| geneid | 23114 |
|---|---|
| ensemblid | ENSG00000163531.17 |
| hgncid | 29866 |
| symbol | NFASC |
| name | neurofascin |
| refseq_nuc | NM_001160331.2 |
| refseq_prot | NP_001153803.1 |
| ensembl_nuc | ENST00000539706.6 |
| ensembl_prot | ENSP00000438614.2 |
| mane_status | MANE Plus Clinical |
| chr | chr1 |
| start | 204870862 |
| end | 205022822 |
| strand | + |
| ver | v1.2 |
| region | chr1:204870862-205022822 |
| region5000 | chr1:204865862-205027822 |
| regionname0 | NFASC_chr1_204870862_205022822 |
| regionname5000 | NFASC_chr1_204865862_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 | 1189 | 254 | 85 | 56 | 68 | 12 | 31 | 46 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0002 | 0/0 | 1189 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0003 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0004 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0005 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0006 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0007 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0008 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0009 | 0/0 | 1189 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 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 | 3570 | 97 | 12 | 17 | 42 | 5 | 21 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0002 | 1/1 | 3570 | 87 | 38 | 17 | 24 | 3 | 3 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0003 | 0/0 | 3570 | 21 | 15 | 4 | 0 | 2 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0004 | 0/0 | 3570 | 11 | 0 | 7 | 2 | 1 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0005 | 0/0 | 3570 | 9 | 9 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0006 | 0/0 | 3570 | 6 | 5 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0007 | 0/0 | 3570 | 3 | 0 | 1 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0008 | 0/0 | 3570 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0009 | 0/0 | 3570 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0010 | 0/0 | 3570 | 3 | 0 | 2 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0011 | 0/0 | 3570 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0012 | 0/0 | 3570 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0013 | 0/0 | 3570 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0014 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0015 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0016 | 0/0 | 3570 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0017 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0018 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0019 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0020 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0021 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0022 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0023 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0024 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0025 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0026 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0027 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| c0028 | 0/0 | 3570 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 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 | 6591 | 100 | 4 | 39 | 38 | 7 | 11 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0002 | 0/0 | 6595 | 31 | 7 | 2 | 10 | 2 | 10 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0003 | 0/0 | 6591 | 12 | 11 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0004 | 0/0 | 6591 | 11 | 11 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0005 | 0/0 | 6588 | 8 | 8 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0006 | 0/0 | 6599 | 7 | 0 | 1 | 5 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0007 | 0/0 | 6595 | 7 | 6 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0008 | 1/0 | 6583 | 7 | 4 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0009 | 0/0 | 6599 | 5 | 5 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0010 | 0/0 | 6592 | 5 | 3 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0011 | 0/0 | 6591 | 4 | 0 | 0 | 4 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0012 | 0/0 | 6595 | 4 | 0 | 3 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0013 | 0/0 | 6587 | 3 | 2 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0014 | 0/0 | 6595 | 3 | 0 | 0 | 3 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0015 | 0/0 | 6591 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0016 | 0/0 | 6583 | 3 | 1 | 0 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0017 | 0/0 | 6603 | 3 | 2 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0018 | 0/0 | 6587 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0019 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0020 | 0/0 | 6595 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0021 | 0/0 | 6599 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0022 | 0/0 | 6587 | 2 | 1 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0023 | 0/0 | 6595 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0024 | 0/0 | 6591 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0025 | 0/0 | 6582 | 2 | 0 | 1 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0026 | 0/0 | 6582 | 2 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0027 | 0/0 | 6591 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0028 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0029 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0030 | 0/0 | 6591 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0031 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0032 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0033 | 0/0 | 6591 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0034 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0035 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0036 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0037 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0038 | 0/0 | 6591 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0039 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0040 | 0/0 | 6591 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0041 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0042 | 0/0 | 6591 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0043 | 0/0 | 6591 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0044 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0045 | 0/0 | 6591 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0046 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0047 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0048 | 0/0 | 6584 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0049 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0050 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0051 | 0/0 | 6592 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0052 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0053 | 0/0 | 6591 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0054 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| t0055 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 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_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 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 | 3570 | 97 | 12 | 17 | 42 | 5 | 21 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002 | 1/1 | 3570 | 87 | 38 | 17 | 24 | 3 | 3 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003 | 0/0 | 3570 | 21 | 15 | 4 | 0 | 2 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0004 | 0/0 | 3570 | 11 | 0 | 7 | 2 | 1 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005 | 0/0 | 3570 | 9 | 9 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0006 | 0/0 | 3570 | 6 | 5 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0007 | 0/0 | 3570 | 3 | 0 | 1 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0008 | 0/0 | 3570 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0009 | 0/0 | 3570 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0010 | 0/0 | 3570 | 3 | 0 | 2 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0011 | 0/0 | 3570 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0012 | 0/0 | 3570 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0014 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0016 | 0/0 | 3570 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0017 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0020 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0021 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0022 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0027 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0002c0013 | 0/0 | 3570 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0002c0025 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0003c0026 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0004c0024 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0005c0018 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0006c0015 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0007c0019 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0008c0023 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0009c0028 | 0/0 | 3570 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10160 | 41 | 1 | 11 | 20 | 2 | 7 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0002 | 0/0 | 10164 | 14 | 0 | 1 | 5 | 1 | 7 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0003 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0005 | 0/0 | 10157 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0006 | 0/0 | 10168 | 4 | 0 | 0 | 4 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0007 | 0/0 | 10164 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0009 | 0/0 | 10168 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0010 | 0/0 | 10161 | 3 | 1 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0011 | 0/0 | 10160 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0012 | 0/0 | 10164 | 2 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0013 | 0/0 | 10156 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0014 | 0/0 | 10164 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0015 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0018 | 0/0 | 10156 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0020 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0023 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0025 | 0/0 | 10151 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0027 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0028 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0029 | 0/0 | 10164 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0036 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0040 | 0/0 | 10160 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0041 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0042 | 0/0 | 10160 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0044 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0045 | 0/0 | 10160 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0046 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0049 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0051 | 0/0 | 10161 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0054 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0001t0055 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0001 | 0/1 | 10160 | 30 | 2 | 10 | 14 | 3 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0002 | 0/0 | 10164 | 16 | 7 | 1 | 5 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0003 | 0/0 | 10160 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0004 | 0/0 | 10160 | 6 | 6 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0005 | 0/0 | 10157 | 5 | 5 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0006 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0008 | 1/0 | 10152 | 6 | 3 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0009 | 0/0 | 10168 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0012 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0013 | 0/0 | 10156 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0014 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0017 | 0/0 | 10172 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0020 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0021 | 0/0 | 10168 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0022 | 0/0 | 10156 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0023 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0032 | 0/0 | 10153 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0039 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0043 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0047 | 0/0 | 10165 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0048 | 0/0 | 10153 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0050 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0002t0053 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0001 | 0/0 | 10160 | 4 | 1 | 2 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0003 | 0/0 | 10160 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0004 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0006 | 0/0 | 10168 | 2 | 0 | 1 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0007 | 0/0 | 10164 | 4 | 3 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0008 | 0/0 | 10152 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0010 | 0/0 | 10161 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0024 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0035 | 0/0 | 10172 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0003t0037 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0004t0001 | 0/0 | 10160 | 10 | 0 | 6 | 2 | 1 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0004t0038 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0003 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0007 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0010 | 0/0 | 10161 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0013 | 0/0 | 10156 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0019 | 0/0 | 10164 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0033 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0005t0052 | 0/0 | 10172 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0006t0003 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0006t0004 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0006t0005 | 0/0 | 10157 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0006t0017 | 0/0 | 10172 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0006t0034 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0007t0016 | 0/0 | 10152 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0007t0026 | 0/0 | 10151 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0008t0001 | 0/0 | 10160 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0009t0001 | 0/0 | 10160 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0010t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0010t0025 | 0/0 | 10151 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0010t0026 | 0/0 | 10151 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0011t0015 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0011t0030 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0012t0001 | 0/0 | 10160 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0014t0004 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0016t0002 | 0/0 | 10164 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0017t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0020t0016 | 0/0 | 10152 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0021t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0022t0031 | 0/0 | 10157 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0001c0027t0004 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0002c0013t0001 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0002c0013t0011 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0002c0025t0012 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0003c0026t0003 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0004c0024t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0005c0018t0001 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0006c0015t0027 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0007c0019t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0008c0023t0011 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 205027822 |
| a0009c0028t0022 | 0/0 | 10156 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | copy fasta | chr1 | 204865862 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0011g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0012g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0013g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0014g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0015g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0018g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0018g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0020g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0023g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0025g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0027g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0028g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0029g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0036g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0040g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0041g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0042g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0044g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0045g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0046g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0049g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0051g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0054g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0055g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0012g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0017g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0020g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0021g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0023g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0032g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0039g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0043g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0047g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0048g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0050g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0053g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0024g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0035g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0037g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0038g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0019g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0033g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0052g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0006t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0006t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0006t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0006t0017g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0006t0017g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0006t0034g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0007t0016g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0007t0016g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0007t0026g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0008t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0008t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0008t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0009t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0009t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0010t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0010t0025g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0010t0026g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0011t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0011t0030g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0012t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0012t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0014t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0016t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0017t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0020t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0021t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0022t0031g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0027t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0002c0013t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0002c0013t0011g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0002c0025t0012g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0003c0026t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0004c0024t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0005c0018t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0006c0015t0027g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0007c0019t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0008c0023t0011g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0009c0028t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0078 | EUR | GBR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0065 | EUR | FIN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0063 | EUR | FIN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00423 | hp1 | a0001 | c0001 | t0014 | g0246 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00423 | hp2 | a0001 | c0001 | t0055 | g0156 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00639 | hp1 | a0001 | c0007 | t0026 | g0123 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0059 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00673 | hp1 | a0001 | c0002 | t0014 | g0204 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00673 | hp2 | a0001 | c0002 | t0039 | g0162 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00735 | hp2 | a0001 | c0008 | t0001 | g0147 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00738 | hp1 | a0006 | c0015 | t0027 | g0074 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0119 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00741 | hp2 | a0002 | c0025 | t0012 | g0148 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0090 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01069 | hp2 | a0001 | c0002 | t0008 | g0253 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01071 | hp1 | a0001 | c0002 | t0008 | g0252 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01074 | hp1 | a0001 | c0010 | t0025 | g0049 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01099 | hp1 | a0001 | c0002 | t0012 | g0125 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0130 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0111 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01109 | hp2 | a0001 | c0002 | t0048 | g0239 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01167 | hp1 | a0001 | c0008 | t0001 | g0145 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01169 | hp1 | a0001 | c0008 | t0001 | g0146 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01169 | hp2 | a0001 | c0001 | t0027 | g0087 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01175 | hp1 | a0007 | c0019 | t0001 | g0229 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01192 | hp1 | a0001 | c0002 | t0017 | g0215 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01192 | hp2 | a0001 | c0021 | t0001 | g0150 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01243 | hp2 | a0001 | c0003 | t0007 | g0181 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01255 | hp2 | a0001 | c0012 | t0001 | g0068 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01257 | hp1 | a0001 | c0002 | t0023 | g0097 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01257 | hp2 | a0001 | c0010 | t0001 | g0091 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0053 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01346 | hp2 | a0001 | c0003 | t0006 | g0102 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01358 | hp1 | a0001 | c0012 | t0001 | g0116 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01358 | hp2 | a0001 | c0017 | t0001 | g0167 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0051 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01433 | hp2 | a0004 | c0024 | t0001 | g0052 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01496 | hp1 | a0001 | c0006 | t0003 | g0260 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0064 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01515 | hp1 | a0001 | c0001 | t0025 | g0088 | EUR | IBS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0127 | EUR | IBS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01928 | hp1 | a0001 | c0001 | t0023 | g0143 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01978 | hp1 | a0001 | c0004 | t0038 | g0132 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02004 | hp2 | a0001 | c0001 | t0012 | g0120 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02055 | hp1 | a0001 | c0011 | t0030 | g0015 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02055 | hp2 | a0001 | c0011 | t0015 | g0176 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02145 | hp2 | a0001 | c0002 | t0021 | g0219 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | CDX | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02165 | hp2 | a0001 | c0001 | t0011 | g0172 | EAS | CDX | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02257 | hp2 | a0001 | c0002 | t0021 | g0173 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02258 | hp1 | a0001 | c0003 | t0007 | g0042 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0201 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02280 | hp1 | a0001 | c0003 | t0007 | g0044 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0035 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0236 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02572 | hp2 | a0001 | c0005 | t0019 | g0212 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02602 | hp2 | a0001 | c0001 | t0010 | g0027 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0046 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02622 | hp1 | a0001 | c0005 | t0013 | g0006 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0242 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02630 | hp2 | a0001 | c0006 | t0005 | g0054 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02717 | hp1 | a0001 | c0005 | t0019 | g0211 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02717 | hp2 | a0001 | c0005 | t0003 | g0218 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0036 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02723 | hp2 | a0001 | c0003 | t0007 | g0012 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02735 | hp1 | a0001 | c0010 | t0026 | g0022 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02735 | hp2 | a0001 | c0001 | t0029 | g0073 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0076 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0099 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0227 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0243 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0231 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02895 | hp2 | a0001 | c0006 | t0017 | g0134 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02897 | hp1 | a0001 | c0006 | t0017 | g0135 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02897 | hp2 | a0001 | c0003 | t0037 | g0225 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02922 | hp1 | a0001 | c0003 | t0035 | g0220 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02922 | hp2 | a0001 | c0002 | t0009 | g0037 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0138 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0240 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0005 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03017 | hp1 | a0001 | c0009 | t0001 | g0118 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03017 | hp2 | a0001 | c0007 | t0016 | g0103 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03041 | hp1 | a0001 | c0005 | t0033 | g0241 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03041 | hp2 | a0001 | c0002 | t0022 | g0039 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03098 | hp2 | a0001 | c0002 | t0043 | g0182 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0025 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03139 | hp1 | a0003 | c0026 | t0003 | g0177 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0133 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03195 | hp1 | a0001 | c0002 | t0032 | g0251 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03195 | hp2 | a0001 | c0005 | t0010 | g0213 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0255 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0230 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03225 | hp2 | a0001 | c0005 | t0052 | g0033 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03239 | hp2 | a0009 | c0028 | t0022 | g0089 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03453 | hp1 | a0001 | c0003 | t0010 | g0040 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0214 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0254 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03491 | hp1 | a0001 | c0009 | t0001 | g0002 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03492 | hp1 | a0001 | c0009 | t0001 | g0002 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03516 | hp2 | a0001 | c0006 | t0034 | g0030 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03540 | hp1 | a0001 | c0005 | t0007 | g0248 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03540 | hp2 | a0001 | c0002 | t0013 | g0217 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0232 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03654 | hp2 | a0001 | c0001 | t0042 | g0114 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03669 | hp1 | a0001 | c0007 | t0016 | g0096 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03688 | hp2 | a0001 | c0001 | t0051 | g0021 | SAS | STU | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03831 | hp2 | a0001 | c0001 | t0045 | g0072 | SAS | BEB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | STU | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | STU | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18522 | hp1 | a0001 | c0003 | t0024 | g0041 | AFR | YRI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | YRI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | CHB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18612 | hp2 | a0001 | c0001 | t0020 | g0085 | EAS | CHB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18906 | hp1 | a0001 | c0003 | t0024 | g0222 | AFR | YRI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18906 | hp2 | a0001 | c0003 | t0008 | g0011 | AFR | YRI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18947 | hp1 | a0001 | c0002 | t0020 | g0057 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18953 | hp2 | a0001 | c0001 | t0044 | g0235 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18969 | hp1 | a0001 | c0001 | t0041 | g0194 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18982 | hp1 | a0001 | c0001 | t0014 | g0098 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18986 | hp2 | a0001 | c0001 | t0036 | g0187 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19002 | hp1 | a0001 | c0001 | t0049 | g0197 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19002 | hp2 | a0001 | c0001 | t0018 | g0153 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0157 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19007 | hp1 | a0001 | c0001 | t0018 | g0154 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19007 | hp2 | a0008 | c0023 | t0011 | g0189 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19009 | hp2 | a0001 | c0002 | t0006 | g0129 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19010 | hp1 | a0002 | c0013 | t0011 | g0185 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0216 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19030 | hp2 | a0001 | c0022 | t0031 | g0136 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19043 | hp2 | a0001 | c0002 | t0008 | g0221 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19054 | hp1 | a0001 | c0002 | t0050 | g0199 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19060 | hp1 | a0001 | c0001 | t0054 | g0207 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19075 | hp1 | a0005 | c0018 | t0001 | g0188 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19091 | hp2 | a0002 | c0013 | t0001 | g0084 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20129 | hp1 | a0001 | c0002 | t0008 | g0043 | AFR | ASW | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20129 | hp2 | a0001 | c0014 | t0004 | g0228 | AFR | ASW | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20752 | hp1 | a0001 | c0016 | t0002 | g0067 | EUR | TSI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | TSI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20805 | hp1 | a0001 | c0003 | t0006 | g0093 | EUR | TSI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | TSI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20905 | hp1 | a0001 | c0001 | t0040 | g0019 | SAS | GIH | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01123 | hp1 | a0001 | c0001 | t0046 | g0171 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0210 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0183 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02559 | hp2 | a0001 | c0002 | t0047 | g0164 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0140 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03471 | hp2 | a0001 | c0002 | t0053 | g0237 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG06807 | hp1 | a0001 | c0027 | t0004 | g0004 | AFR | USA | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | USA | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0038 | AFR | USA | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | USA | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA21309 | hp1 | a0001 | c0006 | t0004 | g0184 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA21309 | hp2 | a0001 | c0020 | t0016 | g0152 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0060 | REF | REF | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0008 | g0108 | REF | REF | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 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 | a0009 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.22C>T | p.Pro8Ser | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/28 | 321/10152 | 22/3570 | 8/1189 | chr1 | 204944337 | ||
| chr1:204952014
|
C | T | 1 | a0003 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.95C>T | p.Thr32Met | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/28 | 394/10152 | 95/3570 | 32/1189 | chr1 | 204952014 | ||
| chr1:204954892
|
C | T | 2 | a0002a0004 | 4 | HG00741.hp2 HG01433.hp2 NA19010.hp1 others(1): Show |
missense_variant | MODERATE | c.458C>T | p.Thr153Met | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/28 | 757/10152 | 458/3570 | 153/1189 | chr1 | 204954892 | ||
| chr1:204968878
|
C | T | 1 | a0008 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.932C>T | p.Ala311Val | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/28 | 1231/10152 | 932/3570 | 311/1189 | chr1 | 204968878 | ||
| chr1:204975276
|
A | C | 1 | a0005 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.1597A>C | p.Thr533Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/28 | 1896/10152 | 1597/3570 | 533/1189 | chr1 | 204975276 | ||
| chr1:204975289
|
G | A | 1 | a0006 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1610G>A | p.Arg537Gln | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/28 | 1909/10152 | 1610/3570 | 537/1189 | chr1 | 204975289 | ||
| chr1:204975313
|
G | A | 1 | a0004 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1634G>A | p.Arg545Lys | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/28 | 1933/10152 | 1634/3570 | 545/1189 | chr1 | 204975313 | ||
| chr1:204975408
|
A | G | 1 | a0004 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1729A>G | p.Ile577Val | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/28 | 2028/10152 | 1729/3570 | 577/1189 | chr1 | 204975408 | ||
| chr1:204981868
|
G | A | 1 | a0007 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.2351G>A | p.Arg784Gln | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/28 | 2650/10152 | 2351/3570 | 784/1189 | chr1 | 204981868 |
| 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 | a0001c0027 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.66C>T | p.Gly22Gly | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/28 | 365/10152 | 66/3570 | 22/1189 | chr1 | 204944381 | ||
| chr1:204954911
|
G | A | 2 | a0001c0011a0001c0014 | 3 | HG02055.hp1 HG02055.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.477G>A | p.Pro159Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/28 | 776/10152 | 477/3570 | 159/1189 | chr1 | 204954911 | ||
| chr1:204970635
|
C | T | 1 | a0001c0005 | 9 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.1056C>T | p.Asp352Asp | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/28 | 1355/10152 | 1056/3570 | 352/1189 | chr1 | 204970635 | ||
| chr1:204973400
|
C | T | 1 | a0001c0022 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1293C>T | p.Asn431Asn | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/28 | 1592/10152 | 1293/3570 | 431/1189 | chr1 | 204973400 | ||
| chr1:204974234
|
C | T | 1 | a0001c0021 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1368C>T | p.Tyr456Tyr | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 12/28 | 1667/10152 | 1368/3570 | 456/1189 | chr1 | 204974234 | ||
| chr1:204974774
|
C | T | 2 | a0001c0006a0001c0022 | 7 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(4): Show |
synonymous_variant | LOW | c.1542C>T | p.Ala514Ala | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/28 | 1841/10152 | 1542/3570 | 514/1189 | chr1 | 204974774 | ||
| chr1:204974819
|
C | A | 10 | a0001c0001a0001c0007a0001c0008others(7): Show | 110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
synonymous_variant | LOW | c.1587C>A | p.Val529Val | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/28 | 1886/10152 | 1587/3570 | 529/1189 | chr1 | 204974819 | ||
| chr1:204975326
|
G | A | 1 | a0004c0024 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1647G>A | p.Thr549Thr | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/28 | 1946/10152 | 1647/3570 | 549/1189 | chr1 | 204975326 | ||
| chr1:204976686
|
C | T | 1 | a0004c0024 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1755C>T | p.Asp585Asp | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/28 | 2054/10152 | 1755/3570 | 585/1189 | chr1 | 204976686 | ||
| chr1:204976693
|
C | T | 1 | a0001c0017 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.1762C>T | p.Leu588Leu | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/28 | 2061/10152 | 1762/3570 | 588/1189 | chr1 | 204976693 | ||
| chr1:204976743
|
C | T | 1 | a0001c0008 | 3 | HG00735.hp2 HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.1812C>T | p.Val604Val | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/28 | 2111/10152 | 1812/3570 | 604/1189 | chr1 | 204976743 | ||
| chr1:204979531
|
A | G | 10 | a0001c0003a0001c0009a0001c0010others(7): Show | 35 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(32): Show |
synonymous_variant | LOW | c.2181A>G | p.Pro727Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/28 | 2480/10152 | 2181/3570 | 727/1189 | chr1 | 204979531 | ||
| chr1:204980374
|
C | T | 1 | a0001c0011 | 2 | HG02055.hp1 HG02055.hp2 |
synonymous_variant | LOW | c.2214C>T | p.Pro738Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/28 | 2513/10152 | 2214/3570 | 738/1189 | chr1 | 204980374 | ||
| chr1:204982010
|
C | T | 2 | a0001c0010a0002c0025 | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.2493C>T | p.Ser831Ser | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/28 | 2792/10152 | 2493/3570 | 831/1189 | chr1 | 204982010 | ||
| chr1:204986107
|
G | A | 1 | a0001c0017 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.2817G>A | p.Pro939Pro | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/28 | 3116/10152 | 2817/3570 | 939/1189 | chr1 | 204986107 | ||
| chr1:204988640
|
G | C | 1 | a0001c0012 | 2 | HG01255.hp2 HG01358.hp1 |
synonymous_variant | LOW | c.2955G>C | p.Gly985Gly | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/28 | 3254/10152 | 2955/3570 | 985/1189 | chr1 | 204988640 | ||
| chr1:205009576
|
G | A | 3 | a0001c0004a0001c0009a0001c0021 | 15 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(12): Show |
synonymous_variant | LOW | c.3156G>A | p.Ala1052Ala | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/28 | 3455/10152 | 3156/3570 | 1052/1189 | chr1 | 205009576 | ||
| chr1:205016506
|
G | A | 2 | a0001c0007a0001c0020 | 4 | HG00639.hp1 HG03017.hp2 HG03669.hp1 others(1): Show |
synonymous_variant | LOW | c.3537G>A | p.Thr1179Thr | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3836/10152 | 3537/3570 | 1179/1189 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204870976
|
C | A | 1 | a0001c0001t0028 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/28 | 73340 | chr1 | 204870976 | |||||
| chr1:204944230
|
G | T | 2 | a0001c0001t0054a0001c0001t0055 | 2 | HG00423.hp2 NA19060.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/28 | chr1 | 204944230 | ||||||
| chr1:204944278
|
G | A | 1 | a0001c0001t0029 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/28 | 38 | chr1 | 204944278 | |||||
| chr1:205016541
|
G | A | 1 | a0001c0001t0018 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2 | chr1 | 205016541 | |||||
| chr1:205016766
|
G | A | 10 | a0001c0001t0005a0001c0001t0018a0001c0002t0005others(7): Show | 17 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 227 | chr1 | 205016766 | |||||
| chr1:205017129
|
G | A | 1 | a0001c0001t0028 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 590 | chr1 | 205017129 | |||||
| chr1:205017231
|
C | T | 18 | a0001c0001t0003a0001c0001t0018a0001c0001t0027others(15): Show | 32 | HG00738.hp1 HG01169.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*692C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 692 | chr1 | 205017231 | |||||
| chr1:205017322
|
A | G | 3 | a0001c0002t0017a0001c0005t0052a0001c0006t0017 | 4 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*783A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 783 | chr1 | 205017322 | |||||
| chr1:205017458
|
T | C | 97 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*919T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 919 | chr1 | 205017458 | |||||
| chr1:205017516
|
A | G | 2 | a0001c0001t0027a0006c0015t0027 | 2 | HG00738.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*977A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 977 | chr1 | 205017516 | |||||
| chr1:205017674
|
T | C | 2 | a0001c0001t0009a0001c0002t0009 | 5 | HG02622.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1135T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1135 | chr1 | 205017674 | |||||
| chr1:205017764
|
C | T | 1 | a0001c0001t0029 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1225 | chr1 | 205017764 | |||||
| chr1:205017991
|
G | A | 14 | a0001c0001t0003a0001c0001t0027a0001c0002t0003others(11): Show | 26 | HG00738.hp1 HG01169.hp2 HG01496.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1452G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1452 | chr1 | 205017991 | |||||
| chr1:205018001
|
G | C | 1 | a0001c0003t0035 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1462 | chr1 | 205018001 | |||||
| chr1:205018038
|
C | T | 1 | a0001c0001t0051 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1499 | chr1 | 205018038 | |||||
| chr1:205018093
|
C | T | 1 | a0001c0005t0052 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1554C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1554 | chr1 | 205018093 | |||||
| chr1:205018260
|
A | G | 1 | a0001c0002t0032 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1721 | chr1 | 205018260 | |||||
| chr1:205018282
|
G | A | 1 | a0001c0001t0036 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1743G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1743 | chr1 | 205018282 | |||||
| chr1:205018366
|
C | T | 1 | a0001c0002t0050 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1827C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1827 | chr1 | 205018366 | |||||
| chr1:205018501
|
T | G | 16 | a0001c0001t0003a0001c0001t0018a0001c0001t0027others(13): Show | 29 | HG00738.hp1 HG01169.hp2 HG01496.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1962T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1962 | chr1 | 205018501 | |||||
| chr1:205018522
|
C | G | 1 | a0001c0001t0049 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 1983 | chr1 | 205018522 | |||||
| chr1:205018825
|
C | T | 40 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(37): Show | 68 | HG00738.hp1 HG00741.hp2 HG01099.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2286C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2286 | chr1 | 205018825 | |||||
| chr1:205018844
|
G | A | 2 | a0001c0001t0020a0001c0002t0020 | 2 | NA18612.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2305G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2305 | chr1 | 205018844 | |||||
| chr1:205018905
|
T | C | 1 | a0001c0001t0036 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2366T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2366 | chr1 | 205018905 | |||||
| chr1:205019055
|
C | A | 54 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(51): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*2516C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2516 | chr1 | 205019055 | |||||
| chr1:205019115
|
AG | A | 4 | a0001c0001t0025a0001c0007t0026a0001c0010t0025others(1): Show | 4 | HG00639.hp1 HG01074.hp1 HG01515.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2578delG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2578 | INFO_REALIGN_3_PRIME | chr1 | 205019115 | ||||
| chr1:205019407
|
T | C | 40 | a0001c0001t0001a0001c0001t0009a0001c0001t0013others(37): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2868T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2868 | chr1 | 205019407 | |||||
| chr1:205019475
|
C | CCATT | 11 | a0001c0001t0005a0001c0001t0013a0001c0001t0018others(8): Show | 17 | HG00280.hp1 HG01109.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2959_*2962dupTTCA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(1): Show |
45 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(42): Show | 144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2955_*2962dupTTCA others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(5): Show |
29 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(26): Show | 68 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2951_*2962dupTTCA others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(9): Show |
7 | a0001c0001t0006a0001c0001t0009a0001c0002t0006others(4): Show | 15 | HG01346.hp2 HG02145.hp2 HG02257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2947_*2962dupTTCA others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019475
|
C | CCATTCAT others(13): Show |
4 | a0001c0002t0017a0001c0003t0035a0001c0005t0052others(1): Show | 5 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2943_*2962dupTTCA others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 2963 | INFO_REALIGN_3_PRIME | chr1 | 205019475 | ||||
| chr1:205019555
|
C | T | 1 | a0001c0001t0045 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3016C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3016 | chr1 | 205019555 | |||||
| chr1:205019854
|
T | C | 8 | a0001c0001t0010a0001c0001t0012a0001c0001t0051others(5): Show | 11 | HG00741.hp2 HG01099.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3315T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3315 | chr1 | 205019854 | |||||
| chr1:205019899
|
G | A | 6 | a0001c0001t0025a0001c0007t0016a0001c0007t0026others(3): Show | 7 | HG00639.hp1 HG01074.hp1 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3360G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3360 | chr1 | 205019899 | |||||
| chr1:205020031
|
T | C | 1 | a0001c0001t0018 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3492T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3492 | chr1 | 205020031 | |||||
| chr1:205020035
|
T | G | 40 | a0001c0001t0001a0001c0001t0009a0001c0001t0013others(37): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*3496T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3496 | chr1 | 205020035 | |||||
| chr1:205020258
|
C | T | 1 | a0001c0001t0044 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3719C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3719 | chr1 | 205020258 | |||||
| chr1:205020290
|
G | T | 2 | a0001c0001t0023a0001c0002t0023 | 2 | HG01257.hp1 HG01928.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3751G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3751 | chr1 | 205020290 | |||||
| chr1:205020407
|
T | G | 1 | a0001c0001t0018 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3868T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3868 | chr1 | 205020407 | |||||
| chr1:205020482
|
C | T | 2 | a0001c0001t0015a0001c0011t0015 | 3 | HG02055.hp2 HG03130.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3943C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3943 | chr1 | 205020482 | |||||
| chr1:205020488
|
AGAG | A | 5 | a0001c0001t0010a0001c0001t0051a0001c0002t0047others(2): Show | 7 | HG01109.hp1 HG02559.hp2 HG02602.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3953_*3955delGAG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3953 | INFO_REALIGN_3_PRIME | chr1 | 205020488 | ||||
| chr1:205020490
|
A | G | 1 | a0001c0001t0046 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3951A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 3951 | chr1 | 205020490 | |||||
| chr1:205020601
|
C | T | 3 | a0001c0001t0015a0001c0003t0024a0001c0011t0015 | 5 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4062C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4062 | chr1 | 205020601 | |||||
| chr1:205020622
|
C | T | 1 | a0001c0002t0053 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4083C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4083 | chr1 | 205020622 | |||||
| chr1:205020783
|
C | A | 9 | a0001c0001t0010a0001c0001t0012a0001c0001t0018others(6): Show | 13 | HG00741.hp2 HG01099.hp1 HG01109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4244C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4244 | chr1 | 205020783 | |||||
| chr1:205020951
|
G | T | 1 | a0001c0002t0043 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4412G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4412 | chr1 | 205020951 | |||||
| chr1:205020968
|
C | T | 2 | a0001c0005t0019a0001c0005t0033 | 3 | HG02572.hp2 HG02717.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4429C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4429 | chr1 | 205020968 | |||||
| chr1:205020984
|
T | A | 1 | a0001c0011t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4445T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4445 | chr1 | 205020984 | |||||
| chr1:205021032
|
TAGAG | T | 4 | a0001c0001t0015a0001c0002t0048a0001c0003t0024others(1): Show | 6 | HG01109.hp2 HG02055.hp2 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4496_*4499delAGAG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4496 | INFO_REALIGN_3_PRIME | chr1 | 205021032 | ||||
| chr1:205021057
|
A | G | 25 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(22): Show | 46 | HG00738.hp1 HG01109.hp2 HG01169.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4518A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4518 | chr1 | 205021057 | |||||
| chr1:205021337
|
A | G | 1 | a0001c0022t0031 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4798A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4798 | chr1 | 205021337 | |||||
| chr1:205021500
|
G | T | 1 | a0001c0001t0042 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4961G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 4961 | chr1 | 205021500 | |||||
| chr1:205021578
|
A | G | 1 | a0001c0001t0041 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5039A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5039 | chr1 | 205021578 | |||||
| chr1:205021704
|
G | C | 1 | a0001c0002t0047 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5165G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5165 | chr1 | 205021704 | |||||
| chr1:205021732
|
G | C | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(96): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*5193G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5193 | chr1 | 205021732 | |||||
| chr1:205021907
|
G | A | 6 | a0001c0001t0005a0001c0002t0005a0001c0002t0032others(3): Show | 11 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5368G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5368 | chr1 | 205021907 | |||||
| chr1:205021983
|
G | A | 1 | a0001c0001t0018 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5444G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5444 | chr1 | 205021983 | |||||
| chr1:205021991
|
C | T | 1 | a0001c0001t0041 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5452C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5452 | chr1 | 205021991 | |||||
| chr1:205022132
|
T | C | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0027others(17): Show | 37 | HG00738.hp1 HG01109.hp2 HG01169.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5593T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5593 | chr1 | 205022132 | |||||
| chr1:205022252
|
C | T | 7 | a0001c0001t0003a0001c0002t0003a0001c0002t0053others(4): Show | 13 | HG01496.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5713C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5713 | chr1 | 205022252 | |||||
| chr1:205022404
|
C | A | 1 | a0001c0001t0018 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5865C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5865 | chr1 | 205022404 | |||||
| chr1:205022435
|
G | A | 1 | a0001c0001t0018 | 2 | NA19002.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5896G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5896 | chr1 | 205022435 | |||||
| chr1:205022468
|
C | G | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(45): Show | 102 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5929C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 5929 | chr1 | 205022468 | |||||
| chr1:205022642
|
C | T | 18 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(15): Show | 51 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*6103C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 6103 | chr1 | 205022642 | |||||
| chr1:205022713
|
G | A | 1 | a0001c0004t0038 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6174G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 6174 | chr1 | 205022713 | |||||
| chr1:205022759
|
T | TA | 6 | a0001c0001t0005a0001c0002t0005a0001c0002t0032others(3): Show | 11 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6227dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 28/28 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204871352
|
G | A | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+282G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204871352 | ||||||
| chr1:204871357
|
C | T | 2 | a0001c0002t0001g0261a0001c0006t0003g0260 | 2 | HG01106.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-91+287C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204871357 | ||||||
| chr1:204871508
|
T | C | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+438T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204871508 | ||||||
| chr1:204871754
|
A | C | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-91+684A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204871754 | ||||||
| chr1:204872067
|
C | T | 4 | a0001c0001t0001g0257a0001c0001t0006g0258a0001c0002t0001g0256others(1): Show | 5 | HG01243.hp1 NA18951.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+997C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872067 | ||||||
| chr1:204872153
|
C | G | 30 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0249others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-91+1083C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872153 | ||||||
| chr1:204872185
|
A | G | 1 | a0001c0002t0009g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-91+1115A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872185 | ||||||
| chr1:204872252
|
T | A | 1 | a0001c0011t0030g0015 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-91+1182T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872252 | ||||||
| chr1:204872661
|
G | T | 1 | a0001c0003t0037g0225 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-91+1591G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872661 | ||||||
| chr1:204872662
|
C | T | 1 | a0001c0003t0037g0225 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-91+1592C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872662 | ||||||
| chr1:204872974
|
G | A | 30 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0249others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-91+1904G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204872974 | ||||||
| chr1:204873009
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-91+1939G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873009 | ||||||
| chr1:204873052
|
A | G | 107 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(104): Show | 108 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-91+1982A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873052 | ||||||
| chr1:204873118
|
G | A | 1 | a0001c0002t0004g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-91+2048G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873118 | ||||||
| chr1:204873156
|
GGC | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(170): Show | 175 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.-91+2087_-91+2088d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873156 | ||||||
| chr1:204873160
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(170): Show | 175 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.-91+2090C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873160 | ||||||
| chr1:204873161
|
CTTGCA | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(170): Show | 175 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.-91+2094_-91+2098d others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204873161 | |||||
| chr1:204873286
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-91+2216C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873286 | ||||||
| chr1:204873341
|
C | A | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+2271C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873341 | ||||||
| chr1:204873426
|
C | T | 2 | a0001c0001t0002g0131a0001c0004t0038g0132 | 2 | HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-91+2356C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873426 | ||||||
| chr1:204873641
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-91+2571G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873641 | ||||||
| chr1:204873658
|
G | A | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+2588G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873658 | ||||||
| chr1:204873676
|
TC | T | 41 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.-91+2608delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204873676 | |||||
| chr1:204873687
|
G | A | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+2617G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873687 | ||||||
| chr1:204873955
|
G | A | 42 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-91+2885G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204873955 | ||||||
| chr1:204874064
|
A | C | 30 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0249others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-91+2994A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874064 | ||||||
| chr1:204874156
|
G | A | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+3086G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874156 | ||||||
| chr1:204874169
|
C | T | 1 | a0001c0004t0001g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-91+3099C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874169 | ||||||
| chr1:204874181
|
G | C | 104 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(101): Show | 105 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-91+3111G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874181 | ||||||
| chr1:204874251
|
A | G | 2 | a0001c0002t0021g0219a0001c0003t0035g0220 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-91+3181A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874251 | ||||||
| chr1:204874266
|
C | G | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+3196C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874266 | ||||||
| chr1:204874531
|
G | A | 7 | a0001c0001t0001g0141a0001c0001t0023g0143a0001c0002t0001g0142others(4): Show | 7 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+3461G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874531 | ||||||
| chr1:204874562
|
C | T | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+3492C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874562 | ||||||
| chr1:204874564
|
C | T | 2 | a0001c0002t0001g0261a0001c0006t0003g0260 | 2 | HG01106.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-91+3494C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874564 | ||||||
| chr1:204874573
|
A | G | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+3503A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874573 | ||||||
| chr1:204874771
|
C | T | 2 | a0001c0002t0002g0128a0001c0002t0006g0129 | 2 | NA18954.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-91+3701C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874771 | ||||||
| chr1:204874777
|
T | C | 1 | a0002c0025t0012g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-91+3707T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874777 | ||||||
| chr1:204874836
|
T | A | 16 | a0001c0001t0005g0139a0001c0001t0009g0010a0001c0002t0001g0013others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-91+3766T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204874836 | ||||||
| chr1:204875073
|
T | TTTG | 45 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0249others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.-91+4039_-91+4041d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
T | TTTGTTG | 19 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0002g0028others(16): Show | 20 | HG00738.hp2 HG01074.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.-91+4036_-91+4041d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
T | TTTGTTGT others(2): Show |
9 | a0001c0001t0001g0016a0001c0001t0002g0017a0001c0001t0002g0131others(6): Show | 9 | HG00733.hp1 HG01175.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-91+4033_-91+4041d others(11): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTG | T | 34 | a0001c0001t0001g0126a0001c0001t0001g0186a0001c0001t0001g0191others(31): Show | 35 | HG00558.hp1 HG00673.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.-91+4039_-91+4041d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTGTTG | T | 20 | a0001c0001t0005g0139a0001c0001t0009g0010a0001c0001t0054g0207others(17): Show | 20 | HG01243.hp2 HG02132.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-91+4036_-91+4041d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTGTTGT others(5): Show |
T | 1 | a0001c0003t0003g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-91+4030_-91+4041d others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875073
|
TTTGTTGT others(8): Show |
T | 1 | a0001c0003t0001g0127 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-91+4027_-91+4041d others(17): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875073 | |||||
| chr1:204875140
|
G | T | 11 | a0001c0002t0004g0214a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+4070G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875140 | ||||||
| chr1:204875499
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-91+4429C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875499 | ||||||
| chr1:204875522
|
T | G | 1 | a0001c0021t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-91+4452T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875522 | ||||||
| chr1:204875665
|
C | A | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+4595C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875665 | ||||||
| chr1:204875665
|
CT | C | 42 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-91+4598delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204875665 | |||||
| chr1:204875719
|
G | A | 1 | a0001c0004t0001g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-91+4649G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875719 | ||||||
| chr1:204875831
|
A | G | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-91+4761A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875831 | ||||||
| chr1:204875846
|
G | A | 1 | a0001c0001t0040g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-91+4776G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875846 | ||||||
| chr1:204875937
|
A | G | 56 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(53): Show | 56 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-91+4867A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875937 | ||||||
| chr1:204875981
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-91+4911A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204875981 | ||||||
| chr1:204876033
|
G | T | 2 | a0001c0001t0040g0019a0001c0002t0001g0018 | 2 | HG06807.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-91+4963G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876033 | ||||||
| chr1:204876219
|
T | C | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+5149T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876219 | ||||||
| chr1:204876573
|
A | G | 5 | a0001c0001t0005g0139a0001c0002t0004g0133a0001c0002t0043g0182others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+5503A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876573 | ||||||
| chr1:204876631
|
A | G | 1 | a0001c0002t0002g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-91+5561A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876631 | ||||||
| chr1:204876664
|
G | A | 74 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(71): Show | 74 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-91+5594G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876664 | ||||||
| chr1:204876724
|
A | G | 3 | a0001c0002t0021g0219a0001c0003t0035g0220a0001c0011t0030g0015 | 3 | HG02055.hp1 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-91+5654A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876724 | ||||||
| chr1:204876903
|
C | T | 4 | a0001c0001t0007g0048a0001c0002t0002g0047a0001c0002t0004g0034others(1): Show | 4 | HG02970.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+5833C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876903 | ||||||
| chr1:204876917
|
C | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+5847C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876917 | ||||||
| chr1:204876960
|
G | A | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+5890G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876960 | ||||||
| chr1:204876994
|
ATGTATAT others(67): Show |
A | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-91+5926_-91+5999d others(76): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876994 | |||||
| chr1:204876996
|
G | A | 81 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(78): Show | 82 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-91+5926G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204876996 | ||||||
| chr1:204876996
|
G | GTA | 13 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0002g0121others(10): Show | 13 | HG00558.hp2 HG00741.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-91+5957_-91+5958d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
G | GTATA | 5 | a0001c0001t0001g0122a0001c0002t0002g0250a0001c0002t0005g0254others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+5955_-91+5958d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTA | G | 47 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0069others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.-91+5957_-91+5958d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTATA | G | 13 | a0001c0001t0002g0028a0001c0001t0003g0045a0001c0001t0007g0032others(10): Show | 13 | HG01099.hp2 HG02559.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.-91+5955_-91+5958d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTATATA | G | 17 | a0001c0001t0006g0024a0001c0001t0007g0048a0001c0002t0001g0018others(14): Show | 17 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-91+5953_-91+5958d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204876996
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(4): Show | 8 | HG00738.hp2 HG01074.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-91+5951_-91+5958d others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204876996 | |||||
| chr1:204877000
|
A | G | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+5930A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877000 | ||||||
| chr1:204877002
|
A | G | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+5932A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877002 | ||||||
| chr1:204877003
|
T | TATATATA others(16): Show |
1 | a0001c0002t0002g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-91+5934_-91+5956d others(25): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877003 | |||||
| chr1:204877011
|
TATATATA others(63): Show |
T | 1 | a0001c0002t0001g0178 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-91+5942_-91+6011d others(72): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877011 | ||||||
| chr1:204877015
|
TATATATA others(59): Show |
T | 1 | a0002c0025t0012g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-91+5946_-91+6011d others(68): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877015 | ||||||
| chr1:204877016
|
ATATATAT others(45): Show |
A | 6 | a0001c0001t0001g0174a0001c0001t0001g0186a0001c0001t0036g0187others(3): Show | 6 | HG01346.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+5965_-91+6016d others(54): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877016 | |||||
| chr1:204877018
|
ATATATAT others(43): Show |
A | 5 | a0001c0001t0011g0172a0001c0002t0005g0210a0001c0008t0001g0145others(2): Show | 5 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+5959_-91+6008d others(52): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877018 | |||||
| chr1:204877020
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0004g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-91+5959_-91+5975d others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877020 | |||||
| chr1:204877020
|
ATATATAT others(41): Show |
A | 3 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0002t0001g0149 | 3 | HG03491.hp2 HG03492.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-91+5959_-91+6006d others(50): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877020 | |||||
| chr1:204877021
|
TATATATA others(53): Show |
T | 12 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0001t0006g0258others(9): Show | 12 | HG00558.hp1 HG00673.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-91+5952_-91+6011d others(62): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877021 | ||||||
| chr1:204877022
|
ATATATAA others(31): Show |
A | 4 | a0001c0001t0001g0141a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG01175.hp2 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+5959_-91+5996d others(40): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877022 | |||||
| chr1:204877022
|
ATATATAA others(39): Show |
A | 1 | a0001c0001t0046g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-91+5959_-91+6004d others(48): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877022 | |||||
| chr1:204877023
|
TATATAAT others(51): Show |
T | 18 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(15): Show | 18 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-91+5954_-91+6011d others(60): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877023 | ||||||
| chr1:204877024
|
ATATAATA others(6): Show |
A | 2 | a0001c0003t0024g0222a0001c0005t0003g0218 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-91+5959_-91+5971d others(15): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(26): Show |
A | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-91+5955_-91+5987d others(35): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877024 | ||||||
| chr1:204877024
|
ATATAATA others(28): Show |
A | 1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-91+5956_-91+5990d others(37): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(29): Show |
A | 5 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0011g0157others(2): Show | 5 | HG00423.hp2 HG01081.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+5959_-91+5994d others(38): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(37): Show |
A | 3 | a0001c0001t0002g0169a0001c0002t0001g0144a0001c0002t0001g0170 | 3 | HG00544.hp2 HG02293.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-91+5959_-91+6002d others(46): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877024 | |||||
| chr1:204877024
|
ATATAATA others(57): Show |
A | 2 | a0001c0002t0043g0182a0001c0003t0007g0181 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+5955_-91+6018d others(66): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877024 | ||||||
| chr1:204877025
|
TATAATAT others(49): Show |
T | 9 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0002t0001g0190others(6): Show | 10 | HG02572.hp2 HG02717.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+5956_-91+6011d others(58): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877025 | ||||||
| chr1:204877026
|
ATAATATA others(4): Show |
A | 1 | a0001c0003t0003g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-91+5959_-91+5969d others(13): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877026 | |||||
| chr1:204877026
|
ATAATATA others(26): Show |
A | 9 | a0001c0001t0009g0010a0001c0002t0002g0007a0001c0002t0002g0008others(6): Show | 9 | HG02145.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-91+5958_-91+5990d others(35): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877026 | |||||
| chr1:204877026
|
ATAATATA others(35): Show |
A | 5 | a0001c0001t0001g0165a0001c0001t0002g0166a0001c0002t0001g0168others(2): Show | 5 | HG01192.hp2 HG01358.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+5959_-91+6000d others(44): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877026 | |||||
| chr1:204877026
|
ATAATATA others(49): Show |
A | 1 | a0001c0001t0001g0086 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-91+5957_-91+6012d others(58): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877026 | ||||||
| chr1:204877027
|
T | A | 3 | a0001c0002t0004g0230a0001c0002t0004g0231a0001c0002t0005g0140 | 3 | HG02886.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-91+5957T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877027 | ||||||
| chr1:204877027
|
T | G | 1 | a0001c0002t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-91+5957T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877027 | ||||||
| chr1:204877027
|
TA | T | 4 | a0001c0006t0017g0134a0001c0006t0017g0135a0001c0007t0026g0123others(1): Show | 4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+5959delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877027 | |||||
| chr1:204877028
|
AATATATA others(24): Show |
A | 1 | a0001c0027t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-91+5959_-91+5989d others(33): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877028 | ||||||
| chr1:204877028
|
AATATATA others(25): Show |
A | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-91+5959_-91+5990d others(34): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877028 | ||||||
| chr1:204877028
|
AATATATA others(33): Show |
A | 5 | a0001c0001t0023g0143a0001c0002t0001g0161a0001c0002t0001g0163others(2): Show | 5 | HG00673.hp2 HG01928.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+5959_-91+5998d others(42): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877028 | ||||||
| chr1:204877029
|
A | T | 1 | a0001c0002t0008g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-91+5959A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877029 | ||||||
| chr1:204877030
|
T | A | 1 | a0001c0002t0008g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-91+5960T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877030 | ||||||
| chr1:204877037
|
T | A | 6 | a0001c0001t0005g0226a0001c0002t0008g0221a0001c0006t0017g0134others(3): Show | 6 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-91+5967T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877037 | ||||||
| chr1:204877039
|
A | T | 2 | a0001c0001t0005g0226a0001c0002t0008g0221 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+5969A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877039 | ||||||
| chr1:204877045
|
ATATAATA others(30): Show |
A | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-91+5976_-91+6012d others(39): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877045 | ||||||
| chr1:204877050
|
ATATATTT others(3): Show |
A | 3 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0022t0031g0136 | 3 | HG02965.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-91+5986_-91+5995d others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877050 | |||||
| chr1:204877059
|
T | A | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-91+5989T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877059 | ||||||
| chr1:204877060
|
T | A | 3 | a0001c0001t0005g0139a0001c0006t0017g0134a0001c0006t0017g0135 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-91+5990T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877060 | ||||||
| chr1:204877068
|
T | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(8): Show | 11 | HG00423.hp2 HG01081.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-91+5998T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877068 | ||||||
| chr1:204877068
|
T | TTATATAT others(18): Show |
1 | a0001c0002t0009g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-91+6004_-91+6028d others(27): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877068 | |||||
| chr1:204877068
|
T | TTATATAT others(20): Show |
3 | a0001c0002t0003g0227a0001c0014t0004g0228a0007c0019t0001g0229 | 3 | HG01175.hp1 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-91+6002_-91+6028d others(29): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877068 | |||||
| chr1:204877068
|
TTA | T | 7 | a0001c0001t0015g0232a0001c0002t0005g0140a0001c0002t0008g0221others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+6009_-91+6010d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204877068 | |||||
| chr1:204877081
|
A | T | 40 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-91+6011A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877081 | ||||||
| chr1:204877087
|
T | A | 2 | a0001c0001t0001g0086a0001c0002t0002g0151 | 2 | HG03239.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-91+6017T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877087 | ||||||
| chr1:204877090
|
T | A | 2 | a0001c0002t0043g0182a0001c0003t0007g0181 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+6020T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877090 | ||||||
| chr1:204877091
|
T | A | 43 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(40): Show | 43 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+6021T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877091 | ||||||
| chr1:204877147
|
A | G | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+6077A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877147 | ||||||
| chr1:204877200
|
C | A | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+6130C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877200 | ||||||
| chr1:204877268
|
C | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+6198C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877268 | ||||||
| chr1:204877290
|
G | A | 1 | a0001c0002t0004g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-91+6220G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877290 | ||||||
| chr1:204877336
|
A | G | 82 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(79): Show | 83 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-91+6266A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877336 | ||||||
| chr1:204877347
|
G | A | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+6277G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877347 | ||||||
| chr1:204877354
|
G | A | 1 | a0001c0003t0007g0181 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-91+6284G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877354 | ||||||
| chr1:204877481
|
G | A | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+6411G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877481 | ||||||
| chr1:204877644
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(32): Show | 36 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.-91+6574C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877644 | ||||||
| chr1:204877755
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-91+6685C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877755 | ||||||
| chr1:204877756
|
G | A | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+6686G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877756 | ||||||
| chr1:204877946
|
A | G | 1 | a0001c0001t0020g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-91+6876A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877946 | ||||||
| chr1:204877973
|
G | A | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+6903G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204877973 | ||||||
| chr1:204878014
|
C | T | 1 | a0002c0013t0001g0084 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-91+6944C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878014 | ||||||
| chr1:204878143
|
T | G | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+7073T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878143 | ||||||
| chr1:204878366
|
G | A | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+7296G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878366 | ||||||
| chr1:204878442
|
T | C | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-91+7372T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878442 | ||||||
| chr1:204878540
|
C | T | 4 | a0001c0002t0003g0227a0001c0002t0009g0255a0001c0014t0004g0228others(1): Show | 4 | HG01175.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+7470C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878540 | ||||||
| chr1:204878601
|
A | G | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+7531A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878601 | ||||||
| chr1:204878660
|
T | G | 17 | a0001c0001t0005g0139a0001c0002t0004g0133a0001c0002t0004g0214others(14): Show | 17 | HG01192.hp1 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-91+7590T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878660 | ||||||
| chr1:204878683
|
C | T | 3 | a0001c0002t0003g0175a0001c0011t0015g0176a0003c0026t0003g0177 | 3 | HG02055.hp2 HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-91+7613C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878683 | ||||||
| chr1:204878691
|
G | A | 41 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-91+7621G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878691 | ||||||
| chr1:204878771
|
G | A | 2 | a0001c0001t0015g0025a0001c0002t0005g0026 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-91+7701G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878771 | ||||||
| chr1:204878787
|
G | A | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+7717G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878787 | ||||||
| chr1:204878947
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-91+7877G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204878947 | ||||||
| chr1:204879003
|
C | G | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+7933C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879003 | ||||||
| chr1:204879059
|
C | G | 41 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-91+7989C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879059 | ||||||
| chr1:204879190
|
A | G | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+8120A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879190 | ||||||
| chr1:204879233
|
T | C | 11 | a0001c0002t0004g0214a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+8163T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879233 | ||||||
| chr1:204879264
|
A | G | 27 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0249others(24): Show | 27 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.-91+8194A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879264 | ||||||
| chr1:204879266
|
T | C | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+8196T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879266 | ||||||
| chr1:204879317
|
TTG | T | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+8251_-91+8252d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204879317 | |||||
| chr1:204879907
|
C | A | 65 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0069others(62): Show | 66 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-91+8837C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879907 | ||||||
| chr1:204879942
|
G | T | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+8872G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879942 | ||||||
| chr1:204879958
|
G | A | 1 | a0001c0002t0013g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-91+8888G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879958 | ||||||
| chr1:204879972
|
C | T | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+8902C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204879972 | ||||||
| chr1:204880028
|
G | T | 40 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-91+8958G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880028 | ||||||
| chr1:204880148
|
G | T | 3 | a0001c0002t0003g0175a0001c0011t0015g0176a0003c0026t0003g0177 | 3 | HG02055.hp2 HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-91+9078G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880148 | ||||||
| chr1:204880197
|
G | T | 2 | a0001c0002t0004g0230a0001c0002t0004g0231 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-91+9127G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880197 | ||||||
| chr1:204880203
|
C | T | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+9133C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880203 | ||||||
| chr1:204880222
|
G | A | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+9152G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880222 | ||||||
| chr1:204880323
|
A | AT | 4 | a0001c0002t0005g0254a0001c0002t0008g0252a0001c0002t0008g0253others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+9261dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204880323 | |||||
| chr1:204880358
|
T | G | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+9288T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880358 | ||||||
| chr1:204880387
|
G | A | 2 | a0001c0001t0001g0058a0001c0002t0020g0057 | 2 | NA18947.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-91+9317G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880387 | ||||||
| chr1:204880465
|
C | T | 7 | a0001c0001t0005g0139a0001c0002t0004g0133a0001c0002t0008g0221others(4): Show | 7 | HG01243.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+9395C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880465 | ||||||
| chr1:204880505
|
G | A | 1 | a0001c0002t0002g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-91+9435G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880505 | ||||||
| chr1:204880507
|
C | T | 1 | a0001c0003t0001g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-91+9437C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880507 | ||||||
| chr1:204880522
|
A | G | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+9452A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880522 | ||||||
| chr1:204880579
|
T | G | 1 | a0001c0001t0042g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-91+9509T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880579 | ||||||
| chr1:204880599
|
G | A | 41 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-91+9529G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880599 | ||||||
| chr1:204880613
|
A | G | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+9543A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880613 | ||||||
| chr1:204880791
|
C | T | 71 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(68): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-91+9721C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880791 | ||||||
| chr1:204880818
|
C | T | 5 | a0001c0001t0054g0207a0001c0002t0001g0208a0001c0002t0001g0209others(2): Show | 5 | HG00558.hp1 NA18612.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+9748C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880818 | ||||||
| chr1:204880819
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-91+9749G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204880819 | ||||||
| chr1:204881144
|
A | G | 1 | a0001c0002t0017g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-91+10074A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881144 | ||||||
| chr1:204881349
|
G | T | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+10279G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881349 | ||||||
| chr1:204881374
|
C | T | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+10304C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881374 | ||||||
| chr1:204881435
|
T | C | 1 | a0001c0004t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-91+10365T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881435 | ||||||
| chr1:204881568
|
G | A | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+10498G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881568 | ||||||
| chr1:204881589
|
C | T | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+10519C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881589 | ||||||
| chr1:204881608
|
C | T | 11 | a0001c0002t0004g0214a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+10538C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204881608 | ||||||
| chr1:204882104
|
C | T | 5 | a0001c0001t0015g0232a0001c0002t0009g0242a0001c0005t0003g0243others(2): Show | 5 | HG02622.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+11034C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882104 | ||||||
| chr1:204882242
|
T | C | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+11172T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882242 | ||||||
| chr1:204882427
|
T | TC | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+11364dupC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204882427 | |||||
| chr1:204882433
|
C | G | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+11363C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882433 | ||||||
| chr1:204882501
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0041g0194 | 3 | HG02132.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-91+11431T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882501 | ||||||
| chr1:204882554
|
A | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+11484A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882554 | ||||||
| chr1:204882602
|
C | G | 5 | a0001c0001t0005g0139a0001c0002t0004g0133a0001c0002t0043g0182others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+11532C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882602 | ||||||
| chr1:204882679
|
G | T | 2 | a0001c0001t0001g0192a0001c0001t0036g0187 | 2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-91+11609G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882679 | ||||||
| chr1:204882811
|
T | G | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+11741T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882811 | ||||||
| chr1:204882815
|
G | A | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+11745G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882815 | ||||||
| chr1:204882893
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-91+11823G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882893 | ||||||
| chr1:204882907
|
C | T | 1 | a0001c0002t0013g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-91+11837C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882907 | ||||||
| chr1:204882962
|
C | T | 26 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0249others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-91+11892C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204882962 | ||||||
| chr1:204883161
|
C | T | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+12091C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883161 | ||||||
| chr1:204883211
|
C | T | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+12141C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883211 | ||||||
| chr1:204883244
|
G | A | 34 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(31): Show | 35 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-91+12174G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883244 | ||||||
| chr1:204883356
|
G | A | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+12286G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883356 | ||||||
| chr1:204883371
|
C | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+12301C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883371 | ||||||
| chr1:204883464
|
C | G | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+12394C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883464 | ||||||
| chr1:204883498
|
A | G | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+12428A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883498 | ||||||
| chr1:204883569
|
G | C | 1 | a0001c0001t0005g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-91+12499G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883569 | ||||||
| chr1:204883636
|
C | G | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-91+12566C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883636 | ||||||
| chr1:204883715
|
T | C | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+12645T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883715 | ||||||
| chr1:204883765
|
G | A | 41 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-91+12695G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883765 | ||||||
| chr1:204883811
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-91+12741A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883811 | ||||||
| chr1:204883813
|
G | A | 34 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(31): Show | 35 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-91+12743G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883813 | ||||||
| chr1:204883924
|
C | T | 2 | a0001c0001t0007g0048a0001c0002t0002g0047 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-91+12854C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204883924 | ||||||
| chr1:204884055
|
T | G | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+12985T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884055 | ||||||
| chr1:204884135
|
G | A | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+13065G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884135 | ||||||
| chr1:204884210
|
A | G | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+13140A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884210 | ||||||
| chr1:204884255
|
C | T | 45 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 46 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-91+13185C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884255 | ||||||
| chr1:204884353
|
A | G | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+13283A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884353 | ||||||
| chr1:204884384
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-91+13314G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884384 | ||||||
| chr1:204884425
|
C | T | 11 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+13355C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884425 | ||||||
| chr1:204884628
|
C | T | 1 | a0001c0004t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-91+13558C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884628 | ||||||
| chr1:204884876
|
G | A | 2 | a0001c0002t0001g0060a0001c0004t0001g0059 | 2 | HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-91+13806G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884876 | ||||||
| chr1:204884932
|
A | T | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+13862A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884932 | ||||||
| chr1:204885143
|
A | C | 11 | a0001c0002t0004g0214a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+14073A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204885143 | ||||||
| chr1:204885230
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0002g0017 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-91+14160T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204885230 | ||||||
| chr1:204885278
|
A | C | 2 | a0001c0009t0001g0002a0001c0009t0001g0118 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-91+14208A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204885278 | ||||||
| chr1:204885389
|
TG | T | 41 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-91+14327delG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204885389 | |||||
| chr1:204885390
|
G | T | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+14320G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204885390 | ||||||
| chr1:204885391
|
G | C | 1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-91+14321G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204885391 | ||||||
| chr1:204885994
|
C | T | 35 | a0001c0001t0001g0058a0001c0001t0001g0186a0001c0001t0001g0191others(32): Show | 36 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-91+14924C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204885994 | ||||||
| chr1:204886001
|
G | A | 1 | a0001c0006t0004g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-91+14931G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204886001 | ||||||
| chr1:204886311
|
A | T | 12 | a0001c0002t0003g0201a0001c0002t0004g0214a0001c0002t0004g0216others(9): Show | 12 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-91+15241A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204886311 | ||||||
| chr1:204886543
|
A | C | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+15473A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204886543 | ||||||
| chr1:204886770
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-91+15700G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204886770 | ||||||
| chr1:204886838
|
G | A | 63 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(60): Show | 64 | HG00558.hp1 HG00673.hp1 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.-91+15768G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204886838 | ||||||
| chr1:204886911
|
C | T | 107 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(104): Show | 108 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-91+15841C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204886911 | ||||||
| chr1:204887206
|
G | T | 2 | a0001c0002t0002g0200a0001c0002t0002g0205 | 2 | HG00558.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-91+16136G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204887206 | ||||||
| chr1:204887307
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-91+16237C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204887307 | ||||||
| chr1:204887586
|
C | CT | 48 | a0001c0001t0001g0001a0001c0001t0001g0082a0001c0001t0001g0100others(45): Show | 49 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-91+16546dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
C | CTT | 18 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0141others(15): Show | 18 | HG00099.hp2 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-91+16545_-91+1654 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
C | CTTT | 25 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(22): Show | 25 | HG00423.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-91+16544_-91+1654 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
C | CTTTT | 8 | a0001c0002t0001g0142a0001c0002t0001g0161a0001c0002t0001g0168others(5): Show | 8 | HG00735.hp2 HG00741.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+16543_-91+1654 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CT | C | 23 | a0001c0001t0001g0122a0001c0001t0009g0010a0001c0001t0027g0087others(20): Show | 23 | HG01169.hp2 HG01192.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-91+16546delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-91+16536_-91+1654 others(15): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CTTTTTTT others(7): Show |
C | 33 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(30): Show | 34 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.-91+16533_-91+1654 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887586
|
CTTTTTTT others(8): Show |
C | 1 | a0005c0018t0001g0188 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-91+16532_-91+1654 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204887586 | |||||
| chr1:204887629
|
T | C | 80 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(77): Show | 81 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-91+16559T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204887629 | ||||||
| chr1:204887830
|
C | T | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+16760C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204887830 | ||||||
| chr1:204887845
|
G | A | 5 | a0001c0003t0001g0137a0001c0003t0003g0138a0001c0006t0017g0134others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+16775G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204887845 | ||||||
| chr1:204888016
|
G | T | 10 | a0001c0001t0009g0010a0001c0002t0001g0013a0001c0002t0002g0007others(7): Show | 10 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+16946G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888016 | ||||||
| chr1:204888031
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-91+16961C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888031 | ||||||
| chr1:204888322
|
C | T | 2 | a0001c0001t0007g0048a0001c0002t0002g0047 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-91+17252C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888322 | ||||||
| chr1:204888323
|
G | A | 1 | a0001c0004t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-91+17253G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888323 | ||||||
| chr1:204888505
|
A | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0002t0001g0105others(1): Show | 4 | HG01257.hp1 HG01261.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+17435A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888505 | ||||||
| chr1:204888569
|
C | T | 2 | a0001c0001t0027g0087a0001c0001t0042g0114 | 2 | HG01169.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-91+17499C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888569 | ||||||
| chr1:204888869
|
G | A | 14 | a0001c0001t0003g0045a0001c0002t0008g0043a0001c0002t0008g0221others(11): Show | 14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-91+17799G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888869 | ||||||
| chr1:204888881
|
T | A | 1 | a0008c0023t0011g0189 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-91+17811T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204888881 | ||||||
| chr1:204889128
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-91+18058C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889128 | ||||||
| chr1:204889197
|
T | C | 14 | a0001c0001t0003g0045a0001c0002t0008g0043a0001c0002t0008g0221others(11): Show | 14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-91+18127T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889197 | ||||||
| chr1:204889258
|
A | G | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+18188A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889258 | ||||||
| chr1:204889690
|
A | C | 2 | a0001c0001t0001g0113a0001c0007t0016g0103 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-91+18620A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889690 | ||||||
| chr1:204889710
|
A | G | 1 | a0008c0023t0011g0189 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-91+18640A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889710 | ||||||
| chr1:204889740
|
A | G | 1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-91+18670A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889740 | ||||||
| chr1:204889806
|
G | A | 1 | a0001c0010t0026g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-91+18736G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889806 | ||||||
| chr1:204889947
|
G | A | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+18877G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204889947 | ||||||
| chr1:204890138
|
T | A | 1 | a0001c0002t0001g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-91+19068T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890138 | ||||||
| chr1:204890380
|
G | A | 4 | a0001c0001t0007g0048a0001c0002t0002g0047a0001c0002t0004g0034others(1): Show | 4 | HG02970.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+19310G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890380 | ||||||
| chr1:204890385
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-91+19315C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890385 | ||||||
| chr1:204890486
|
G | T | 2 | a0001c0001t0001g0126a0001c0001t0002g0121 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-91+19416G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890486 | ||||||
| chr1:204890541
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-91+19471G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890541 | ||||||
| chr1:204890565
|
CT | C | 60 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0141others(57): Show | 60 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-91+19507delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204890565 | |||||
| chr1:204890621
|
A | G | 153 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(150): Show | 154 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.-91+19551A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890621 | ||||||
| chr1:204890669
|
C | A | 4 | a0001c0001t0002g0028a0001c0001t0010g0027a0001c0002t0001g0023others(1): Show | 4 | HG02602.hp2 HG02735.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+19599C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890669 | ||||||
| chr1:204890694
|
C | T | 11 | a0001c0001t0028g0183a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+19624C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890694 | ||||||
| chr1:204890780
|
G | A | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+19710G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204890780 | ||||||
| chr1:204891104
|
C | T | 11 | a0001c0001t0028g0183a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+20034C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891104 | ||||||
| chr1:204891119
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-91+20049G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891119 | ||||||
| chr1:204891194
|
G | A | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-91+20124G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891194 | ||||||
| chr1:204891397
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-91+20327G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891397 | ||||||
| chr1:204891593
|
C | T | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+20523C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891593 | ||||||
| chr1:204891594
|
G | T | 2 | a0001c0006t0017g0134a0001c0006t0017g0135 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-91+20524G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891594 | ||||||
| chr1:204891697
|
A | G | 1 | a0001c0002t0005g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-91+20627A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891697 | ||||||
| chr1:204891840
|
G | A | 110 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(107): Show | 111 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.-91+20770G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891840 | ||||||
| chr1:204891851
|
A | T | 1 | a0001c0001t0012g0120 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-91+20781A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891851 | ||||||
| chr1:204891955
|
C | T | 110 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(107): Show | 111 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.-91+20885C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891955 | ||||||
| chr1:204891963
|
A | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+20893A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204891963 | ||||||
| chr1:204892106
|
G | A | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+21036G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892106 | ||||||
| chr1:204892134
|
A | G | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+21064A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892134 | ||||||
| chr1:204892192
|
A | G | 1 | a0001c0001t0027g0087 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-91+21122A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892192 | ||||||
| chr1:204892243
|
C | T | 110 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(107): Show | 111 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.-91+21173C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892243 | ||||||
| chr1:204892256
|
C | T | 110 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(107): Show | 111 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.-91+21186C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892256 | ||||||
| chr1:204892399
|
G | C | 2 | a0001c0001t0007g0048a0001c0002t0002g0047 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-91+21329G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892399 | ||||||
| chr1:204892691
|
A | G | 42 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-91+21621A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892691 | ||||||
| chr1:204892819
|
G | A | 1 | a0001c0004t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-91+21749G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204892819 | ||||||
| chr1:204893326
|
G | A | 2 | a0001c0001t0001g0058a0001c0002t0020g0057 | 2 | NA18947.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-91+22256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204893326 | ||||||
| chr1:204893516
|
A | C | 47 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(44): Show | 47 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-91+22446A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204893516 | ||||||
| chr1:204893598
|
G | A | 2 | a0001c0002t0002g0200a0001c0002t0002g0205 | 2 | HG00558.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-91+22528G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204893598 | ||||||
| chr1:204893645
|
G | A | 11 | a0001c0001t0028g0183a0001c0002t0004g0216a0001c0002t0005g0210others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-91+22575G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204893645 | ||||||
| chr1:204893690
|
G | A | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+22620G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204893690 | ||||||
| chr1:204893993
|
A | G | 110 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(107): Show | 111 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.-91+22923A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204893993 | ||||||
| chr1:204894001
|
C | A | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+22931C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204894001 | ||||||
| chr1:204894076
|
A | C | 51 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(48): Show | 52 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.-91+23006A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204894076 | ||||||
| chr1:204894162
|
T | C | 1 | a0001c0003t0001g0127 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-91+23092T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204894162 | ||||||
| chr1:204894178
|
T | A | 123 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(120): Show | 124 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-91+23108T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204894178 | ||||||
| chr1:204895024
|
A | G | 123 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(120): Show | 124 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-91+23954A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204895024 | ||||||
| chr1:204895593
|
G | A | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+24523G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204895593 | ||||||
| chr1:204895952
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(4): Show | 8 | HG00738.hp2 HG01074.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.-91+24882A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204895952 | ||||||
| chr1:204896044
|
G | A | 4 | a0001c0003t0003g0138a0001c0006t0017g0134a0001c0006t0017g0135others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+24974G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896044 | ||||||
| chr1:204896083
|
T | G | 2 | a0001c0006t0017g0134a0001c0006t0017g0135 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-91+25013T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896083 | ||||||
| chr1:204896156
|
A | C | 93 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(90): Show | 94 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-91+25086A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896156 | ||||||
| chr1:204896314
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-91+25244G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896314 | ||||||
| chr1:204896420
|
C | G | 30 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 31 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-91+25350C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896420 | ||||||
| chr1:204896530
|
T | A | 38 | a0001c0001t0001g0061a0001c0001t0001g0141a0001c0001t0001g0155others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-91+25460T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896530 | ||||||
| chr1:204896776
|
C | T | 14 | a0001c0001t0005g0139a0001c0001t0028g0183a0001c0002t0004g0216others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-91+25706C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896776 | ||||||
| chr1:204896923
|
G | A | 4 | a0001c0003t0003g0138a0001c0006t0017g0134a0001c0006t0017g0135others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+25853G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204896923 | ||||||
| chr1:204897056
|
C | G | 1 | a0001c0007t0016g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-91+25986C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897056 | ||||||
| chr1:204897237
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(169): Show | 174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.-91+26167T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897237 | ||||||
| chr1:204897275
|
A | C | 4 | a0001c0003t0003g0138a0001c0006t0017g0134a0001c0006t0017g0135others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+26205A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897275 | ||||||
| chr1:204897296
|
C | T | 2 | a0001c0002t0008g0221a0001c0003t0024g0222 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+26226C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897296 | ||||||
| chr1:204897355
|
A | C | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-91+26285A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897355 | ||||||
| chr1:204897578
|
C | CT | 5 | a0001c0001t0005g0139a0001c0001t0028g0183a0001c0002t0013g0217others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+26522dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204897578 | |||||
| chr1:204897578
|
CT | C | 24 | a0001c0001t0002g0245a0001c0001t0002g0249a0001c0001t0005g0226others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-91+26522delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204897578 | |||||
| chr1:204897640
|
C | T | 21 | a0001c0001t0002g0245a0001c0001t0002g0249a0001c0001t0006g0247others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-91+26570C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897640 | ||||||
| chr1:204897749
|
T | G | 3 | a0001c0001t0003g0045a0001c0001t0015g0232a0001c0003t0001g0071 | 3 | HG01123.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-91+26679T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897749 | ||||||
| chr1:204897751
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-91+26681G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897751 | ||||||
| chr1:204897791
|
A | C | 1 | a0001c0002t0013g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-91+26721A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897791 | ||||||
| chr1:204897798
|
T | C | 1 | a0001c0002t0003g0227 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-91+26728T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204897798 | ||||||
| chr1:204898145
|
A | G | 34 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(31): Show | 35 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-91+27075A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204898145 | ||||||
| chr1:204898301
|
G | A | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+27231G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204898301 | ||||||
| chr1:204898309
|
T | C | 2 | a0001c0002t0002g0077a0001c0003t0001g0127 | 2 | HG01106.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-91+27239T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204898309 | ||||||
| chr1:204898509
|
TATC | T | 3 | a0001c0001t0007g0032a0001c0001t0010g0029a0001c0002t0002g0031 | 3 | HG02630.hp1 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-91+27442_-91+2744 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204898509 | |||||
| chr1:204898553
|
G | C | 1 | a0002c0025t0012g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-91+27483G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204898553 | ||||||
| chr1:204898957
|
G | C | 2 | a0001c0002t0004g0133a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-91+27887G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204898957 | ||||||
| chr1:204899164
|
G | A | 2 | a0001c0001t0006g0247a0001c0001t0014g0246 | 2 | HG00423.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-91+28094G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899164 | ||||||
| chr1:204899369
|
G | C | 50 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(47): Show | 51 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-91+28299G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899369 | ||||||
| chr1:204899420
|
A | AG | 151 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0141others(148): Show | 153 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.-91+28351dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204899420 | |||||
| chr1:204899439
|
C | T | 6 | a0001c0002t0002g0238a0001c0002t0003g0236a0001c0002t0008g0240others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-91+28369C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899439 | ||||||
| chr1:204899449
|
C | T | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-91+28379C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899449 | ||||||
| chr1:204899709
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0141others(47): Show | 51 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-91+28639T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899709 | ||||||
| chr1:204899757
|
C | T | 7 | a0001c0001t0001g0191a0001c0001t0054g0207a0001c0002t0001g0208others(4): Show | 7 | HG00558.hp1 NA18612.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.-91+28687C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899757 | ||||||
| chr1:204899960
|
C | T | 1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-91+28890C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204899960 | ||||||
| chr1:204900009
|
A | G | 1 | a0001c0003t0037g0225 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-91+28939A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204900009 | ||||||
| chr1:204900067
|
T | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0141others(111): Show | 116 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-91+28997T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204900067 | ||||||
| chr1:204900176
|
A | G | 3 | a0001c0002t0008g0043a0001c0003t0007g0042a0001c0003t0007g0044 | 3 | HG02258.hp1 HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-91+29106A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204900176 | ||||||
| chr1:204900326
|
T | G | 14 | a0001c0001t0005g0139a0001c0001t0028g0183a0001c0002t0004g0216others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-91+29256T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204900326 | ||||||
| chr1:204900431
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0141others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+29361A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204900431 | ||||||
| chr1:204900879
|
G | A | 12 | a0001c0001t0003g0045a0001c0002t0008g0043a0001c0002t0009g0037others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-91+29809G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204900879 | ||||||
| chr1:204901529
|
A | G | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-91+30459A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204901529 | ||||||
| chr1:204901860
|
G | A | 36 | a0001c0001t0002g0028a0001c0001t0002g0062a0001c0001t0007g0032others(33): Show | 37 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-91+30790G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204901860 | ||||||
| chr1:204901930
|
C | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(96): Show | 102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-91+30860C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204901930 | ||||||
| chr1:204902018
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(127): Show | 133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-91+30948C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902018 | ||||||
| chr1:204902122
|
C | T | 42 | a0001c0001t0001g0104a0001c0001t0001g0124a0001c0001t0001g0155others(39): Show | 42 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-91+31052C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902122 | ||||||
| chr1:204902123
|
G | A | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+31053G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902123 | ||||||
| chr1:204902130
|
C | T | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-91+31060C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902130 | ||||||
| chr1:204902366
|
C | T | 1 | a0001c0002t0001g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-91+31296C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902366 | ||||||
| chr1:204902542
|
T | C | 1 | a0001c0002t0002g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-91+31472T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902542 | ||||||
| chr1:204902648
|
T | C | 5 | a0001c0001t0003g0045a0001c0002t0009g0037a0001c0003t0003g0035others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+31578T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902648 | ||||||
| chr1:204902676
|
A | C | 13 | a0001c0001t0005g0226a0001c0001t0007g0048a0001c0001t0010g0111others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-91+31606A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902676 | ||||||
| chr1:204902681
|
G | A | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-91+31611G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902681 | ||||||
| chr1:204902702
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-91+31632T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902702 | ||||||
| chr1:204902853
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0058others(56): Show | 62 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-91+31783G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902853 | ||||||
| chr1:204902900
|
G | A | 2 | a0001c0002t0004g0230a0001c0002t0004g0231 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-91+31830G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902900 | ||||||
| chr1:204902940
|
A | G | 20 | a0001c0001t0003g0045a0001c0001t0005g0226a0001c0001t0007g0048others(17): Show | 20 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-91+31870A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902940 | ||||||
| chr1:204902960
|
A | C | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-91+31890A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902960 | ||||||
| chr1:204903329
|
G | A | 1 | a0001c0001t0014g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-91+32259G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903329 | ||||||
| chr1:204903359
|
C | T | 7 | a0001c0001t0002g0131a0001c0002t0001g0063a0001c0002t0002g0077others(4): Show | 7 | HG00323.hp1 HG00733.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+32289C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903359 | ||||||
| chr1:204903504
|
G | T | 3 | a0001c0001t0015g0025a0001c0002t0005g0026a0001c0006t0034g0030 | 3 | HG02559.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-91+32434G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903504 | ||||||
| chr1:204903529
|
A | G | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-91+32459A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903529 | ||||||
| chr1:204903714
|
G | A | 20 | a0001c0001t0001g0086a0001c0001t0001g0109a0001c0001t0001g0165others(17): Show | 20 | HG00544.hp1 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.-91+32644G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903714 | ||||||
| chr1:204903878
|
G | A | 1 | a0001c0004t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-91+32808G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903878 | ||||||
| chr1:204903894
|
A | G | 2 | a0001c0002t0003g0201a0001c0003t0010g0040 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-91+32824A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903894 | ||||||
| chr1:204903906
|
G | C | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+32836G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204903906 | ||||||
| chr1:204904345
|
G | A | 1 | a0001c0001t0040g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-91+33275G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204904345 | ||||||
| chr1:204904462
|
G | A | 1 | a0001c0007t0016g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-91+33392G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204904462 | ||||||
| chr1:204904565
|
A | C | 2 | a0001c0001t0046g0171a0001c0017t0001g0167 | 2 | HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-91+33495A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204904565 | ||||||
| chr1:204904630
|
C | A | 1 | a0001c0001t0002g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-91+33560C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204904630 | ||||||
| chr1:204904819
|
T | C | 20 | a0001c0001t0002g0131a0001c0001t0010g0111a0001c0001t0013g0065others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.-91+33749T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204904819 | ||||||
| chr1:204904883
|
TC | T | 150 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0086others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-91+33815delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204904883 | |||||
| chr1:204905072
|
G | T | 1 | a0001c0002t0002g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-91+34002G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905072 | ||||||
| chr1:204905132
|
T | A | 18 | a0001c0001t0007g0048a0001c0001t0009g0010a0001c0002t0001g0013others(15): Show | 18 | HG01192.hp1 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-91+34062T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905132 | ||||||
| chr1:204905164
|
A | C | 4 | a0001c0001t0011g0157a0001c0001t0011g0172a0001c0002t0001g0161others(1): Show | 4 | HG02135.hp1 HG02165.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-91+34094A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905164 | ||||||
| chr1:204905183
|
C | G | 53 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0075others(50): Show | 53 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-91+34113C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905183 | ||||||
| chr1:204905189
|
A | G | 1 | a0001c0005t0010g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-91+34119A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905189 | ||||||
| chr1:204905331
|
G | T | 54 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0001g0112others(51): Show | 55 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-91+34261G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905331 | ||||||
| chr1:204905370
|
G | GT | 7 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0003t0007g0012others(4): Show | 7 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+34312dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204905370 | |||||
| chr1:204905370
|
GT | G | 61 | a0001c0001t0001g0086a0001c0001t0001g0109a0001c0001t0001g0165others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-91+34312delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204905370 | |||||
| chr1:204905420
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-91+34350G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905420 | ||||||
| chr1:204905443
|
C | T | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0003t0007g0012others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-91+34373C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905443 | ||||||
| chr1:204905466
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-91+34396G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905466 | ||||||
| chr1:204905477
|
T | C | 54 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0001g0112others(51): Show | 55 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-91+34407T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905477 | ||||||
| chr1:204905480
|
A | G | 1 | a0001c0001t0042g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-91+34410A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905480 | ||||||
| chr1:204905728
|
G | A | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-91+34658G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204905728 | ||||||
| chr1:204906048
|
G | A | 1 | a0001c0006t0034g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-91+34978G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906048 | ||||||
| chr1:204906132
|
G | A | 4 | a0001c0001t0002g0131a0001c0002t0002g0077a0001c0004t0001g0078others(1): Show | 4 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+35062G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906132 | ||||||
| chr1:204906202
|
A | T | 20 | a0001c0001t0002g0131a0001c0001t0010g0111a0001c0001t0013g0065others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.-91+35132A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906202 | ||||||
| chr1:204906204
|
G | T | 1 | a0001c0001t0029g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-91+35134G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906204 | ||||||
| chr1:204906272
|
C | A | 2 | a0001c0002t0004g0230a0001c0002t0004g0231 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-91+35202C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906272 | ||||||
| chr1:204906443
|
G | A | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-91+35373G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906443 | ||||||
| chr1:204906517
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-91+35447G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906517 | ||||||
| chr1:204906687
|
A | AT | 5 | a0001c0001t0001g0198a0001c0002t0009g0242a0001c0003t0003g0138others(2): Show | 5 | HG02622.hp2 HG02965.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+35630dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204906687 | |||||
| chr1:204906687
|
AT | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0058others(92): Show | 97 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-91+35630delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204906687 | |||||
| chr1:204906736
|
G | A | 2 | a0001c0002t0003g0201a0001c0003t0010g0040 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-91+35666G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906736 | ||||||
| chr1:204906750
|
TCGGCTCA others(18): Show |
T | 6 | a0001c0001t0005g0139a0001c0002t0003g0227a0001c0002t0009g0255others(3): Show | 6 | HG01175.hp1 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+35681_-91+3570 others(29): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906750 | ||||||
| chr1:204906751
|
CGGCTCAC others(18): Show |
C | 99 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0082others(96): Show | 100 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-91+35688_-91+3571 others(29): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204906751 | |||||
| chr1:204906776
|
G | T | 6 | a0001c0001t0005g0139a0001c0002t0003g0227a0001c0002t0009g0255others(3): Show | 6 | HG01175.hp1 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+35706G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906776 | ||||||
| chr1:204906779
|
C | T | 61 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0104others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-91+35709C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906779 | ||||||
| chr1:204906805
|
CCCCGAGT others(17): Show |
C | 1 | a0001c0002t0001g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-91+35740_-91+3576 others(28): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204906805 | |||||
| chr1:204906839
|
C | A | 2 | a0001c0001t0001g0196a0001c0002t0005g0140 | 2 | HG02129.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-91+35769C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906839 | ||||||
| chr1:204906840
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-91+35770T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906840 | ||||||
| chr1:204906844
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-91+35774C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906844 | ||||||
| chr1:204906877
|
G | T | 10 | a0001c0001t0015g0025a0001c0002t0002g0007a0001c0002t0002g0008others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-91+35807G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906877 | ||||||
| chr1:204906882
|
A | G | 14 | a0001c0001t0003g0045a0001c0001t0009g0010a0001c0001t0009g0110others(11): Show | 14 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-91+35812A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906882 | ||||||
| chr1:204906884
|
C | T | 1 | a0001c0001t0044g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-91+35814C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906884 | ||||||
| chr1:204906885
|
A | G | 9 | a0001c0001t0001g0174a0001c0001t0005g0139a0001c0001t0044g0235others(6): Show | 9 | HG01243.hp2 HG01346.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-91+35815A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906885 | ||||||
| chr1:204906904
|
G | C | 40 | a0001c0001t0001g0086a0001c0001t0001g0109a0001c0001t0002g0249others(37): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-91+35834G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906904 | ||||||
| chr1:204906904
|
G | T | 95 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0104others(92): Show | 96 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-91+35834G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906904 | ||||||
| chr1:204906905
|
C | G | 135 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0086others(132): Show | 136 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-91+35835C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906905 | ||||||
| chr1:204906930
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-91+35860G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906930 | ||||||
| chr1:204906934
|
T | C | 2 | a0001c0001t0001g0113a0001c0002t0001g0206 | 2 | HG02132.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-91+35864T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906934 | ||||||
| chr1:204906935
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-91+35865G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204906935 | ||||||
| chr1:204907296
|
A | G | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0003t0007g0012others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-91+36226A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204907296 | ||||||
| chr1:204907308
|
GTTGT | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0094a0001c0001t0001g0155others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.-91+36245_-91+3624 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204907308 | |||||
| chr1:204907521
|
G | A | 2 | a0001c0002t0003g0175a0001c0014t0004g0228 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-91+36451G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204907521 | ||||||
| chr1:204907570
|
G | T | 1 | a0001c0001t0054g0207 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-91+36500G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204907570 | ||||||
| chr1:204907838
|
T | G | 33 | a0001c0001t0001g0122a0001c0001t0002g0121a0001c0001t0002g0131others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.-90-36388T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204907838 | ||||||
| chr1:204907941
|
T | C | 113 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(110): Show | 114 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-90-36285T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204907941 | ||||||
| chr1:204907944
|
A | ATG | 25 | a0001c0001t0005g0139a0001c0002t0001g0013a0001c0002t0002g0007others(22): Show | 25 | HG01175.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-90-36260_-90-3625 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204907944 | |||||
| chr1:204907944
|
A | ATGTG | 3 | a0001c0001t0015g0025a0001c0002t0048g0239a0001c0006t0034g0030 | 3 | HG01109.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-90-36262_-90-3625 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204907944 | |||||
| chr1:204907944
|
ATG | A | 110 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(107): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-90-36260_-90-3625 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204907944 | |||||
| chr1:204908014
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(219): Show | 225 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-90-36212T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908014 | ||||||
| chr1:204908068
|
A | G | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-36158A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908068 | ||||||
| chr1:204908212
|
G | A | 1 | a0001c0002t0021g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-90-36014G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908212 | ||||||
| chr1:204908262
|
A | T | 2 | a0001c0001t0015g0025a0001c0006t0034g0030 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-90-35964A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908262 | ||||||
| chr1:204908297
|
A | G | 1 | a0001c0001t0027g0087 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-90-35929A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908297 | ||||||
| chr1:204908350
|
C | T | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-35876C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908350 | ||||||
| chr1:204908524
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(224): Show | 230 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-90-35702G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908524 | ||||||
| chr1:204908542
|
T | G | 115 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(112): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-90-35684T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908542 | ||||||
| chr1:204908565
|
T | C | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-35661T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908565 | ||||||
| chr1:204908808
|
T | G | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90-35418T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908808 | ||||||
| chr1:204908901
|
C | A | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-35325C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908901 | ||||||
| chr1:204908917
|
A | G | 30 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0005g0139others(27): Show | 31 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.-90-35309A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204908917 | ||||||
| chr1:204909175
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-90-35051C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909175 | ||||||
| chr1:204909399
|
A | G | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-34827A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909399 | ||||||
| chr1:204909474
|
GAAAGTTC others(3): Show |
G | 4 | a0001c0002t0001g0013a0001c0002t0003g0175a0001c0014t0004g0228others(1): Show | 4 | HG02257.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-34750_-90-3474 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204909474 | |||||
| chr1:204909485
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-90-34741A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909485 | ||||||
| chr1:204909545
|
C | T | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-90-34681C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909545 | ||||||
| chr1:204909576
|
A | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-34650A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909576 | ||||||
| chr1:204909592
|
G | A | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90-34634G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909592 | ||||||
| chr1:204909652
|
T | C | 1 | a0001c0002t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-90-34574T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909652 | ||||||
| chr1:204909660
|
A | G | 4 | a0001c0002t0005g0140a0001c0002t0009g0242a0001c0003t0003g0138others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-34566A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909660 | ||||||
| chr1:204909761
|
A | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-34465A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909761 | ||||||
| chr1:204909763
|
T | A | 5 | a0001c0001t0003g0045a0001c0002t0003g0236a0001c0002t0008g0043others(2): Show | 5 | HG02451.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-34463T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909763 | ||||||
| chr1:204909809
|
A | G | 4 | a0001c0002t0005g0140a0001c0002t0009g0242a0001c0003t0003g0138others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-34417A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909809 | ||||||
| chr1:204909893
|
T | C | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-34333T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909893 | ||||||
| chr1:204909961
|
A | G | 84 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(81): Show | 84 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.-90-34265A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204909961 | ||||||
| chr1:204910027
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-90-34199A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910027 | ||||||
| chr1:204910046
|
A | G | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-34180A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910046 | ||||||
| chr1:204910155
|
G | GTA | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-34061_-90-3406 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204910155 | |||||
| chr1:204910381
|
G | C | 3 | a0001c0002t0005g0254a0001c0002t0008g0252a0001c0002t0008g0253 | 3 | HG01069.hp2 HG01071.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-90-33845G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910381 | ||||||
| chr1:204910425
|
T | G | 1 | a0001c0002t0009g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90-33801T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910425 | ||||||
| chr1:204910516
|
A | ATCT | 123 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(120): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-90-33708_-90-3370 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204910516 | |||||
| chr1:204910621
|
A | G | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-33605A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910621 | ||||||
| chr1:204910695
|
A | T | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-33531A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910695 | ||||||
| chr1:204910824
|
A | AT | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-33393dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204910824 | |||||
| chr1:204910906
|
G | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-33320G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910906 | ||||||
| chr1:204910947
|
A | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-33279A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204910947 | ||||||
| chr1:204911079
|
C | T | 4 | a0001c0002t0005g0140a0001c0002t0009g0242a0001c0003t0003g0138others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-33147C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204911079 | ||||||
| chr1:204911260
|
T | C | 30 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0005g0139others(27): Show | 31 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.-90-32966T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204911260 | ||||||
| chr1:204911376
|
G | A | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-32850G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204911376 | ||||||
| chr1:204911408
|
A | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-32818A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204911408 | ||||||
| chr1:204911582
|
G | A | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90-32644G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204911582 | ||||||
| chr1:204912077
|
A | G | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-32149A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912077 | ||||||
| chr1:204912079
|
G | A | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-32147G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912079 | ||||||
| chr1:204912139
|
T | C | 13 | a0001c0001t0015g0025a0001c0002t0002g0007a0001c0002t0002g0008others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-90-32087T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912139 | ||||||
| chr1:204912210
|
C | T | 119 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(116): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-90-32016C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912210 | ||||||
| chr1:204912214
|
G | A | 13 | a0001c0001t0015g0025a0001c0002t0002g0007a0001c0002t0002g0008others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-90-32012G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912214 | ||||||
| chr1:204912274
|
A | G | 4 | a0001c0002t0005g0140a0001c0002t0009g0242a0001c0003t0003g0138others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-31952A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912274 | ||||||
| chr1:204912285
|
T | G | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-31941T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912285 | ||||||
| chr1:204912471
|
T | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-31755T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912471 | ||||||
| chr1:204912480
|
T | C | 3 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0003t0007g0181 | 3 | HG01243.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-90-31746T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912480 | ||||||
| chr1:204912523
|
G | A | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-31703G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912523 | ||||||
| chr1:204912566
|
G | A | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-31660G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912566 | ||||||
| chr1:204912571
|
C | G | 30 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0005g0139others(27): Show | 31 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.-90-31655C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912571 | ||||||
| chr1:204912865
|
A | AT | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-31361_-90-3136 others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912865 | ||||||
| chr1:204912867
|
AT | A | 3 | a0001c0002t0003g0175a0001c0014t0004g0228a0001c0022t0031g0136 | 3 | HG02257.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-31358delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912867 | ||||||
| chr1:204912880
|
T | C | 73 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(70): Show | 73 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.-90-31346T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912880 | ||||||
| chr1:204912884
|
T | C | 29 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0005g0139others(26): Show | 30 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.-90-31342T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912884 | ||||||
| chr1:204912889
|
G | A | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-31337G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912889 | ||||||
| chr1:204912905
|
A | G | 1 | a0001c0003t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-90-31321A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204912905 | ||||||
| chr1:204913042
|
A | T | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90-31184A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913042 | ||||||
| chr1:204913100
|
A | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-31126A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913100 | ||||||
| chr1:204913104
|
A | G | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-31122A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913104 | ||||||
| chr1:204913148
|
T | TAAC | 115 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(112): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-90-31076_-90-3107 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204913148 | |||||
| chr1:204913164
|
C | T | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-31062C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913164 | ||||||
| chr1:204913382
|
G | A | 115 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(112): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-90-30844G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913382 | ||||||
| chr1:204913405
|
A | G | 114 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-90-30821A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913405 | ||||||
| chr1:204913761
|
T | C | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-30465T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913761 | ||||||
| chr1:204913823
|
A | G | 123 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(120): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-90-30403A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204913823 | ||||||
| chr1:204914051
|
A | G | 2 | a0001c0001t0002g0028a0001c0001t0010g0027 | 2 | HG02602.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-90-30175A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914051 | ||||||
| chr1:204914098
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-90-30128C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914098 | ||||||
| chr1:204914264
|
T | C | 1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-90-29962T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914264 | ||||||
| chr1:204914283
|
A | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-29943A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914283 | ||||||
| chr1:204914320
|
G | A | 4 | a0001c0002t0005g0140a0001c0002t0009g0242a0001c0003t0003g0138others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-29906G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914320 | ||||||
| chr1:204914467
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-90-29759A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914467 | ||||||
| chr1:204914730
|
C | T | 2 | a0001c0002t0021g0219a0001c0003t0035g0220 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-90-29496C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914730 | ||||||
| chr1:204914753
|
G | A | 1 | a0009c0028t0022g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-90-29473G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914753 | ||||||
| chr1:204914825
|
T | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(169): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-90-29401T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914825 | ||||||
| chr1:204914835
|
G | C | 1 | a0001c0004t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-90-29391G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914835 | ||||||
| chr1:204914903
|
G | A | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-29323G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914903 | ||||||
| chr1:204914976
|
A | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-90-29250A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204914976 | ||||||
| chr1:204915000
|
G | T | 1 | a0001c0002t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-90-29226G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915000 | ||||||
| chr1:204915049
|
A | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-90-29177A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915049 | ||||||
| chr1:204915097
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-90-29129G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915097 | ||||||
| chr1:204915163
|
C | T | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-29063C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915163 | ||||||
| chr1:204915216
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-90-29010G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915216 | ||||||
| chr1:204915225
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-90-29001G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915225 | ||||||
| chr1:204915271
|
ACT | A | 3 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0037g0225 | 3 | HG02451.hp1 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-90-28952_-90-2895 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204915271 | |||||
| chr1:204915297
|
A | T | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28929A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915297 | ||||||
| chr1:204915302
|
A | T | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28924A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915302 | ||||||
| chr1:204915471
|
A | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28755A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915471 | ||||||
| chr1:204915516
|
C | T | 5 | a0001c0002t0005g0254a0001c0002t0008g0252a0001c0002t0008g0253others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-28710C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915516 | ||||||
| chr1:204915581
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0069others(45): Show | 50 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90-28645G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915581 | ||||||
| chr1:204915693
|
T | G | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28533T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915693 | ||||||
| chr1:204915708
|
T | A | 124 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(121): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-90-28518T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915708 | ||||||
| chr1:204915722
|
G | T | 4 | a0001c0002t0003g0227a0001c0002t0009g0255a0001c0005t0003g0218others(1): Show | 4 | HG01175.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-28504G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915722 | ||||||
| chr1:204915743
|
G | A | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28483G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915743 | ||||||
| chr1:204915909
|
T | C | 13 | a0001c0001t0015g0025a0001c0002t0002g0007a0001c0002t0002g0008others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-90-28317T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915909 | ||||||
| chr1:204915976
|
A | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-90-28250A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204915976 | ||||||
| chr1:204916006
|
G | A | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28220G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916006 | ||||||
| chr1:204916045
|
T | C | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90-28181T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916045 | ||||||
| chr1:204916082
|
G | A | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-28144G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916082 | ||||||
| chr1:204916237
|
T | C | 2 | a0001c0001t0003g0045a0001c0002t0009g0037 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-90-27989T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916237 | ||||||
| chr1:204916355
|
G | A | 2 | a0001c0001t0007g0032a0001c0002t0002g0031 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-90-27871G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916355 | ||||||
| chr1:204916356
|
G | A | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-27870G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916356 | ||||||
| chr1:204916392
|
A | G | 1 | a0001c0001t0011g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-90-27834A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916392 | ||||||
| chr1:204916405
|
A | G | 1 | a0001c0002t0001g0203 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-90-27821A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916405 | ||||||
| chr1:204916722
|
G | GTTTGTTT | 226 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-90-27493_-90-2748 others(11): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204916722 | |||||
| chr1:204916754
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-90-27472G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916754 | ||||||
| chr1:204916830
|
T | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-90-27396T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916830 | ||||||
| chr1:204916853
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0055g0156 | 2 | HG00423.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-90-27373G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204916853 | ||||||
| chr1:204917114
|
G | T | 2 | a0001c0002t0003g0175a0001c0014t0004g0228 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-27112G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204917114 | ||||||
| chr1:204917285
|
A | G | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-26941A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204917285 | ||||||
| chr1:204917441
|
A | T | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-26785A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204917441 | ||||||
| chr1:204917728
|
C | T | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-26498C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204917728 | ||||||
| chr1:204917933
|
A | G | 2 | a0001c0001t0007g0032a0001c0002t0002g0031 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-90-26293A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204917933 | ||||||
| chr1:204917944
|
A | C | 6 | a0001c0002t0004g0034a0001c0002t0005g0140a0001c0002t0009g0242others(3): Show | 6 | HG02622.hp2 HG02965.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-26282A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204917944 | ||||||
| chr1:204918302
|
G | A | 2 | a0001c0001t0002g0062a0001c0016t0002g0067 | 2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-90-25924G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204918302 | ||||||
| chr1:204918474
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-90-25752G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204918474 | ||||||
| chr1:204918551
|
A | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-90-25675A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204918551 | ||||||
| chr1:204918584
|
C | CT | 111 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0058others(108): Show | 113 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-90-25623dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204918584 | |||||
| chr1:204918584
|
CT | C | 7 | a0001c0001t0001g0124a0001c0001t0012g0120a0001c0001t0041g0194others(4): Show | 7 | HG00323.hp2 HG02004.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90-25623delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204918584 | |||||
| chr1:204918765
|
T | C | 2 | a0001c0002t0001g0161a0001c0002t0002g0055 | 2 | HG04199.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-90-25461T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204918765 | ||||||
| chr1:204918805
|
C | T | 6 | a0001c0002t0004g0034a0001c0002t0005g0140a0001c0002t0009g0242others(3): Show | 6 | HG02622.hp2 HG02965.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-25421C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204918805 | ||||||
| chr1:204918840
|
C | T | 1 | a0001c0002t0053g0237 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-90-25386C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204918840 | ||||||
| chr1:204919216
|
G | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0069others(45): Show | 50 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90-25010G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204919216 | ||||||
| chr1:204919408
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0069others(75): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-90-24818G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204919408 | ||||||
| chr1:204919520
|
A | G | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-24706A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204919520 | ||||||
| chr1:204919524
|
A | C | 2 | a0001c0001t0046g0171a0001c0017t0001g0167 | 2 | HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-90-24702A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204919524 | ||||||
| chr1:204919626
|
G | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0069others(46): Show | 51 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-90-24600G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204919626 | ||||||
| chr1:204919753
|
C | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-24473C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204919753 | ||||||
| chr1:204920205
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-90-24021G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920205 | ||||||
| chr1:204920404
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0069others(75): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-90-23822C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920404 | ||||||
| chr1:204920427
|
C | CT | 55 | a0001c0001t0001g0020a0001c0001t0001g0094a0001c0001t0001g0109others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.-90-23779dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204920427 | |||||
| chr1:204920427
|
CT | C | 8 | a0001c0001t0005g0139a0001c0001t0009g0010a0001c0002t0008g0240others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-23779delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204920427 | |||||
| chr1:204920427
|
CTT | C | 25 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0013g0065others(22): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.-90-23780_-90-2377 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204920427 | |||||
| chr1:204920447
|
T | C | 3 | a0001c0006t0017g0134a0001c0006t0017g0135a0001c0011t0015g0176 | 3 | HG02055.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-90-23779T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920447 | ||||||
| chr1:204920447
|
T | TC | 80 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0075others(77): Show | 80 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.-90-23778dupC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204920447 | |||||
| chr1:204920458
|
GCTTTGAA others(3): Show |
G | 1 | a0001c0002t0002g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-90-23759_-90-2375 others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204920458 | |||||
| chr1:204920608
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0041g0194 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-90-23618C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920608 | ||||||
| chr1:204920781
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0040g0019a0001c0001t0045g0072others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-23445G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920781 | ||||||
| chr1:204920793
|
G | T | 1 | a0001c0001t0023g0143 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-90-23433G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920793 | ||||||
| chr1:204920843
|
C | G | 1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-90-23383C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920843 | ||||||
| chr1:204920960
|
G | A | 1 | a0001c0002t0021g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-90-23266G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204920960 | ||||||
| chr1:204921226
|
C | G | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-23000C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921226 | ||||||
| chr1:204921512
|
G | A | 4 | a0001c0002t0001g0013a0001c0002t0003g0175a0001c0014t0004g0228others(1): Show | 4 | HG02257.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-22714G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921512 | ||||||
| chr1:204921522
|
T | G | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-22704T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921522 | ||||||
| chr1:204921603
|
A | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0082others(83): Show | 86 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.-90-22623A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921603 | ||||||
| chr1:204921664
|
G | A | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-22562G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921664 | ||||||
| chr1:204921670
|
C | A | 2 | a0001c0002t0003g0175a0001c0014t0004g0228 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-22556C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921670 | ||||||
| chr1:204921843
|
T | C | 1 | a0001c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-90-22383T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921843 | ||||||
| chr1:204921868
|
G | A | 1 | a0001c0003t0007g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-90-22358G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921868 | ||||||
| chr1:204921950
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0193a0001c0002t0002g0115 | 3 | HG02015.hp2 HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-90-22276G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204921950 | ||||||
| chr1:204922030
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-90-22196G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922030 | ||||||
| chr1:204922093
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-90-22133C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922093 | ||||||
| chr1:204922107
|
C | T | 36 | a0001c0001t0001g0069a0001c0001t0001g0113a0001c0001t0001g0158others(33): Show | 37 | HG00558.hp2 HG00741.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.-90-22119C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922107 | ||||||
| chr1:204922182
|
G | A | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18612.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-90-22044G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922182 | ||||||
| chr1:204922292
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0002g0062a0001c0016t0002g0067 | 3 | HG00099.hp1 HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-90-21934C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922292 | ||||||
| chr1:204922320
|
C | G | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-21906C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922320 | ||||||
| chr1:204922419
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-90-21807A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922419 | ||||||
| chr1:204922429
|
C | G | 2 | a0001c0002t0003g0175a0001c0014t0004g0228 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-21797C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922429 | ||||||
| chr1:204922649
|
G | C | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-21577G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922649 | ||||||
| chr1:204922829
|
A | G | 3 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0037g0225 | 3 | HG02451.hp1 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-90-21397A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922829 | ||||||
| chr1:204922953
|
C | T | 2 | a0001c0001t0025g0088a0001c0010t0026g0022 | 2 | HG01515.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-90-21273C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922953 | ||||||
| chr1:204922987
|
C | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90-21239C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204922987 | ||||||
| chr1:204923201
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(162): Show | 168 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-90-21025C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923201 | ||||||
| chr1:204923322
|
G | T | 8 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90-20904G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923322 | ||||||
| chr1:204923375
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0012g0099others(5): Show | 9 | HG00738.hp2 HG01074.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90-20851C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923375 | ||||||
| chr1:204923434
|
C | T | 1 | a0001c0001t0049g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-90-20792C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923434 | ||||||
| chr1:204923518
|
T | A | 6 | a0001c0002t0001g0013a0001c0002t0003g0175a0001c0002t0004g0034others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-20708T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923518 | ||||||
| chr1:204923575
|
C | T | 4 | a0001c0001t0028g0183a0001c0002t0004g0230a0001c0002t0004g0231others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-20651C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923575 | ||||||
| chr1:204923713
|
G | A | 3 | a0001c0002t0009g0242a0001c0003t0003g0138a0001c0003t0024g0222 | 3 | HG02622.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-90-20513G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923713 | ||||||
| chr1:204923715
|
C | A | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-20511C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923715 | ||||||
| chr1:204923928
|
C | T | 1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-90-20298C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204923928 | ||||||
| chr1:204924078
|
C | G | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90-20148C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924078 | ||||||
| chr1:204924186
|
C | T | 1 | a0001c0001t0012g0120 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-90-20040C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924186 | ||||||
| chr1:204924274
|
A | T | 1 | a0001c0002t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-90-19952A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924274 | ||||||
| chr1:204924395
|
A | C | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90-19831A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924395 | ||||||
| chr1:204924421
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-90-19805T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924421 | ||||||
| chr1:204924524
|
G | C | 3 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0037g0225 | 3 | HG02451.hp1 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-90-19702G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924524 | ||||||
| chr1:204924576
|
G | A | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-90-19650G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924576 | ||||||
| chr1:204924757
|
A | C | 43 | a0001c0001t0001g0020a0001c0001t0001g0094a0001c0001t0001g0122others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.-90-19469A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204924757 | ||||||
| chr1:204925056
|
A | G | 4 | a0001c0001t0001g0155a0001c0001t0001g0257a0001c0001t0006g0258others(1): Show | 4 | HG02015.hp1 NA18990.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-19170A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925056 | ||||||
| chr1:204925066
|
G | T | 19 | a0001c0001t0007g0032a0001c0001t0009g0110a0001c0001t0010g0029others(16): Show | 19 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-90-19160G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925066 | ||||||
| chr1:204925184
|
G | A | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-19042G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925184 | ||||||
| chr1:204925271
|
A | G | 2 | a0001c0002t0003g0175a0001c0014t0004g0228 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-18955A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925271 | ||||||
| chr1:204925371
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-90-18855C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925371 | ||||||
| chr1:204925388
|
A | C | 20 | a0001c0001t0007g0032a0001c0001t0009g0110a0001c0001t0010g0029others(17): Show | 20 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-90-18838A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925388 | ||||||
| chr1:204925442
|
C | T | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-18784C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925442 | ||||||
| chr1:204925500
|
T | C | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-18726T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925500 | ||||||
| chr1:204925802
|
C | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-18424C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204925802 | ||||||
| chr1:204926036
|
A | C | 1 | a0001c0003t0003g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-90-18190A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926036 | ||||||
| chr1:204926088
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(48): Show | 53 | HG00558.hp2 HG00738.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.-90-18138G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926088 | ||||||
| chr1:204926380
|
G | GTA | 40 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0001g0106others(37): Show | 40 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-90-17820_-90-1781 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
G | GTATA | 15 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0174others(12): Show | 15 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90-17822_-90-1781 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
G | GTATATA | 12 | a0001c0001t0001g0061a0001c0001t0001g0257a0001c0001t0006g0070others(9): Show | 12 | HG00558.hp1 HG02165.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90-17824_-90-1781 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
G | GTATATAT others(13): Show |
1 | a0001c0002t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-90-17838_-90-1781 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926380
|
GTA | G | 5 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-17820_-90-1781 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926380 | |||||
| chr1:204926394
|
ATATATAT others(15): Show |
A | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-17830_-90-1780 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926394 | |||||
| chr1:204926396
|
ATATATAT others(9): Show |
A | 1 | a0001c0005t0033g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-90-17828_-90-1781 others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926396
|
ATATATAT others(13): Show |
A | 10 | a0001c0001t0001g0109a0001c0001t0040g0019a0001c0001t0045g0072others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90-17828_-90-1780 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926396
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-90-17828_-90-1780 others(25): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926396
|
ATATATAT others(15): Show |
A | 7 | a0001c0001t0002g0121a0001c0001t0005g0139a0001c0002t0043g0182others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90-17828_-90-1780 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926396 | |||||
| chr1:204926398
|
ATATATAT others(14): Show |
A | 42 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(39): Show | 44 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-90-17826_-90-1780 others(25): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926398 | |||||
| chr1:204926398
|
ATATATAT others(15): Show |
A | 20 | a0001c0001t0002g0131a0001c0001t0013g0065a0001c0001t0025g0088others(17): Show | 21 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.-90-17826_-90-1780 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926398 | |||||
| chr1:204926400
|
ATATATAT others(12): Show |
A | 11 | a0001c0001t0001g0069a0001c0001t0002g0101a0001c0001t0014g0098others(8): Show | 11 | HG00558.hp2 HG00741.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90-17824_-90-1780 others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926400 | |||||
| chr1:204926400
|
ATATATAT others(14): Show |
A | 2 | a0001c0002t0008g0240a0001c0002t0009g0037 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-90-17824_-90-1780 others(25): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926400 | |||||
| chr1:204926400
|
ATATATAT others(15): Show |
A | 1 | a0001c0021t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-90-17824_-90-1780 others(26): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926400 | |||||
| chr1:204926406
|
A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(23): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(22): Show |
1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(33): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(27): Show |
1 | a0001c0005t0003g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(38): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(34): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(24): Show |
1 | a0001c0005t0013g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(35): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(25): Show |
1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(36): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATATATAT others(7): Show |
1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATT | 8 | a0001c0001t0001g0075a0001c0001t0001g0122a0001c0001t0011g0157others(5): Show | 8 | HG00423.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-17794_-90-1779 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | ATTT | 6 | a0001c0001t0001g0159a0001c0001t0001g0193a0001c0002t0001g0144others(3): Show | 6 | HG00735.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-17795_-90-1779 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926406
|
A | T | 9 | a0001c0001t0007g0048a0001c0002t0001g0060a0001c0002t0017g0215others(6): Show | 9 | HG00639.hp2 HG01192.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90-17820A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926406 | ||||||
| chr1:204926406
|
AT | A | 5 | a0001c0001t0002g0081a0001c0001t0015g0232a0001c0002t0002g0047others(2): Show | 5 | HG03516.hp1 HG03579.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-17793delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204926406 | |||||
| chr1:204926407
|
T | TA | 11 | a0001c0001t0001g0202a0001c0001t0001g0259a0001c0001t0036g0187others(8): Show | 11 | HG01358.hp1 HG02723.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90-17819_-90-1781 others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATA | 10 | a0001c0001t0001g0141a0001c0001t0001g0165a0001c0001t0001g0195others(7): Show | 10 | HG01071.hp2 HG01123.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-17819_-90-1781 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATA | 5 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0223others(2): Show | 5 | HG00323.hp2 HG03491.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-17819_-90-1781 others(9): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATATA others(4): Show |
1 | a0001c0001t0009g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(15): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATATA others(6): Show |
2 | a0001c0001t0010g0029a0001c0003t0010g0040 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-90-17819_-90-1781 others(17): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926407 | ||||||
| chr1:204926407
|
T | TATATATA others(8): Show |
1 | a0001c0005t0007g0248 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-90-17819_-90-1781 others(19): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926407 | ||||||
| chr1:204926408
|
T | A | 46 | a0001c0001t0001g0061a0001c0001t0001g0082a0001c0001t0001g0100others(43): Show | 46 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-90-17818T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926408 | ||||||
| chr1:204926409
|
T | A | 27 | a0001c0001t0001g0086a0001c0001t0001g0126a0001c0001t0001g0165others(24): Show | 27 | HG01123.hp1 HG01175.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-90-17817T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926409 | ||||||
| chr1:204926410
|
T | A | 11 | a0001c0001t0001g0117a0001c0001t0001g0191a0001c0001t0027g0087others(8): Show | 11 | HG00423.hp2 HG00558.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90-17816T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926410 | ||||||
| chr1:204926411
|
T | A | 3 | a0001c0001t0009g0110a0001c0003t0007g0012a0001c0005t0007g0248 | 3 | HG02723.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-90-17815T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926411 | ||||||
| chr1:204926412
|
T | A | 1 | a0001c0001t0055g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-90-17814T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926412 | ||||||
| chr1:204926616
|
G | C | 2 | a0001c0006t0017g0134a0001c0006t0017g0135 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-90-17610G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926616 | ||||||
| chr1:204926768
|
T | G | 9 | a0001c0002t0001g0013a0001c0002t0003g0201a0001c0002t0005g0140others(6): Show | 9 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90-17458T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926768 | ||||||
| chr1:204926793
|
G | A | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90-17433G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926793 | ||||||
| chr1:204926943
|
C | G | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90-17283C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926943 | ||||||
| chr1:204926967
|
C | T | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-90-17259C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204926967 | ||||||
| chr1:204927053
|
T | C | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-17173T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927053 | ||||||
| chr1:204927094
|
A | C | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-90-17132A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927094 | ||||||
| chr1:204927191
|
C | T | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-17035C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927191 | ||||||
| chr1:204927196
|
A | G | 5 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-17030A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927196 | ||||||
| chr1:204927308
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-90-16918A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927308 | ||||||
| chr1:204927362
|
C | G | 1 | a0001c0001t0002g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-90-16864C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927362 | ||||||
| chr1:204927486
|
G | C | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-16740G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927486 | ||||||
| chr1:204927711
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-90-16515C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927711 | ||||||
| chr1:204927737
|
A | G | 1 | a0001c0001t0010g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-90-16489A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927737 | ||||||
| chr1:204927810
|
G | A | 19 | a0001c0001t0007g0032a0001c0001t0009g0110a0001c0001t0010g0029others(16): Show | 19 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-90-16416G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927810 | ||||||
| chr1:204927970
|
G | A | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-90-16256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204927970 | ||||||
| chr1:204928001
|
G | C | 4 | a0001c0002t0003g0201a0001c0002t0004g0034a0001c0003t0010g0040others(1): Show | 4 | HG02258.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-16225G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928001 | ||||||
| chr1:204928206
|
G | A | 6 | a0001c0001t0007g0048a0001c0002t0017g0215a0001c0005t0010g0213others(3): Show | 6 | HG01192.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-16020G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928206 | ||||||
| chr1:204928294
|
G | T | 1 | a0001c0003t0007g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-90-15932G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928294 | ||||||
| chr1:204928444
|
G | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(82): Show | 88 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-90-15782G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928444 | ||||||
| chr1:204928518
|
G | A | 3 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0037g0225 | 3 | HG02451.hp1 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-90-15708G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928518 | ||||||
| chr1:204928620
|
G | A | 1 | a0001c0002t0002g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-90-15606G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928620 | ||||||
| chr1:204928902
|
G | A | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-15324G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204928902 | ||||||
| chr1:204929002
|
A | G | 3 | a0001c0003t0001g0071a0001c0004t0001g0051a0001c0004t0001g0053 | 3 | HG01123.hp2 HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-90-15224A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204929002 | ||||||
| chr1:204929129
|
G | T | 3 | a0001c0002t0003g0227a0001c0002t0009g0255a0007c0019t0001g0229 | 3 | HG01175.hp1 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-90-15097G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204929129 | ||||||
| chr1:204929295
|
C | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-14931C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204929295 | ||||||
| chr1:204929715
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-90-14511C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204929715 | ||||||
| chr1:204929919
|
G | A | 3 | a0001c0003t0003g0035a0001c0003t0003g0036a0001c0003t0037g0225 | 3 | HG02451.hp1 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-90-14307G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204929919 | ||||||
| chr1:204929956
|
C | T | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-90-14270C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204929956 | ||||||
| chr1:204930016
|
A | G | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-14210A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930016 | ||||||
| chr1:204930018
|
G | A | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-90-14208G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930018 | ||||||
| chr1:204930187
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-90-14039T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930187 | ||||||
| chr1:204930308
|
C | T | 1 | a0002c0013t0011g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-90-13918C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930308 | ||||||
| chr1:204930513
|
G | A | 1 | a0001c0003t0037g0225 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-90-13713G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930513 | ||||||
| chr1:204930650
|
G | A | 7 | a0001c0002t0003g0201a0001c0002t0005g0254a0001c0002t0008g0252others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90-13576G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930650 | ||||||
| chr1:204930757
|
A | C | 2 | a0001c0001t0001g0195a0001c0001t0041g0194 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-90-13469A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930757 | ||||||
| chr1:204930789
|
C | T | 25 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.-90-13437C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930789 | ||||||
| chr1:204930829
|
A | G | 2 | a0001c0002t0021g0219a0001c0014t0004g0228 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-90-13397A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204930829 | ||||||
| chr1:204931085
|
A | G | 13 | a0001c0001t0010g0029a0001c0002t0005g0140a0001c0002t0009g0037others(10): Show | 13 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90-13141A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204931085 | ||||||
| chr1:204931218
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-90-13008G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204931218 | ||||||
| chr1:204931374
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-90-12852C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204931374 | ||||||
| chr1:204931655
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-90-12571C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204931655 | ||||||
| chr1:204931882
|
A | G | 1 | a0001c0001t0027g0087 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-90-12344A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204931882 | ||||||
| chr1:204931927
|
A | G | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90-12299A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204931927 | ||||||
| chr1:204932060
|
T | C | 3 | a0001c0002t0009g0255a0001c0005t0003g0218a0001c0022t0031g0136 | 3 | HG02717.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-90-12166T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932060 | ||||||
| chr1:204932113
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-90-12113G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932113 | ||||||
| chr1:204932154
|
C | T | 2 | a0001c0001t0015g0232a0001c0002t0004g0214 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-90-12072C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932154 | ||||||
| chr1:204932280
|
A | G | 30 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(27): Show | 30 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-90-11946A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932280 | ||||||
| chr1:204932489
|
T | A | 5 | a0001c0002t0009g0255a0001c0005t0003g0218a0002c0013t0001g0084others(2): Show | 5 | HG01433.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-11737T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932489 | ||||||
| chr1:204932519
|
A | T | 1 | a0001c0006t0003g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-90-11707A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932519 | ||||||
| chr1:204932564
|
G | C | 1 | a0001c0002t0021g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-90-11662G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204932564 | ||||||
| chr1:204933196
|
G | A | 3 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG02258.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-90-11030G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204933196 | ||||||
| chr1:204933233
|
C | G | 2 | a0001c0002t0009g0255a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-90-10993C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204933233 | ||||||
| chr1:204933298
|
G | C | 33 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(30): Show | 33 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-90-10928G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204933298 | ||||||
| chr1:204933473
|
A | G | 65 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0075others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-90-10753A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204933473 | ||||||
| chr1:204933789
|
T | A | 1 | a0001c0005t0003g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-90-10437T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204933789 | ||||||
| chr1:204933906
|
C | T | 1 | a0001c0002t0020g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-90-10320C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204933906 | ||||||
| chr1:204934069
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(7): Show | 11 | HG00738.hp2 HG01074.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90-10157C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934069 | ||||||
| chr1:204934132
|
C | T | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-90-10094C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934132 | ||||||
| chr1:204934137
|
C | CA | 46 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0075others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.-90-10072dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204934137 | |||||
| chr1:204934137
|
C | CAA | 82 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0109others(79): Show | 84 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-90-10073_-90-1007 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204934137 | |||||
| chr1:204934294
|
G | T | 23 | a0001c0001t0002g0081a0001c0001t0028g0183a0001c0001t0040g0019others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-90-9932G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934294 | ||||||
| chr1:204934487
|
G | A | 1 | a0001c0010t0025g0049 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-90-9739G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934487 | ||||||
| chr1:204934695
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.-90-9531A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934695 | ||||||
| chr1:204934715
|
C | G | 2 | a0001c0002t0009g0255a0001c0005t0003g0218 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-90-9511C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934715 | ||||||
| chr1:204934746
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-90-9480C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934746 | ||||||
| chr1:204934757
|
G | T | 1 | a0001c0014t0004g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-90-9469G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934757 | ||||||
| chr1:204934775
|
G | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-9451G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934775 | ||||||
| chr1:204934830
|
T | C | 27 | a0001c0001t0001g0109a0001c0001t0028g0183a0001c0001t0040g0019others(24): Show | 27 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-90-9396T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934830 | ||||||
| chr1:204934947
|
T | C | 4 | a0001c0002t0008g0240a0001c0002t0009g0255a0001c0005t0003g0218others(1): Show | 4 | HG02717.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-9279T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204934947 | ||||||
| chr1:204935208
|
A | G | 4 | a0001c0002t0009g0037a0001c0002t0009g0242a0001c0003t0003g0138others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-9018A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935208 | ||||||
| chr1:204935253
|
G | A | 1 | a0001c0003t0004g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-90-8973G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935253 | ||||||
| chr1:204935399
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(60): Show | 65 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-90-8827T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935399 | ||||||
| chr1:204935489
|
C | T | 6 | a0001c0001t0001g0193a0001c0002t0001g0168a0001c0002t0002g0115others(3): Show | 6 | HG00673.hp1 HG00673.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-8737C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935489 | ||||||
| chr1:204935575
|
T | C | 14 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0002t0001g0206others(11): Show | 14 | HG01192.hp1 HG02132.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-90-8651T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935575 | ||||||
| chr1:204935707
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(78): Show | 83 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-90-8519G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935707 | ||||||
| chr1:204935877
|
G | A | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-8349G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935877 | ||||||
| chr1:204935892
|
T | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0109others(87): Show | 92 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-90-8334T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204935892 | ||||||
| chr1:204936036
|
G | A | 4 | a0001c0001t0001g0257a0001c0001t0006g0258a0001c0001t0020g0085others(1): Show | 4 | NA18612.hp2 NA18990.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-8190G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936036 | ||||||
| chr1:204936063
|
G | C | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-8163G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936063 | ||||||
| chr1:204936141
|
G | A | 1 | a0001c0001t0014g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-90-8085G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936141 | ||||||
| chr1:204936180
|
TTCCC | T | 15 | a0001c0001t0010g0029a0001c0002t0003g0175a0001c0002t0003g0236others(12): Show | 15 | HG01175.hp1 HG01496.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90-8043_-90-8040d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936180 | |||||
| chr1:204936183
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-90-8043C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936183 | ||||||
| chr1:204936192
|
C | T | 140 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0061others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-90-8034C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936192 | ||||||
| chr1:204936196
|
TTC | T | 5 | a0001c0001t0001g0124a0001c0001t0001g0165a0001c0001t0025g0088others(2): Show | 5 | HG00323.hp2 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-8028_-90-8027d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936196 | |||||
| chr1:204936197
|
TC | T | 124 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0061others(121): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-90-8028delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936197 | ||||||
| chr1:204936198
|
C | CTTT | 54 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(51): Show | 56 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-90-8025_-90-8023d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936198 | |||||
| chr1:204936198
|
C | CTTTT | 6 | a0001c0001t0001g0223a0001c0002t0001g0190a0001c0002t0001g0233others(3): Show | 6 | HG00544.hp1 HG01109.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-8026_-90-8023d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936198 | |||||
| chr1:204936198
|
C | T | 11 | a0001c0001t0001g0122a0001c0001t0001g0191a0001c0001t0001g0192others(8): Show | 11 | HG00099.hp1 HG01123.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90-8028C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936198 | ||||||
| chr1:204936201
|
TTTC | T | 13 | a0001c0001t0010g0029a0001c0002t0003g0175a0001c0002t0008g0043others(10): Show | 13 | HG01175.hp1 HG01496.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-90-8022_-90-8020d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936201 | |||||
| chr1:204936202
|
TTC | T | 9 | a0001c0001t0007g0048a0001c0002t0003g0201a0001c0002t0004g0034others(6): Show | 9 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-90-8022_-90-8021d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936202 | |||||
| chr1:204936203
|
TC | T | 6 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0003t0035g0220others(3): Show | 6 | HG01433.hp2 HG02132.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90-8022delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936203 | ||||||
| chr1:204936204
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-90-8022C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936204 | ||||||
| chr1:204936204
|
CT | C | 5 | a0001c0005t0007g0248a0001c0005t0013g0006a0001c0005t0019g0211others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-8007delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936204 | |||||
| chr1:204936258
|
G | A | 2 | a0001c0001t0015g0232a0001c0002t0004g0214 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-90-7968G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936258 | ||||||
| chr1:204936327
|
G | A | 26 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0001t0010g0029others(23): Show | 26 | HG01175.hp1 HG01192.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.-90-7899G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936327 | ||||||
| chr1:204936342
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-90-7884C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936342 | ||||||
| chr1:204936391
|
G | A | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-7835G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936391 | ||||||
| chr1:204936418
|
C | T | 56 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(53): Show | 56 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.-90-7808C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936418 | ||||||
| chr1:204936475
|
T | C | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-7751T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936475 | ||||||
| chr1:204936689
|
C | T | 2 | a0001c0003t0001g0137a0003c0026t0003g0177 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-90-7537C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936689 | ||||||
| chr1:204936716
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-7510T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936716 | ||||||
| chr1:204936780
|
A | G | 48 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(45): Show | 48 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.-90-7446A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936780 | ||||||
| chr1:204936792
|
G | A | 47 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(44): Show | 47 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-90-7434G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936792 | ||||||
| chr1:204936866
|
ACT | A | 3 | a0001c0002t0003g0175a0001c0020t0016g0152a0007c0019t0001g0229 | 3 | HG01175.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-90-7351_-90-7350d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204936866 | |||||
| chr1:204936868
|
T | G | 2 | a0001c0005t0019g0211a0001c0005t0019g0212 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-90-7358T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936868 | ||||||
| chr1:204936906
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-90-7320C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936906 | ||||||
| chr1:204936925
|
A | G | 45 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(42): Show | 45 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-90-7301A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204936925 | ||||||
| chr1:204937047
|
T | TA | 54 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(51): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-90-7178dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204937047 | |||||
| chr1:204937071
|
G | T | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-7155G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937071 | ||||||
| chr1:204937106
|
G | A | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-7120G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937106 | ||||||
| chr1:204937153
|
T | TAAA | 53 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0001t0010g0029others(50): Show | 53 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.-90-7064_-90-7062d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204937153 | |||||
| chr1:204937170
|
C | G | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-7056C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937170 | ||||||
| chr1:204937208
|
T | A | 1 | a0001c0001t0002g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-90-7018T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937208 | ||||||
| chr1:204937268
|
C | A | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6958C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937268 | ||||||
| chr1:204937371
|
T | C | 47 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(44): Show | 47 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-90-6855T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937371 | ||||||
| chr1:204937385
|
A | G | 43 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(40): Show | 43 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-90-6841A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937385 | ||||||
| chr1:204937466
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6760T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937466 | ||||||
| chr1:204937472
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6754T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937472 | ||||||
| chr1:204937486
|
C | T | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6740C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937486 | ||||||
| chr1:204937501
|
G | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6725G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937501 | ||||||
| chr1:204937538
|
G | C | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-6688G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937538 | ||||||
| chr1:204937604
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6622T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937604 | ||||||
| chr1:204937688
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6538T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937688 | ||||||
| chr1:204937700
|
G | A | 1 | a0001c0017t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-90-6526G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937700 | ||||||
| chr1:204937759
|
C | T | 1 | a0001c0002t0004g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-90-6467C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937759 | ||||||
| chr1:204937794
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6432T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937794 | ||||||
| chr1:204937811
|
G | T | 32 | a0001c0001t0001g0109a0001c0001t0028g0183a0001c0001t0040g0019others(29): Show | 32 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-90-6415G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937811 | ||||||
| chr1:204937818
|
A | G | 15 | a0001c0001t0010g0029a0001c0002t0003g0175a0001c0002t0003g0236others(12): Show | 15 | HG01175.hp1 HG01496.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90-6408A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937818 | ||||||
| chr1:204937826
|
A | G | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-90-6400A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937826 | ||||||
| chr1:204937869
|
A | G | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6357A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937869 | ||||||
| chr1:204937915
|
A | G | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6311A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937915 | ||||||
| chr1:204937946
|
C | G | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-6280C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204937946 | ||||||
| chr1:204938121
|
G | A | 1 | a0001c0001t0029g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-90-6105G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938121 | ||||||
| chr1:204938173
|
G | A | 3 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG02258.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-90-6053G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938173 | ||||||
| chr1:204938185
|
C | G | 58 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0001t0010g0029others(55): Show | 58 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.-90-6041C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938185 | ||||||
| chr1:204938195
|
A | T | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-90-6031A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938195 | ||||||
| chr1:204938263
|
G | A | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-5963G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938263 | ||||||
| chr1:204938466
|
A | G | 1 | a0001c0007t0026g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90-5760A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938466 | ||||||
| chr1:204938533
|
C | G | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-5693C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938533 | ||||||
| chr1:204938554
|
A | G | 47 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(44): Show | 47 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-90-5672A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938554 | ||||||
| chr1:204938561
|
A | T | 28 | a0001c0001t0001g0109a0001c0001t0028g0183a0001c0001t0040g0019others(25): Show | 28 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-90-5665A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938561 | ||||||
| chr1:204938655
|
C | A | 11 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0002t0001g0206others(8): Show | 11 | HG01192.hp1 HG02132.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90-5571C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938655 | ||||||
| chr1:204938656
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0109others(117): Show | 122 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.-90-5570A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938656 | ||||||
| chr1:204938688
|
G | A | 4 | a0001c0001t0010g0029a0001c0003t0003g0035a0001c0003t0003g0036others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-5538G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938688 | ||||||
| chr1:204938768
|
C | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-90-5458C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938768 | ||||||
| chr1:204938837
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-90-5389A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938837 | ||||||
| chr1:204938844
|
T | A | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-5382T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938844 | ||||||
| chr1:204938862
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-5364T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204938862 | ||||||
| chr1:204939033
|
G | GATGT | 17 | a0001c0001t0001g0109a0001c0001t0040g0019a0001c0001t0045g0072others(14): Show | 17 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-90-5190_-90-5189i others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939033 | |||||
| chr1:204939037
|
G | T | 44 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(41): Show | 44 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-90-5189G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939037 | ||||||
| chr1:204939038
|
A | ATG | 28 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.-90-5140_-90-5139d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGGATG | 5 | a0001c0001t0001g0001a0001c0001t0002g0028a0001c0001t0010g0027others(2): Show | 6 | HG00738.hp2 HG01074.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-5186_-90-5185i others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGGATGT others(1): Show |
4 | a0001c0001t0002g0080a0001c0001t0012g0099a0001c0002t0048g0239others(1): Show | 4 | HG01109.hp2 HG02738.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-5186_-90-5185i others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATG | 16 | a0001c0001t0003g0045a0001c0001t0010g0029a0001c0002t0001g0023others(13): Show | 16 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(1): Show |
25 | a0001c0001t0001g0158a0001c0001t0001g0223a0001c0001t0002g0101others(22): Show | 25 | HG00741.hp2 HG01074.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(3): Show |
9 | a0001c0002t0001g0050a0001c0002t0001g0209a0001c0002t0001g0234others(6): Show | 10 | HG00544.hp1 HG00741.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(5): Show |
3 | a0001c0002t0001g0107a0001c0002t0002g0055a0001c0002t0012g0125 | 3 | HG01099.hp1 HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTATGT others(7): Show |
1 | a0001c0002t0001g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-90-5185_-90-5184i others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTG | 30 | a0001c0001t0001g0075a0001c0001t0001g0082a0001c0001t0001g0086others(27): Show | 30 | HG00544.hp2 HG00735.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-90-5142_-90-5139d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTG | 20 | a0001c0001t0001g0061a0001c0001t0001g0160a0001c0001t0001g0180others(17): Show | 20 | HG01071.hp2 HG01358.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-90-5144_-90-5139d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(1): Show |
13 | a0001c0001t0001g0104a0001c0001t0001g0113a0001c0001t0001g0165others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90-5146_-90-5139d others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0069a0001c0002t0004g0216a0001c0002t0008g0221others(1): Show | 4 | HG03139.hp1 NA18974.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90-5148_-90-5139d others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0013g0065a0001c0005t0052g0033 | 2 | HG00280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-90-5150_-90-5139d others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0124a0001c0003t0001g0137 | 2 | HG00323.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-90-5152_-90-5139d others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
ATG | A | 17 | a0001c0001t0001g0100a0001c0001t0002g0081a0001c0001t0002g0249others(14): Show | 17 | HG00099.hp2 HG01099.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90-5140_-90-5139d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939038
|
ATGTG | A | 8 | a0001c0002t0043g0182a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90-5142_-90-5139d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939038 | |||||
| chr1:204939040
|
G | A | 2 | a0001c0020t0016g0152a0004c0024t0001g0052 | 2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-90-5186G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939040 | ||||||
| chr1:204939040
|
G | GTA | 5 | a0001c0002t0003g0236a0001c0002t0008g0043a0001c0002t0022g0039others(2): Show | 5 | HG02451.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-5185_-90-5184i others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204939040 | |||||
| chr1:204939042
|
G | A | 9 | a0001c0001t0028g0183a0001c0002t0009g0037a0001c0002t0009g0242others(6): Show | 9 | HG01175.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-90-5184G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939042 | ||||||
| chr1:204939044
|
G | A | 2 | a0001c0020t0016g0152a0004c0024t0001g0052 | 2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-90-5182G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939044 | ||||||
| chr1:204939288
|
A | G | 47 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(44): Show | 47 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-90-4938A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939288 | ||||||
| chr1:204939507
|
T | C | 1 | a0001c0002t0013g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-90-4719T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939507 | ||||||
| chr1:204939741
|
G | A | 12 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0002t0001g0206others(9): Show | 12 | HG01192.hp1 HG02132.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90-4485G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939741 | ||||||
| chr1:204939832
|
T | C | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-4394T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939832 | ||||||
| chr1:204939930
|
T | C | 59 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-90-4296T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204939930 | ||||||
| chr1:204940028
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-90-4198G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940028 | ||||||
| chr1:204940139
|
A | G | 8 | a0001c0001t0015g0025a0001c0002t0002g0007a0001c0002t0002g0008others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-4087A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940139 | ||||||
| chr1:204940180
|
C | T | 1 | a0001c0006t0003g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-90-4046C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940180 | ||||||
| chr1:204940218
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(56): Show | 61 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-90-4008C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940218 | ||||||
| chr1:204940435
|
A | G | 2 | a0001c0011t0015g0176a0001c0011t0030g0015 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-90-3791A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940435 | ||||||
| chr1:204940580
|
G | A | 46 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(43): Show | 46 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.-90-3646G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940580 | ||||||
| chr1:204940588
|
CCTT | C | 46 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(43): Show | 46 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.-90-3635_-90-3633d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204940588 | |||||
| chr1:204940601
|
C | T | 46 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(43): Show | 46 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.-90-3625C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940601 | ||||||
| chr1:204940642
|
A | T | 2 | a0001c0002t0002g0055a0001c0002t0002g0151 | 2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-90-3584A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940642 | ||||||
| chr1:204940643
|
G | A | 67 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(64): Show | 67 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.-90-3583G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940643 | ||||||
| chr1:204940644
|
T | C | 43 | a0001c0001t0001g0109a0001c0001t0010g0029a0001c0001t0028g0183others(40): Show | 43 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-90-3582T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940644 | ||||||
| chr1:204940688
|
A | G | 8 | a0001c0001t0015g0025a0001c0002t0002g0007a0001c0002t0002g0008others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-3538A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940688 | ||||||
| chr1:204940898
|
G | A | 1 | a0001c0002t0039g0162 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-90-3328G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940898 | ||||||
| chr1:204940924
|
T | G | 1 | a0001c0002t0002g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-90-3302T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204940924 | ||||||
| chr1:204941228
|
T | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0109others(119): Show | 124 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-90-2998T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941228 | ||||||
| chr1:204941233
|
T | A | 32 | a0001c0001t0001g0109a0001c0001t0007g0048a0001c0001t0028g0183others(29): Show | 32 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-90-2993T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941233 | ||||||
| chr1:204941263
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-90-2963T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941263 | ||||||
| chr1:204941384
|
T | C | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90-2842T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941384 | ||||||
| chr1:204941448
|
A | G | 72 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0005g0139others(69): Show | 72 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.-90-2778A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941448 | ||||||
| chr1:204941473
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0224 | 2 | HG00733.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-90-2753A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941473 | ||||||
| chr1:204941560
|
T | C | 72 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0005g0139others(69): Show | 72 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.-90-2666T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941560 | ||||||
| chr1:204941688
|
G | T | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-90-2538G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941688 | ||||||
| chr1:204941779
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-90-2447A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204941779 | ||||||
| chr1:204942025
|
T | C | 1 | a0001c0003t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-90-2201T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942025 | ||||||
| chr1:204942096
|
G | A | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-90-2130G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942096 | ||||||
| chr1:204942203
|
G | C | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-90-2023G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942203 | ||||||
| chr1:204942378
|
A | C | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-90-1848A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942378 | ||||||
| chr1:204942660
|
GA | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(45): Show | 50 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90-1562delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 204942660 | |||||
| chr1:204942671
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(121): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-90-1555C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942671 | ||||||
| chr1:204942813
|
C | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0238 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-90-1413C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942813 | ||||||
| chr1:204942838
|
G | A | 2 | a0001c0010t0001g0091a0002c0025t0012g0148 | 2 | HG00741.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.-90-1388G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942838 | ||||||
| chr1:204942849
|
T | C | 7 | a0001c0002t0003g0236a0001c0002t0008g0043a0001c0002t0009g0037others(4): Show | 7 | HG02451.hp2 HG02622.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90-1377T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942849 | ||||||
| chr1:204942966
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-90-1260C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942966 | ||||||
| chr1:204942972
|
C | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-90-1254C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204942972 | ||||||
| chr1:204943278
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-90-948G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943278 | ||||||
| chr1:204943439
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(184): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-90-787C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943439 | ||||||
| chr1:204943497
|
C | G | 1 | a0001c0002t0002g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-90-729C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943497 | ||||||
| chr1:204943637
|
A | C | 66 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-90-589A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943637 | ||||||
| chr1:204943691
|
C | T | 6 | a0001c0002t0003g0236a0001c0002t0008g0043a0001c0002t0009g0242others(3): Show | 6 | HG02451.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-535C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943691 | ||||||
| chr1:204943700
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(55): Show | 60 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-90-526C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943700 | ||||||
| chr1:204943715
|
G | A | 66 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-90-511G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943715 | ||||||
| chr1:204943973
|
G | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(49): Show | 54 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-90-253G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204943973 | ||||||
| chr1:204944118
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0002g0083 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-90-108T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204944118 | ||||||
| chr1:204944143
|
C | G | 91 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(88): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-90-83C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204944143 | ||||||
| chr1:204944460
|
T | G | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+54T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944460 | ||||||
| chr1:204944508
|
T | G | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+102T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944508 | ||||||
| chr1:204944524
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(184): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.91+118A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944524 | ||||||
| chr1:204944624
|
G | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0109others(86): Show | 91 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.91+218G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944624 | ||||||
| chr1:204944666
|
G | A | 4 | a0001c0001t0010g0029a0001c0003t0003g0035a0001c0003t0003g0036others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+260G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944666 | ||||||
| chr1:204944678
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+272G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944678 | ||||||
| chr1:204944754
|
C | T | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+348C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944754 | ||||||
| chr1:204944833
|
C | A | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.91+427C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944833 | ||||||
| chr1:204944867
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0002g0062a0001c0016t0002g0067 | 3 | HG00099.hp1 HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.91+461A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944867 | ||||||
| chr1:204945037
|
T | G | 4 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0002t0048g0239others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+631T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945037 | ||||||
| chr1:204945074
|
C | CA | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.91+669dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204945074 | |||||
| chr1:204945144
|
G | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91+738G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945144 | ||||||
| chr1:204945391
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.91+985T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945391 | ||||||
| chr1:204945514
|
GCTGCCC | G | 79 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.91+1116_91+1121del others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204945514 | |||||
| chr1:204945565
|
T | G | 3 | a0001c0004t0001g0051a0001c0004t0001g0053a0001c0004t0001g0078 | 3 | HG00099.hp2 HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.91+1159T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945565 | ||||||
| chr1:204945638
|
C | T | 1 | a0001c0003t0006g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.91+1232C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945638 | ||||||
| chr1:204945690
|
C | T | 3 | a0001c0006t0003g0260a0001c0020t0016g0152a0007c0019t0001g0229 | 3 | HG01175.hp1 HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.91+1284C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945690 | ||||||
| chr1:204945916
|
C | T | 1 | a0001c0002t0022g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+1510C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945916 | ||||||
| chr1:204945964
|
G | A | 9 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(6): Show | 9 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+1558G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204945964 | ||||||
| chr1:204946219
|
G | A | 1 | a0001c0001t0042g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.91+1813G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946219 | ||||||
| chr1:204946265
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.91+1859A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946265 | ||||||
| chr1:204946365
|
G | A | 9 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(6): Show | 9 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+1959G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946365 | ||||||
| chr1:204946513
|
A | G | 2 | a0001c0001t0007g0032a0001c0002t0002g0031 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.91+2107A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946513 | ||||||
| chr1:204946530
|
C | A | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.91+2124C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946530 | ||||||
| chr1:204946620
|
T | A | 1 | a0001c0005t0019g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+2214T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946620 | ||||||
| chr1:204946629
|
G | A | 29 | a0001c0001t0001g0109a0001c0001t0007g0048a0001c0001t0028g0183others(26): Show | 29 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.91+2223G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946629 | ||||||
| chr1:204946717
|
A | G | 4 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0002t0048g0239others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+2311A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946717 | ||||||
| chr1:204946776
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.91+2370A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946776 | ||||||
| chr1:204946792
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.91+2386T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946792 | ||||||
| chr1:204946811
|
T | C | 67 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(64): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.91+2405T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946811 | ||||||
| chr1:204946813
|
C | T | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91+2407C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946813 | ||||||
| chr1:204946823
|
C | G | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+2417C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946823 | ||||||
| chr1:204946969
|
A | G | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91+2563A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946969 | ||||||
| chr1:204947010
|
G | C | 1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+2604G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947010 | ||||||
| chr1:204947111
|
G | A | 7 | a0001c0002t0003g0236a0001c0002t0008g0043a0001c0002t0009g0037others(4): Show | 7 | HG02451.hp2 HG02622.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+2705G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947111 | ||||||
| chr1:204947179
|
G | T | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+2773G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947179 | ||||||
| chr1:204947331
|
A | G | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+2925A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947331 | ||||||
| chr1:204947397
|
G | A | 10 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+2991G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947397 | ||||||
| chr1:204947398
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.91+2992T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947398 | ||||||
| chr1:204947460
|
C | T | 6 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0009g0255others(3): Show | 6 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+3054C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947460 | ||||||
| chr1:204947461
|
G | T | 6 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+3055G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947461 | ||||||
| chr1:204947472
|
C | T | 10 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+3066C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947472 | ||||||
| chr1:204947546
|
C | T | 1 | a0001c0001t0006g0247 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.91+3140C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947546 | ||||||
| chr1:204947599
|
C | A | 1 | a0001c0002t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.91+3193C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947599 | ||||||
| chr1:204947644
|
C | A | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.91+3238C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947644 | ||||||
| chr1:204947690
|
G | A | 2 | a0001c0001t0015g0232a0001c0002t0004g0214 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.91+3284G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947690 | ||||||
| chr1:204947844
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(57): Show | 62 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.91+3438A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947844 | ||||||
| chr1:204947980
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.91+3574G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947980 | ||||||
| chr1:204948013
|
T | C | 1 | a0001c0002t0009g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.91+3607T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948013 | ||||||
| chr1:204948143
|
G | A | 89 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0075others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.91+3737G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948143 | ||||||
| chr1:204948220
|
A | G | 5 | a0001c0002t0005g0254a0001c0002t0008g0252a0001c0002t0008g0253others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-3791A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948220 | ||||||
| chr1:204948298
|
T | C | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.92-3713T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948298 | ||||||
| chr1:204948452
|
T | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(8): Show | 12 | HG00738.hp2 HG01074.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-3559T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948452 | ||||||
| chr1:204948552
|
C | T | 60 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.92-3459C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948552 | ||||||
| chr1:204948571
|
G | A | 11 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0002t0003g0175others(8): Show | 11 | HG02132.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-3440G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948571 | ||||||
| chr1:204948572
|
G | T | 11 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0002t0003g0175others(8): Show | 11 | HG02132.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-3439G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948572 | ||||||
| chr1:204948580
|
AAAAAC | A | 23 | a0001c0001t0001g0109a0001c0001t0015g0025a0001c0001t0028g0183others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.92-3411_92-3407del others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204948580 | |||||
| chr1:204948781
|
T | C | 41 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0010g0029others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.92-3230T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204948781 | ||||||
| chr1:204949072
|
G | T | 1 | a0002c0025t0012g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92-2939G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949072 | ||||||
| chr1:204949199
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-2812G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949199 | ||||||
| chr1:204949206
|
C | T | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.92-2805C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949206 | ||||||
| chr1:204949417
|
G | A | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.92-2594G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949417 | ||||||
| chr1:204949631
|
G | C | 10 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-2380G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949631 | ||||||
| chr1:204949942
|
T | C | 52 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0010g0029others(49): Show | 52 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.92-2069T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949942 | ||||||
| chr1:204949968
|
T | A | 1 | a0001c0001t0002g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.92-2043T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204949968 | ||||||
| chr1:204950104
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.92-1907G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950104 | ||||||
| chr1:204950271
|
A | G | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.92-1740A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950271 | ||||||
| chr1:204950282
|
A | G | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-1729A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950282 | ||||||
| chr1:204950328
|
G | A | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.92-1683G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950328 | ||||||
| chr1:204950335
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.92-1676G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950335 | ||||||
| chr1:204950366
|
C | T | 23 | a0001c0001t0001g0109a0001c0001t0015g0025a0001c0001t0028g0183others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.92-1645C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950366 | ||||||
| chr1:204950624
|
A | G | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-1387A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950624 | ||||||
| chr1:204950824
|
GT | G | 4 | a0001c0001t0010g0029a0001c0003t0003g0035a0001c0003t0003g0036others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-1184delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204950824 | |||||
| chr1:204950879
|
G | A | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-1132G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950879 | ||||||
| chr1:204950991
|
A | G | 24 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(21): Show | 25 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.92-1020A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204950991 | ||||||
| chr1:204951083
|
G | A | 10 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-928G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951083 | ||||||
| chr1:204951150
|
A | AT | 13 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0257others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-842dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951150
|
A | ATT | 37 | a0001c0001t0001g0001a0001c0001t0001g0158a0001c0001t0001g0223others(34): Show | 39 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.92-843_92-842dupTT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951150
|
A | ATTT | 5 | a0001c0001t0001g0058a0001c0002t0001g0060a0001c0002t0001g0142others(2): Show | 5 | HG01175.hp2 HG01346.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-844_92-842dupTT others(1): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951150
|
AT | A | 47 | a0001c0001t0001g0109a0001c0001t0001g0117a0001c0001t0002g0081others(44): Show | 47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.92-842delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951150 | |||||
| chr1:204951194
|
G | C | 62 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.92-817G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951194 | ||||||
| chr1:204951315
|
A | AT | 9 | a0001c0001t0001g0126a0001c0001t0001g0165a0001c0001t0001g0180others(6): Show | 9 | HG00544.hp2 HG01192.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-674dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951315 | |||||
| chr1:204951315
|
AT | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(57): Show | 62 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.92-674delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951315 | |||||
| chr1:204951315
|
ATT | A | 47 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0010g0029others(44): Show | 47 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.92-675_92-674delTT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951315 | |||||
| chr1:204951355
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0041g0194 | 2 | HG02132.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.92-656G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951355 | ||||||
| chr1:204951369
|
G | C | 10 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-642G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951369 | ||||||
| chr1:204951470
|
AT | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(60): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.92-525delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 204951470 | |||||
| chr1:204951471
|
T | TA | 4 | a0001c0001t0010g0029a0001c0003t0003g0035a0001c0003t0003g0036others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-540_92-539insA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951471 | ||||||
| chr1:204951472
|
T | A | 10 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0002t0003g0236others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-539T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951472 | ||||||
| chr1:204951486
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0109others(95): Show | 100 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.92-525T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951486 | ||||||
| chr1:204951486
|
T | TG | 10 | a0001c0001t0007g0048a0001c0002t0005g0140a0001c0003t0010g0040others(7): Show | 10 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-525_92-524insG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951486 | ||||||
| chr1:204951487
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.92-524A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951487 | ||||||
| chr1:204951507
|
C | T | 6 | a0001c0002t0001g0013a0001c0003t0001g0119a0001c0003t0001g0127others(3): Show | 6 | HG00741.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-504C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951507 | ||||||
| chr1:204951564
|
G | A | 3 | a0001c0002t0009g0242a0001c0003t0003g0138a0001c0003t0024g0222 | 3 | HG02622.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.92-447G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951564 | ||||||
| chr1:204951587
|
G | A | 6 | a0001c0005t0003g0243a0001c0005t0007g0248a0001c0005t0013g0006others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-424G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951587 | ||||||
| chr1:204951593
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(53): Show | 58 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.92-418C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951593 | ||||||
| chr1:204951626
|
G | A | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-385G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951626 | ||||||
| chr1:204951641
|
T | G | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-370T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951641 | ||||||
| chr1:204951645
|
T | G | 1 | a0001c0001t0006g0024 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.92-366T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951645 | ||||||
| chr1:204951678
|
C | T | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-333C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951678 | ||||||
| chr1:204951705
|
G | A | 7 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(4): Show | 7 | HG01192.hp1 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-306G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951705 | ||||||
| chr1:204951711
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(53): Show | 58 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.92-300G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951711 | ||||||
| chr1:204951761
|
G | A | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.92-250G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951761 | ||||||
| chr1:204951814
|
G | A | 6 | a0001c0005t0003g0243a0001c0005t0007g0248a0001c0005t0013g0006others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-197G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204951814 | ||||||
| chr1:204952130
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(44): Show | 49 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.197+14A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952130 | ||||||
| chr1:204952154
|
G | A | 10 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0002t0003g0236others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.197+38G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952154 | ||||||
| chr1:204952184
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0224a0001c0017t0001g0167 | 3 | HG00733.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.197+68C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952184 | ||||||
| chr1:204952403
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(68): Show | 73 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.197+287T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952403 | ||||||
| chr1:204952457
|
TC | T | 38 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0010g0029others(35): Show | 38 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+342delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952457 | ||||||
| chr1:204952561
|
T | C | 1 | a0001c0002t0006g0129 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.197+445T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952561 | ||||||
| chr1:204952578
|
G | A | 3 | a0002c0013t0001g0084a0002c0013t0011g0185a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.197+462G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952578 | ||||||
| chr1:204952635
|
A | AG | 10 | a0001c0001t0049g0197a0001c0002t0001g0013a0001c0002t0002g0047others(7): Show | 10 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.197+523dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 204952635 | |||||
| chr1:204952670
|
G | T | 6 | a0001c0002t0003g0236a0001c0002t0008g0043a0001c0002t0009g0242others(3): Show | 6 | HG02451.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+554G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952670 | ||||||
| chr1:204952681
|
G | A | 46 | a0001c0001t0001g0109a0001c0001t0002g0081a0001c0001t0007g0048others(43): Show | 46 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.197+565G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952681 | ||||||
| chr1:204952699
|
C | T | 10 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0002t0003g0236others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.197+583C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952699 | ||||||
| chr1:204952744
|
G | A | 3 | a0001c0002t0001g0013a0001c0002t0004g0034a0001c0005t0052g0033 | 3 | HG02280.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+628G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204952744 | ||||||
| chr1:204953000
|
T | A | 10 | a0001c0001t0002g0081a0001c0002t0001g0206a0001c0002t0003g0236others(7): Show | 10 | HG02132.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.197+884T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953000 | ||||||
| chr1:204953158
|
T | C | 4 | a0001c0001t0005g0139a0001c0002t0043g0182a0001c0002t0048g0239others(1): Show | 4 | HG01109.hp2 HG01433.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1030T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953158 | ||||||
| chr1:204953286
|
T | G | 3 | a0001c0002t0002g0047a0001c0002t0002g0238a0001c0002t0004g0216 | 3 | HG02572.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.198-902T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953286 | ||||||
| chr1:204953286
|
T | TTTTG | 9 | a0001c0001t0049g0197a0001c0003t0007g0012a0001c0003t0007g0181others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-886_198-883dup others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 204953286 | |||||
| chr1:204953328
|
G | A | 14 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.198-860G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953328 | ||||||
| chr1:204953512
|
G | A | 1 | a0001c0002t0009g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-676G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953512 | ||||||
| chr1:204953575
|
C | T | 10 | a0001c0001t0007g0048a0001c0002t0005g0140a0001c0003t0010g0040others(7): Show | 10 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-613C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953575 | ||||||
| chr1:204953679
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198-509G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953679 | ||||||
| chr1:204953863
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0158others(41): Show | 46 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.198-325A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953863 | ||||||
| chr1:204953898
|
C | G | 43 | a0001c0001t0002g0081a0001c0001t0007g0048a0001c0001t0010g0029others(40): Show | 43 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.198-290C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204953898 | ||||||
| chr1:204954028
|
C | T | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.198-160C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204954028 | ||||||
| chr1:204954154
|
C | T | 4 | a0001c0002t0001g0013a0001c0011t0015g0176a0001c0011t0030g0015others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-34C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 3/27 | chr1 | 204954154 | ||||||
| chr1:204954431
|
G | A | 1 | a0001c0001t0036g0187 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.394+47G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 4/27 | chr1 | 204954431 | ||||||
| chr1:204954521
|
C | A | 13 | a0001c0001t0007g0048a0001c0002t0005g0140a0001c0003t0010g0040others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.394+137C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 4/27 | chr1 | 204954521 | ||||||
| chr1:204954602
|
G | A | 13 | a0001c0001t0007g0048a0001c0002t0005g0140a0001c0003t0010g0040others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.394+218G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 4/27 | chr1 | 204954602 | ||||||
| chr1:204954666
|
C | T | 3 | a0001c0011t0015g0176a0001c0011t0030g0015a0001c0014t0004g0228 | 3 | HG02055.hp1 HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.395-163C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 4/27 | chr1 | 204954666 | ||||||
| chr1:204954769
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.395-60C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 4/27 | chr1 | 204954769 | ||||||
| chr1:204955105
|
G | A | 4 | a0001c0002t0003g0175a0001c0006t0003g0260a0001c0020t0016g0152others(1): Show | 4 | HG01175.hp1 HG01496.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+154G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204955105 | ||||||
| chr1:204955134
|
C | A | 10 | a0001c0001t0007g0048a0001c0002t0005g0140a0001c0003t0010g0040others(7): Show | 10 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+183C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204955134 | ||||||
| chr1:204955162
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.517+211G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204955162 | ||||||
| chr1:204955366
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.517+415G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204955366 | ||||||
| chr1:204955557
|
G | A | 66 | a0001c0001t0001g0158a0001c0001t0002g0081a0001c0001t0002g0101others(63): Show | 68 | HG00323.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.517+606G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204955557 | ||||||
| chr1:204955659
|
GC | G | 16 | a0001c0001t0007g0048a0001c0002t0005g0140a0001c0003t0010g0040others(13): Show | 16 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+709delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204955659 | ||||||
| chr1:204956569
|
C | T | 1 | a0001c0001t0029g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.518-1087C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204956569 | ||||||
| chr1:204956805
|
G | A | 8 | a0001c0001t0007g0048a0001c0005t0003g0243a0001c0005t0007g0248others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-851G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204956805 | ||||||
| chr1:204956818
|
C | T | 57 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(54): Show | 57 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.518-838C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204956818 | ||||||
| chr1:204956907
|
G | GA | 41 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-739dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr1 | 204956907 | |||||
| chr1:204957176
|
A | G | 1 | a0001c0001t0042g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.518-480A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204957176 | ||||||
| chr1:204957195
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.518-461C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204957195 | ||||||
| chr1:204957245
|
A | G | 53 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(50): Show | 53 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.518-411A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204957245 | ||||||
| chr1:204957379
|
G | A | 3 | a0001c0002t0009g0242a0001c0003t0003g0138a0001c0003t0024g0222 | 3 | HG02622.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.518-277G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204957379 | ||||||
| chr1:204957555
|
C | T | 1 | a0001c0001t0025g0088 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.518-101C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204957555 | ||||||
| chr1:204957586
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.518-70G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 5/27 | chr1 | 204957586 | ||||||
| chr1:204957852
|
C | T | 53 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(50): Show | 53 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.688+26C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204957852 | ||||||
| chr1:204957870
|
A | C | 2 | a0001c0002t0003g0227a0001c0002t0047g0164 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.688+44A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204957870 | ||||||
| chr1:204957909
|
T | C | 4 | a0001c0001t0049g0197a0002c0013t0001g0084a0002c0013t0011g0185others(1): Show | 4 | HG01433.hp2 NA19002.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+83T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204957909 | ||||||
| chr1:204958008
|
A | G | 57 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(54): Show | 57 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.688+182A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958008 | ||||||
| chr1:204958046
|
C | T | 1 | a0001c0002t0009g0037 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.688+220C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958046 | ||||||
| chr1:204958290
|
A | G | 53 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(50): Show | 53 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.688+464A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958290 | ||||||
| chr1:204958309
|
T | C | 4 | a0001c0002t0001g0105a0001c0002t0001g0144a0001c0002t0001g0163others(1): Show | 4 | HG01257.hp1 HG01978.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+483T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958309 | ||||||
| chr1:204958320
|
A | G | 3 | a0001c0001t0049g0197a0002c0013t0001g0084a0002c0013t0011g0185 | 3 | NA19002.hp1 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.688+494A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958320 | ||||||
| chr1:204958475
|
C | T | 1 | a0001c0002t0006g0129 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.688+649C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958475 | ||||||
| chr1:204958774
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.688+948G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958774 | ||||||
| chr1:204958920
|
C | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.688+1094C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204958920 | ||||||
| chr1:204959027
|
A | G | 52 | a0001c0001t0001g0158a0001c0001t0002g0081a0001c0001t0002g0101others(49): Show | 54 | HG00323.hp1 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.688+1201A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959027 | ||||||
| chr1:204959061
|
G | GT | 88 | a0001c0001t0001g0158a0001c0001t0001g0198a0001c0001t0002g0081others(85): Show | 90 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.688+1246dupT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr1 | 204959061 | |||||
| chr1:204959148
|
T | C | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.688+1322T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959148 | ||||||
| chr1:204959150
|
C | G | 2 | a0001c0001t0025g0088a0001c0007t0016g0103 | 2 | HG01515.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.688+1324C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959150 | ||||||
| chr1:204959198
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.688+1372A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959198 | ||||||
| chr1:204959204
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.688+1378C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959204 | ||||||
| chr1:204959331
|
C | T | 78 | a0001c0001t0001g0158a0001c0001t0001g0198a0001c0001t0002g0081others(75): Show | 80 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.688+1505C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959331 | ||||||
| chr1:204959554
|
G | A | 28 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.688+1728G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959554 | ||||||
| chr1:204959577
|
G | T | 1 | a0001c0002t0008g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.688+1751G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959577 | ||||||
| chr1:204959580
|
C | T | 27 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0006g0024others(24): Show | 27 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.688+1754C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959580 | ||||||
| chr1:204959622
|
C | G | 3 | a0001c0002t0001g0050a0001c0002t0001g0107a0001c0002t0001g0261 | 3 | HG01106.hp2 HG01167.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.688+1796C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959622 | ||||||
| chr1:204959658
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.688+1832C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959658 | ||||||
| chr1:204959694
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.688+1868T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959694 | ||||||
| chr1:204959708
|
G | T | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.688+1882G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959708 | ||||||
| chr1:204960007
|
G | A | 65 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.689-2101G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204960007 | ||||||
| chr1:204960068
|
G | C | 63 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0075others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.689-2040G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204960068 | ||||||
| chr1:204960091
|
G | A | 2 | a0001c0002t0003g0175a0007c0019t0001g0229 | 2 | HG01175.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.689-2017G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204960091 | ||||||
| chr1:204960318
|
T | A | 2 | a0001c0001t0015g0232a0001c0002t0004g0214 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.689-1790T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204960318 | ||||||
| chr1:204960474
|
G | A | 1 | a0001c0001t0023g0143 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.689-1634G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204960474 | ||||||
| chr1:204961015
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0106others(105): Show | 111 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.689-1093T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961015 | ||||||
| chr1:204961147
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0165others(11): Show | 15 | HG00738.hp2 HG01074.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-961A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961147 | ||||||
| chr1:204961311
|
A | G | 1 | a0001c0017t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.689-797A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961311 | ||||||
| chr1:204961450
|
A | C | 1 | a0001c0002t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.689-658A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961450 | ||||||
| chr1:204961540
|
C | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0094others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.689-568C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961540 | ||||||
| chr1:204961776
|
C | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.689-332C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961776 | ||||||
| chr1:204961949
|
G | A | 26 | a0001c0001t0001g0198a0001c0001t0002g0131a0001c0001t0003g0045others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.689-159G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204961949 | ||||||
| chr1:204962002
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.689-106C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204962002 | ||||||
| chr1:204962009
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0165others(41): Show | 45 | HG00738.hp2 HG01074.hp2 HG02004.hp2 others(42): Show |
intron_variant | MODIFIER | c.689-99A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204962009 | ||||||
| chr1:204962263
|
C | T | 4 | a0001c0002t0043g0182a0001c0002t0048g0239a0001c0003t0003g0035others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+105C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962263 | ||||||
| chr1:204962436
|
G | T | 1 | a0001c0001t0051g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.739+278G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962436 | ||||||
| chr1:204962478
|
A | G | 12 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(9): Show | 12 | HG01192.hp1 HG01433.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.739+320A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962478 | ||||||
| chr1:204962548
|
A | G | 1 | a0001c0001t0014g0098 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.739+390A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962548 | ||||||
| chr1:204962631
|
T | G | 1 | a0001c0002t0021g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.739+473T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962631 | ||||||
| chr1:204962744
|
G | A | 7 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+586G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962744 | ||||||
| chr1:204962813
|
C | A | 1 | a0001c0005t0003g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.739+655C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204962813 | ||||||
| chr1:204963235
|
A | G | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.739+1077A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963235 | ||||||
| chr1:204963273
|
G | T | 9 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.739+1115G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963273 | ||||||
| chr1:204963481
|
A | G | 1 | a0001c0010t0026g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.739+1323A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963481 | ||||||
| chr1:204963483
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(37): Show | 41 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.739+1325A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963483 | ||||||
| chr1:204963493
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(36): Show | 40 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.739+1335G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963493 | ||||||
| chr1:204963516
|
A | G | 1 | a0001c0002t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.739+1358A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963516 | ||||||
| chr1:204963621
|
A | G | 2 | a0001c0012t0001g0068a0001c0012t0001g0116 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.739+1463A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963621 | ||||||
| chr1:204963677
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(35): Show | 39 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.739+1519C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963677 | ||||||
| chr1:204963682
|
G | A | 9 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.739+1524G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963682 | ||||||
| chr1:204963786
|
A | G | 2 | a0001c0001t0003g0045a0001c0001t0010g0029 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.739+1628A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204963786 | ||||||
| chr1:204964129
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.739+1971C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204964129 | ||||||
| chr1:204964261
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.739+2103G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204964261 | ||||||
| chr1:204964595
|
A | G | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.739+2437A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204964595 | ||||||
| chr1:204964731
|
C | T | 6 | a0001c0002t0001g0105a0001c0002t0001g0142a0001c0002t0001g0144others(3): Show | 6 | HG01175.hp2 HG01243.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.739+2573C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204964731 | ||||||
| chr1:204964742
|
A | C | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+2584A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204964742 | ||||||
| chr1:204964905
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0006g0070a0001c0001t0018g0153others(1): Show | 4 | NA19002.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+2747G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204964905 | ||||||
| chr1:204965059
|
G | T | 3 | a0001c0002t0003g0236a0001c0002t0008g0043a0001c0002t0053g0237 | 3 | HG02451.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.739+2901G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965059 | ||||||
| chr1:204965123
|
G | A | 18 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(15): Show | 18 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.739+2965G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965123 | ||||||
| chr1:204965180
|
G | A | 1 | a0001c0002t0008g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.739+3022G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965180 | ||||||
| chr1:204965372
|
C | G | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.740-2877C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965372 | ||||||
| chr1:204965380
|
G | T | 9 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-2869G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965380 | ||||||
| chr1:204965402
|
T | C | 9 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(6): Show | 9 | HG01433.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-2847T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965402 | ||||||
| chr1:204965420
|
A | G | 1 | a0001c0017t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.740-2829A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965420 | ||||||
| chr1:204965589
|
C | T | 2 | a0001c0001t0003g0045a0001c0001t0010g0029 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.740-2660C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965589 | ||||||
| chr1:204965719
|
T | G | 1 | a0001c0002t0001g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.740-2530T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204965719 | ||||||
| chr1:204966006
|
C | G | 1 | a0001c0002t0001g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.740-2243C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966006 | ||||||
| chr1:204966072
|
T | G | 2 | a0001c0002t0001g0178a0005c0018t0001g0188 | 2 | NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.740-2177T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966072 | ||||||
| chr1:204966300
|
G | A | 9 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-1949G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966300 | ||||||
| chr1:204966338
|
G | T | 1 | a0001c0002t0008g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.740-1911G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966338 | ||||||
| chr1:204966394
|
A | G | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.740-1855A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966394 | ||||||
| chr1:204966406
|
G | T | 17 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(14): Show | 17 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.740-1843G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966406 | ||||||
| chr1:204966494
|
G | A | 1 | a0001c0027t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.740-1755G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966494 | ||||||
| chr1:204966519
|
G | A | 7 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-1730G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966519 | ||||||
| chr1:204966807
|
C | G | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.740-1442C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966807 | ||||||
| chr1:204966814
|
G | A | 1 | a0001c0001t0055g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.740-1435G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966814 | ||||||
| chr1:204966828
|
A | G | 2 | a0001c0002t0005g0026a0001c0002t0005g0046 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.740-1421A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966828 | ||||||
| chr1:204966902
|
G | A | 3 | a0001c0001t0049g0197a0002c0013t0001g0084a0002c0013t0011g0185 | 3 | NA19002.hp1 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.740-1347G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204966902 | ||||||
| chr1:204967028
|
C | T | 4 | a0001c0002t0001g0013a0001c0002t0009g0037a0001c0002t0009g0242others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-1221C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967028 | ||||||
| chr1:204967030
|
C | T | 10 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(7): Show | 10 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.740-1219C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967030 | ||||||
| chr1:204967207
|
A | G | 18 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(15): Show | 18 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.740-1042A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967207 | ||||||
| chr1:204967220
|
C | T | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.740-1029C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967220 | ||||||
| chr1:204967479
|
A | G | 41 | a0001c0001t0001g0109a0001c0001t0002g0131a0001c0002t0001g0066others(38): Show | 41 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.740-770A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967479 | ||||||
| chr1:204967510
|
G | A | 1 | a0001c0001t0005g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.740-739G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967510 | ||||||
| chr1:204967636
|
G | A | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.740-613G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967636 | ||||||
| chr1:204967707
|
C | T | 40 | a0001c0001t0001g0109a0001c0001t0002g0131a0001c0002t0001g0066others(37): Show | 40 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.740-542C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967707 | ||||||
| chr1:204967750
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.740-499G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967750 | ||||||
| chr1:204967765
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.740-484A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967765 | ||||||
| chr1:204967947
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.740-302A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204967947 | ||||||
| chr1:204968056
|
A | T | 1 | a0001c0001t0013g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.740-193A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204968056 | ||||||
| chr1:204968090
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.740-159A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204968090 | ||||||
| chr1:204968115
|
G | T | 9 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-134G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204968115 | ||||||
| chr1:204968221
|
C | T | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.740-28C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 7/27 | chr1 | 204968221 | ||||||
| chr1:204968524
|
C | A | 2 | a0001c0001t0002g0028a0001c0001t0010g0027 | 2 | HG02602.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.851+164C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 8/27 | chr1 | 204968524 | ||||||
| chr1:204968600
|
C | G | 5 | a0001c0002t0001g0013a0001c0002t0009g0037a0001c0002t0009g0242others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-198C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 8/27 | chr1 | 204968600 | ||||||
| chr1:204968620
|
C | T | 3 | a0001c0002t0003g0227a0001c0002t0004g0034a0001c0002t0047g0164 | 3 | HG02559.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-178C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 8/27 | chr1 | 204968620 | ||||||
| chr1:204968686
|
A | G | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-112A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 8/27 | chr1 | 204968686 | ||||||
| chr1:204968747
|
A | T | 6 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-51A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 8/27 | chr1 | 204968747 | ||||||
| chr1:204969178
|
G | C | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18612.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1036+196G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969178 | ||||||
| chr1:204969243
|
G | A | 18 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(15): Show | 18 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1036+261G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969243 | ||||||
| chr1:204969312
|
C | T | 14 | a0001c0002t0001g0092a0001c0002t0001g0105a0001c0002t0001g0142others(11): Show | 15 | HG00558.hp2 HG01175.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1036+330C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969312 | ||||||
| chr1:204969336
|
C | T | 2 | a0001c0011t0015g0176a0001c0011t0030g0015 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1036+354C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969336 | ||||||
| chr1:204969345
|
T | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0193a0001c0001t0041g0194 | 3 | HG02015.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1036+363T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969345 | ||||||
| chr1:204969514
|
C | A | 2 | a0001c0001t0001g0259a0005c0018t0001g0188 | 2 | NA18953.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1036+532C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969514 | ||||||
| chr1:204969611
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0042g0114 | 4 | HG00738.hp2 HG01074.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+629T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969611 | ||||||
| chr1:204969677
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1036+695A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969677 | ||||||
| chr1:204969689
|
G | A | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+707G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969689 | ||||||
| chr1:204969710
|
G | T | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1036+728G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204969710 | ||||||
| chr1:204970008
|
G | A | 6 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-608G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204970008 | ||||||
| chr1:204970033
|
G | A | 27 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(24): Show | 27 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1037-583G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204970033 | ||||||
| chr1:204970049
|
C | T | 6 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-567C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204970049 | ||||||
| chr1:204970053
|
C | T | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1037-563C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204970053 | ||||||
| chr1:204970074
|
C | CA | 5 | a0001c0001t0042g0114a0001c0002t0004g0214a0001c0002t0009g0242others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-517dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr1 | 204970074 | |||||
| chr1:204970074
|
CA | C | 152 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0061others(149): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1037-517delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr1 | 204970074 | |||||
| chr1:204970074
|
CAA | C | 8 | a0001c0001t0001g0198a0001c0001t0005g0139a0001c0001t0006g0070others(5): Show | 8 | HG01167.hp2 HG02895.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1037-518_1037-517d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr1 | 204970074 | |||||
| chr1:204970208
|
T | A | 43 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(40): Show | 45 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1037-408T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204970208 | ||||||
| chr1:204970344
|
T | TA | 20 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(17): Show | 20 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1037-265dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr1 | 204970344 | |||||
| chr1:204970506
|
C | T | 1 | a0001c0005t0052g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1037-110C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 9/27 | chr1 | 204970506 | ||||||
| chr1:204970771
|
T | C | 27 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(24): Show | 27 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168+24T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204970771 | ||||||
| chr1:204970789
|
G | C | 27 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(24): Show | 27 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168+42G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204970789 | ||||||
| chr1:204970807
|
T | G | 1 | a0002c0025t0012g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1168+60T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204970807 | ||||||
| chr1:204970846
|
C | G | 1 | a0001c0001t0049g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1168+99C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204970846 | ||||||
| chr1:204971040
|
C | T | 6 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168+293C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971040 | ||||||
| chr1:204971066
|
T | A | 1 | a0001c0002t0039g0162 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1168+319T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971066 | ||||||
| chr1:204971162
|
G | A | 4 | a0001c0002t0021g0219a0001c0003t0007g0012a0001c0003t0007g0181others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168+415G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971162 | ||||||
| chr1:204971251
|
G | C | 2 | a0001c0002t0005g0026a0001c0002t0005g0046 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1168+504G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971251 | ||||||
| chr1:204971317
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1168+570G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971317 | ||||||
| chr1:204971432
|
A | T | 27 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(24): Show | 27 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168+685A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971432 | ||||||
| chr1:204971458
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1168+711A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971458 | ||||||
| chr1:204971487
|
G | A | 19 | a0001c0001t0049g0197a0001c0002t0001g0206a0001c0002t0021g0219others(16): Show | 19 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1168+740G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971487 | ||||||
| chr1:204971537
|
G | A | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1168+790G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971537 | ||||||
| chr1:204971555
|
G | A | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1168+808G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971555 | ||||||
| chr1:204971571
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1168+824A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971571 | ||||||
| chr1:204971575
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1168+828A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971575 | ||||||
| chr1:204971585
|
A | T | 29 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(26): Show | 29 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1168+838A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971585 | ||||||
| chr1:204971617
|
C | T | 19 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(16): Show | 19 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1168+870C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971617 | ||||||
| chr1:204971652
|
T | G | 30 | a0001c0001t0015g0025a0001c0001t0015g0232a0001c0002t0003g0236others(27): Show | 30 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1168+905T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971652 | ||||||
| chr1:204971658
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1168+911A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971658 | ||||||
| chr1:204971659
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1168+912A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971659 | ||||||
| chr1:204971833
|
A | G | 27 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(24): Show | 27 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168+1086A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971833 | ||||||
| chr1:204971844
|
C | T | 42 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(39): Show | 43 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1168+1097C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971844 | ||||||
| chr1:204971915
|
T | C | 26 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(23): Show | 26 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168+1168T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971915 | ||||||
| chr1:204971999
|
T | A | 25 | a0001c0002t0003g0236a0001c0002t0004g0133a0001c0002t0004g0214others(22): Show | 25 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1168+1252T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204971999 | ||||||
| chr1:204972012
|
G | A | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-1264G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972012 | ||||||
| chr1:204972088
|
G | A | 5 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169-1188G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972088 | ||||||
| chr1:204972231
|
C | G | 39 | a0001c0002t0003g0201a0001c0002t0003g0236a0001c0002t0004g0133others(36): Show | 39 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1169-1045C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972231 | ||||||
| chr1:204972384
|
G | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1169-892G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972384 | ||||||
| chr1:204972403
|
T | C | 32 | a0001c0002t0003g0201a0001c0002t0003g0236a0001c0002t0004g0133others(29): Show | 32 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.1169-873T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972403 | ||||||
| chr1:204972416
|
GA | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(9): Show | 13 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1169-857delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr1 | 204972416 | |||||
| chr1:204972440
|
A | G | 1 | a0001c0001t0036g0187 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1169-836A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972440 | ||||||
| chr1:204972659
|
AG | A | 7 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-615delG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr1 | 204972659 | |||||
| chr1:204972675
|
G | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0160a0001c0001t0001g0196others(3): Show | 6 | HG02129.hp1 HG02135.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1169-601G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972675 | ||||||
| chr1:204972685
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(256): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1169-591A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972685 | ||||||
| chr1:204972947
|
G | C | 2 | a0001c0002t0004g0034a0001c0002t0005g0140 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1169-329G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972947 | ||||||
| chr1:204972992
|
A | G | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18612.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1169-284A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204972992 | ||||||
| chr1:204973035
|
C | T | 44 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(41): Show | 45 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1169-241C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204973035 | ||||||
| chr1:204973036
|
G | A | 2 | a0001c0006t0017g0134a0001c0006t0017g0135 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1169-240G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 10/27 | chr1 | 204973036 | ||||||
| chr1:204973463
|
C | T | 1 | a0001c0001t0013g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1312+44C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973463 | ||||||
| chr1:204973540
|
A | G | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312+121A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973540 | ||||||
| chr1:204973569
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1312+150G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973569 | ||||||
| chr1:204973643
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0101 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1312+224C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973643 | ||||||
| chr1:204973663
|
A | G | 2 | a0001c0011t0015g0176a0001c0011t0030g0015 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1312+244A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973663 | ||||||
| chr1:204973711
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1312+292C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973711 | ||||||
| chr1:204973737
|
C | A | 12 | a0001c0002t0001g0092a0001c0002t0001g0105a0001c0002t0001g0142others(9): Show | 13 | HG00558.hp2 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1312+318C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973737 | ||||||
| chr1:204973800
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1313-379C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973800 | ||||||
| chr1:204973826
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1313-353G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973826 | ||||||
| chr1:204973851
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1313-328G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973851 | ||||||
| chr1:204973905
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1313-274A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973905 | ||||||
| chr1:204973968
|
T | C | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1313-211T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973968 | ||||||
| chr1:204973988
|
G | A | 94 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0061others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1313-191G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973988 | ||||||
| chr1:204973993
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1313-186C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973993 | ||||||
| chr1:204974010
|
T | C | 1 | a0005c0018t0001g0188 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1313-169T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204974010 | ||||||
| chr1:204974073
|
G | A | 1 | a0001c0001t0015g0025 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1313-106G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204974073 | ||||||
| chr1:204974157
|
A | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1313-22A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204974157 | ||||||
| chr1:204974377
|
A | G | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424+87A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 12/27 | chr1 | 204974377 | ||||||
| chr1:204974485
|
G | C | 3 | a0001c0008t0001g0145a0001c0008t0001g0146a0001c0008t0001g0147 | 3 | HG00735.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1425-172G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 12/27 | chr1 | 204974485 | ||||||
| chr1:204974644
|
G | T | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1425-13G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 12/27 | chr1 | 204974644 | ||||||
| chr1:204974833
|
AG | A | 9 | a0001c0002t0003g0201a0001c0002t0003g0236a0001c0002t0004g0216others(6): Show | 9 | HG01192.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1591+13delG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr1 | 204974833 | |||||
| chr1:204974863
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(118): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1591+40C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204974863 | ||||||
| chr1:204974864
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1591+41A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204974864 | ||||||
| chr1:204974881
|
A | G | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1591+58A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204974881 | ||||||
| chr1:204974891
|
A | G | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1591+68A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204974891 | ||||||
| chr1:204975058
|
A | G | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1592-213A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204975058 | ||||||
| chr1:204975140
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1592-131A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204975140 | ||||||
| chr1:204975180
|
G | T | 10 | a0001c0002t0003g0227a0001c0002t0005g0210a0001c0002t0047g0164others(7): Show | 10 | HG01496.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1592-91G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204975180 | ||||||
| chr1:204975187
|
G | A | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1592-84G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 13/27 | chr1 | 204975187 | ||||||
| chr1:204975429
|
C | G | 1 | a0001c0001t0014g0098 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1739+11C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975429 | ||||||
| chr1:204975518
|
C | T | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1739+100C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975518 | ||||||
| chr1:204975583
|
C | T | 1 | a0001c0010t0001g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1739+165C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975583 | ||||||
| chr1:204975711
|
A | G | 10 | a0001c0002t0003g0227a0001c0002t0005g0026a0001c0002t0005g0046others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739+293A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975711 | ||||||
| chr1:204975847
|
C | G | 3 | a0001c0001t0001g0191a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | NA18969.hp2 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1739+429C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975847 | ||||||
| chr1:204975897
|
G | A | 6 | a0001c0006t0003g0260a0001c0006t0004g0184a0001c0006t0005g0054others(3): Show | 6 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1739+479G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975897 | ||||||
| chr1:204975946
|
G | A | 2 | a0001c0002t0004g0034a0001c0002t0005g0140 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1739+528G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975946 | ||||||
| chr1:204975951
|
G | T | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1739+533G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975951 | ||||||
| chr1:204975977
|
G | A | 5 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1739+559G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204975977 | ||||||
| chr1:204976003
|
T | TTC | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1739+586_1739+587d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 204976003 | |||||
| chr1:204976114
|
A | G | 7 | a0001c0002t0005g0026a0001c0002t0005g0046a0001c0002t0005g0254others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1740-557A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976114 | ||||||
| chr1:204976188
|
T | C | 36 | a0001c0002t0001g0206a0001c0002t0004g0034a0001c0002t0005g0140others(33): Show | 37 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1740-483T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976188 | ||||||
| chr1:204976191
|
G | C | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1740-480G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976191 | ||||||
| chr1:204976210
|
CTA | C | 24 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1740-458_1740-457d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 204976210 | |||||
| chr1:204976213
|
T | C | 4 | a0001c0002t0001g0013a0001c0002t0009g0037a0001c0002t0009g0242others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1740-458T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976213 | ||||||
| chr1:204976225
|
C | A | 2 | a0001c0002t0004g0034a0001c0002t0005g0140 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1740-446C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976225 | ||||||
| chr1:204976330
|
T | C | 29 | a0001c0002t0001g0206a0001c0003t0001g0071a0001c0003t0001g0119others(26): Show | 30 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1740-341T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976330 | ||||||
| chr1:204976361
|
C | A | 35 | a0001c0002t0001g0206a0001c0002t0004g0034a0001c0002t0005g0140others(32): Show | 36 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1740-310C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976361 | ||||||
| chr1:204976373
|
G | T | 2 | a0001c0001t0028g0183a0001c0014t0004g0228 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1740-298G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976373 | ||||||
| chr1:204976490
|
G | A | 44 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(41): Show | 45 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1740-181G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976490 | ||||||
| chr1:204976497
|
C | G | 6 | a0001c0006t0003g0260a0001c0006t0004g0184a0001c0006t0005g0054others(3): Show | 6 | HG01496.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1740-174C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976497 | ||||||
| chr1:204976537
|
G | A | 31 | a0001c0002t0001g0206a0001c0002t0004g0034a0001c0002t0005g0140others(28): Show | 32 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1740-134G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976537 | ||||||
| chr1:204976550
|
A | AT | 36 | a0001c0002t0001g0206a0001c0002t0004g0034a0001c0002t0005g0140others(33): Show | 37 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1740-121_1740-120i others(3): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976550 | ||||||
| chr1:204976591
|
C | A | 8 | a0001c0002t0003g0236a0001c0002t0004g0216a0001c0002t0004g0230others(5): Show | 8 | HG01192.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1740-80C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976591 | ||||||
| chr1:204976618
|
G | C | 35 | a0001c0002t0001g0206a0001c0002t0004g0034a0001c0002t0005g0140others(32): Show | 36 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1740-53G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 14/27 | chr1 | 204976618 | ||||||
| chr1:204976806
|
A | G | 32 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(29): Show | 33 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1864+11A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204976806 | ||||||
| chr1:204976865
|
C | T | 1 | a0001c0020t0016g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1864+70C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204976865 | ||||||
| chr1:204976914
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1864+119G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204976914 | ||||||
| chr1:204976979
|
C | A | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1864+184C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204976979 | ||||||
| chr1:204977002
|
G | A | 1 | a0001c0001t0029g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1864+207G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977002 | ||||||
| chr1:204977172
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1864+377A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977172 | ||||||
| chr1:204977212
|
T | C | 4 | a0001c0002t0001g0013a0001c0002t0009g0037a0001c0002t0009g0242others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1864+417T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977212 | ||||||
| chr1:204977259
|
C | T | 32 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(29): Show | 33 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1865-422C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977259 | ||||||
| chr1:204977265
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1865-416G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977265 | ||||||
| chr1:204977425
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1865-256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977425 | ||||||
| chr1:204977540
|
T | C | 29 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(26): Show | 30 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1865-141T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977540 | ||||||
| chr1:204977636
|
T | C | 35 | a0001c0002t0004g0034a0001c0002t0005g0140a0001c0003t0001g0071others(32): Show | 36 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1865-45T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 15/27 | chr1 | 204977636 | ||||||
| chr1:204977879
|
C | T | 24 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1909+154C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204977879 | ||||||
| chr1:204977944
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1909+219G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204977944 | ||||||
| chr1:204978045
|
C | T | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+320C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204978045 | ||||||
| chr1:204978046
|
G | A | 1 | a0001c0001t0007g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1909+321G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204978046 | ||||||
| chr1:204978361
|
C | G | 45 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(42): Show | 46 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1910-607C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204978361 | ||||||
| chr1:204978574
|
G | A | 26 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1910-394G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204978574 | ||||||
| chr1:204978754
|
T | TG | 23 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(20): Show | 24 | HG00741.hp1 HG01123.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1910-205dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr1 | 204978754 | |||||
| chr1:204978757
|
G | T | 4 | a0001c0002t0003g0236a0001c0002t0004g0216a0001c0002t0008g0043others(1): Show | 4 | HG02451.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1910-211G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204978757 | ||||||
| chr1:204978960
|
G | A | 1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | splice_region_variant&intron_variant | LOW | c.1910-8G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 16/27 | chr1 | 204978960 | ||||||
| chr1:204979110
|
C | T | 2 | a0001c0002t0004g0034a0001c0002t0005g0140 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2011+41C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 17/27 | chr1 | 204979110 | ||||||
| chr1:204979607
|
A | G | 29 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(26): Show | 30 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.2209+48A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/27 | chr1 | 204979607 | ||||||
| chr1:204979828
|
A | T | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2209+269A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/27 | chr1 | 204979828 | ||||||
| chr1:204979924
|
C | A | 8 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209+365C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/27 | chr1 | 204979924 | ||||||
| chr1:204979928
|
T | C | 1 | a0001c0006t0003g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2209+369T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/27 | chr1 | 204979928 | ||||||
| chr1:204980029
|
G | C | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2210-341G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/27 | chr1 | 204980029 | ||||||
| chr1:204980211
|
A | G | 5 | a0001c0002t0001g0013a0001c0002t0009g0037a0001c0002t0009g0242others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2210-159A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 18/27 | chr1 | 204980211 | ||||||
| chr1:204980517
|
G | A | 35 | a0001c0002t0005g0026a0001c0002t0005g0046a0001c0002t0005g0254others(32): Show | 36 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.2280+77G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204980517 | ||||||
| chr1:204980639
|
T | C | 98 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(95): Show | 100 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.2280+199T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204980639 | ||||||
| chr1:204980698
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(10): Show | 14 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2280+258T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204980698 | ||||||
| chr1:204980984
|
C | T | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280+544C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204980984 | ||||||
| chr1:204981118
|
G | A | 5 | a0001c0002t0001g0013a0001c0002t0009g0037a0001c0002t0009g0242others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2280+678G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981118 | ||||||
| chr1:204981128
|
A | G | 8 | a0001c0002t0005g0026a0001c0002t0005g0046a0001c0002t0005g0254others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2281-670A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981128 | ||||||
| chr1:204981188
|
G | A | 2 | a0001c0001t0010g0111a0001c0002t0002g0077 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2281-610G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981188 | ||||||
| chr1:204981301
|
C | T | 1 | a0001c0003t0003g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2281-497C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981301 | ||||||
| chr1:204981434
|
T | C | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2281-364T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981434 | ||||||
| chr1:204981462
|
A | G | 1 | a0001c0010t0025g0049 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2281-336A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981462 | ||||||
| chr1:204981581
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(257): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2281-217G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981581 | ||||||
| chr1:204981602
|
C | T | 1 | a0009c0028t0022g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2281-196C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981602 | ||||||
| chr1:204981620
|
C | T | 7 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2281-178C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981620 | ||||||
| chr1:204981670
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2281-128C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981670 | ||||||
| chr1:204981684
|
G | A | 5 | a0001c0003t0001g0071a0001c0003t0001g0127a0001c0009t0001g0002others(2): Show | 6 | HG01123.hp2 HG01515.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2281-114G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 19/27 | chr1 | 204981684 | ||||||
| chr1:204982056
|
CT | C | 32 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(29): Show | 33 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.2503+38delT | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr1 | 204982056 | |||||
| chr1:204982081
|
C | T | 45 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(42): Show | 46 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2503+61C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204982081 | ||||||
| chr1:204982266
|
A | G | 2 | a0001c0002t0003g0227a0001c0002t0047g0164 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2503+246A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204982266 | ||||||
| chr1:204982412
|
A | G | 75 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(72): Show | 77 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2503+392A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204982412 | ||||||
| chr1:204982750
|
T | A | 1 | a0001c0002t0002g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2503+730T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204982750 | ||||||
| chr1:204982856
|
T | TG | 5 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+841dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr1 | 204982856 | |||||
| chr1:204982898
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2503+878A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204982898 | ||||||
| chr1:204983108
|
C | G | 7 | a0001c0002t0005g0026a0001c0002t0005g0046a0001c0002t0005g0254others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-919C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983108 | ||||||
| chr1:204983207
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2504-820G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983207 | ||||||
| chr1:204983250
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2504-777G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983250 | ||||||
| chr1:204983413
|
T | C | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2504-614T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983413 | ||||||
| chr1:204983597
|
C | T | 7 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2504-430C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983597 | ||||||
| chr1:204983609
|
T | C | 80 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(77): Show | 82 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.2504-418T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983609 | ||||||
| chr1:204983656
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2504-371A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983656 | ||||||
| chr1:204983684
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2504-343C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983684 | ||||||
| chr1:204983721
|
C | A | 75 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(72): Show | 77 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2504-306C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 20/27 | chr1 | 204983721 | ||||||
| chr1:204984159
|
C | T | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2619+17C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984159 | ||||||
| chr1:204984218
|
A | G | 10 | a0001c0002t0003g0227a0001c0002t0005g0026a0001c0002t0005g0046others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2619+76A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984218 | ||||||
| chr1:204984316
|
A | T | 19 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(16): Show | 20 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.2619+174A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984316 | ||||||
| chr1:204984331
|
A | ATG | 14 | a0001c0002t0001g0066a0001c0002t0012g0125a0001c0003t0004g0005others(11): Show | 14 | HG00639.hp2 HG01069.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.2619+203_2619+204d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984331 | |||||
| chr1:204984345
|
G | A | 4 | a0001c0006t0004g0184a0001c0006t0017g0134a0001c0006t0017g0135others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2619+203G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984345 | ||||||
| chr1:204984345
|
G | GTGTA | 71 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(68): Show | 72 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2619+204_2619+205i others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984345 | |||||
| chr1:204984347
|
A | G | 1 | a0001c0004t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2619+205A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984347 | ||||||
| chr1:204984355
|
ATATGTGT others(5): Show |
A | 1 | a0001c0004t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2619+215_2619+226d others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984355 | |||||
| chr1:204984357
|
A | ATG | 23 | a0001c0001t0013g0065a0001c0002t0001g0013a0001c0002t0003g0201others(20): Show | 23 | HG00280.hp1 HG01109.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.2619+227_2619+228d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984357 | |||||
| chr1:204984357
|
A | ATGTG | 8 | a0001c0002t0008g0221a0001c0005t0003g0243a0001c0005t0007g0248others(5): Show | 8 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2619+225_2619+228d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984357 | |||||
| chr1:204984357
|
A | G | 79 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2619+215A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984357 | ||||||
| chr1:204984368
|
T | C | 1 | a0001c0004t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2619+226T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984368 | ||||||
| chr1:204984369
|
G | GTA | 25 | a0001c0002t0001g0066a0001c0002t0012g0125a0001c0003t0001g0071others(22): Show | 26 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2619+236_2619+237d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984369 | |||||
| chr1:204984370
|
T | C | 1 | a0001c0004t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2619+228T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984370 | ||||||
| chr1:204984380
|
C | CGCATATA others(15): Show |
1 | a0001c0001t0054g0207 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2619+239_2619+260d others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984380 | |||||
| chr1:204984382
|
C | CAT | 26 | a0001c0001t0001g0020a0001c0001t0001g0100a0001c0001t0001g0104others(23): Show | 26 | HG00544.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2619+268_2619+269d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATAT | 8 | a0001c0001t0001g0109a0001c0002t0001g0203a0001c0002t0002g0047others(5): Show | 8 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2619+266_2619+269d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATAT | 6 | a0001c0001t0025g0088a0001c0002t0005g0026a0001c0002t0005g0046others(3): Show | 6 | HG00099.hp2 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2619+264_2619+269d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(1): Show |
8 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(5): Show | 8 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2619+262_2619+269d others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(3): Show |
6 | a0001c0002t0005g0254a0001c0002t0008g0252a0001c0002t0008g0253others(3): Show | 6 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2619+260_2619+269d others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(7): Show |
4 | a0001c0002t0003g0227a0001c0002t0004g0133a0001c0002t0004g0214others(1): Show | 4 | HG02809.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2619+256_2619+269d others(16): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(9): Show |
1 | a0001c0002t0043g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2619+254_2619+269d others(18): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
C | CATATATA others(11): Show |
2 | a0001c0002t0047g0164a0001c0002t0048g0239 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2619+252_2619+269d others(20): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
CAT | C | 32 | a0001c0001t0001g0069a0001c0001t0001g0122a0001c0001t0001g0193others(29): Show | 32 | HG00280.hp1 HG00733.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.2619+268_2619+269d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
CATAT | C | 17 | a0001c0001t0001g0094a0001c0001t0002g0062a0001c0002t0001g0079others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.2619+266_2619+269d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984382
|
CATATAT | C | 66 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(63): Show | 68 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2619+264_2619+269d others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984382 | |||||
| chr1:204984383
|
A | G | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2619+241A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984383 | ||||||
| chr1:204984393
|
A | ATATATAT others(5): Show |
1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2619+259_2619+260i others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984393 | |||||
| chr1:204984523
|
C | T | 19 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(16): Show | 20 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.2619+381C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984523 | ||||||
| chr1:204984599
|
C | T | 55 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(52): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2619+457C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984599 | ||||||
| chr1:204984649
|
GA | G | 59 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(56): Show | 60 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2619+510delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204984649 | |||||
| chr1:204984772
|
A | G | 2 | a0001c0001t0015g0025a0001c0001t0015g0232 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2619+630A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984772 | ||||||
| chr1:204984831
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2619+689C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984831 | ||||||
| chr1:204984838
|
C | T | 3 | a0001c0002t0003g0227a0001c0002t0005g0210a0001c0002t0047g0164 | 3 | HG02109.hp1 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2619+696C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984838 | ||||||
| chr1:204985074
|
T | TACTTGCT others(5): Show |
1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2620-834_2620-823d others(14): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr1 | 204985074 | |||||
| chr1:204985082
|
T | A | 7 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2620-828T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985082 | ||||||
| chr1:204985086
|
G | C | 2 | a0001c0006t0004g0184a0001c0006t0034g0030 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2620-824G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985086 | ||||||
| chr1:204985462
|
C | T | 1 | a0001c0002t0004g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2620-448C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985462 | ||||||
| chr1:204985491
|
C | G | 1 | a0001c0001t0054g0207 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2620-419C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985491 | ||||||
| chr1:204985510
|
A | G | 1 | a0009c0028t0022g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2620-400A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985510 | ||||||
| chr1:204985587
|
G | A | 2 | a0001c0001t0011g0157a0008c0023t0011g0189 | 2 | NA19003.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2620-323G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985587 | ||||||
| chr1:204985660
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0193 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2620-250A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985660 | ||||||
| chr1:204985865
|
A | G | 105 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(102): Show | 107 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2620-45A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985865 | ||||||
| chr1:204986191
|
G | A | 59 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(56): Show | 60 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2824+77G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986191 | ||||||
| chr1:204986201
|
A | G | 59 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(56): Show | 60 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2824+87A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986201 | ||||||
| chr1:204986241
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0027g0087 | 2 | HG00733.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2824+127G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986241 | ||||||
| chr1:204986288
|
G | A | 59 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(56): Show | 60 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2824+174G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986288 | ||||||
| chr1:204986301
|
G | T | 2 | a0001c0001t0006g0247a0001c0001t0036g0187 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2824+187G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986301 | ||||||
| chr1:204986362
|
C | T | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2824+248C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986362 | ||||||
| chr1:204986363
|
G | A | 1 | a0001c0001t0020g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2824+249G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986363 | ||||||
| chr1:204986574
|
C | A | 8 | a0001c0002t0003g0236a0001c0002t0004g0216a0001c0002t0004g0230others(5): Show | 8 | HG01192.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2824+460C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986574 | ||||||
| chr1:204986588
|
G | A | 20 | a0001c0003t0001g0071a0001c0003t0001g0119a0001c0003t0001g0127others(17): Show | 21 | HG00741.hp1 HG01123.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.2824+474G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986588 | ||||||
| chr1:204986885
|
G | A | 1 | a0001c0002t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2825-533G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986885 | ||||||
| chr1:204986958
|
G | A | 2 | a0001c0001t0028g0183a0001c0014t0004g0228 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2825-460G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986958 | ||||||
| chr1:204987197
|
G | C | 56 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(53): Show | 56 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2825-221G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204987197 | ||||||
| chr1:204987208
|
G | A | 2 | a0001c0003t0004g0005a0001c0027t0004g0004 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2825-210G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204987208 | ||||||
| chr1:204987263
|
C | T | 1 | a0001c0002t0004g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2825-155C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204987263 | ||||||
| chr1:204987917
|
C | CACAG | 117 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0094others(114): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2947+378_2947+381d others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr1 | 204987917 | |||||
| chr1:204987927
|
A | T | 13 | a0001c0002t0001g0013a0001c0003t0004g0005a0001c0003t0004g0038others(10): Show | 13 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2947+387A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204987927 | ||||||
| chr1:204987999
|
C | G | 3 | a0001c0002t0003g0227a0001c0002t0005g0210a0001c0002t0047g0164 | 3 | HG02109.hp1 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2947+459C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204987999 | ||||||
| chr1:204988045
|
A | G | 26 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2947+505A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988045 | ||||||
| chr1:204988175
|
T | G | 1 | a0001c0002t0001g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2948-458T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988175 | ||||||
| chr1:204988303
|
G | A | 1 | a0001c0002t0002g0200 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2948-330G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988303 | ||||||
| chr1:204988358
|
A | G | 1 | a0001c0003t0007g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2948-275A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988358 | ||||||
| chr1:204988448
|
A | G | 10 | a0001c0001t0028g0183a0001c0002t0005g0026a0001c0002t0005g0046others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2948-185A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988448 | ||||||
| chr1:204988458
|
A | G | 1 | a0001c0001t0003g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2948-175A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988458 | ||||||
| chr1:204988476
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2948-157G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 23/27 | chr1 | 204988476 | ||||||
| chr1:204988980
|
T | C | 2 | a0001c0002t0001g0092a0001c0002t0001g0179 | 2 | HG00558.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.3121+174T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204988980 | ||||||
| chr1:204988981
|
G | T | 5 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(2): Show | 5 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3121+175G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204988981 | ||||||
| chr1:204989016
|
T | A | 9 | a0001c0003t0010g0040a0001c0006t0003g0260a0001c0006t0004g0184others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3121+210T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989016 | ||||||
| chr1:204989017
|
C | T | 9 | a0001c0003t0010g0040a0001c0006t0003g0260a0001c0006t0004g0184others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3121+211C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989017 | ||||||
| chr1:204989107
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3121+301G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989107 | ||||||
| chr1:204989249
|
G | A | 2 | a0001c0003t0024g0222a0004c0024t0001g0052 | 2 | HG01433.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3121+443G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989249 | ||||||
| chr1:204989273
|
G | A | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3121+467G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989273 | ||||||
| chr1:204989306
|
G | A | 5 | a0001c0002t0004g0230a0001c0002t0004g0231a0001c0002t0013g0217others(2): Show | 5 | HG01192.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3121+500G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989306 | ||||||
| chr1:204989409
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3121+603G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989409 | ||||||
| chr1:204989432
|
G | A | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3121+626G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989432 | ||||||
| chr1:204989453
|
C | A | 1 | a0001c0001t0046g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3121+647C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989453 | ||||||
| chr1:204989514
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(8): Show | 12 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.3121+708C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989514 | ||||||
| chr1:204989552
|
C | T | 15 | a0001c0002t0048g0239a0001c0003t0001g0119a0001c0003t0003g0035others(12): Show | 15 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.3121+746C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989552 | ||||||
| chr1:204989883
|
G | T | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3121+1077G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989883 | ||||||
| chr1:204989886
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(9): Show | 13 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.3121+1080T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989886 | ||||||
| chr1:204989915
|
C | T | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3121+1109C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989915 | ||||||
| chr1:204989916
|
C | T | 2 | a0001c0002t0003g0227a0001c0002t0047g0164 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3121+1110C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989916 | ||||||
| chr1:204989938
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3121+1132C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204989938 | ||||||
| chr1:204990014
|
G | T | 10 | a0001c0002t0003g0201a0001c0003t0010g0040a0001c0006t0003g0260others(7): Show | 10 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.3121+1208G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990014 | ||||||
| chr1:204990147
|
C | T | 39 | a0001c0001t0001g0069a0001c0001t0001g0094a0001c0001t0001g0100others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3122-1145C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990147 | ||||||
| chr1:204990182
|
G | A | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3122-1110G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990182 | ||||||
| chr1:204990314
|
G | T | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3122-978G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990314 | ||||||
| chr1:204990339
|
C | A | 9 | a0001c0001t0028g0183a0001c0002t0005g0026a0001c0002t0005g0046others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3122-953C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990339 | ||||||
| chr1:204990360
|
A | G | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3122-932A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990360 | ||||||
| chr1:204990430
|
C | T | 20 | a0001c0002t0003g0236a0001c0002t0004g0216a0001c0002t0008g0043others(17): Show | 20 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.3122-862C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990430 | ||||||
| chr1:204990441
|
A | G | 7 | a0001c0005t0003g0243a0001c0005t0007g0248a0001c0005t0010g0213others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3122-851A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990441 | ||||||
| chr1:204990563
|
C | CA | 216 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.3122-713dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr1 | 204990563 | |||||
| chr1:204990563
|
C | CAA | 14 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0009g0010others(11): Show | 14 | HG01496.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3122-714_3122-713d others(4): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr1 | 204990563 | |||||
| chr1:204990574
|
A | G | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3122-718A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990574 | ||||||
| chr1:204990586
|
G | A | 1 | a0001c0004t0038g0132 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3122-706G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990586 | ||||||
| chr1:204990713
|
C | T | 1 | a0001c0002t0004g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3122-579C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990713 | ||||||
| chr1:204990735
|
G | C | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3122-557G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990735 | ||||||
| chr1:204990939
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3122-353G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990939 | ||||||
| chr1:204990941
|
T | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3122-351T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204990941 | ||||||
| chr1:204991043
|
G | A | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3122-249G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204991043 | ||||||
| chr1:204991111
|
C | T | 25 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0094others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.3122-181C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204991111 | ||||||
| chr1:204991234
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3122-58C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204991234 | ||||||
| chr1:204991277
|
C | T | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3122-15C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 24/27 | chr1 | 204991277 | ||||||
| chr1:204991317
|
A | G | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3136+11A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204991317 | ||||||
| chr1:204991645
|
C | T | 25 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.3136+339C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204991645 | ||||||
| chr1:204991690
|
C | G | 1 | a0001c0001t0013g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3136+384C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204991690 | ||||||
| chr1:204991761
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+455A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204991761 | ||||||
| chr1:204991802
|
G | A | 93 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0075others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.3136+496G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204991802 | ||||||
| chr1:204991987
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+681A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204991987 | ||||||
| chr1:204992305
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3136+999C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204992305 | ||||||
| chr1:204992912
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3136+1606A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204992912 | ||||||
| chr1:204992934
|
C | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3136+1628C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204992934 | ||||||
| chr1:204992953
|
C | T | 1 | a0001c0002t0001g0208 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3136+1647C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204992953 | ||||||
| chr1:204992970
|
G | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+1664G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204992970 | ||||||
| chr1:204993053
|
G | A | 7 | a0001c0005t0003g0243a0001c0005t0007g0248a0001c0005t0010g0213others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3136+1747G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993053 | ||||||
| chr1:204993099
|
G | C | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+1793G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993099 | ||||||
| chr1:204993116
|
G | A | 11 | a0001c0001t0028g0183a0001c0002t0003g0227a0001c0002t0005g0026others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3136+1810G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993116 | ||||||
| chr1:204993154
|
G | A | 5 | a0001c0002t0004g0230a0001c0002t0004g0231a0001c0002t0013g0217others(2): Show | 5 | HG01192.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3136+1848G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993154 | ||||||
| chr1:204993222
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0002g0028others(8): Show | 12 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.3136+1916C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993222 | ||||||
| chr1:204993237
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3136+1931T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993237 | ||||||
| chr1:204993243
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3136+1937T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993243 | ||||||
| chr1:204993277
|
A | G | 43 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(40): Show | 44 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.3136+1971A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993277 | ||||||
| chr1:204993305
|
C | T | 1 | a0005c0018t0001g0188 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3136+1999C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993305 | ||||||
| chr1:204993409
|
G | C | 4 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3136+2103G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993409 | ||||||
| chr1:204993446
|
A | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+2140A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993446 | ||||||
| chr1:204993453
|
A | G | 1 | a0001c0001t0009g0010 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3136+2147A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993453 | ||||||
| chr1:204993526
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3136+2220T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993526 | ||||||
| chr1:204993531
|
C | T | 1 | a0001c0002t0006g0129 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3136+2225C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993531 | ||||||
| chr1:204993532
|
G | A | 44 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0002t0001g0018others(41): Show | 45 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.3136+2226G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993532 | ||||||
| chr1:204993534
|
A | G | 118 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0075others(115): Show | 119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.3136+2228A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993534 | ||||||
| chr1:204993589
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+2283C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993589 | ||||||
| chr1:204993590
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(256): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.3136+2284A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993590 | ||||||
| chr1:204993741
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0003t0004g0005others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.3136+2435G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993741 | ||||||
| chr1:204993822
|
G | A | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3136+2516G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993822 | ||||||
| chr1:204994151
|
G | A | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3136+2845G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204994151 | ||||||
| chr1:204994186
|
C | T | 7 | a0001c0005t0003g0243a0001c0005t0007g0248a0001c0005t0010g0213others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3136+2880C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204994186 | ||||||
| chr1:204994212
|
C | A | 2 | a0001c0001t0012g0099a0001c0001t0027g0087 | 2 | HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3136+2906C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204994212 | ||||||
| chr1:204994474
|
T | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0094others(81): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3136+3168T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204994474 | ||||||
| chr1:204994534
|
A | T | 1 | a0001c0002t0001g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3136+3228A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204994534 | ||||||
| chr1:204994949
|
C | T | 24 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0094others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.3136+3643C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204994949 | ||||||
| chr1:204995171
|
G | T | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3136+3865G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995171 | ||||||
| chr1:204995203
|
G | A | 2 | a0001c0001t0006g0024a0001c0001t0049g0197 | 2 | NA18962.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.3136+3897G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995203 | ||||||
| chr1:204995313
|
A | G | 1 | a0001c0003t0007g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3136+4007A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995313 | ||||||
| chr1:204995315
|
A | AGT | 18 | a0001c0002t0002g0077a0001c0002t0003g0175a0001c0002t0009g0037others(15): Show | 19 | HG00639.hp2 HG01099.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.3136+4046_3136+404 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
A | AGTGT | 44 | a0001c0001t0001g0069a0001c0001t0001g0094a0001c0001t0001g0100others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.3136+4044_3136+404 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
A | AGTGTGT | 4 | a0001c0001t0001g0016a0001c0001t0044g0235a0001c0001t0049g0197others(1): Show | 4 | HG03942.hp2 HG04199.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.3136+4042_3136+404 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
A | AGTGTGTG others(1): Show |
4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3136+4040_3136+404 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGT | A | 24 | a0001c0001t0001g0082a0001c0001t0028g0183a0001c0001t0055g0156others(21): Show | 24 | HG00423.hp2 HG00673.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3136+4046_3136+404 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGT | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0058others(129): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3136+4044_3136+404 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGTGT | A | 15 | a0001c0001t0003g0045a0001c0001t0005g0139a0001c0001t0005g0226others(12): Show | 15 | HG01109.hp1 HG01192.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3136+4042_3136+404 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0028others(4): Show | 7 | HG00323.hp1 HG02602.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3136+4040_3136+404 others(12): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995315
|
AGTGTGTG others(11): Show |
A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+4030_3136+404 others(22): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995315 | |||||
| chr1:204995335
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3136+4029T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995335 | ||||||
| chr1:204995343
|
TGTGTGTG others(13): Show |
T | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3136+4041_3136+406 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204995343 | |||||
| chr1:204995354
|
A | G | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3136+4048A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995354 | ||||||
| chr1:204995503
|
C | T | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3136+4197C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995503 | ||||||
| chr1:204995546
|
G | A | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3136+4240G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995546 | ||||||
| chr1:204995731
|
G | A | 6 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3136+4425G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204995731 | ||||||
| chr1:204996024
|
G | T | 28 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(25): Show | 28 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.3136+4718G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996024 | ||||||
| chr1:204996026
|
C | A | 28 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(25): Show | 28 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.3136+4720C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996026 | ||||||
| chr1:204996288
|
A | G | 6 | a0001c0003t0004g0005a0001c0003t0004g0038a0001c0003t0007g0042others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3136+4982A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996288 | ||||||
| chr1:204996296
|
C | A | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+4990C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996296 | ||||||
| chr1:204996396
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(254): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3136+5090T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996396 | ||||||
| chr1:204996529
|
A | G | 155 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0075others(152): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3136+5223A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996529 | ||||||
| chr1:204996599
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0058 | 3 | HG00738.hp2 HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3136+5293C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996599 | ||||||
| chr1:204996626
|
T | C | 41 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0007others(38): Show | 42 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.3136+5320T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996626 | ||||||
| chr1:204996740
|
C | T | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+5434C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996740 | ||||||
| chr1:204996910
|
T | C | 10 | a0001c0001t0001g0191a0001c0002t0001g0105a0001c0002t0001g0142others(7): Show | 10 | HG01175.hp2 HG01243.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3136+5604T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996910 | ||||||
| chr1:204997042
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0126others(54): Show | 59 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.3136+5736T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997042 | ||||||
| chr1:204997145
|
C | T | 2 | a0001c0001t0001g0124a0001c0006t0005g0054 | 2 | HG00323.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3136+5839C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997145 | ||||||
| chr1:204997172
|
C | T | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3136+5866C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997172 | ||||||
| chr1:204997225
|
C | T | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3136+5919C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997225 | ||||||
| chr1:204997274
|
A | G | 22 | a0001c0001t0028g0183a0001c0002t0003g0175a0001c0002t0004g0034others(19): Show | 22 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.3136+5968A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997274 | ||||||
| chr1:204997300
|
C | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0069others(73): Show | 78 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.3136+5994C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997300 | ||||||
| chr1:204997316
|
G | A | 1 | a0001c0002t0023g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3136+6010G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997316 | ||||||
| chr1:204997454
|
C | G | 2 | a0001c0009t0001g0002a0001c0009t0001g0118 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3136+6148C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997454 | ||||||
| chr1:204997469
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3136+6163G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997469 | ||||||
| chr1:204997514
|
T | G | 2 | a0001c0002t0004g0034a0001c0005t0052g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3136+6208T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997514 | ||||||
| chr1:204997562
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.3136+6256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997562 | ||||||
| chr1:204997621
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(223): Show | 229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.3136+6315A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997621 | ||||||
| chr1:204997640
|
C | A | 3 | a0001c0002t0004g0133a0001c0002t0004g0214a0001c0002t0043g0182 | 3 | HG03098.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3136+6334C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997640 | ||||||
| chr1:204997791
|
G | A | 2 | a0001c0003t0001g0127a0007c0019t0001g0229 | 2 | HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3136+6485G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997791 | ||||||
| chr1:204997796
|
C | T | 9 | a0001c0001t0009g0010a0001c0002t0003g0201a0001c0002t0004g0230others(6): Show | 9 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3136+6490C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997796 | ||||||
| chr1:204997870
|
C | T | 2 | a0001c0001t0028g0183a0001c0006t0034g0030 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3136+6564C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997870 | ||||||
| chr1:204998032
|
CA | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(158): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.3136+6729delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204998032 | |||||
| chr1:204998058
|
A | T | 23 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0002g0047others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.3136+6752A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998058 | ||||||
| chr1:204998111
|
G | T | 3 | a0001c0001t0018g0153a0001c0001t0018g0154a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3136+6805G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998111 | ||||||
| chr1:204998128
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.3136+6822G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998128 | ||||||
| chr1:204998527
|
G | T | 1 | a0001c0002t0022g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3136+7221G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998527 | ||||||
| chr1:204998585
|
G | A | 2 | a0001c0001t0015g0025a0001c0001t0015g0232 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3136+7279G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998585 | ||||||
| chr1:204998657
|
G | A | 2 | a0001c0011t0015g0176a0001c0011t0030g0015 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.3136+7351G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998657 | ||||||
| chr1:204998730
|
TAA | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3136+7428_3136+742 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204998730 | |||||
| chr1:204998854
|
T | G | 1 | a0004c0024t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3136+7548T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998854 | ||||||
| chr1:204998909
|
C | T | 2 | a0001c0001t0001g0001a0001c0017t0001g0167 | 3 | HG00738.hp2 HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.3136+7603C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204998909 | ||||||
| chr1:204999002
|
A | C | 3 | a0001c0001t0018g0153a0001c0001t0018g0154a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3136+7696A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999002 | ||||||
| chr1:204999063
|
T | C | 6 | a0001c0002t0001g0079a0001c0003t0010g0040a0001c0006t0003g0260others(3): Show | 6 | HG01074.hp1 HG01257.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3136+7757T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999063 | ||||||
| chr1:204999130
|
C | A | 53 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(50): Show | 53 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.3136+7824C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999130 | ||||||
| chr1:204999211
|
C | T | 50 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(47): Show | 50 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.3136+7905C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999211 | ||||||
| chr1:204999264
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.3136+7958C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999264 | ||||||
| chr1:204999414
|
G | A | 6 | a0001c0002t0001g0079a0001c0003t0010g0040a0001c0006t0003g0260others(3): Show | 6 | HG01074.hp1 HG01257.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3136+8108G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999414 | ||||||
| chr1:204999415
|
G | A | 28 | a0001c0001t0001g0126a0001c0001t0003g0045a0001c0001t0005g0139others(25): Show | 28 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3136+8109G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999415 | ||||||
| chr1:204999557
|
G | C | 1 | a0001c0002t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3136+8251G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999557 | ||||||
| chr1:204999631
|
G | A | 2 | a0001c0002t0004g0230a0001c0002t0004g0231 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3136+8325G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999631 | ||||||
| chr1:204999659
|
T | C | 51 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(48): Show | 51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.3136+8353T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999659 | ||||||
| chr1:204999668
|
TAA | T | 2 | a0001c0009t0001g0002a0001c0009t0001g0118 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3136+8363_3136+836 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999668 | ||||||
| chr1:204999668
|
TAATATG | T | 16 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0005g0140others(13): Show | 16 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.3136+8366_3136+837 others(10): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 204999668 | |||||
| chr1:204999817
|
A | G | 51 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(48): Show | 51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.3136+8511A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999817 | ||||||
| chr1:204999929
|
G | T | 1 | a0001c0001t0010g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3136+8623G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999929 | ||||||
| chr1:204999938
|
A | G | 51 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(48): Show | 51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.3136+8632A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999938 | ||||||
| chr1:204999963
|
T | A | 17 | a0001c0002t0001g0066a0001c0002t0001g0203a0001c0002t0003g0175others(14): Show | 17 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.3136+8657T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999963 | ||||||
| chr1:205000032
|
C | T | 1 | a0001c0001t0006g0247 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3136+8726C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000032 | ||||||
| chr1:205000116
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3136+8810T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000116 | ||||||
| chr1:205000154
|
G | A | 2 | a0001c0002t0004g0230a0001c0002t0004g0231 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3136+8848G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000154 | ||||||
| chr1:205000189
|
G | A | 51 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(48): Show | 51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.3136+8883G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000189 | ||||||
| chr1:205000242
|
T | G | 6 | a0001c0002t0003g0201a0001c0002t0004g0230a0001c0002t0004g0231others(3): Show | 6 | HG01192.hp1 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3136+8936T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000242 | ||||||
| chr1:205000264
|
G | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0193 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3136+8958G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000264 | ||||||
| chr1:205000291
|
C | T | 48 | a0001c0001t0001g0180a0001c0001t0002g0080a0001c0001t0002g0081others(45): Show | 48 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.3136+8985C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000291 | ||||||
| chr1:205000458
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0061others(90): Show | 95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3137-9099C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000458 | ||||||
| chr1:205000561
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0061others(90): Show | 95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3137-8996G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000561 | ||||||
| chr1:205000776
|
G | A | 5 | a0001c0001t0009g0110a0001c0002t0009g0037a0001c0002t0009g0242others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3137-8781G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000776 | ||||||
| chr1:205000794
|
T | C | 3 | a0001c0001t0018g0153a0001c0001t0018g0154a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3137-8763T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000794 | ||||||
| chr1:205000826
|
C | CA | 5 | a0001c0001t0009g0110a0001c0002t0009g0037a0001c0002t0009g0242others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3137-8718dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205000826 | |||||
| chr1:205000826
|
CA | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0061others(114): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.3137-8718delA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205000826 | |||||
| chr1:205000826
|
CAA | C | 53 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(50): Show | 53 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.3137-8719_3137-871 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205000826 | |||||
| chr1:205000839
|
A | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0061others(89): Show | 94 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3137-8718A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000839 | ||||||
| chr1:205000839
|
A | T | 1 | a0007c0019t0001g0229 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3137-8718A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000839 | ||||||
| chr1:205000885
|
C | G | 1 | a0001c0005t0052g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3137-8672C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205000885 | ||||||
| chr1:205001020
|
TC | T | 49 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(46): Show | 49 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.3137-8533delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205001020 | |||||
| chr1:205001115
|
A | G | 52 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3137-8442A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001115 | ||||||
| chr1:205001174
|
T | C | 52 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3137-8383T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001174 | ||||||
| chr1:205001195
|
C | T | 1 | a0001c0003t0010g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3137-8362C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001195 | ||||||
| chr1:205001302
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3137-8255C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001302 | ||||||
| chr1:205001325
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3137-8232C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001325 | ||||||
| chr1:205001367
|
C | A | 52 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3137-8190C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001367 | ||||||
| chr1:205001437
|
T | C | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3137-8120T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001437 | ||||||
| chr1:205001516
|
A | G | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3137-8041A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001516 | ||||||
| chr1:205001580
|
G | A | 49 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(46): Show | 49 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.3137-7977G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001580 | ||||||
| chr1:205001649
|
T | A | 52 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3137-7908T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001649 | ||||||
| chr1:205001716
|
C | A | 49 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(46): Show | 49 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.3137-7841C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001716 | ||||||
| chr1:205001742
|
C | T | 1 | a0001c0002t0022g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3137-7815C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001742 | ||||||
| chr1:205001761
|
G | A | 3 | a0001c0001t0012g0099a0001c0001t0012g0120a0001c0001t0027g0087 | 3 | HG01169.hp2 HG02004.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3137-7796G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001761 | ||||||
| chr1:205001981
|
G | A | 3 | a0001c0001t0018g0153a0001c0001t0018g0154a0004c0024t0001g0052 | 3 | HG01433.hp2 NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3137-7576G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001981 | ||||||
| chr1:205002214
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0061others(89): Show | 94 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3137-7343A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002214 | ||||||
| chr1:205002266
|
G | A | 5 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(2): Show | 5 | HG01074.hp1 HG01257.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3137-7291G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002266 | ||||||
| chr1:205002285
|
A | G | 53 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0017others(50): Show | 53 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.3137-7272A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002285 | ||||||
| chr1:205002315
|
T | C | 1 | a0001c0002t0001g0203 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3137-7242T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002315 | ||||||
| chr1:205002324
|
A | G | 54 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(51): Show | 54 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.3137-7233A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002324 | ||||||
| chr1:205002327
|
T | C | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3137-7230T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002327 | ||||||
| chr1:205002357
|
C | A | 52 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0080others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3137-7200C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002357 | ||||||
| chr1:205002377
|
G | A | 5 | a0001c0001t0009g0110a0001c0002t0009g0037a0001c0002t0009g0242others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3137-7180G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002377 | ||||||
| chr1:205002408
|
G | A | 3 | a0001c0005t0052g0033a0001c0006t0017g0134a0001c0006t0017g0135 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3137-7149G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002408 | ||||||
| chr1:205002408
|
G | C | 24 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0009g0110others(21): Show | 24 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.3137-7149G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002408 | ||||||
| chr1:205002425
|
A | G | 55 | a0001c0001t0001g0180a0001c0001t0001g0223a0001c0001t0002g0017others(52): Show | 55 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.3137-7132A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002425 | ||||||
| chr1:205002576
|
T | C | 5 | a0001c0002t0003g0175a0001c0002t0004g0214a0001c0002t0043g0182others(2): Show | 5 | HG01496.hp1 HG02257.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3137-6981T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002576 | ||||||
| chr1:205002666
|
C | T | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3137-6891C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002666 | ||||||
| chr1:205002895
|
T | C | 2 | a0001c0001t0015g0025a0001c0003t0037g0225 | 2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3137-6662T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002895 | ||||||
| chr1:205002965
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3137-6592A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205002965 | ||||||
| chr1:205003005
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3137-6552T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003005 | ||||||
| chr1:205003160
|
G | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(145): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.3137-6397G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003160 | ||||||
| chr1:205003201
|
C | G | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3137-6356C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003201 | ||||||
| chr1:205003289
|
A | G | 11 | a0001c0001t0018g0153a0001c0001t0018g0154a0001c0002t0004g0216others(8): Show | 11 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3137-6268A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003289 | ||||||
| chr1:205003357
|
G | C | 1 | a0001c0003t0003g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3137-6200G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003357 | ||||||
| chr1:205003456
|
G | A | 7 | a0001c0001t0007g0032a0001c0001t0007g0048a0001c0002t0048g0239others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3137-6101G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003456 | ||||||
| chr1:205003515
|
C | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.3137-6042C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003515 | ||||||
| chr1:205003528
|
A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3137-6029A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003528 | ||||||
| chr1:205003569
|
G | A | 1 | a0001c0002t0002g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3137-5988G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003569 | ||||||
| chr1:205003718
|
C | T | 16 | a0001c0001t0009g0110a0001c0002t0004g0216a0001c0002t0004g0230others(13): Show | 16 | HG02572.hp2 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.3137-5839C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003718 | ||||||
| chr1:205003775
|
G | A | 12 | a0001c0002t0004g0216a0001c0002t0004g0230a0001c0002t0004g0231others(9): Show | 12 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.3137-5782G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003775 | ||||||
| chr1:205003877
|
C | T | 4 | a0001c0001t0009g0110a0001c0002t0009g0037a0001c0002t0009g0242others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-5680C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003877 | ||||||
| chr1:205004010
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0061others(155): Show | 159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.3137-5547A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004010 | ||||||
| chr1:205004046
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.3137-5511T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004046 | ||||||
| chr1:205004409
|
G | C | 2 | a0001c0001t0011g0157a0008c0023t0011g0189 | 2 | NA19003.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3137-5148G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004409 | ||||||
| chr1:205004441
|
A | G | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3137-5116A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004441 | ||||||
| chr1:205004481
|
G | A | 51 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0007g0032others(48): Show | 51 | HG00639.hp1 HG00741.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.3137-5076G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004481 | ||||||
| chr1:205004553
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3137-5004G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004553 | ||||||
| chr1:205004699
|
G | A | 1 | a0001c0002t0047g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3137-4858G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004699 | ||||||
| chr1:205004702
|
T | G | 13 | a0001c0001t0009g0010a0001c0002t0004g0216a0001c0002t0004g0230others(10): Show | 13 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.3137-4855T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004702 | ||||||
| chr1:205004753
|
C | T | 98 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0109others(95): Show | 100 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.3137-4804C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004753 | ||||||
| chr1:205004764
|
ACAGG | A | 44 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(41): Show | 46 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.3137-4789_3137-478 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205004764 | |||||
| chr1:205004794
|
G | A | 99 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0109others(96): Show | 101 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.3137-4763G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004794 | ||||||
| chr1:205004883
|
G | A | 44 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(41): Show | 46 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.3137-4674G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004883 | ||||||
| chr1:205005052
|
G | T | 1 | a0001c0004t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3137-4505G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005052 | ||||||
| chr1:205005057
|
G | A | 98 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0109others(95): Show | 100 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.3137-4500G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005057 | ||||||
| chr1:205005266
|
C | T | 1 | a0001c0001t0055g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3137-4291C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005266 | ||||||
| chr1:205005270
|
ATTC | A | 13 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(10): Show | 13 | HG01192.hp1 HG01496.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3137-4282_3137-428 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205005270 | |||||
| chr1:205005380
|
C | T | 105 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0082others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.3137-4177C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005380 | ||||||
| chr1:205005389
|
G | A | 18 | a0001c0001t0007g0032a0001c0001t0007g0048a0001c0002t0001g0013others(15): Show | 18 | HG01109.hp2 HG01175.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137-4168G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005389 | ||||||
| chr1:205005418
|
C | CA | 18 | a0001c0001t0007g0032a0001c0001t0007g0048a0001c0002t0001g0013others(15): Show | 18 | HG01109.hp2 HG01175.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137-4138dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205005418 | |||||
| chr1:205005418
|
C | T | 4 | a0001c0002t0001g0018a0001c0002t0001g0066a0001c0012t0001g0068others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-4139C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005418 | ||||||
| chr1:205005452
|
G | A | 92 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0082others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.3137-4105G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005452 | ||||||
| chr1:205005465
|
G | A | 1 | a0001c0003t0003g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3137-4092G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005465 | ||||||
| chr1:205005556
|
G | A | 1 | a0001c0003t0024g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3137-4001G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005556 | ||||||
| chr1:205005603
|
G | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0186a0001c0001t0001g0192others(1): Show | 4 | HG00544.hp1 NA18955.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.3137-3954G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005603 | ||||||
| chr1:205005671
|
C | G | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3137-3886C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005671 | ||||||
| chr1:205005901
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3137-3656T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205005901 | ||||||
| chr1:205006046
|
G | A | 1 | a0001c0002t0008g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3137-3511G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006046 | ||||||
| chr1:205006046
|
G | T | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3137-3511G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006046 | ||||||
| chr1:205006136
|
C | G | 15 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(12): Show | 15 | HG01192.hp1 HG01496.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3137-3421C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006136 | ||||||
| chr1:205006136
|
C | T | 86 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0082others(83): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.3137-3421C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006136 | ||||||
| chr1:205006153
|
A | T | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3137-3404A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006153 | ||||||
| chr1:205006218
|
T | C | 1 | a0001c0002t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3137-3339T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006218 | ||||||
| chr1:205006240
|
T | G | 67 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0007g0032others(64): Show | 67 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.3137-3317T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006240 | ||||||
| chr1:205006523
|
G | A | 2 | a0001c0002t0001g0149a0001c0002t0002g0115 | 2 | HG02523.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3137-3034G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006523 | ||||||
| chr1:205006607
|
G | A | 44 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(41): Show | 46 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.3137-2950G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006607 | ||||||
| chr1:205006794
|
A | G | 1 | a0001c0002t0002g0238 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3137-2763A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006794 | ||||||
| chr1:205006810
|
T | G | 19 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(16): Show | 19 | HG01192.hp1 HG01496.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3137-2747T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006810 | ||||||
| chr1:205006841
|
A | G | 4 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022others(1): Show | 4 | HG01074.hp1 HG01175.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-2716A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006841 | ||||||
| chr1:205006852
|
A | G | 47 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0001t0001g0082others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.3137-2705A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006852 | ||||||
| chr1:205006924
|
A | T | 8 | a0001c0001t0003g0045a0001c0002t0003g0201a0001c0002t0003g0236others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3137-2633A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205006924 | ||||||
| chr1:205006964
|
TGGA | T | 46 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(43): Show | 48 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.3137-2590_3137-258 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205006964 | |||||
| chr1:205007010
|
G | A | 89 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0082others(86): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.3137-2547G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007010 | ||||||
| chr1:205007078
|
T | C | 19 | a0001c0001t0009g0010a0001c0001t0015g0025a0001c0001t0015g0232others(16): Show | 19 | HG01496.hp1 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3137-2479T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007078 | ||||||
| chr1:205007085
|
G | A | 1 | a0001c0002t0017g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3137-2472G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007085 | ||||||
| chr1:205007101
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3137-2456T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007101 | ||||||
| chr1:205007136
|
G | C | 110 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0082others(107): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.3137-2421G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007136 | ||||||
| chr1:205007230
|
T | TA | 18 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(15): Show | 18 | HG01192.hp1 HG01496.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3137-2323dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205007230 | |||||
| chr1:205007235
|
T | A | 110 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0082others(107): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.3137-2322T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007235 | ||||||
| chr1:205007236
|
T | A | 18 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(15): Show | 18 | HG01192.hp1 HG01496.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3137-2321T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007236 | ||||||
| chr1:205007244
|
C | A | 18 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(15): Show | 18 | HG01192.hp1 HG01496.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3137-2313C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007244 | ||||||
| chr1:205007350
|
A | AAC | 24 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(21): Show | 24 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.3137-2204_3137-220 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205007350 | |||||
| chr1:205007445
|
A | G | 17 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3137-2112A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007445 | ||||||
| chr1:205007573
|
T | C | 1 | a0001c0007t0026g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3137-1984T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007573 | ||||||
| chr1:205007615
|
CTTTG | C | 17 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3137-1938_3137-193 others(8): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205007615 | |||||
| chr1:205007655
|
A | G | 17 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3137-1902A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007655 | ||||||
| chr1:205007763
|
G | A | 12 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0010g0027others(9): Show | 12 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3137-1794G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007763 | ||||||
| chr1:205007782
|
A | G | 41 | a0001c0001t0007g0032a0001c0001t0007g0048a0001c0001t0010g0029others(38): Show | 41 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.3137-1775A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007782 | ||||||
| chr1:205007812
|
G | T | 1 | a0001c0002t0023g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3137-1745G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205007812 | ||||||
| chr1:205008004
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3137-1553G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008004 | ||||||
| chr1:205008025
|
C | T | 1 | a0001c0002t0022g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3137-1532C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008025 | ||||||
| chr1:205008051
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0002g0249a0001c0001t0014g0098others(1): Show | 4 | NA18955.hp2 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-1506G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008051 | ||||||
| chr1:205008056
|
G | T | 23 | a0001c0001t0002g0131a0001c0001t0003g0045a0001c0001t0005g0139others(20): Show | 23 | HG00733.hp1 HG01106.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.3137-1501G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008056 | ||||||
| chr1:205008319
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3137-1238C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008319 | ||||||
| chr1:205008543
|
C | T | 47 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(44): Show | 49 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.3137-1014C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008543 | ||||||
| chr1:205008559
|
G | A | 44 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(41): Show | 45 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3137-998G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008559 | ||||||
| chr1:205008579
|
G | C | 47 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(44): Show | 49 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.3137-978G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008579 | ||||||
| chr1:205008594
|
AC | A | 66 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(63): Show | 68 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.3137-956delC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205008594 | |||||
| chr1:205008599
|
C | A | 14 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0010g0027others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3137-958C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008599 | ||||||
| chr1:205008599
|
C | G | 1 | a0001c0001t0049g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3137-958C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008599 | ||||||
| chr1:205008600
|
C | T | 1 | a0001c0001t0010g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3137-957C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008600 | ||||||
| chr1:205008628
|
T | C | 66 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(63): Show | 68 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.3137-929T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008628 | ||||||
| chr1:205008640
|
C | T | 17 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3137-917C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008640 | ||||||
| chr1:205008671
|
A | G | 166 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0069others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.3137-886A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008671 | ||||||
| chr1:205008808
|
C | CG | 38 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0009g0010others(35): Show | 38 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.3137-742dupG | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205008808 | |||||
| chr1:205008814
|
G | T | 12 | a0001c0001t0003g0045a0001c0002t0003g0201a0001c0002t0003g0236others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3137-743G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008814 | ||||||
| chr1:205008954
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3137-603A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205008954 | ||||||
| chr1:205009079
|
C | T | 4 | a0001c0002t0001g0018a0001c0002t0001g0066a0001c0012t0001g0068others(1): Show | 4 | HG01081.hp2 HG01255.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.3137-478C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205009079 | ||||||
| chr1:205009108
|
A | C | 1 | a0001c0002t0001g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3137-449A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205009108 | ||||||
| chr1:205009108
|
A | G | 1 | a0001c0001t0014g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3137-449A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205009108 | ||||||
| chr1:205009206
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3137-351G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205009206 | ||||||
| chr1:205009314
|
T | TCTG | 26 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0009g0010others(23): Show | 26 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.3137-240_3137-238d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205009314 | |||||
| chr1:205009317
|
G | GCTT | 40 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.3137-239_3137-237d others(5): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | 205009317 | |||||
| chr1:205009405
|
A | G | 170 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0069others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.3137-152A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205009405 | ||||||
| chr1:205009515
|
C | A | 47 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(44): Show | 49 | HG00099.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.3137-42C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205009515 | ||||||
| chr1:205009818
|
C | A | 3 | a0001c0010t0001g0091a0001c0010t0025g0049a0001c0010t0026g0022 | 3 | HG01074.hp1 HG01257.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.3268+130C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205009818 | ||||||
| chr1:205009943
|
A | G | 72 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(69): Show | 74 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.3268+255A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205009943 | ||||||
| chr1:205010003
|
T | C | 1 | a0001c0004t0001g0003 | 2 | NA18951.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3268+315T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010003 | ||||||
| chr1:205010074
|
G | A | 2 | a0001c0001t0006g0024a0001c0001t0006g0070 | 2 | NA18962.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.3268+386G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010074 | ||||||
| chr1:205010325
|
C | T | 35 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.3268+637C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010325 | ||||||
| chr1:205010555
|
T | C | 4 | a0001c0001t0009g0110a0001c0002t0009g0037a0001c0002t0009g0242others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3268+867T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010555 | ||||||
| chr1:205010564
|
G | A | 35 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.3268+876G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010564 | ||||||
| chr1:205010601
|
T | A | 2 | a0001c0002t0003g0175a0001c0006t0004g0184 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3268+913T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010601 | ||||||
| chr1:205010624
|
G | A | 7 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 7 | HG00733.hp2 HG00738.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3268+936G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010624 | ||||||
| chr1:205010689
|
G | A | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3268+1001G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010689 | ||||||
| chr1:205010772
|
A | G | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3268+1084A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010772 | ||||||
| chr1:205010858
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3268+1170G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010858 | ||||||
| chr1:205010881
|
C | T | 1 | a0001c0001t0028g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3268+1193C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010881 | ||||||
| chr1:205010910
|
G | GA | 71 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(68): Show | 73 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.3268+1237dupA | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr1 | 205010910 | |||||
| chr1:205010974
|
A | G | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3268+1286A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205010974 | ||||||
| chr1:205011207
|
A | AC | 94 | a0001c0001t0001g0016a0001c0001t0001g0112a0001c0001t0001g0113others(91): Show | 96 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.3268+1527dupC | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr1 | 205011207 | |||||
| chr1:205011207
|
A | ACC | 18 | a0001c0001t0001g0109a0001c0001t0009g0010a0001c0002t0004g0133others(15): Show | 18 | HG00738.hp1 HG02572.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.3268+1526_3268+152 others(6): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr1 | 205011207 | |||||
| chr1:205011207
|
A | ACCC | 12 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0012g0099others(9): Show | 12 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3268+1525_3268+152 others(7): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr1 | 205011207 | |||||
| chr1:205011214
|
C | G | 2 | a0001c0001t0001g0082a0001c0001t0002g0083 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3268+1526C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011214 | ||||||
| chr1:205011232
|
G | A | 70 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0112others(67): Show | 72 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.3268+1544G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011232 | ||||||
| chr1:205011420
|
C | T | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3269-1377C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011420 | ||||||
| chr1:205011448
|
G | A | 17 | a0001c0001t0015g0025a0001c0001t0015g0232a0001c0002t0003g0175others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3269-1349G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011448 | ||||||
| chr1:205011449
|
T | A | 1 | a0001c0001t0013g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3269-1348T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011449 | ||||||
| chr1:205011450
|
C | T | 1 | a0001c0001t0013g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3269-1347C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011450 | ||||||
| chr1:205011582
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3269-1215G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011582 | ||||||
| chr1:205011779
|
G | A | 156 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0069others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.3269-1018G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011779 | ||||||
| chr1:205011807
|
C | T | 13 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0010g0027others(10): Show | 13 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.3269-990C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011807 | ||||||
| chr1:205011875
|
T | G | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3269-922T>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011875 | ||||||
| chr1:205011887
|
T | C | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3269-910T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011887 | ||||||
| chr1:205011952
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3269-845G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205011952 | ||||||
| chr1:205012004
|
G | A | 35 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.3269-793G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012004 | ||||||
| chr1:205012123
|
A | G | 34 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.3269-674A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012123 | ||||||
| chr1:205012206
|
C | T | 1 | a0001c0003t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3269-591C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012206 | ||||||
| chr1:205012228
|
A | G | 2 | a0001c0002t0003g0175a0001c0003t0024g0222 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3269-569A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012228 | ||||||
| chr1:205012308
|
G | A | 1 | a0001c0001t0051g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3269-489G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012308 | ||||||
| chr1:205012410
|
G | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0193a0001c0001t0041g0194others(1): Show | 4 | HG02015.hp2 HG02523.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.3269-387G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012410 | ||||||
| chr1:205012417
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3269-380A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012417 | ||||||
| chr1:205012461
|
A | T | 4 | a0001c0003t0035g0220a0001c0007t0016g0096a0001c0007t0016g0103others(1): Show | 4 | HG02922.hp1 HG03017.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3269-336A>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012461 | ||||||
| chr1:205012474
|
G | A | 26 | a0001c0001t0003g0045a0001c0001t0007g0032a0001c0001t0007g0048others(23): Show | 26 | HG00639.hp1 HG01109.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.3269-323G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012474 | ||||||
| chr1:205012676
|
A | G | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3269-121A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012676 | ||||||
| chr1:205012760
|
C | T | 1 | a0001c0002t0012g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3269-37C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 26/27 | chr1 | 205012760 | ||||||
| chr1:205012926
|
C | T | 6 | a0001c0003t0035g0220a0001c0007t0016g0096a0001c0007t0016g0103others(3): Show | 6 | HG01074.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338+60C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205012926 | ||||||
| chr1:205013035
|
G | C | 4 | a0001c0002t0004g0034a0001c0002t0017g0215a0001c0003t0010g0040others(1): Show | 4 | HG01192.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3338+169G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013035 | ||||||
| chr1:205013104
|
C | T | 34 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(31): Show | 34 | HG01074.hp1 HG01192.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.3338+238C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013104 | ||||||
| chr1:205013347
|
G | A | 6 | a0001c0003t0035g0220a0001c0007t0016g0096a0001c0007t0016g0103others(3): Show | 6 | HG01074.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338+481G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013347 | ||||||
| chr1:205013497
|
A | G | 1 | a0001c0003t0004g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3338+631A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013497 | ||||||
| chr1:205013585
|
A | G | 157 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0082others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.3338+719A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013585 | ||||||
| chr1:205013712
|
G | C | 2 | a0001c0002t0005g0140a0001c0003t0003g0036 | 2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3338+846G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013712 | ||||||
| chr1:205013715
|
C | T | 19 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(16): Show | 19 | HG01192.hp1 HG01496.hp1 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.3338+849C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013715 | ||||||
| chr1:205013870
|
T | C | 1 | a0001c0002t0021g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3338+1004T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205013870 | ||||||
| chr1:205014051
|
G | T | 15 | a0001c0001t0003g0045a0001c0001t0028g0183a0001c0002t0003g0201others(12): Show | 15 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3338+1185G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014051 | ||||||
| chr1:205014114
|
G | A | 2 | a0001c0001t0003g0045a0003c0026t0003g0177 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3338+1248G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014114 | ||||||
| chr1:205014227
|
C | A | 1 | a0001c0022t0031g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3338+1361C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014227 | ||||||
| chr1:205014246
|
C | G | 185 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0069others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.3338+1380C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014246 | ||||||
| chr1:205014275
|
G | C | 47 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.3338+1409G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014275 | ||||||
| chr1:205014293
|
G | A | 1 | a0001c0002t0023g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3338+1427G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014293 | ||||||
| chr1:205014367
|
A | G | 30 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0094others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.3338+1501A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014367 | ||||||
| chr1:205014485
|
C | T | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3338+1619C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014485 | ||||||
| chr1:205014597
|
T | A | 1 | a0001c0006t0005g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3339-1711T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014597 | ||||||
| chr1:205014651
|
C | A | 2 | a0001c0007t0016g0096a0001c0007t0016g0103 | 2 | HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3339-1657C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014651 | ||||||
| chr1:205014696
|
A | C | 16 | a0001c0001t0010g0029a0001c0001t0015g0025a0001c0001t0015g0232others(13): Show | 16 | HG01496.hp1 HG02723.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.3339-1612A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014696 | ||||||
| chr1:205014712
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3339-1596G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014712 | ||||||
| chr1:205014877
|
G | A | 23 | a0001c0001t0009g0010a0001c0001t0009g0110a0001c0001t0010g0029others(20): Show | 23 | HG01496.hp1 HG02055.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.3339-1431G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014877 | ||||||
| chr1:205014912
|
C | T | 4 | a0001c0002t0004g0034a0001c0002t0017g0215a0001c0003t0010g0040others(1): Show | 4 | HG01192.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3339-1396C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205014912 | ||||||
| chr1:205015087
|
C | T | 1 | a0001c0006t0005g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3339-1221C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015087 | ||||||
| chr1:205015145
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3339-1163C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015145 | ||||||
| chr1:205015194
|
G | C | 1 | a0001c0002t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3339-1114G>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015194 | ||||||
| chr1:205015205
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0018g0154 | 2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3339-1103G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015205 | ||||||
| chr1:205015285
|
GAGACCCA others(14): Show |
G | 1 | a0001c0002t0005g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3339-1000_3339-980 others(24): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr1 | 205015285 | |||||
| chr1:205015364
|
C | T | 12 | a0001c0001t0007g0032a0001c0001t0007g0048a0001c0002t0003g0175others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3339-944C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015364 | ||||||
| chr1:205015416
|
A | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0110a0001c0002t0009g0037others(3): Show | 6 | HG02055.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3339-892A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015416 | ||||||
| chr1:205015427
|
A | G | 1 | a0001c0001t0051g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3339-881A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015427 | ||||||
| chr1:205015439
|
C | T | 25 | a0001c0001t0001g0058a0001c0001t0002g0028a0001c0001t0007g0032others(22): Show | 25 | HG00741.hp2 HG01099.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.3339-869C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015439 | ||||||
| chr1:205015444
|
G | A | 66 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0001g0109others(63): Show | 68 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.3339-864G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015444 | ||||||
| chr1:205015490
|
A | G | 7 | a0001c0001t0009g0010a0001c0001t0009g0110a0001c0002t0009g0037others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3339-818A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015490 | ||||||
| chr1:205015671
|
C | A | 41 | a0001c0001t0003g0045a0001c0001t0007g0032a0001c0001t0007g0048others(38): Show | 41 | HG00738.hp1 HG01109.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.3339-637C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015671 | ||||||
| chr1:205015744
|
A | G | 1 | a0001c0003t0024g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3339-564A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015744 | ||||||
| chr1:205015755
|
A | G | 4 | a0001c0002t0017g0215a0001c0005t0052g0033a0001c0006t0017g0134others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3339-553A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205015755 | ||||||
| chr1:205016022
|
C | G | 42 | a0001c0001t0002g0131a0001c0001t0005g0139a0001c0001t0005g0226others(39): Show | 42 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.3339-286C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205016022 | ||||||
| chr1:205016037
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3339-271T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205016037 | ||||||
| chr1:205016098
|
A | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0058others(47): Show | 53 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3339-210A>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205016098 | ||||||
| chr1:205016187
|
G | A | 3 | a0001c0005t0019g0211a0001c0005t0019g0212a0001c0005t0033g0241 | 3 | HG02572.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3339-121G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205016187 | ||||||
| chr1:205016295
|
T | C | 1 | a0001c0002t0048g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3339-13T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205016295 |