001c0002t0011g0144a0001c0002t0025g0042others(4): Show | 7 | HG02451.hp2 HG02622.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+2705G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947111 | ||||||
| chr1:204947179
|
G | T | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+2773G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947179 | ||||||
| chr1:204947331
|
A | G | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+2925A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947331 | ||||||
| chr1:204947397
|
G | A | 10 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+2991G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947397 | ||||||
| chr1:204947398
|
T | A | 1 | a0002c0003t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.91+2992T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947398 | ||||||
| chr1:204947460
|
C | T | 6 | a0001c0004t0005g0153a0001c0015t0005g0114a0001c0043t0027g0224others(3): Show | 6 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+3054C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947460 | ||||||
| chr1:204947461
|
G | T | 5 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+3055G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947461 | ||||||
| chr1:204947470
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.91+3064G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947470 | ||||||
| chr1:204947472
|
C | T | 10 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+3066C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947472 | ||||||
| chr1:204947546
|
C | T | 1 | a0001c0001t0006g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.92-3011C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947546 | ||||||
| chr1:204947599
|
C | A | 1 | a0001c0004t0001g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.92-2958C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947599 | ||||||
| chr1:204947644
|
C | A | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.92-2913C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947644 | ||||||
| chr1:204947690
|
G | A | 2 | a0001c0001t0023g0109a0003c0018t0003g0136 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.92-2867G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947690 | ||||||
| chr1:204947844
|
A | G | 48 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(45): Show | 50 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-2713A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947844 | ||||||
| chr1:204947912
|
ACACT | A | 2 | a0002c0003t0002g0124a0002c0003t0002g0125 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.92-2641_92-2638del others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 204947912 | |||||
| chr1:204947980
|
G | A | 216 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(213): Show | 218 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.92-2577G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204947980 | ||||||
| chr1:204948013
|
T | C | 1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.92-2544T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948013 | ||||||
| chr1:204948143
|
G | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(77): Show | 80 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.92-2414G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948143 | ||||||
| chr1:204948220
|
A | G | 5 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-2337A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948220 | ||||||
| chr1:204948452
|
T | G | 5 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0027t0014g0184others(2): Show | 6 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-2105T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948452 | ||||||
| chr1:204948552
|
C | T | 48 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-2005C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948552 | ||||||
| chr1:204948571
|
G | A | 11 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(8): Show | 11 | HG02132.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-1986G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948571 | ||||||
| chr1:204948572
|
G | T | 11 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(8): Show | 11 | HG02132.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-1985G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948572 | ||||||
| chr1:204948580
|
AAAAAC | A | 21 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0004g0107others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.92-1957_92-1953del others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 204948580 | |||||
| chr1:204948781
|
T | C | 37 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0001g0023others(34): Show | 37 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.92-1776T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204948781 | ||||||
| chr1:204949072
|
G | T | 1 | a0005c0047t0021g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.92-1485G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949072 | ||||||
| chr1:204949199
|
G | A | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-1358G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949199 | ||||||
| chr1:204949206
|
C | T | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-1351C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949206 | ||||||
| chr1:204949417
|
G | A | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-1140G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949417 | ||||||
| chr1:204949631
|
G | C | 10 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-926G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949631 | ||||||
| chr1:204949942
|
T | C | 48 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0001g0023others(45): Show | 48 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.92-615T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949942 | ||||||
| chr1:204949968
|
T | A | 1 | a0002c0003t0002g0050 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.92-589T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204949968 | ||||||
| chr1:204950104
|
G | A | 94 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0082others(91): Show | 96 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.92-453G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204950104 | ||||||
| chr1:204950271
|
A | G | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.92-286A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204950271 | ||||||
| chr1:204950282
|
A | G | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-275A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204950282 | ||||||
| chr1:204950328
|
G | A | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.92-229G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204950328 | ||||||
| chr1:204950335
|
G | A | 1 | a0001c0004t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.92-222G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204950335 | ||||||
| chr1:204950366
|
C | T | 21 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0004g0107others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.92-191C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 3/29 | chr1 | 204950366 | ||||||
| chr1:204950624
|
A | G | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+50A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204950624 | ||||||
| chr1:204950824
|
GT | G | 3 | a0001c0005t0005g0131a0001c0005t0034g0135a0002c0003t0010g0088 | 3 | HG02451.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.109+253delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204950824 | |||||
| chr1:204950991
|
A | G | 20 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0002t0001g0027others(17): Show | 20 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.109+417A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204950991 | ||||||
| chr1:204951083
|
G | A | 10 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+509G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951083 | ||||||
| chr1:204951150
|
A | AT | 11 | a0001c0001t0001g0163a0001c0001t0004g0064a0001c0002t0002g0191others(8): Show | 11 | HG01109.hp2 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+595dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951150
|
A | ATT | 30 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0010g0147others(27): Show | 32 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.109+594_109+595dup others(2): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951150
|
AT | A | 44 | a0001c0001t0001g0044a0001c0001t0001g0202a0001c0001t0023g0156others(41): Show | 44 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.109+595delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951194
|
G | C | 49 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(46): Show | 49 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.109+620G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951194 | ||||||
| chr1:204951315
|
A | AT | 9 | a0001c0001t0001g0079a0001c0001t0001g0215a0001c0001t0006g0168others(6): Show | 9 | HG00544.hp2 HG01192.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-674dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951315 | |||||
| chr1:204951315
|
AT | A | 45 | a0001c0001t0001g0082a0001c0001t0004g0064a0001c0001t0006g0121others(42): Show | 47 | HG00558.hp2 HG00738.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.110-674delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951315 | |||||
| chr1:204951315
|
ATT | A | 45 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0001g0023others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.110-675_110-674del others(2): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951315 | |||||
| chr1:204951355
|
G | C | 2 | a0001c0001t0001g0081a0001c0001t0040g0113 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.110-656G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951355 | ||||||
| chr1:204951369
|
G | C | 10 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-642G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951369 | ||||||
| chr1:204951470
|
AT | A | 50 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(47): Show | 50 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.110-525delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr1 | 204951470 | |||||
| chr1:204951471
|
T | TA | 3 | a0001c0005t0005g0131a0001c0005t0034g0135a0002c0003t0010g0088 | 3 | HG02451.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.110-540_110-539ins others(1): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951471 | ||||||
| chr1:204951472
|
T | A | 10 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-539T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951472 | ||||||
| chr1:204951486
|
T | G | 85 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0146others(82): Show | 87 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.110-525T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951486 | ||||||
| chr1:204951486
|
T | TG | 8 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-525_110-524ins others(1): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951486 | ||||||
| chr1:204951507
|
C | T | 5 | a0001c0004t0001g0139a0001c0005t0006g0152a0001c0005t0006g0172others(2): Show | 5 | HG00741.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-504C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951507 | ||||||
| chr1:204951564
|
G | A | 3 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102 | 3 | HG02622.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.110-447G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951564 | ||||||
| chr1:204951587
|
G | A | 6 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-424G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951587 | ||||||
| chr1:204951593
|
C | T | 45 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(42): Show | 47 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.110-418C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951593 | ||||||
| chr1:204951626
|
G | A | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-385G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951626 | ||||||
| chr1:204951645
|
T | G | 1 | a0002c0003t0006g0221 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.110-366T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951645 | ||||||
| chr1:204951678
|
C | T | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-333C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951678 | ||||||
| chr1:204951705
|
G | A | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0005g0114others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-306G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951705 | ||||||
| chr1:204951711
|
G | A | 45 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(42): Show | 47 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.110-300G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951711 | ||||||
| chr1:204951761
|
G | A | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110-250G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951761 | ||||||
| chr1:204951814
|
G | A | 6 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-197G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 4/29 | chr1 | 204951814 | ||||||
| chr1:204952130
|
A | G | 37 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(34): Show | 39 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.215+14A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952130 | ||||||
| chr1:204952154
|
G | A | 10 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+38G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952154 | ||||||
| chr1:204952184
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0201a0001c0030t0001g0030 | 3 | HG01071.hp2 HG01358.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.215+68C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952184 | ||||||
| chr1:204952403
|
T | C | 59 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0004g0064others(56): Show | 61 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.215+287T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952403 | ||||||
| chr1:204952457
|
TC | T | 35 | a0001c0001t0001g0202a0001c0001t0023g0156a0001c0002t0001g0023others(32): Show | 35 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.215+342delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952457 | ||||||
| chr1:204952561
|
T | C | 1 | a0001c0002t0006g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.215+445T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952561 | ||||||
| chr1:204952578
|
G | A | 2 | a0005c0046t0001g0034a0007c0045t0013g0015 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.215+462G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952578 | ||||||
| chr1:204952635
|
A | AG | 9 | a0001c0002t0002g0140a0001c0002t0002g0219a0001c0004t0001g0139others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.215+523dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr1 | 204952635 | |||||
| chr1:204952670
|
G | T | 6 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0050g0099others(3): Show | 6 | HG02451.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+554G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952670 | ||||||
| chr1:204952681
|
G | A | 41 | a0001c0001t0001g0202a0001c0002t0001g0023a0001c0002t0004g0107others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.215+565G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952681 | ||||||
| chr1:204952699
|
C | T | 10 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+583C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952699 | ||||||
| chr1:204952744
|
G | A | 3 | a0001c0004t0001g0139a0001c0015t0049g0119a0003c0019t0003g0116 | 3 | HG02280.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215+628G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204952744 | ||||||
| chr1:204953000
|
T | A | 10 | a0001c0002t0001g0023a0001c0002t0008g0137a0001c0002t0011g0144others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+884T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953000 | ||||||
| chr1:204953158
|
T | C | 3 | a0001c0001t0004g0064a0001c0002t0045g0098a0001c0004t0041g0065 | 3 | HG01109.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.216-1030T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953158 | ||||||
| chr1:204953286
|
T | G | 3 | a0001c0002t0002g0140a0001c0002t0002g0219a0001c0002t0003g0009 | 3 | HG02572.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.216-902T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953286 | ||||||
| chr1:204953286
|
T | TTTTG | 7 | a0001c0005t0007g0066a0001c0005t0022g0134a0001c0010t0004g0194others(4): Show | 7 | HG01243.hp1 HG02630.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-886_216-883dup others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr1 | 204953286 | |||||
| chr1:204953328
|
G | A | 12 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(9): Show | 12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.216-860G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953328 | ||||||
| chr1:204953512
|
G | A | 1 | a0002c0008t0011g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-676G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953512 | ||||||
| chr1:204953575
|
C | T | 8 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-613C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953575 | ||||||
| chr1:204953679
|
G | A | 1 | a0001c0001t0004g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.216-509G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953679 | ||||||
| chr1:204953863
|
A | G | 35 | a0001c0001t0001g0082a0001c0001t0002g0146a0001c0001t0010g0147others(32): Show | 37 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.216-325A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953863 | ||||||
| chr1:204953898
|
C | G | 36 | a0001c0002t0001g0023a0001c0002t0002g0148a0001c0002t0002g0189others(33): Show | 36 | HG02055.hp1 HG02055.hp2 HG02132.hp1 others(33): Show |
intron_variant | MODIFIER | c.216-290C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204953898 | ||||||
| chr1:204954028
|
C | T | 1 | a0001c0039t0032g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.216-160C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204954028 | ||||||
| chr1:204954154
|
C | T | 4 | a0001c0004t0001g0139a0003c0016t0026g0141a0003c0016t0053g0041others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-34C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 5/29 | chr1 | 204954154 | ||||||
| chr1:204954431
|
G | A | 1 | a0001c0001t0033g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.412+47G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 6/29 | chr1 | 204954431 | ||||||
| chr1:204954521
|
C | A | 11 | a0001c0015t0029g0101a0003c0016t0026g0141a0003c0016t0053g0041others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+137C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 6/29 | chr1 | 204954521 | ||||||
| chr1:204954602
|
G | A | 11 | a0001c0015t0029g0101a0003c0016t0026g0141a0003c0016t0053g0041others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+218G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 6/29 | chr1 | 204954602 | ||||||
| chr1:204954666
|
C | T | 3 | a0003c0016t0026g0141a0003c0016t0053g0041a0003c0024t0003g0115 | 3 | HG02055.hp1 HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-163C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 6/29 | chr1 | 204954666 | ||||||
| chr1:204954769
|
C | T | 1 | a0001c0005t0001g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.413-60C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 6/29 | chr1 | 204954769 | ||||||
| chr1:204955105
|
G | A | 4 | a0001c0010t0005g0175a0001c0038t0014g0078a0003c0019t0005g0007others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+154G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204955105 | ||||||
| chr1:204955134
|
C | A | 8 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+183C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204955134 | ||||||
| chr1:204955366
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.535+415G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204955366 | ||||||
| chr1:204955557
|
G | A | 59 | a0001c0001t0001g0082a0001c0002t0001g0023a0001c0002t0001g0057others(56): Show | 60 | HG00323.hp1 HG00558.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.535+606G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204955557 | ||||||
| chr1:204955659
|
GC | G | 13 | a0001c0015t0029g0101a0003c0016t0026g0141a0003c0016t0053g0041others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+709delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204955659 | ||||||
| chr1:204956805
|
G | A | 7 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-851G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204956805 | ||||||
| chr1:204956818
|
C | T | 45 | a0001c0001t0005g0133a0001c0002t0001g0027a0001c0002t0001g0180others(42): Show | 45 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.536-838C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204956818 | ||||||
| chr1:204956907
|
G | GA | 30 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.536-739dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr1 | 204956907 | |||||
| chr1:204957245
|
A | G | 42 | a0001c0001t0005g0133a0001c0002t0001g0027a0001c0002t0001g0180others(39): Show | 42 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.536-411A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204957245 | ||||||
| chr1:204957379
|
G | A | 3 | a0001c0005t0005g0061a0001c0005t0022g0089a0002c0008t0011g0102 | 3 | HG02622.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.536-277G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 7/29 | chr1 | 204957379 | ||||||
| chr1:204957852
|
C | T | 42 | a0001c0001t0005g0133a0001c0002t0001g0027a0001c0002t0001g0180others(39): Show | 42 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.706+26C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204957852 | ||||||
| chr1:204957870
|
A | C | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.706+44A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204957870 | ||||||
| chr1:204957909
|
T | C | 3 | a0002c0003t0046g0016a0005c0046t0001g0034a0007c0045t0013g0015 | 3 | NA19002.hp1 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.706+83T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204957909 | ||||||
| chr1:204958008
|
A | G | 45 | a0001c0001t0005g0133a0001c0002t0001g0027a0001c0002t0001g0180others(42): Show | 45 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.706+182A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958008 | ||||||
| chr1:204958046
|
C | T | 1 | a0001c0002t0011g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.706+220C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958046 | ||||||
| chr1:204958290
|
A | G | 42 | a0001c0001t0005g0133a0001c0002t0001g0027a0001c0002t0001g0180others(39): Show | 42 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.706+464A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958290 | ||||||
| chr1:204958309
|
T | C | 5 | a0001c0002t0009g0193a0001c0004t0001g0046a0001c0004t0001g0083others(2): Show | 5 | HG01256.hp1 HG01257.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.706+483T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958309 | ||||||
| chr1:204958320
|
A | G | 3 | a0002c0003t0046g0016a0005c0046t0001g0034a0007c0045t0013g0015 | 3 | NA19002.hp1 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.706+494A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958320 | ||||||
| chr1:204958475
|
C | T | 1 | a0001c0002t0006g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.706+649C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958475 | ||||||
| chr1:204958774
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.706+948G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204958774 | ||||||
| chr1:204959027
|
A | G | 48 | a0001c0001t0001g0082a0001c0002t0001g0023a0001c0002t0001g0057others(45): Show | 49 | HG00323.hp1 HG00558.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.706+1201A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959027 | ||||||
| chr1:204959061
|
G | GT | 76 | a0001c0001t0001g0082a0001c0001t0005g0133a0001c0002t0001g0023others(73): Show | 77 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.706+1246dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 204959061 | |||||
| chr1:204959150
|
C | G | 1 | a0001c0027t0014g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.706+1324C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959150 | ||||||
| chr1:204959204
|
C | T | 1 | a0001c0004t0001g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.706+1378C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959204 | ||||||
| chr1:204959331
|
C | T | 68 | a0001c0001t0001g0082a0001c0001t0005g0133a0001c0002t0001g0023others(65): Show | 69 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.706+1505C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959331 | ||||||
| chr1:204959554
|
G | A | 20 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(17): Show | 20 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.706+1728G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959554 | ||||||
| chr1:204959580
|
C | T | 21 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(18): Show | 21 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.706+1754C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959580 | ||||||
| chr1:204959622
|
C | G | 2 | a0001c0004t0001g0174a0001c0004t0001g0176 | 2 | HG01106.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.706+1796C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959622 | ||||||
| chr1:204959658
|
C | T | 1 | a0002c0003t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.706+1832C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959658 | ||||||
| chr1:204959694
|
T | C | 143 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0081others(140): Show | 145 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.706+1868T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959694 | ||||||
| chr1:204959708
|
G | T | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.706+1882G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204959708 | ||||||
| chr1:204960007
|
G | A | 52 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.706+2181G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204960007 | ||||||
| chr1:204960068
|
G | C | 59 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(56): Show | 59 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.706+2242G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204960068 | ||||||
| chr1:204960091
|
G | A | 2 | a0003c0019t0005g0007a0009c0031t0001g0209 | 2 | HG01175.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.706+2265G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204960091 | ||||||
| chr1:204960318
|
T | A | 2 | a0001c0001t0023g0109a0003c0018t0003g0136 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.706+2492T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204960318 | ||||||
| chr1:204960474
|
G | A | 1 | a0002c0003t0009g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.706+2648G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204960474 | ||||||
| chr1:204961015
|
T | C | 89 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0002g0146others(86): Show | 91 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.706+3189T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204961015 | ||||||
| chr1:204961147
|
A | G | 9 | a0001c0001t0001g0079a0001c0001t0002g0146a0001c0001t0006g0168others(6): Show | 10 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+3321A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204961147 | ||||||
| chr1:204961311
|
A | G | 1 | a0001c0030t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.706+3485A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204961311 | ||||||
| chr1:204961540
|
C | T | 20 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0163others(17): Show | 20 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.706+3714C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204961540 | ||||||
| chr1:204961949
|
G | A | 20 | a0001c0001t0005g0133a0001c0001t0023g0109a0001c0002t0001g0027others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.706+4123G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204961949 | ||||||
| chr1:204962002
|
C | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.706+4176C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962002 | ||||||
| chr1:204962009
|
A | G | 35 | a0001c0001t0001g0079a0001c0001t0002g0146a0001c0001t0006g0168others(32): Show | 36 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.706+4183A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962009 | ||||||
| chr1:204962263
|
C | T | 4 | a0001c0002t0045g0098a0001c0004t0041g0065a0001c0005t0005g0131others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.706+4437C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962263 | ||||||
| chr1:204962478
|
A | G | 11 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0015t0029g0101others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.706+4652A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962478 | ||||||
| chr1:204962548
|
A | G | 1 | a0002c0003t0012g0222 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.706+4722A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962548 | ||||||
| chr1:204962631
|
T | G | 1 | a0001c0002t0019g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.706+4805T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962631 | ||||||
| chr1:204962744
|
G | A | 7 | a0001c0002t0045g0098a0001c0004t0041g0065a0001c0005t0005g0131others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.706+4918G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962744 | ||||||
| chr1:204962813
|
C | A | 1 | a0001c0015t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.706+4987C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204962813 | ||||||
| chr1:204963235
|
A | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.707-5014A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963235 | ||||||
| chr1:204963273
|
G | T | 9 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.707-4976G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963273 | ||||||
| chr1:204963483
|
A | G | 32 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0002t0004g0157others(29): Show | 33 | HG00738.hp2 HG01074.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.707-4766A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963483 | ||||||
| chr1:204963493
|
G | A | 31 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0002t0004g0157others(28): Show | 32 | HG00738.hp2 HG01074.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.707-4756G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963493 | ||||||
| chr1:204963516
|
A | G | 1 | a0001c0002t0002g0158 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.707-4733A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963516 | ||||||
| chr1:204963621
|
A | G | 2 | a0001c0032t0001g0196a0002c0033t0001g0169 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.707-4628A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963621 | ||||||
| chr1:204963677
|
C | T | 30 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0002t0008g0137others(27): Show | 31 | HG00738.hp2 HG01074.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.707-4572C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963677 | ||||||
| chr1:204963682
|
G | A | 9 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.707-4567G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963682 | ||||||
| chr1:204963786
|
A | G | 2 | a0001c0001t0005g0133a0002c0003t0010g0088 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.707-4463A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204963786 | ||||||
| chr1:204964129
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.707-4120C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204964129 | ||||||
| chr1:204964261
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.707-3988G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204964261 | ||||||
| chr1:204964595
|
A | G | 1 | a0001c0021t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.707-3654A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204964595 | ||||||
| chr1:204964731
|
C | T | 7 | a0001c0002t0009g0193a0001c0004t0001g0013a0001c0004t0001g0046others(4): Show | 7 | HG01175.hp1 HG01243.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.707-3518C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204964731 | ||||||
| chr1:204964742
|
A | C | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-3507A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204964742 | ||||||
| chr1:204964905
|
G | A | 4 | a0001c0001t0001g0079a0001c0001t0006g0168a0002c0007t0016g0074others(1): Show | 4 | NA19002.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-3344G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204964905 | ||||||
| chr1:204965059
|
G | T | 3 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0050g0099 | 3 | HG02451.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.707-3190G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965059 | ||||||
| chr1:204965123
|
G | A | 16 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(13): Show | 16 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.707-3126G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965123 | ||||||
| chr1:204965180
|
G | A | 1 | a0001c0002t0008g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.707-3069G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965180 | ||||||
| chr1:204965372
|
C | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.707-2877C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965372 | ||||||
| chr1:204965380
|
G | T | 9 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.707-2869G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965380 | ||||||
| chr1:204965402
|
T | C | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-2847T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965402 | ||||||
| chr1:204965420
|
A | G | 2 | a0001c0001t0001g0084a0001c0030t0001g0030 | 2 | HG01358.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.707-2829A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965420 | ||||||
| chr1:204965589
|
C | T | 2 | a0001c0001t0005g0133a0002c0003t0010g0088 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.707-2660C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965589 | ||||||
| chr1:204965719
|
T | G | 1 | a0002c0006t0001g0070 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.707-2530T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204965719 | ||||||
| chr1:204966006
|
C | G | 1 | a0002c0006t0001g0070 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.707-2243C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966006 | ||||||
| chr1:204966300
|
G | A | 9 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.707-1949G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966300 | ||||||
| chr1:204966338
|
G | T | 1 | a0001c0002t0008g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.707-1911G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966338 | ||||||
| chr1:204966394
|
A | G | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-1855A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966394 | ||||||
| chr1:204966406
|
G | T | 16 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(13): Show | 16 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.707-1843G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966406 | ||||||
| chr1:204966494
|
G | A | 1 | a0003c0049t0003g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.707-1755G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966494 | ||||||
| chr1:204966519
|
G | A | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-1730G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966519 | ||||||
| chr1:204966807
|
C | G | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-1442C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966807 | ||||||
| chr1:204966814
|
G | A | 1 | a0001c0001t0052g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.707-1435G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966814 | ||||||
| chr1:204966828
|
A | G | 2 | a0001c0002t0004g0157a0001c0002t0004g0185 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.707-1421A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966828 | ||||||
| chr1:204966902
|
G | A | 3 | a0002c0003t0046g0016a0005c0046t0001g0034a0007c0045t0013g0015 | 3 | NA19002.hp1 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.707-1347G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204966902 | ||||||
| chr1:204967028
|
C | T | 4 | a0001c0002t0011g0144a0001c0004t0001g0139a0002c0008t0011g0102others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-1221C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967028 | ||||||
| chr1:204967030
|
C | T | 9 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.707-1219C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967030 | ||||||
| chr1:204967207
|
A | G | 16 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(13): Show | 16 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.707-1042A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967207 | ||||||
| chr1:204967220
|
C | T | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-1029C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967220 | ||||||
| chr1:204967479
|
A | G | 32 | a0001c0001t0001g0202a0001c0002t0001g0027a0001c0002t0001g0180others(29): Show | 32 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.707-770A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967479 | ||||||
| chr1:204967510
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.707-739G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967510 | ||||||
| chr1:204967636
|
G | A | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.707-613G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967636 | ||||||
| chr1:204967707
|
C | T | 32 | a0001c0001t0001g0202a0001c0002t0001g0027a0001c0002t0001g0180others(29): Show | 32 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.707-542C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967707 | ||||||
| chr1:204967765
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.707-484A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967765 | ||||||
| chr1:204967947
|
A | G | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.707-302A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204967947 | ||||||
| chr1:204968090
|
A | G | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.707-159A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204968090 | ||||||
| chr1:204968115
|
G | T | 9 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.707-134G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204968115 | ||||||
| chr1:204968221
|
C | T | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.707-28C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 8/29 | chr1 | 204968221 | ||||||
| chr1:204968524
|
C | A | 2 | a0001c0001t0002g0146a0001c0001t0010g0147 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.818+164C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 9/29 | chr1 | 204968524 | ||||||
| chr1:204968600
|
C | G | 5 | a0001c0002t0011g0144a0001c0004t0001g0139a0001c0043t0027g0224others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-198C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 9/29 | chr1 | 204968600 | ||||||
| chr1:204968620
|
C | T | 2 | a0001c0036t0044g0220a0003c0019t0003g0116 | 2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.819-178C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 9/29 | chr1 | 204968620 | ||||||
| chr1:204968686
|
A | G | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.819-112A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 9/29 | chr1 | 204968686 | ||||||
| chr1:204968747
|
A | T | 6 | a0001c0002t0045g0098a0001c0004t0041g0065a0002c0006t0003g0128others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-51A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 9/29 | chr1 | 204968747 | ||||||
| chr1:204969178
|
G | C | 1 | a0002c0006t0001g0037 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1003+196G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969178 | ||||||
| chr1:204969243
|
G | A | 16 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(13): Show | 16 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1003+261G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969243 | ||||||
| chr1:204969312
|
C | T | 14 | a0001c0002t0001g0057a0001c0002t0006g0195a0001c0002t0009g0193others(11): Show | 14 | HG00558.hp2 HG01175.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1003+330C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969312 | ||||||
| chr1:204969336
|
C | T | 2 | a0003c0016t0026g0141a0003c0016t0053g0041 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1003+354C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969336 | ||||||
| chr1:204969345
|
T | G | 3 | a0001c0001t0040g0113a0002c0003t0001g0059a0002c0003t0001g0166 | 3 | HG02015.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1003+363T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969345 | ||||||
| chr1:204969611
|
T | C | 1 | a0002c0003t0001g0001 | 2 | HG00738.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1003+629T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969611 | ||||||
| chr1:204969677
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1003+695A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969677 | ||||||
| chr1:204969689
|
G | A | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1003+707G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969689 | ||||||
| chr1:204969710
|
G | T | 1 | a0001c0039t0032g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1003+728G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204969710 | ||||||
| chr1:204970008
|
G | A | 6 | a0001c0002t0045g0098a0001c0004t0041g0065a0002c0006t0003g0128others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004-608G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204970008 | ||||||
| chr1:204970033
|
G | A | 25 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(22): Show | 25 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1004-583G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204970033 | ||||||
| chr1:204970049
|
C | T | 6 | a0001c0002t0045g0098a0001c0004t0041g0065a0002c0006t0003g0128others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004-567C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204970049 | ||||||
| chr1:204970053
|
C | T | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1004-563C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204970053 | ||||||
| chr1:204970074
|
CA | C | 133 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0044others(130): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1004-517delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 204970074 | |||||
| chr1:204970074
|
CAA | C | 6 | a0001c0001t0004g0064a0001c0001t0006g0168a0001c0004t0001g0112others(3): Show | 6 | HG01167.hp2 HG02976.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004-518_1004-517d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 204970074 | |||||
| chr1:204970208
|
T | A | 36 | a0001c0002t0001g0057a0001c0002t0001g0060a0001c0002t0001g0122others(33): Show | 37 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1004-408T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204970208 | ||||||
| chr1:204970344
|
T | TA | 20 | a0001c0002t0004g0157a0001c0002t0004g0185a0001c0002t0008g0137others(17): Show | 20 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1004-265dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 204970344 | |||||
| chr1:204970506
|
C | T | 1 | a0001c0015t0049g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1004-110C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 10/29 | chr1 | 204970506 | ||||||
| chr1:204970771
|
T | C | 25 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(22): Show | 25 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1135+24T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204970771 | ||||||
| chr1:204970789
|
G | C | 25 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(22): Show | 25 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1135+42G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204970789 | ||||||
| chr1:204970807
|
T | G | 1 | a0005c0047t0021g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1135+60T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204970807 | ||||||
| chr1:204970846
|
C | G | 1 | a0002c0003t0046g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1135+99C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204970846 | ||||||
| chr1:204971040
|
C | T | 6 | a0001c0002t0045g0098a0001c0004t0041g0065a0002c0006t0003g0128others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+293C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971040 | ||||||
| chr1:204971066
|
T | A | 1 | a0001c0004t0038g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1135+319T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971066 | ||||||
| chr1:204971162
|
G | A | 3 | a0001c0002t0019g0008a0001c0005t0007g0066a0001c0005t0022g0134 | 3 | HG01243.hp1 HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1135+415G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971162 | ||||||
| chr1:204971251
|
G | C | 2 | a0001c0002t0004g0157a0001c0002t0004g0185 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1135+504G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971251 | ||||||
| chr1:204971317
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1135+570G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971317 | ||||||
| chr1:204971432
|
A | T | 25 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(22): Show | 25 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1135+685A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971432 | ||||||
| chr1:204971458
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1135+711A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971458 | ||||||
| chr1:204971487
|
G | A | 16 | a0001c0002t0001g0023a0001c0002t0019g0008a0001c0005t0001g0062others(13): Show | 16 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1135+740G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971487 | ||||||
| chr1:204971537
|
G | A | 1 | a0001c0002t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1135+790G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971537 | ||||||
| chr1:204971555
|
G | A | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135+808G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971555 | ||||||
| chr1:204971571
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1135+824A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971571 | ||||||
| chr1:204971575
|
A | G | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1135+828A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971575 | ||||||
| chr1:204971585
|
A | T | 27 | a0001c0002t0004g0157a0001c0002t0004g0185a0001c0002t0008g0137others(24): Show | 27 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1135+838A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971585 | ||||||
| chr1:204971617
|
C | T | 18 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(15): Show | 18 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1135+870C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971617 | ||||||
| chr1:204971652
|
T | G | 28 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0004others(25): Show | 28 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1135+905T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971652 | ||||||
| chr1:204971833
|
A | G | 25 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(22): Show | 25 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1135+1086A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971833 | ||||||
| chr1:204971844
|
C | T | 36 | a0001c0002t0001g0057a0001c0002t0001g0060a0001c0002t0001g0122others(33): Show | 36 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1135+1097C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971844 | ||||||
| chr1:204971874
|
G | A | 1 | a0001c0001t0007g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1135+1127G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971874 | ||||||
| chr1:204971915
|
T | C | 24 | a0001c0002t0008g0137a0001c0002t0025g0042a0001c0002t0045g0098others(21): Show | 24 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1135+1168T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971915 | ||||||
| chr1:204971999
|
T | A | 23 | a0001c0002t0025g0042a0001c0002t0045g0098a0001c0002t0050g0099others(20): Show | 23 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1135+1252T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204971999 | ||||||
| chr1:204972012
|
G | A | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136-1264G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972012 | ||||||
| chr1:204972088
|
G | A | 4 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136-1188G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972088 | ||||||
| chr1:204972231
|
C | G | 37 | a0001c0002t0003g0009a0001c0002t0004g0107a0001c0002t0004g0157others(34): Show | 37 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1136-1045C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972231 | ||||||
| chr1:204972403
|
T | C | 30 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0025g0042others(27): Show | 30 | HG01109.hp2 HG01192.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1136-873T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972403 | ||||||
| chr1:204972416
|
GA | G | 7 | a0001c0001t0002g0146a0001c0001t0010g0147a0002c0003t0001g0001others(4): Show | 8 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136-857delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 204972416 | |||||
| chr1:204972440
|
A | G | 1 | a0001c0001t0033g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1136-836A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972440 | ||||||
| chr1:204972659
|
AG | A | 7 | a0001c0002t0045g0098a0001c0004t0041g0065a0001c0015t0049g0119others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136-615delG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 204972659 | |||||
| chr1:204972675
|
G | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0149others(3): Show | 6 | HG02129.hp2 HG02135.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136-601G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972675 | ||||||
| chr1:204972685
|
A | G | 222 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(219): Show | 224 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.1136-591A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972685 | ||||||
| chr1:204972947
|
G | C | 2 | a0003c0019t0003g0116a0011c0037t0004g0110 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1136-329G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972947 | ||||||
| chr1:204972992
|
A | G | 1 | a0002c0006t0001g0037 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1136-284A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204972992 | ||||||
| chr1:204973035
|
C | T | 39 | a0001c0002t0001g0057a0001c0002t0001g0060a0001c0002t0001g0122others(36): Show | 39 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1136-241C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204973035 | ||||||
| chr1:204973036
|
G | A | 1 | a0001c0010t0024g0151 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1136-240G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 11/29 | chr1 | 204973036 | ||||||
| chr1:204973540
|
A | G | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1279+121A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973540 | ||||||
| chr1:204973643
|
C | T | 1 | a0001c0026t0002g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1279+224C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973643 | ||||||
| chr1:204973663
|
A | G | 2 | a0003c0016t0026g0141a0003c0016t0053g0041 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1279+244A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973663 | ||||||
| chr1:204973737
|
C | A | 12 | a0001c0002t0001g0057a0001c0002t0002g0158a0001c0002t0009g0193others(9): Show | 12 | HG00558.hp2 HG01175.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1279+318C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973737 | ||||||
| chr1:204973800
|
C | T | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-379C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973800 | ||||||
| chr1:204973826
|
G | T | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-353G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973826 | ||||||
| chr1:204973851
|
G | A | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-328G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973851 | ||||||
| chr1:204973905
|
A | G | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-274A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973905 | ||||||
| chr1:204973968
|
T | C | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-211T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973968 | ||||||
| chr1:204973988
|
G | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(79): Show | 82 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1280-191G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973988 | ||||||
| chr1:204973993
|
C | T | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-186C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204973993 | ||||||
| chr1:204974073
|
G | A | 1 | a0001c0001t0023g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1280-106G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204974073 | ||||||
| chr1:204974157
|
A | T | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-22A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 12/29 | chr1 | 204974157 | ||||||
| chr1:204974377
|
A | G | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1391+87A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 13/29 | chr1 | 204974377 | ||||||
| chr1:204974485
|
G | C | 3 | a0001c0012t0001g0054a0001c0012t0001g0055a0001c0012t0001g0056 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1392-172G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 13/29 | chr1 | 204974485 | ||||||
| chr1:204974644
|
G | T | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1392-13G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 13/29 | chr1 | 204974644 | ||||||
| chr1:204974833
|
AG | A | 9 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0025g0042others(6): Show | 9 | HG01192.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558+13delG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr1 | 204974833 | |||||
| chr1:204974863
|
C | T | 101 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(98): Show | 102 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1558+40C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204974863 | ||||||
| chr1:204974864
|
A | G | 192 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(189): Show | 194 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1558+41A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204974864 | ||||||
| chr1:204974881
|
A | G | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558+58A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204974881 | ||||||
| chr1:204974891
|
A | G | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558+68A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204974891 | ||||||
| chr1:204975058
|
A | G | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1559-213A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204975058 | ||||||
| chr1:204975180
|
G | T | 8 | a0001c0002t0004g0004a0001c0010t0004g0194a0001c0010t0005g0175others(5): Show | 8 | HG01496.hp1 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1559-91G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204975180 | ||||||
| chr1:204975187
|
G | A | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1559-84G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 14/29 | chr1 | 204975187 | ||||||
| chr1:204975429
|
C | G | 1 | a0002c0003t0012g0222 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1706+11C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975429 | ||||||
| chr1:204975518
|
C | T | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1706+100C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975518 | ||||||
| chr1:204975583
|
C | T | 1 | a0001c0022t0001g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1706+165C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975583 | ||||||
| chr1:204975711
|
A | G | 9 | a0001c0002t0004g0004a0001c0002t0004g0107a0001c0002t0004g0157others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1706+293A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975711 | ||||||
| chr1:204975847
|
C | G | 3 | a0001c0001t0001g0058a0002c0003t0002g0124a0002c0003t0002g0125 | 3 | NA18969.hp2 NA18970.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1706+429C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975847 | ||||||
| chr1:204975897
|
G | A | 5 | a0001c0010t0004g0194a0001c0010t0005g0175a0001c0010t0024g0151others(2): Show | 5 | HG01496.hp1 HG02630.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1706+479G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975897 | ||||||
| chr1:204975946
|
G | A | 2 | a0003c0019t0003g0116a0011c0037t0004g0110 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1706+528G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975946 | ||||||
| chr1:204975951
|
G | T | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1706+533G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975951 | ||||||
| chr1:204975977
|
G | A | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1706+559G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204975977 | ||||||
| chr1:204976003
|
T | TTC | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1706+586_1706+587d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr1 | 204976003 | |||||
| chr1:204976114
|
A | G | 7 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707-557A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976114 | ||||||
| chr1:204976188
|
T | C | 30 | a0001c0002t0001g0023a0001c0005t0001g0062a0001c0005t0005g0061others(27): Show | 31 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1707-483T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976188 | ||||||
| chr1:204976210
|
CTA | C | 18 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(15): Show | 18 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1707-458_1707-457d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr1 | 204976210 | |||||
| chr1:204976213
|
T | C | 4 | a0001c0002t0011g0144a0001c0004t0001g0139a0002c0008t0011g0102others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707-458T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976213 | ||||||
| chr1:204976225
|
C | A | 2 | a0003c0019t0003g0116a0011c0037t0004g0110 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1707-446C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976225 | ||||||
| chr1:204976330
|
T | C | 25 | a0001c0002t0001g0023a0001c0005t0001g0062a0001c0005t0005g0061others(22): Show | 26 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1707-341T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976330 | ||||||
| chr1:204976361
|
C | A | 30 | a0001c0002t0001g0023a0001c0005t0001g0062a0001c0005t0005g0061others(27): Show | 31 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1707-310C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976361 | ||||||
| chr1:204976373
|
G | T | 2 | a0003c0024t0003g0115a0003c0029t0031g0005 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1707-298G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976373 | ||||||
| chr1:204976490
|
G | A | 38 | a0001c0002t0001g0057a0001c0002t0001g0060a0001c0002t0001g0122others(35): Show | 38 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1707-181G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976490 | ||||||
| chr1:204976497
|
C | G | 5 | a0001c0010t0004g0194a0001c0010t0005g0175a0001c0010t0024g0151others(2): Show | 5 | HG01496.hp1 HG02630.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1707-174C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976497 | ||||||
| chr1:204976537
|
G | A | 27 | a0001c0002t0001g0023a0001c0005t0001g0062a0001c0005t0005g0061others(24): Show | 28 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1707-134G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976537 | ||||||
| chr1:204976550
|
A | AT | 30 | a0001c0002t0001g0023a0001c0005t0001g0062a0001c0005t0005g0061others(27): Show | 31 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1707-121_1707-120i others(3): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976550 | ||||||
| chr1:204976591
|
C | A | 8 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0025g0042others(5): Show | 8 | HG01192.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707-80C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976591 | ||||||
| chr1:204976618
|
G | C | 30 | a0001c0002t0001g0023a0001c0005t0001g0062a0001c0005t0005g0061others(27): Show | 31 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1707-53G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 15/29 | chr1 | 204976618 | ||||||
| chr1:204976806
|
A | G | 27 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0005t0005g0131others(24): Show | 28 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1831+11A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204976806 | ||||||
| chr1:204976865
|
C | T | 1 | a0001c0038t0014g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1831+70C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204976865 | ||||||
| chr1:204976914
|
G | A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1831+119G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204976914 | ||||||
| chr1:204977212
|
T | C | 4 | a0001c0002t0011g0144a0001c0004t0001g0139a0002c0008t0011g0102others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1831+417T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204977212 | ||||||
| chr1:204977259
|
C | T | 27 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0005t0005g0131others(24): Show | 28 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1832-422C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204977259 | ||||||
| chr1:204977425
|
G | A | 1 | a0002c0007t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1832-256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204977425 | ||||||
| chr1:204977449
|
A | C | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1832-232A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204977449 | ||||||
| chr1:204977540
|
T | C | 24 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0005t0005g0131others(21): Show | 25 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1832-141T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204977540 | ||||||
| chr1:204977636
|
T | C | 29 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0005t0005g0131others(26): Show | 30 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1832-45T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 16/29 | chr1 | 204977636 | ||||||
| chr1:204977879
|
C | T | 18 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(15): Show | 18 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1876+154C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204977879 | ||||||
| chr1:204978045
|
C | T | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1876+320C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204978045 | ||||||
| chr1:204978046
|
G | A | 1 | a0001c0001t0007g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1876+321G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204978046 | ||||||
| chr1:204978361
|
C | G | 39 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(36): Show | 39 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1877-607C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204978361 | ||||||
| chr1:204978574
|
G | A | 20 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(17): Show | 20 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1877-394G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204978574 | ||||||
| chr1:204978754
|
T | TG | 18 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0005t0005g0131others(15): Show | 19 | HG00741.hp2 HG01123.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1877-205dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr1 | 204978754 | |||||
| chr1:204978757
|
G | T | 4 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0025g0042others(1): Show | 4 | HG02451.hp2 HG03471.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1877-211G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204978757 | ||||||
| chr1:204978960
|
G | A | 1 | a0001c0004t0005g0153 | 1 | HG02258.hp2 | splice_region_variant&intron_variant | LOW | c.1877-8G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 17/29 | chr1 | 204978960 | ||||||
| chr1:204979110
|
C | T | 2 | a0003c0019t0003g0116a0011c0037t0004g0110 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1978+41C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 18/29 | chr1 | 204979110 | ||||||
| chr1:204979607
|
A | G | 24 | a0001c0005t0001g0062a0001c0005t0005g0061a0001c0005t0005g0131others(21): Show | 25 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.2176+48A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 19/29 | chr1 | 204979607 | ||||||
| chr1:204979828
|
A | T | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2176+269A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 19/29 | chr1 | 204979828 | ||||||
| chr1:204979924
|
C | A | 7 | a0001c0005t0022g0089a0002c0040t0004g0052a0003c0009t0003g0187others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176+365C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 19/29 | chr1 | 204979924 | ||||||
| chr1:204979928
|
T | C | 1 | a0001c0010t0005g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2176+369T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 19/29 | chr1 | 204979928 | ||||||
| chr1:204980211
|
A | G | 5 | a0001c0002t0011g0144a0001c0004t0001g0139a0001c0005t0001g0062others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2177-159A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 19/29 | chr1 | 204980211 | ||||||
| chr1:204980517
|
G | A | 30 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(27): Show | 31 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.2247+77G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204980517 | ||||||
| chr1:204980639
|
T | C | 84 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(81): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2247+199T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204980639 | ||||||
| chr1:204980698
|
T | C | 8 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0027t0014g0184others(5): Show | 9 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.2247+258T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204980698 | ||||||
| chr1:204980984
|
C | T | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2247+544C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204980984 | ||||||
| chr1:204981118
|
G | A | 5 | a0001c0002t0011g0144a0001c0004t0001g0139a0001c0005t0001g0062others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2247+678G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981118 | ||||||
| chr1:204981128
|
A | G | 8 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2248-670A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981128 | ||||||
| chr1:204981188
|
G | A | 3 | a0001c0001t0010g0127a0001c0002t0002g0069a0001c0002t0002g0192 | 3 | HG01106.hp1 HG01109.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2248-610G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981188 | ||||||
| chr1:204981434
|
T | C | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2248-364T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981434 | ||||||
| chr1:204981462
|
A | G | 1 | a0001c0022t0048g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2248-336A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981462 | ||||||
| chr1:204981581
|
G | C | 223 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(220): Show | 225 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.2248-217G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981581 | ||||||
| chr1:204981602
|
C | T | 1 | a0013c0050t0020g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2248-196C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981602 | ||||||
| chr1:204981620
|
C | T | 7 | a0001c0002t0045g0098a0001c0004t0041g0065a0001c0015t0049g0119others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2248-178C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981620 | ||||||
| chr1:204981684
|
G | A | 3 | a0001c0014t0001g0002a0001c0014t0001g0200a0001c0021t0001g0170 | 4 | HG01123.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.2248-114G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 20/29 | chr1 | 204981684 | ||||||
| chr1:204982056
|
CT | C | 26 | a0001c0005t0005g0061a0001c0005t0005g0131a0001c0005t0006g0152others(23): Show | 27 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2470+38delT | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204982056 | |||||
| chr1:204982081
|
C | T | 39 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(36): Show | 39 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.2470+61C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204982081 | ||||||
| chr1:204982266
|
A | G | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2470+246A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204982266 | ||||||
| chr1:204982412
|
A | G | 63 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(60): Show | 64 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2470+392A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204982412 | ||||||
| chr1:204982898
|
A | G | 212 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(209): Show | 214 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.2470+878A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204982898 | ||||||
| chr1:204983093
|
A | G | 1 | a0001c0001t0009g0029 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2470+1073A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983093 | ||||||
| chr1:204983108
|
C | G | 7 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2470+1088C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983108 | ||||||
| chr1:204983597
|
C | T | 7 | a0001c0002t0045g0098a0001c0004t0041g0065a0001c0015t0049g0119others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2470+1577C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983597 | ||||||
| chr1:204983609
|
T | C | 66 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(63): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2470+1589T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983609 | ||||||
| chr1:204983656
|
A | G | 1 | a0002c0003t0001g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2470+1636A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983656 | ||||||
| chr1:204983684
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2470+1664C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983684 | ||||||
| chr1:204983721
|
C | A | 63 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(60): Show | 64 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2470+1701C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204983721 | ||||||
| chr1:204984218
|
A | G | 9 | a0001c0002t0004g0004a0001c0002t0004g0107a0001c0002t0004g0157others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2470+2198A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984218 | ||||||
| chr1:204984242
|
G | A | 1 | a0002c0040t0004g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2470+2222G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984242 | ||||||
| chr1:204984316
|
A | T | 15 | a0001c0005t0005g0061a0001c0005t0005g0131a0001c0005t0006g0152others(12): Show | 16 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2470+2296A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984316 | ||||||
| chr1:204984331
|
A | ATG | 11 | a0001c0002t0001g0180a0001c0005t0022g0089a0001c0017t0001g0173others(8): Show | 11 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2470+2325_2470+232 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984331 | |||||
| chr1:204984345
|
G | A | 3 | a0001c0010t0024g0151a0001c0010t0030g0217a0001c0041t0003g0118 | 3 | HG02897.hp1 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2470+2325G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984345 | ||||||
| chr1:204984345
|
G | GTGTA | 59 | a0001c0002t0001g0023a0001c0002t0001g0027a0001c0002t0001g0057others(56): Show | 59 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2470+2326_2470+232 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984345 | |||||
| chr1:204984357
|
A | ATG | 22 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0011g0144others(19): Show | 22 | HG01109.hp2 HG01192.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.2470+2349_2470+235 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984357 | |||||
| chr1:204984357
|
A | ATGTG | 8 | a0001c0002t0008g0143a0001c0015t0029g0101a0003c0023t0007g0108others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2470+2347_2470+235 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984357 | |||||
| chr1:204984357
|
A | G | 66 | a0001c0002t0001g0023a0001c0002t0001g0027a0001c0002t0001g0057others(63): Show | 66 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2470+2337A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984357 | ||||||
| chr1:204984369
|
G | GTA | 19 | a0001c0002t0001g0180a0001c0005t0005g0061a0001c0005t0005g0131others(16): Show | 20 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.2470+2358_2470+235 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984369 | |||||
| chr1:204984380
|
C | CGCATATA others(15): Show |
1 | a0001c0001t0051g0036 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2470+2361_2470+238 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984380 | |||||
| chr1:204984382
|
C | CAT | 21 | a0001c0001t0001g0149a0001c0001t0002g0210a0001c0001t0006g0121others(18): Show | 21 | HG00544.hp2 HG00639.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2470+2390_2470+239 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATAT | 6 | a0001c0001t0001g0202a0001c0002t0001g0027a0001c0002t0002g0140others(3): Show | 6 | HG01074.hp2 HG01257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2470+2388_2470+239 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATAT | 4 | a0001c0002t0004g0004a0001c0002t0004g0157a0001c0002t0004g0185others(1): Show | 4 | HG01261.hp1 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2470+2386_2470+239 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(1): Show |
7 | a0001c0002t0002g0148a0001c0002t0002g0189a0001c0002t0002g0191others(4): Show | 7 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2470+2384_2470+239 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(3): Show |
6 | a0001c0002t0004g0107a0001c0002t0008g0105a0001c0002t0008g0106others(3): Show | 6 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2470+2382_2470+239 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(7): Show |
3 | a0001c0015t0049g0119a0002c0006t0003g0128a0003c0018t0003g0136 | 3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2470+2378_2470+239 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(9): Show |
1 | a0001c0004t0041g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2470+2376_2470+239 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(11): Show |
2 | a0001c0002t0045g0098a0001c0036t0044g0220 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2470+2374_2470+239 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
CAT | C | 25 | a0001c0001t0002g0146a0001c0001t0004g0064a0001c0001t0004g0117others(22): Show | 25 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2470+2390_2470+239 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
CATAT | C | 14 | a0001c0002t0001g0205a0001c0002t0020g0100a0001c0015t0029g0101others(11): Show | 14 | HG01981.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470+2388_2470+239 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
CATATAT | C | 55 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(52): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2470+2386_2470+239 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984383
|
A | G | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2470+2363A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984383 | ||||||
| chr1:204984523
|
C | T | 15 | a0001c0005t0005g0061a0001c0005t0005g0131a0001c0005t0006g0152others(12): Show | 16 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2470+2503C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984523 | ||||||
| chr1:204984599
|
C | T | 47 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(44): Show | 47 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2470+2579C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984599 | ||||||
| chr1:204984649
|
GA | G | 50 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2470+2632delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204984649 | |||||
| chr1:204984772
|
A | G | 2 | a0001c0001t0023g0109a0001c0001t0023g0156 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2471-2646A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984772 | ||||||
| chr1:204984838
|
C | T | 2 | a0001c0002t0004g0004a0001c0036t0044g0220 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2471-2580C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204984838 | ||||||
| chr1:204985074
|
T | TACTTGCT others(5): Show |
2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2471-2342_2471-233 others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 204985074 | |||||
| chr1:204985082
|
T | A | 7 | a0001c0002t0045g0098a0001c0004t0041g0065a0001c0015t0049g0119others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2471-2336T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985082 | ||||||
| chr1:204985086
|
G | C | 2 | a0001c0010t0030g0217a0001c0041t0003g0118 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2471-2332G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985086 | ||||||
| chr1:204985462
|
C | T | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2471-1956C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985462 | ||||||
| chr1:204985491
|
C | G | 1 | a0001c0001t0051g0036 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2471-1927C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985491 | ||||||
| chr1:204985510
|
A | G | 1 | a0013c0050t0020g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2471-1908A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985510 | ||||||
| chr1:204985587
|
G | A | 2 | a0002c0003t0013g0132a0012c0044t0013g0010 | 2 | NA19003.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2471-1831G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985587 | ||||||
| chr1:204985660
|
A | G | 2 | a0002c0003t0001g0059a0002c0003t0001g0166 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2471-1758A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985660 | ||||||
| chr1:204985865
|
A | G | 91 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(88): Show | 92 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.2471-1553A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204985865 | ||||||
| chr1:204986107
|
G | A | 1 | a0001c0030t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2471-1311G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986107 | ||||||
| chr1:204986191
|
G | A | 50 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2471-1227G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986191 | ||||||
| chr1:204986201
|
A | G | 50 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2471-1217A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986201 | ||||||
| chr1:204986241
|
G | A | 2 | a0001c0001t0015g0093a0001c0001t0015g0212 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2471-1177G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986241 | ||||||
| chr1:204986288
|
G | A | 50 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2471-1130G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986288 | ||||||
| chr1:204986301
|
G | T | 2 | a0001c0001t0006g0121a0001c0001t0033g0038 | 2 | NA18962.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2471-1117G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986301 | ||||||
| chr1:204986362
|
C | T | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2471-1056C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986362 | ||||||
| chr1:204986363
|
G | A | 1 | a0002c0003t0035g0207 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2471-1055G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986363 | ||||||
| chr1:204986574
|
C | A | 8 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0025g0042others(5): Show | 8 | HG01192.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2471-844C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986574 | ||||||
| chr1:204986588
|
G | A | 16 | a0001c0005t0005g0061a0001c0005t0005g0131a0001c0005t0006g0152others(13): Show | 17 | HG00741.hp2 HG01123.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2471-830G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986588 | ||||||
| chr1:204986885
|
G | A | 1 | a0002c0006t0001g0037 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2471-533G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986885 | ||||||
| chr1:204986958
|
G | A | 2 | a0003c0024t0003g0115a0003c0029t0031g0005 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2471-460G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204986958 | ||||||
| chr1:204987197
|
G | C | 47 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(44): Show | 47 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2471-221G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204987197 | ||||||
| chr1:204987208
|
G | A | 2 | a0003c0009t0003g0187a0003c0049t0003g0186 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2471-210G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204987208 | ||||||
| chr1:204987263
|
C | T | 1 | a0002c0006t0003g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2471-155C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 21/29 | chr1 | 204987263 | ||||||
| chr1:204987917
|
C | CACAG | 97 | a0001c0001t0001g0163a0001c0001t0015g0093a0001c0001t0015g0212others(94): Show | 98 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.2593+378_2593+381d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr1 | 204987917 | |||||
| chr1:204987927
|
A | T | 11 | a0001c0004t0001g0139a0001c0005t0022g0089a0001c0022t0001g0092others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2593+387A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204987927 | ||||||
| chr1:204987999
|
C | G | 2 | a0001c0002t0004g0004a0001c0036t0044g0220 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2593+459C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204987999 | ||||||
| chr1:204988045
|
A | G | 20 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(17): Show | 20 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.2593+505A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204988045 | ||||||
| chr1:204988175
|
T | G | 1 | a0001c0004t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2594-458T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204988175 | ||||||
| chr1:204988303
|
G | A | 1 | a0001c0004t0002g0032 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2594-330G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204988303 | ||||||
| chr1:204988448
|
A | G | 10 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2594-185A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204988448 | ||||||
| chr1:204988458
|
A | G | 1 | a0001c0001t0005g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2594-175A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 22/29 | chr1 | 204988458 | ||||||
| chr1:204988980
|
T | C | 2 | a0001c0002t0001g0057a0001c0004t0001g0179 | 2 | HG00558.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2767+174T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204988980 | ||||||
| chr1:204988981
|
G | T | 5 | a0001c0004t0003g0203a0001c0004t0005g0153a0003c0018t0018g0145others(2): Show | 5 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2767+175G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204988981 | ||||||
| chr1:204989016
|
T | A | 7 | a0001c0010t0004g0194a0001c0010t0005g0175a0001c0010t0024g0151others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2767+210T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989016 | ||||||
| chr1:204989017
|
C | T | 7 | a0001c0010t0004g0194a0001c0010t0005g0175a0001c0010t0024g0151others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2767+211C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989017 | ||||||
| chr1:204989107
|
G | A | 1 | a0003c0019t0005g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2767+301G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989107 | ||||||
| chr1:204989249
|
G | A | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2767+443G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989249 | ||||||
| chr1:204989273
|
G | A | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2767+467G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989273 | ||||||
| chr1:204989306
|
G | A | 5 | a0001c0004t0003g0203a0003c0018t0018g0145a0003c0024t0003g0115others(2): Show | 5 | HG01192.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2767+500G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989306 | ||||||
| chr1:204989409
|
G | A | 1 | a0001c0002t0001g0027 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2767+603G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989409 | ||||||
| chr1:204989432
|
G | A | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2767+626G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989432 | ||||||
| chr1:204989453
|
C | A | 1 | a0001c0001t0043g0028 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2767+647C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989453 | ||||||
| chr1:204989514
|
C | T | 6 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0027t0014g0184others(3): Show | 7 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2767+708C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989514 | ||||||
| chr1:204989552
|
C | T | 12 | a0001c0002t0045g0098a0001c0005t0005g0061a0001c0005t0005g0131others(9): Show | 12 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2767+746C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989552 | ||||||
| chr1:204989883
|
G | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2767+1077G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989883 | ||||||
| chr1:204989886
|
T | C | 6 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0027t0014g0184others(3): Show | 7 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2767+1080T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989886 | ||||||
| chr1:204989915
|
C | T | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2767+1109C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989915 | ||||||
| chr1:204989916
|
C | T | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2767+1110C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989916 | ||||||
| chr1:204989938
|
C | T | 1 | a0002c0003t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2767+1132C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204989938 | ||||||
| chr1:204990014
|
G | T | 8 | a0001c0004t0005g0153a0001c0010t0004g0194a0001c0010t0005g0175others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2767+1208G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990014 | ||||||
| chr1:204990147
|
C | T | 30 | a0001c0001t0015g0093a0001c0001t0015g0212a0001c0001t0040g0113others(27): Show | 30 | HG01168.hp1 HG01169.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.2768-1145C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990147 | ||||||
| chr1:204990182
|
G | A | 1 | a0001c0021t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2768-1110G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990182 | ||||||
| chr1:204990314
|
G | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2768-978G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990314 | ||||||
| chr1:204990339
|
C | A | 9 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2768-953C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990339 | ||||||
| chr1:204990360
|
A | G | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2768-932A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990360 | ||||||
| chr1:204990430
|
C | T | 17 | a0001c0002t0003g0009a0001c0002t0008g0137a0001c0002t0025g0042others(14): Show | 17 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2768-862C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990430 | ||||||
| chr1:204990441
|
A | G | 7 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2768-851A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990441 | ||||||
| chr1:204990563
|
C | CA | 185 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.2768-713dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 204990563 | |||||
| chr1:204990563
|
C | CAA | 9 | a0001c0002t0003g0009a0001c0004t0005g0153a0001c0010t0004g0194others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2768-714_2768-713d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 204990563 | |||||
| chr1:204990574
|
A | G | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2768-718A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990574 | ||||||
| chr1:204990586
|
G | A | 1 | a0001c0035t0036g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2768-706G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990586 | ||||||
| chr1:204990713
|
C | T | 1 | a0004c0020t0003g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2768-579C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990713 | ||||||
| chr1:204990735
|
G | C | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2768-557G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204990735 | ||||||
| chr1:204991043
|
G | A | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2768-249G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204991043 | ||||||
| chr1:204991111
|
C | T | 18 | a0001c0001t0001g0163a0001c0001t0015g0093a0001c0001t0015g0212others(15): Show | 18 | HG01168.hp1 HG01169.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.2768-181C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204991111 | ||||||
| chr1:204991277
|
C | T | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2768-15C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 23/29 | chr1 | 204991277 | ||||||
| chr1:204991317
|
A | G | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2782+11A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204991317 | ||||||
| chr1:204991645
|
C | T | 18 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(15): Show | 18 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2782+339C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204991645 | ||||||
| chr1:204991802
|
G | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(84): Show | 87 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.2782+496G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204991802 | ||||||
| chr1:204992305
|
C | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2782+999C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204992305 | ||||||
| chr1:204992912
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2782+1606A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204992912 | ||||||
| chr1:204992934
|
C | T | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2782+1628C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204992934 | ||||||
| chr1:204993053
|
G | A | 7 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2782+1747G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993053 | ||||||
| chr1:204993116
|
G | A | 10 | a0001c0002t0004g0107a0001c0002t0004g0157a0001c0002t0004g0185others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2782+1810G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993116 | ||||||
| chr1:204993154
|
G | A | 5 | a0001c0004t0003g0203a0003c0018t0018g0145a0003c0024t0003g0115others(2): Show | 5 | HG01192.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2782+1848G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993154 | ||||||
| chr1:204993222
|
C | T | 6 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0027t0014g0184others(3): Show | 7 | HG00738.hp2 HG01074.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2782+1916C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993222 | ||||||
| chr1:204993237
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2782+1931T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993237 | ||||||
| chr1:204993243
|
T | C | 221 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(218): Show | 223 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.2782+1937T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993243 | ||||||
| chr1:204993277
|
A | G | 36 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(33): Show | 36 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.2782+1971A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993277 | ||||||
| chr1:204993409
|
G | C | 4 | a0001c0004t0041g0065a0001c0015t0049g0119a0002c0006t0003g0128others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782+2103G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993409 | ||||||
| chr1:204993526
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2782+2220T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993526 | ||||||
| chr1:204993531
|
C | T | 1 | a0001c0002t0006g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2782+2225C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993531 | ||||||
| chr1:204993532
|
G | A | 38 | a0001c0002t0001g0023a0001c0002t0001g0057a0001c0002t0001g0060others(35): Show | 38 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2782+2226G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993532 | ||||||
| chr1:204993534
|
A | G | 107 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(104): Show | 108 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2782+2228A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993534 | ||||||
| chr1:204993590
|
A | G | 222 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(219): Show | 224 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.2782+2284A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993590 | ||||||
| chr1:204993741
|
G | A | 5 | a0003c0009t0003g0187a0003c0009t0007g0138a0003c0009t0007g0165others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2782+2435G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993741 | ||||||
| chr1:204993822
|
G | A | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2782+2516G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204993822 | ||||||
| chr1:204994151
|
G | A | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2782+2845G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204994151 | ||||||
| chr1:204994186
|
C | T | 7 | a0001c0015t0029g0101a0003c0023t0007g0108a0003c0023t0018g0188others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2782+2880C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204994186 | ||||||
| chr1:204994212
|
C | A | 2 | a0001c0001t0015g0093a0001c0001t0015g0212 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2782+2906C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204994212 | ||||||
| chr1:204994474
|
T | C | 69 | a0001c0001t0001g0163a0001c0001t0015g0093a0001c0001t0015g0212others(66): Show | 69 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2783-2696T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204994474 | ||||||
| chr1:204994534
|
A | T | 1 | a0001c0002t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2783-2636A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204994534 | ||||||
| chr1:204994949
|
C | T | 17 | a0001c0001t0001g0163a0001c0001t0040g0113a0001c0002t0002g0073others(14): Show | 17 | HG01261.hp2 HG01928.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.2783-2221C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204994949 | ||||||
| chr1:204995171
|
G | T | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2783-1999G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995171 | ||||||
| chr1:204995203
|
G | A | 2 | a0002c0003t0006g0221a0002c0003t0046g0016 | 2 | NA18962.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2783-1967G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995203 | ||||||
| chr1:204995313
|
A | G | 1 | a0003c0009t0007g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2783-1857A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995313 | ||||||
| chr1:204995315
|
A | AGT | 16 | a0001c0002t0002g0069a0001c0002t0002g0192a0001c0002t0011g0144others(13): Show | 17 | HG00639.hp2 HG01106.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.2783-1818_2783-181 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
A | AGTGT | 34 | a0001c0001t0040g0113a0001c0002t0001g0027a0001c0002t0002g0073others(31): Show | 34 | HG01069.hp2 HG01175.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.2783-1820_2783-181 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
A | AGTGTGT | 2 | a0001c0001t0001g0163a0002c0003t0046g0016 | 2 | HG03942.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2783-1822_2783-181 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
A | AGTGTGTG others(1): Show |
3 | a0001c0022t0001g0092a0001c0022t0048g0150a0005c0047t0021g0077 | 3 | HG00741.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2783-1824_2783-181 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGT | A | 21 | a0001c0001t0052g0085a0001c0002t0004g0107a0001c0002t0004g0157others(18): Show | 21 | HG00423.hp1 HG00673.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.2783-1818_2783-181 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGT | A | 115 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(112): Show | 116 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.2783-1820_2783-181 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGTGT | A | 13 | a0001c0001t0004g0064a0001c0001t0004g0117a0001c0001t0005g0133others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2783-1822_2783-181 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0002t0009g0193others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2783-1824_2783-181 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995335
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2783-1835T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995335 | ||||||
| chr1:204995343
|
TGTGTGTG others(13): Show |
T | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2783-1823_2783-180 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr1 | 204995343 | |||||
| chr1:204995354
|
A | G | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2783-1816A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995354 | ||||||
| chr1:204995503
|
C | T | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2783-1667C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995503 | ||||||
| chr1:204995546
|
G | A | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2783-1624G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995546 | ||||||
| chr1:204995731
|
G | A | 5 | a0003c0009t0003g0187a0003c0009t0007g0138a0003c0009t0007g0165others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2783-1439G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204995731 | ||||||
| chr1:204996024
|
G | T | 22 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(19): Show | 22 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.2783-1146G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996024 | ||||||
| chr1:204996026
|
C | A | 22 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(19): Show | 22 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.2783-1144C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996026 | ||||||
| chr1:204996288
|
A | G | 5 | a0003c0009t0003g0187a0003c0009t0007g0138a0003c0009t0007g0165others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2783-882A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996288 | ||||||
| chr1:204996396
|
T | C | 221 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(218): Show | 223 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.2783-774T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996396 | ||||||
| chr1:204996529
|
A | G | 140 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(137): Show | 141 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.2783-641A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996529 | ||||||
| chr1:204996599
|
C | T | 1 | a0002c0003t0001g0001 | 2 | HG00738.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2783-571C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996599 | ||||||
| chr1:204996626
|
T | C | 33 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0069others(30): Show | 34 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.2783-544T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996626 | ||||||
| chr1:204996910
|
T | C | 11 | a0001c0001t0001g0058a0001c0002t0009g0193a0001c0004t0001g0013others(8): Show | 11 | HG01175.hp1 HG01243.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.2783-260T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204996910 | ||||||
| chr1:204997042
|
T | C | 51 | a0001c0001t0001g0163a0001c0001t0001g0215a0001c0001t0005g0133others(48): Show | 52 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2783-128T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204997042 | ||||||
| chr1:204997145
|
C | T | 2 | a0001c0001t0001g0162a0001c0010t0004g0194 | 2 | HG00323.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2783-25C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 24/29 | chr1 | 204997145 | ||||||
| chr1:204997454
|
C | G | 2 | a0001c0014t0001g0002a0001c0014t0001g0200 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3019+48C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997454 | ||||||
| chr1:204997469
|
G | A | 1 | a0002c0003t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3019+63G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997469 | ||||||
| chr1:204997514
|
T | G | 2 | a0001c0015t0049g0119a0003c0019t0003g0116 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3019+108T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997514 | ||||||
| chr1:204997562
|
G | A | 188 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(185): Show | 190 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.3019+156G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997562 | ||||||
| chr1:204997621
|
A | G | 198 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(195): Show | 200 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.3019+215A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997621 | ||||||
| chr1:204997640
|
C | A | 3 | a0001c0004t0041g0065a0002c0006t0003g0128a0003c0018t0003g0136 | 3 | HG03098.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3019+234C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997640 | ||||||
| chr1:204997791
|
G | A | 1 | a0009c0031t0001g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3019+385G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997791 | ||||||
| chr1:204997796
|
C | T | 7 | a0001c0004t0003g0203a0001c0004t0005g0153a0001c0010t0024g0151others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3019+390C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997796 | ||||||
| chr1:204997870
|
C | T | 2 | a0001c0010t0030g0217a0003c0029t0031g0005 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3019+464C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204997870 | ||||||
| chr1:204998032
|
CA | C | 135 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(132): Show | 137 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.3019+629delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr1 | 204998032 | |||||
| chr1:204998058
|
A | T | 16 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0002t0002g0140others(13): Show | 16 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.3019+652A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998058 | ||||||
| chr1:204998111
|
G | T | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3019+705G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998111 | ||||||
| chr1:204998128
|
G | A | 130 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(127): Show | 132 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.3019+722G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998128 | ||||||
| chr1:204998527
|
G | T | 1 | a0001c0002t0020g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3019+1121G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998527 | ||||||
| chr1:204998585
|
G | A | 2 | a0001c0001t0023g0109a0001c0001t0023g0156 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3019+1179G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998585 | ||||||
| chr1:204998657
|
G | A | 2 | a0003c0016t0026g0141a0003c0016t0053g0041 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.3019+1251G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998657 | ||||||
| chr1:204998730
|
TAA | T | 221 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(218): Show | 223 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.3019+1328_3019+132 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr1 | 204998730 | |||||
| chr1:204998909
|
C | T | 3 | a0001c0001t0001g0084a0001c0030t0001g0030a0002c0003t0001g0001 | 4 | HG00738.hp2 HG01074.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019+1503C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204998909 | ||||||
| chr1:204999002
|
A | C | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3019+1596A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999002 | ||||||
| chr1:204999063
|
T | C | 4 | a0001c0002t0001g0205a0001c0010t0005g0175a0001c0022t0001g0092others(1): Show | 4 | HG01074.hp2 HG01257.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019+1657T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999063 | ||||||
| chr1:204999130
|
C | A | 44 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(41): Show | 44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3019+1724C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999130 | ||||||
| chr1:204999211
|
C | T | 42 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(39): Show | 42 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.3019+1805C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999211 | ||||||
| chr1:204999264
|
C | T | 177 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(174): Show | 179 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.3019+1858C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999264 | ||||||
| chr1:204999414
|
G | A | 4 | a0001c0002t0001g0205a0001c0010t0005g0175a0001c0022t0001g0092others(1): Show | 4 | HG01074.hp2 HG01257.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3020-1756G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999414 | ||||||
| chr1:204999415
|
G | A | 27 | a0001c0001t0001g0215a0001c0001t0004g0064a0001c0001t0004g0117others(24): Show | 27 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.3020-1755G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999415 | ||||||
| chr1:204999557
|
G | C | 1 | a0001c0004t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3020-1613G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999557 | ||||||
| chr1:204999631
|
G | A | 2 | a0001c0004t0003g0203a0004c0020t0003g0197 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3020-1539G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999631 | ||||||
| chr1:204999659
|
T | C | 43 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(40): Show | 43 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3020-1511T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999659 | ||||||
| chr1:204999668
|
TAA | T | 2 | a0001c0014t0001g0002a0001c0014t0001g0200 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3020-1501_3020-150 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999668 | ||||||
| chr1:204999668
|
TAATATG | T | 10 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0017t0001g0173others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.3020-1498_3020-149 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr1 | 204999668 | |||||
| chr1:204999817
|
A | G | 43 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(40): Show | 43 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3020-1353A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999817 | ||||||
| chr1:204999929
|
G | T | 1 | a0001c0001t0010g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3020-1241G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999929 | ||||||
| chr1:204999938
|
A | G | 43 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(40): Show | 43 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3020-1232A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999938 | ||||||
| chr1:204999963
|
T | A | 11 | a0001c0002t0001g0027a0001c0002t0001g0180a0001c0017t0001g0173others(8): Show | 11 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3020-1207T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 204999963 | ||||||
| chr1:205000032
|
C | T | 1 | a0001c0001t0006g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3020-1138C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000032 | ||||||
| chr1:205000116
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3020-1054T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000116 | ||||||
| chr1:205000154
|
G | A | 2 | a0001c0004t0003g0203a0004c0020t0003g0197 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3020-1016G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000154 | ||||||
| chr1:205000189
|
G | A | 43 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(40): Show | 43 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3020-981G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000189 | ||||||
| chr1:205000242
|
T | G | 6 | a0001c0004t0003g0203a0001c0004t0005g0153a0003c0018t0018g0145others(3): Show | 6 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3020-928T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000242 | ||||||
| chr1:205000264
|
G | C | 2 | a0002c0003t0001g0059a0002c0003t0001g0166 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3020-906G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000264 | ||||||
| chr1:205000291
|
C | T | 41 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(38): Show | 41 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.3020-879C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000291 | ||||||
| chr1:205000458
|
C | T | 85 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(82): Show | 87 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3020-712C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000458 | ||||||
| chr1:205000561
|
G | A | 85 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(82): Show | 87 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3020-609G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000561 | ||||||
| chr1:205000776
|
G | A | 4 | a0001c0002t0011g0144a0001c0005t0001g0062a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3020-394G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000776 | ||||||
| chr1:205000794
|
T | C | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3020-376T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000794 | ||||||
| chr1:205000826
|
CA | C | 100 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(97): Show | 102 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.3020-331delA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr1 | 205000826 | |||||
| chr1:205000826
|
CAA | C | 45 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(42): Show | 45 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.3020-332_3020-331d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr1 | 205000826 | |||||
| chr1:205000839
|
A | C | 84 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 86 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3020-331A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000839 | ||||||
| chr1:205000839
|
A | T | 1 | a0009c0031t0001g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3020-331A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000839 | ||||||
| chr1:205000885
|
C | G | 1 | a0001c0015t0049g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3020-285C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205000885 | ||||||
| chr1:205001020
|
TC | T | 42 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(39): Show | 42 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.3020-146delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr1 | 205001020 | |||||
| chr1:205001115
|
A | G | 44 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(41): Show | 44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3020-55A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 25/29 | chr1 | 205001115 | ||||||
| chr1:205001302
|
C | T | 1 | a0001c0002t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3136+16C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001302 | ||||||
| chr1:205001325
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3136+39C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001325 | ||||||
| chr1:205001367
|
C | A | 44 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(41): Show | 44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3136+81C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001367 | ||||||
| chr1:205001437
|
T | C | 1 | a0001c0039t0032g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3136+151T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001437 | ||||||
| chr1:205001516
|
A | G | 1 | a0001c0039t0032g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3136+230A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001516 | ||||||
| chr1:205001580
|
G | A | 42 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(39): Show | 42 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.3136+294G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001580 | ||||||
| chr1:205001649
|
T | A | 44 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(41): Show | 44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3136+363T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001649 | ||||||
| chr1:205001716
|
C | A | 42 | a0001c0004t0001g0013a0001c0004t0001g0046a0001c0004t0001g0071others(39): Show | 42 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.3136+430C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001716 | ||||||
| chr1:205001742
|
C | T | 1 | a0001c0002t0020g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3136+456C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001742 | ||||||
| chr1:205001761
|
G | A | 3 | a0001c0001t0015g0093a0001c0001t0015g0212a0002c0003t0021g0159 | 3 | HG01168.hp1 HG01169.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.3136+475G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001761 | ||||||
| chr1:205001981
|
G | A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3137-615G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205001981 | ||||||
| chr1:205002180
|
C | CA | 2 | a0002c0003t0001g0033a0002c0003t0037g0068 | 2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3137-415dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 205002180 | |||||
| chr1:205002214
|
A | G | 84 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 86 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3137-382A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002214 | ||||||
| chr1:205002266
|
G | A | 4 | a0001c0022t0001g0092a0001c0022t0048g0150a0003c0016t0026g0141others(1): Show | 4 | HG01074.hp2 HG01257.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3137-330G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002266 | ||||||
| chr1:205002285
|
A | G | 46 | a0001c0001t0002g0210a0001c0002t0003g0009a0001c0004t0001g0013others(43): Show | 46 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.3137-311A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002285 | ||||||
| chr1:205002315
|
T | C | 1 | a0001c0002t0001g0027 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3137-281T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002315 | ||||||
| chr1:205002324
|
A | G | 46 | a0001c0002t0002g0073a0001c0002t0003g0009a0001c0004t0001g0013others(43): Show | 46 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.3137-272A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002324 | ||||||
| chr1:205002327
|
T | C | 2 | a0001c0005t0022g0089a0002c0040t0004g0052 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3137-269T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002327 | ||||||
| chr1:205002357
|
C | A | 45 | a0001c0002t0003g0009a0001c0004t0001g0013a0001c0004t0001g0046others(42): Show | 45 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.3137-239C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002357 | ||||||
| chr1:205002377
|
G | A | 4 | a0001c0002t0011g0144a0001c0005t0001g0062a0002c0008t0011g0102others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-219G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002377 | ||||||
| chr1:205002408
|
G | A | 2 | a0001c0010t0024g0151a0001c0015t0049g0119 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3137-188G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002408 | ||||||
| chr1:205002408
|
G | C | 17 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0001t0015g0093others(14): Show | 17 | HG00741.hp1 HG01074.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.3137-188G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002408 | ||||||
| chr1:205002425
|
A | G | 46 | a0001c0001t0002g0210a0001c0002t0002g0073a0001c0002t0003g0009others(43): Show | 46 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.3137-171A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002425 | ||||||
| chr1:205002576
|
T | C | 4 | a0001c0004t0041g0065a0001c0010t0005g0175a0003c0018t0003g0136others(1): Show | 4 | HG01496.hp1 HG02257.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-20T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 26/29 | chr1 | 205002576 | ||||||
| chr1:205002895
|
T | C | 2 | a0001c0001t0023g0156a0001c0005t0034g0135 | 2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3289+147T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205002895 | ||||||
| chr1:205002965
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3289+217A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205002965 | ||||||
| chr1:205003005
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3289+257T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003005 | ||||||
| chr1:205003160
|
G | T | 127 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(124): Show | 129 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.3289+412G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003160 | ||||||
| chr1:205003201
|
C | G | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3289+453C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003201 | ||||||
| chr1:205003289
|
A | G | 12 | a0001c0002t0003g0009a0001c0004t0003g0203a0001c0005t0022g0089others(9): Show | 12 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3289+541A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003289 | ||||||
| chr1:205003357
|
G | C | 1 | a0001c0005t0005g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3289+609G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003357 | ||||||
| chr1:205003456
|
G | A | 6 | a0001c0001t0007g0130a0001c0001t0007g0160a0001c0002t0045g0098others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3289+708G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003456 | ||||||
| chr1:205003515
|
C | G | 174 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(171): Show | 176 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.3289+767C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003515 | ||||||
| chr1:205003528
|
A | T | 179 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(176): Show | 181 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.3289+780A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003528 | ||||||
| chr1:205003569
|
G | A | 2 | a0001c0002t0002g0069a0001c0002t0002g0192 | 2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.3289+821G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003569 | ||||||
| chr1:205003718
|
C | T | 15 | a0001c0002t0003g0009a0001c0002t0011g0144a0001c0004t0003g0203others(12): Show | 15 | HG02572.hp2 HG02622.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.3289+970C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003718 | ||||||
| chr1:205003775
|
G | A | 12 | a0001c0002t0003g0009a0001c0004t0003g0203a0001c0015t0029g0101others(9): Show | 12 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3289+1027G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003775 | ||||||
| chr1:205003877
|
C | T | 3 | a0001c0002t0011g0144a0002c0008t0011g0102a0002c0008t0011g0126 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3289+1129C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205003877 | ||||||
| chr1:205004010
|
A | G | 145 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(142): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.3289+1262A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004010 | ||||||
| chr1:205004046
|
T | C | 199 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(196): Show | 201 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.3289+1298T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004046 | ||||||
| chr1:205004409
|
G | C | 2 | a0002c0003t0013g0132a0012c0044t0013g0010 | 2 | NA19003.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3289+1661G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004409 | ||||||
| chr1:205004441
|
A | G | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3289+1693A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004441 | ||||||
| chr1:205004481
|
G | A | 40 | a0001c0001t0002g0146a0001c0001t0007g0130a0001c0001t0007g0160others(37): Show | 40 | HG00639.hp1 HG00741.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.3289+1733G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004481 | ||||||
| chr1:205004699
|
G | A | 1 | a0001c0036t0044g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3289+1951G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004699 | ||||||
| chr1:205004702
|
T | G | 12 | a0001c0002t0003g0009a0001c0004t0003g0203a0001c0015t0029g0101others(9): Show | 12 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3289+1954T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004702 | ||||||
| chr1:205004753
|
C | T | 76 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(73): Show | 77 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3289+2005C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004753 | ||||||
| chr1:205004764
|
ACAGG | A | 33 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(30): Show | 34 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.3289+2020_3289+202 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205004764 | |||||
| chr1:205004794
|
G | A | 77 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(74): Show | 78 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.3289+2046G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004794 | ||||||
| chr1:205004883
|
G | A | 33 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(30): Show | 34 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.3289+2135G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205004883 | ||||||
| chr1:205005057
|
G | A | 76 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(73): Show | 77 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3289+2309G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005057 | ||||||
| chr1:205005266
|
C | T | 1 | a0001c0001t0052g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3289+2518C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005266 | ||||||
| chr1:205005270
|
ATTC | A | 10 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0010t0004g0194others(7): Show | 10 | HG01192.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+2527_3289+252 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205005270 | |||||
| chr1:205005380
|
C | T | 84 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0146others(81): Show | 84 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.3289+2632C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005380 | ||||||
| chr1:205005389
|
G | A | 16 | a0001c0001t0007g0130a0001c0001t0007g0160a0001c0002t0045g0098others(13): Show | 16 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3289+2641G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005389 | ||||||
| chr1:205005418
|
C | CA | 16 | a0001c0001t0007g0130a0001c0001t0007g0160a0001c0002t0045g0098others(13): Show | 16 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3289+2671dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205005418 | |||||
| chr1:205005418
|
C | T | 3 | a0001c0002t0001g0180a0001c0004t0001g0071a0001c0032t0001g0196 | 3 | HG01081.hp2 HG01255.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3289+2670C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005418 | ||||||
| chr1:205005452
|
G | A | 72 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0146others(69): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.3289+2704G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005452 | ||||||
| chr1:205005465
|
G | A | 1 | a0001c0005t0005g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3289+2717G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005465 | ||||||
| chr1:205005556
|
G | A | 1 | a0001c0005t0022g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3289+2808G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005556 | ||||||
| chr1:205005603
|
G | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0039others(2): Show | 5 | HG00544.hp1 NA18955.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+2855G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005603 | ||||||
| chr1:205005671
|
C | G | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3289+2923C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005671 | ||||||
| chr1:205005901
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3289+3153T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205005901 | ||||||
| chr1:205006046
|
G | A | 1 | a0001c0002t0008g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3289+3298G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006046 | ||||||
| chr1:205006046
|
G | T | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3289+3298G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006046 | ||||||
| chr1:205006136
|
C | G | 12 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0005t0022g0089others(9): Show | 12 | HG01192.hp1 HG01496.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3289+3388C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006136 | ||||||
| chr1:205006136
|
C | T | 65 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(62): Show | 66 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.3289+3388C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006136 | ||||||
| chr1:205006153
|
A | T | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3290-3404A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006153 | ||||||
| chr1:205006218
|
T | C | 1 | a0003c0019t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3290-3339T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006218 | ||||||
| chr1:205006240
|
T | G | 56 | a0001c0001t0002g0146a0001c0001t0007g0130a0001c0001t0007g0160others(53): Show | 56 | HG00741.hp1 HG01074.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.3290-3317T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006240 | ||||||
| chr1:205006523
|
G | A | 2 | a0001c0004t0001g0112a0001c0004t0002g0204 | 2 | HG02523.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.3290-3034G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006523 | ||||||
| chr1:205006607
|
G | A | 33 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(30): Show | 34 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.3290-2950G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006607 | ||||||
| chr1:205006794
|
A | G | 1 | a0001c0002t0002g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3290-2763A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006794 | ||||||
| chr1:205006810
|
T | G | 15 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0002g0148others(12): Show | 15 | HG01192.hp1 HG01496.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3290-2747T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006810 | ||||||
| chr1:205006841
|
A | G | 3 | a0001c0022t0001g0092a0001c0022t0048g0150a0009c0031t0001g0209 | 3 | HG01074.hp2 HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3290-2716A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006841 | ||||||
| chr1:205006852
|
A | G | 36 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(33): Show | 36 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.3290-2705A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006852 | ||||||
| chr1:205006924
|
A | T | 7 | a0001c0001t0005g0133a0001c0002t0008g0137a0001c0002t0025g0042others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3290-2633A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205006924 | ||||||
| chr1:205006964
|
TGGA | T | 35 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(32): Show | 36 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.3290-2590_3290-258 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205006964 | |||||
| chr1:205007010
|
G | A | 68 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(65): Show | 69 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.3290-2547G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007010 | ||||||
| chr1:205007078
|
T | C | 16 | a0001c0001t0007g0130a0001c0001t0023g0109a0001c0001t0023g0156others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.3290-2479T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007078 | ||||||
| chr1:205007085
|
G | A | 1 | a0004c0020t0024g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3290-2472G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007085 | ||||||
| chr1:205007101
|
T | C | 1 | a0002c0003t0002g0050 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3290-2456T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007101 | ||||||
| chr1:205007136
|
G | C | 85 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(82): Show | 86 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.3290-2421G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007136 | ||||||
| chr1:205007230
|
T | TA | 15 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0002g0148others(12): Show | 15 | HG01192.hp1 HG01496.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3290-2323dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205007230 | |||||
| chr1:205007235
|
T | A | 86 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(83): Show | 87 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.3290-2322T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007235 | ||||||
| chr1:205007236
|
T | A | 15 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0002g0148others(12): Show | 15 | HG01192.hp1 HG01496.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3290-2321T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007236 | ||||||
| chr1:205007244
|
C | A | 15 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0002g0148others(12): Show | 15 | HG01192.hp1 HG01496.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3290-2313C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007244 | ||||||
| chr1:205007350
|
A | AAC | 22 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0002g0148others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.3290-2204_3290-220 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205007350 | |||||
| chr1:205007445
|
A | G | 16 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0107others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3290-2112A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007445 | ||||||
| chr1:205007573
|
T | C | 1 | a0002c0028t0014g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3290-1984T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007573 | ||||||
| chr1:205007615
|
CTTTG | C | 16 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0107others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3290-1938_3290-193 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205007615 | |||||
| chr1:205007655
|
A | G | 16 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0107others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3290-1902A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007655 | ||||||
| chr1:205007763
|
G | A | 8 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0001t0015g0093others(5): Show | 8 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3290-1794G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007763 | ||||||
| chr1:205007782
|
A | G | 37 | a0001c0001t0007g0130a0001c0001t0007g0160a0001c0001t0023g0109others(34): Show | 37 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.3290-1775A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007782 | ||||||
| chr1:205007812
|
G | T | 1 | a0010c0034t0009g0214 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3290-1745G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205007812 | ||||||
| chr1:205008004
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3290-1553G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008004 | ||||||
| chr1:205008025
|
C | T | 1 | a0001c0002t0020g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3290-1532C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008025 | ||||||
| chr1:205008051
|
G | A | 4 | a0001c0001t0002g0120a0001c0004t0001g0076a0002c0003t0001g0164others(1): Show | 4 | NA18955.hp2 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.3290-1506G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008051 | ||||||
| chr1:205008056
|
G | T | 20 | a0001c0001t0004g0064a0001c0001t0004g0117a0001c0001t0005g0133others(17): Show | 20 | HG01106.hp1 HG01256.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.3290-1501G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008056 | ||||||
| chr1:205008543
|
C | T | 36 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(33): Show | 37 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.3290-1014C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008543 | ||||||
| chr1:205008559
|
G | A | 33 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(30): Show | 33 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.3290-998G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008559 | ||||||
| chr1:205008579
|
G | C | 36 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(33): Show | 37 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.3290-978G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008579 | ||||||
| chr1:205008594
|
AC | A | 54 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(51): Show | 55 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.3290-956delC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205008594 | |||||
| chr1:205008599
|
C | A | 10 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0001t0015g0093others(7): Show | 10 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.3290-958C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008599 | ||||||
| chr1:205008599
|
C | G | 1 | a0002c0003t0046g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3290-958C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008599 | ||||||
| chr1:205008600
|
C | T | 1 | a0001c0001t0010g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3290-957C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008600 | ||||||
| chr1:205008628
|
T | C | 54 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(51): Show | 55 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.3290-929T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008628 | ||||||
| chr1:205008640
|
C | T | 16 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0107others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3290-917C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008640 | ||||||
| chr1:205008671
|
A | G | 135 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(132): Show | 136 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.3290-886A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008671 | ||||||
| chr1:205008808
|
C | CG | 31 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0001t0015g0093others(28): Show | 31 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.3290-742dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205008808 | |||||
| chr1:205008808
|
C | CGG | 14 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0107others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.3290-743_3290-742d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205008808 | |||||
| chr1:205008814
|
G | T | 11 | a0001c0001t0005g0133a0001c0002t0008g0137a0001c0002t0025g0042others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3290-743G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008814 | ||||||
| chr1:205008954
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3290-603A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205008954 | ||||||
| chr1:205009079
|
C | T | 3 | a0001c0002t0001g0180a0001c0004t0001g0071a0001c0032t0001g0196 | 3 | HG01081.hp2 HG01255.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3290-478C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205009079 | ||||||
| chr1:205009108
|
A | C | 1 | a0001c0004t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3290-449A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205009108 | ||||||
| chr1:205009108
|
A | G | 1 | a0001c0001t0012g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3290-449A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205009108 | ||||||
| chr1:205009206
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3290-351G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205009206 | ||||||
| chr1:205009314
|
T | TCTG | 21 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0001t0015g0093others(18): Show | 21 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.3290-240_3290-238d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205009314 | |||||
| chr1:205009317
|
G | GCTT | 31 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(28): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.3290-239_3290-237d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr1 | 205009317 | |||||
| chr1:205009405
|
A | G | 138 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(135): Show | 139 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.3290-152A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205009405 | ||||||
| chr1:205009515
|
C | A | 35 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(32): Show | 36 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.3290-42C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 27/29 | chr1 | 205009515 | ||||||
| chr1:205009818
|
C | A | 2 | a0001c0022t0001g0092a0001c0022t0048g0150 | 2 | HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3421+130C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205009818 | ||||||
| chr1:205009943
|
A | G | 57 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(54): Show | 58 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.3421+255A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205009943 | ||||||
| chr1:205010003
|
T | C | 1 | a0002c0013t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3421+315T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010003 | ||||||
| chr1:205010074
|
G | A | 2 | a0001c0001t0006g0168a0002c0003t0006g0221 | 2 | NA18962.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.3421+386G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010074 | ||||||
| chr1:205010325
|
C | T | 27 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(24): Show | 27 | HG00323.hp2 HG00544.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.3421+637C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010325 | ||||||
| chr1:205010555
|
T | C | 3 | a0001c0002t0011g0144a0002c0008t0011g0102a0002c0008t0011g0126 | 3 | HG02622.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3421+867T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010555 | ||||||
| chr1:205010564
|
G | A | 27 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(24): Show | 27 | HG00323.hp2 HG00544.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.3421+876G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010564 | ||||||
| chr1:205010601
|
T | A | 2 | a0001c0041t0003g0118a0003c0019t0005g0007 | 2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3421+913T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010601 | ||||||
| chr1:205010624
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0002c0003t0001g0171others(3): Show | 6 | HG00738.hp1 HG01071.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3421+936G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010624 | ||||||
| chr1:205010689
|
G | A | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3421+1001G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010689 | ||||||
| chr1:205010772
|
A | G | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3421+1084A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010772 | ||||||
| chr1:205010858
|
G | A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3421+1170G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010858 | ||||||
| chr1:205010881
|
C | T | 1 | a0003c0029t0031g0005 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3421+1193C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010881 | ||||||
| chr1:205010910
|
G | GA | 55 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(52): Show | 56 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.3421+1237dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr1 | 205010910 | |||||
| chr1:205010974
|
A | G | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3421+1286A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205010974 | ||||||
| chr1:205011207
|
A | AC | 76 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(73): Show | 77 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3421+1527dupC | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr1 | 205011207 | |||||
| chr1:205011207
|
A | ACC | 16 | a0001c0001t0001g0202a0001c0002t0003g0009a0001c0004t0003g0203others(13): Show | 16 | HG00738.hp1 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.3421+1526_3421+152 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr1 | 205011207 | |||||
| chr1:205011232
|
G | A | 55 | a0001c0001t0001g0081a0001c0001t0001g0163a0001c0001t0001g0201others(52): Show | 56 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.3421+1544G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011232 | ||||||
| chr1:205011420
|
C | T | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3422-1377C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011420 | ||||||
| chr1:205011448
|
G | A | 16 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0004g0107others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3422-1349G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011448 | ||||||
| chr1:205011779
|
G | A | 123 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(120): Show | 124 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.3422-1018G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011779 | ||||||
| chr1:205011807
|
C | T | 9 | a0001c0001t0002g0146a0001c0001t0010g0147a0001c0001t0015g0093others(6): Show | 9 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.3422-990C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011807 | ||||||
| chr1:205011875
|
T | G | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3422-922T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011875 | ||||||
| chr1:205011887
|
T | C | 1 | a0001c0039t0032g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3422-910T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011887 | ||||||
| chr1:205011952
|
G | A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3422-845G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205011952 | ||||||
| chr1:205012004
|
G | A | 26 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(23): Show | 26 | HG00323.hp2 HG00544.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.3422-793G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012004 | ||||||
| chr1:205012123
|
A | G | 26 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(23): Show | 26 | HG00323.hp2 HG00544.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.3422-674A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012123 | ||||||
| chr1:205012206
|
C | T | 1 | a0001c0039t0032g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3422-591C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012206 | ||||||
| chr1:205012228
|
A | G | 2 | a0001c0005t0022g0089a0003c0019t0005g0007 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3422-569A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012228 | ||||||
| chr1:205012410
|
G | A | 4 | a0001c0001t0040g0113a0002c0003t0001g0059a0002c0003t0001g0166others(1): Show | 4 | HG02015.hp2 HG02523.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.3422-387G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012410 | ||||||
| chr1:205012461
|
A | T | 3 | a0001c0027t0014g0184a0001c0038t0014g0078a0001c0039t0032g0006 | 3 | HG02922.hp1 HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3422-336A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012461 | ||||||
| chr1:205012474
|
G | A | 24 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0001t0007g0160others(21): Show | 24 | HG00639.hp1 HG01109.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.3422-323G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012474 | ||||||
| chr1:205012676
|
A | G | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3422-121A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | chr1 | 205012676 | ||||||
| chr1:205012768
|
CTG | C | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3422-25_3422-24del others(2): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr1 | 205012768 | |||||
| chr1:205012926
|
C | T | 4 | a0001c0022t0048g0150a0001c0027t0014g0184a0001c0038t0014g0078others(1): Show | 4 | HG01074.hp2 HG02922.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.3491+60C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205012926 | ||||||
| chr1:205013035
|
G | C | 3 | a0001c0043t0027g0224a0003c0019t0003g0116a0004c0020t0024g0020 | 3 | HG01192.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3491+169G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013035 | ||||||
| chr1:205013104
|
C | T | 27 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0010t0005g0175others(24): Show | 27 | HG01074.hp2 HG01192.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.3491+238C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013104 | ||||||
| chr1:205013347
|
G | A | 4 | a0001c0022t0048g0150a0001c0027t0014g0184a0001c0038t0014g0078others(1): Show | 4 | HG01074.hp2 HG02922.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.3491+481G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013347 | ||||||
| chr1:205013497
|
A | G | 1 | a0003c0009t0003g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3491+631A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013497 | ||||||
| chr1:205013585
|
A | G | 126 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(123): Show | 127 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.3491+719A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013585 | ||||||
| chr1:205013712
|
G | C | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3491+846G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013712 | ||||||
| chr1:205013715
|
C | T | 15 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0010t0005g0175others(12): Show | 15 | HG01192.hp1 HG01496.hp1 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.3491+849C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013715 | ||||||
| chr1:205013870
|
T | C | 1 | a0001c0002t0019g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3491+1004T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205013870 | ||||||
| chr1:205014051
|
G | T | 14 | a0001c0001t0005g0133a0001c0002t0003g0009a0001c0002t0008g0137others(11): Show | 14 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3491+1185G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014051 | ||||||
| chr1:205014114
|
G | A | 2 | a0001c0001t0005g0133a0006c0048t0025g0040 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3491+1248G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014114 | ||||||
| chr1:205014227
|
C | A | 1 | a0001c0043t0027g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3491+1361C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014227 | ||||||
| chr1:205014246
|
C | G | 151 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(148): Show | 152 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.3491+1380C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014246 | ||||||
| chr1:205014275
|
G | C | 36 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(33): Show | 36 | HG00323.hp2 HG00544.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.3491+1409G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014275 | ||||||
| chr1:205014293
|
G | A | 3 | a0001c0001t0009g0029a0001c0002t0009g0193a0010c0034t0009g0214 | 3 | HG01256.hp1 HG01257.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.3491+1427G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014293 | ||||||
| chr1:205014367
|
A | G | 22 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0210others(19): Show | 22 | HG00323.hp2 HG00544.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.3491+1501A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014367 | ||||||
| chr1:205014485
|
C | T | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3491+1619C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014485 | ||||||
| chr1:205014597
|
T | A | 1 | a0001c0010t0004g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3492-1711T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014597 | ||||||
| chr1:205014651
|
C | A | 1 | a0001c0027t0014g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3492-1657C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014651 | ||||||
| chr1:205014696
|
A | C | 13 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0005t0034g0135others(10): Show | 13 | HG01496.hp1 HG02897.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.3492-1612A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014696 | ||||||
| chr1:205014712
|
G | A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3492-1596G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014712 | ||||||
| chr1:205014877
|
G | A | 18 | a0001c0001t0023g0109a0001c0001t0023g0156a0001c0002t0011g0144others(15): Show | 18 | HG01496.hp1 HG02055.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.3492-1431G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014877 | ||||||
| chr1:205014912
|
C | T | 3 | a0001c0043t0027g0224a0003c0019t0003g0116a0004c0020t0024g0020 | 3 | HG01192.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3492-1396C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205014912 | ||||||
| chr1:205015087
|
C | T | 1 | a0001c0010t0004g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3492-1221C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015087 | ||||||
| chr1:205015145
|
C | T | 1 | a0002c0003t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3492-1163C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015145 | ||||||
| chr1:205015194
|
G | C | 1 | a0001c0004t0001g0181 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3492-1114G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015194 | ||||||
| chr1:205015205
|
G | A | 2 | a0002c0007t0016g0074a0002c0007t0016g0075 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3492-1103G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015205 | ||||||
| chr1:205015285
|
GAGACCCA others(14): Show |
G | 1 | a0011c0037t0004g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3492-1000_3492-980 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr1 | 205015285 | |||||
| chr1:205015364
|
C | T | 11 | a0001c0001t0007g0130a0001c0001t0007g0160a0001c0002t0045g0098others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3492-944C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015364 | ||||||
| chr1:205015416
|
A | G | 4 | a0001c0002t0011g0144a0002c0008t0011g0102a0002c0008t0011g0126others(1): Show | 4 | HG02055.hp1 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3492-892A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015416 | ||||||
| chr1:205015439
|
C | T | 20 | a0001c0001t0002g0146a0001c0001t0007g0130a0001c0001t0007g0160others(17): Show | 20 | HG00741.hp1 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3492-869C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015439 | ||||||
| chr1:205015444
|
G | A | 55 | a0001c0001t0001g0084a0001c0001t0001g0149a0001c0001t0001g0201others(52): Show | 56 | HG00639.hp2 HG00673.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.3492-864G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015444 | ||||||
| chr1:205015490
|
A | G | 5 | a0001c0002t0011g0144a0002c0008t0011g0102a0002c0008t0011g0126others(2): Show | 5 | HG02055.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3492-818A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015490 | ||||||
| chr1:205015671
|
C | A | 37 | a0001c0001t0005g0133a0001c0001t0007g0130a0001c0001t0007g0160others(34): Show | 37 | HG00738.hp1 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.3492-637C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015671 | ||||||
| chr1:205015744
|
A | G | 1 | a0001c0005t0022g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3492-564A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015744 | ||||||
| chr1:205015755
|
A | G | 3 | a0001c0010t0024g0151a0001c0015t0049g0119a0004c0020t0024g0020 | 3 | HG01192.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3492-553A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205015755 | ||||||
| chr1:205016022
|
C | G | 37 | a0001c0001t0004g0064a0001c0001t0004g0117a0001c0001t0007g0130others(34): Show | 37 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.3492-286C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205016022 | ||||||
| chr1:205016037
|
T | C | 1 | a0002c0003t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3492-271T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205016037 | ||||||
| chr1:205016098
|
A | C | 38 | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0001g0163others(35): Show | 40 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.3492-210A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205016098 | ||||||
| chr1:205016187
|
G | A | 3 | a0001c0015t0029g0101a0004c0011t0017g0018a0004c0011t0017g0019 | 3 | HG02572.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3492-121G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205016187 | ||||||
| chr1:205016295
|
T | C | 1 | a0001c0002t0045g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3492-13T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 29/29 | chr1 | 205016295 |