Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0002 | 0/0 | 1189 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0003 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0004 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0005 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0006 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0007 | 0/0 | 1189 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0008 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| a0009 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | MARQP others(1184): Show |
chr1 | 204865862 | 205027822 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3567 | 97 | 12 | 17 | 42 | 5 | 21 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0002 | 1/1 | 3567 | 87 | 38 | 17 | 24 | 3 | 3 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0003 | 0/0 | 3567 | 21 | 15 | 4 | 0 | 2 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0004 | 0/0 | 3567 | 11 | 0 | 7 | 2 | 1 | 1 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0005 | 0/0 | 3567 | 9 | 9 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0006 | 0/0 | 3567 | 6 | 5 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0007 | 0/0 | 3567 | 3 | 0 | 1 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0008 | 0/0 | 3567 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0009 | 0/0 | 3567 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0010 | 0/0 | 3567 | 3 | 0 | 2 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0011 | 0/0 | 3567 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0012 | 0/0 | 3567 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0014 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0016 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0017 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0020 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0021 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0022 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0001c0027 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0002c0013 | 0/0 | 3567 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0002c0025 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0003c0015 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0004c0019 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0005c0024 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0006c0026 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0007c0028 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0008c0023 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
chr1 | 204865862 | 205027822 | ||
| a0009c0018 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | ATGGC others(3562): Show |
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 | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0002 | 0/0 | 10164 | 14 | 0 | 1 | 5 | 1 | 7 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0003 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0005 | 0/0 | 10157 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10152): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0006 | 0/0 | 10168 | 4 | 0 | 0 | 4 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10163): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0007 | 0/0 | 10164 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0009 | 0/0 | 10168 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10163): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0010 | 0/0 | 10161 | 3 | 1 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10156): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0011 | 0/0 | 10164 | 3 | 0 | 1 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0012 | 0/0 | 10160 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0013 | 0/0 | 10164 | 2 | 0 | 1 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0014 | 0/0 | 10156 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10151): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0015 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0018 | 0/0 | 10156 | 2 | 0 | 0 | 2 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10151): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0020 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0023 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0025 | 0/0 | 10151 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10146): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0027 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0028 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0029 | 0/0 | 10164 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0036 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0040 | 0/0 | 10160 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0041 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0042 | 0/0 | 10160 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0044 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0045 | 0/0 | 10160 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0048 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0050 | 0/0 | 10161 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10156): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0053 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0001t0054 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0001 | 0/1 | 10160 | 30 | 2 | 10 | 14 | 3 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0002 | 0/0 | 10164 | 16 | 7 | 1 | 5 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0003 | 0/0 | 10160 | 4 | 4 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0004 | 0/0 | 10160 | 6 | 6 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0005 | 0/0 | 10157 | 5 | 5 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10152): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0006 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10163): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0008 | 1/0 | 10152 | 6 | 3 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10147): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0009 | 0/0 | 10168 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10163): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0011 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0013 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0014 | 0/0 | 10156 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10151): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0017 | 0/0 | 10172 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10167): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0020 | 0/0 | 10164 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0021 | 0/0 | 10168 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10163): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0022 | 0/0 | 10156 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10151): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0023 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0032 | 0/0 | 10153 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10148): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0039 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0043 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0046 | 0/0 | 10165 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10160): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0047 | 0/0 | 10153 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10148): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0049 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0002t0052 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0001 | 0/0 | 10160 | 4 | 1 | 2 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0003 | 0/0 | 10160 | 3 | 3 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0004 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0006 | 0/0 | 10168 | 2 | 0 | 1 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10163): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0007 | 0/0 | 10164 | 4 | 3 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0008 | 0/0 | 10152 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10147): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0010 | 0/0 | 10161 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10156): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0024 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0035 | 0/0 | 10172 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10167): Show |
chr1 | 204865862 | 205027822 |
| a0001c0003t0037 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0004t0001 | 0/0 | 10160 | 10 | 0 | 6 | 2 | 1 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0004t0038 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0003 | 0/0 | 10160 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0007 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0010 | 0/0 | 10161 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10156): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0014 | 0/0 | 10156 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10151): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0019 | 0/0 | 10164 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0033 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0005t0051 | 0/0 | 10172 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10167): Show |
chr1 | 204865862 | 205027822 |
| a0001c0006t0003 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0006t0004 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0006t0005 | 0/0 | 10157 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10152): Show |
chr1 | 204865862 | 205027822 |
| a0001c0006t0017 | 0/0 | 10172 | 2 | 2 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10167): Show |
chr1 | 204865862 | 205027822 |
| a0001c0006t0034 | 0/0 | 10164 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0007t0016 | 0/0 | 10152 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10147): Show |
chr1 | 204865862 | 205027822 |
| a0001c0007t0026 | 0/0 | 10151 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10146): Show |
chr1 | 204865862 | 205027822 |
| a0001c0008t0001 | 0/0 | 10160 | 3 | 0 | 3 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0009t0001 | 0/0 | 10160 | 3 | 0 | 0 | 0 | 0 | 3 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0010t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0010t0025 | 0/0 | 10151 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10146): Show |
chr1 | 204865862 | 205027822 |
| a0001c0010t0026 | 0/0 | 10151 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10146): Show |
chr1 | 204865862 | 205027822 |
| a0001c0011t0015 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0011t0030 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0012t0001 | 0/0 | 10160 | 2 | 0 | 2 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0014t0004 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0016t0002 | 0/0 | 10164 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0001c0017t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0020t0016 | 0/0 | 10152 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10147): Show |
chr1 | 204865862 | 205027822 |
| a0001c0021t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0001c0022t0031 | 0/0 | 10157 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10152): Show |
chr1 | 204865862 | 205027822 |
| a0001c0027t0004 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0002c0013t0001 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0002c0013t0012 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0002c0025t0013 | 0/0 | 10164 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10159): Show |
chr1 | 204865862 | 205027822 |
| a0003c0015t0027 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0004c0019t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0005c0024t0001 | 0/0 | 10160 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0006c0026t0003 | 0/0 | 10160 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0007c0028t0022 | 0/0 | 10156 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10151): Show |
chr1 | 204865862 | 205027822 |
| a0008c0023t0012 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| a0009c0018t0001 | 0/0 | 10160 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | GATTC others(10155): Show |
chr1 | 204865862 | 205027822 |
| actghapid | grch38/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 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0068 | 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 |
| a0001c0001t0001g0083 | 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 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0123 | 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 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0001g0189 | 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 |
| a0001c0001t0001g0194 | 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 |
| a0001c0001t0001g0201 | 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 |
| a0001c0001t0001g0258 | 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 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0061 | 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 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0122 | 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 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0002g0241 | 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 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0006g0257 | 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 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0010g0028 | 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 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0011g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0012g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0013g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0013g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0018g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0018g0162 | 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 |
| a0001c0001t0023g0144 | 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 |
| a0001c0001t0036g0203 | 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 |
| a0001c0001t0041g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0042g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0044g0233 | 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 |
| a0001c0001t0048g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0050g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0053g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0001t0054g0164 | 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 |
| a0001c0002t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0065 | 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 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0108 | 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 |
| a0001c0002t0001g0147 | 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 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0174 | 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 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0199 | 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 |
| a0001c0002t0001g0207 | 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 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0001g0232 | 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 |
| a0001c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 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 |
| 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 |
| a0001c0002t0002g0071 | 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 |
| a0001c0002t0002g0116 | 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 |
| a0001c0002t0002g0204 | 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 |
| a0001c0002t0002g0236 | 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 |
| a0001c0002t0003g0190 | 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 |
| a0001c0002t0003g0234 | 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 |
| a0001c0002t0004g0217 | 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 |
| a0001c0002t0004g0248 | 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 |
| a0001c0002t0005g0213 | 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 |
| a0001c0002t0008g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0008g0238 | 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 |
| a0001c0002t0009g0245 | 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 |
| a0001c0002t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0013g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0014g0216 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0020g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0021g0156 | 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 |
| a0001c0002t0023g0098 | 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 |
| a0001c0002t0039g0160 | 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 |
| a0001c0002t0046g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0047g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0049g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0002t0052g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0003t0001g0120 | 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 |
| a0001c0003t0004g0004 | 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 |
| a0001c0003t0008g0010 | 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 |
| a0001c0003t0024g0221 | 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 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0004t0001g0063 | 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 |
| a0001c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0019g0210 | 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 |
| a0001c0005t0033g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0005t0051g0033 | 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 |
| a0001c0007t0016g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0007t0016g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0007t0026g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0008t0001g0143 | 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 |
| a0001c0009t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0009t0001g0119 | 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 |
| a0001c0012t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0001c0012t0001g0117 | 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 |
| a0001c0016t0002g0066 | 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 |
| a0001c0020t0016g0157 | 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 |
| a0001c0027t0004g0011 | 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 |
| a0002c0013t0012g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0002c0025t0013g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0003c0015t0027g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0004c0019t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0005c0024t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0006c0026t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0007c0028t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0008c0023t0012g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| a0009c0018t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0061 | 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 | t0014 | g0064 | EUR | FIN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0062 | 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 | t0011 | g0242 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00423 | hp2 | a0001 | c0001 | t0054 | g0164 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0204 | 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 | g0094 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0058 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00673 | hp1 | a0001 | c0002 | t0011 | g0198 | EAS | CHS | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00673 | hp2 | a0001 | c0002 | t0039 | g0160 | 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 | g0113 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00735 | hp2 | a0001 | c0008 | t0001 | g0146 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00738 | hp1 | a0003 | 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 | g0120 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG00741 | hp2 | a0002 | c0025 | t0013 | 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 | g0170 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01099 | hp1 | a0001 | c0002 | t0013 | 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 | g0112 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01109 | hp2 | a0001 | c0002 | t0047 | g0237 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01167 | hp1 | a0001 | c0008 | t0001 | g0143 | 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 | g0145 | 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 | a0004 | c0019 | t0001 | g0229 | AMR | PUR | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0147 | 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 | g0158 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01255 | hp2 | a0001 | c0012 | t0001 | g0067 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01257 | hp1 | a0001 | c0002 | t0023 | g0098 | 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 | g0107 | 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 | g0159 | 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 | g0117 | 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 | a0005 | 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 | g0063 | 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 | g0144 | 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 | g0106 | 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 | g0171 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02004 | hp2 | a0001 | c0001 | t0013 | g0121 | 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 | g0123 | 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 | g0193 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0163 | 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 | g0189 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0006 | 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 | g0231 | EAS | CDX | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02165 | hp2 | a0001 | c0001 | t0012 | g0165 | 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 | g0156 | 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 | g0190 | 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 | g0118 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0234 | AFR | ACB | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | KHV | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02572 | hp2 | a0001 | c0005 | t0019 | g0210 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02602 | hp2 | a0001 | c0001 | t0010 | g0028 | 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 | t0014 | g0005 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0245 | 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 | g0035 | 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 | t0013 | g0100 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0111 | 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 | g0246 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0248 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0009 | 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 | g0238 | 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 | g0004 | AFR | ESN | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03017 | hp1 | a0001 | c0009 | t0001 | g0119 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03017 | hp2 | a0001 | c0007 | t0016 | g0104 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03041 | hp1 | a0001 | c0005 | t0033 | g0244 | 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 | g0008 | 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 | a0006 | 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 | g0212 | 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 | t0051 | 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 | a0007 | 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 | g0007 | 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 | g0247 | AFR | GWD | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03540 | hp2 | a0001 | c0002 | t0014 | g0216 | 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 | g0239 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03654 | hp2 | a0001 | c0001 | t0042 | g0115 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03669 | hp1 | a0001 | c0007 | t0016 | g0097 | 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 | g0083 | SAS | STU | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03688 | hp2 | a0001 | c0001 | t0050 | 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 | g0055 | SAS | PJL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0027 | 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 | g0110 | 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 | g0071 | SAS | STU | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0082 | 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 | g0208 | 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 | g0221 | AFR | YRI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18906 | hp2 | a0001 | c0003 | t0008 | g0010 | AFR | YRI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18947 | hp1 | a0001 | c0002 | t0020 | g0056 | 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 | g0101 | 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 | g0233 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0196 | 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 | g0243 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18969 | hp1 | a0001 | c0001 | t0041 | g0188 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0194 | 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 | t0011 | g0099 | 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 | g0207 | 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 | g0203 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19002 | hp1 | a0001 | c0001 | t0048 | g0195 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19002 | hp2 | a0001 | c0001 | t0018 | g0162 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19003 | hp2 | a0001 | c0001 | t0012 | g0166 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19007 | hp1 | a0001 | c0001 | t0018 | g0161 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19007 | hp2 | a0008 | c0023 | t0012 | g0192 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0258 | 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 | t0012 | g0185 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0173 | 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 | g0217 | 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 | g0222 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19054 | hp1 | a0001 | c0002 | t0049 | g0200 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19060 | hp1 | a0001 | c0001 | t0053 | g0209 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA19075 | hp1 | a0009 | c0018 | t0001 | g0191 | 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 | g0066 | EUR | TSI | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0108 | 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 | g0114 | SAS | GIH | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0168 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0070 | AMR | CLM | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0213 | 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 | t0046 | g0172 | 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 | t0052 | g0235 | AFR | MSL | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| HG06807 | hp1 | a0001 | c0027 | t0004 | g0011 | 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 | g0202 | 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 | g0057 | 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 | g0157 | AFR | LWK | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0059 | REF | REF | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0008 | g0109 | REF | REF | NFASC_chr1_204865862_205027822 | NFASC | chr1 | 204865862 | 205027822 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204944337 | C | T | 1 | a0007 | 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 | a0006 | 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 | a0002 a0005 |
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 | a0009 | 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 | a0003 | 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 | a0005 | 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 | a0005 | 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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0011 a0001c0014 |
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 | a0001c0006 a0001c0022 |
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 | a0001c0001 a0001c0007 a0001c0008 others(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 | a0005c0024 | 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 | a0005c0024 | 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 | a0001c0003 a0001c0009 a0001c0010 others(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 | a0001c0010 a0002c0025 |
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 | a0001c0004 a0001c0009 a0001c0021 |
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 | a0001c0007 a0001c0020 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0053 a0001c0001t0054 |
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 | a0001c0001t0005 a0001c0001t0018 a0001c0002t0005 others(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 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0027 others(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 | a0001c0002t0017 a0001c0005t0051 a0001c0006t0017 |
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 | 96 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(93): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): 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 | a0001c0001t0027 a0003c0015t0027 |
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 | a0001c0001t0009 a0001c0002t0009 |
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 | a0001c0001t0003 a0001c0001t0027 a0001c0002t0003 others(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 | a0001c0001t0050 | 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 | a0001c0005t0051 | 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 | a0001c0002t0049 | 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 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0027 others(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 | a0001c0001t0048 | 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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(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 | a0001c0001t0020 a0001c0002t0020 |
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 | 53 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(50): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): 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 | a0001c0001t0025 a0001c0007t0026 a0001c0010t0025 others(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 | 39 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(36): Show |
131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): 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 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(42): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): 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 |
28 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(25): 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 | a0001c0001t0006 a0001c0001t0009 a0001c0002t0006 others(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 | a0001c0002t0017 a0001c0003t0035 a0001c0005t0051 others(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 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0050 others(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 | a0001c0001t0025 a0001c0007t0016 a0001c0007t0026 others(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 | 39 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(36): Show |
131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): 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 | a0001c0001t0023 a0001c0002t0023 |
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 | a0001c0001t0015 a0001c0011t0015 |
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 | a0001c0001t0010 a0001c0001t0050 a0001c0002t0046 others(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 | a0001c0001t0011 | 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 | a0001c0001t0015 a0001c0003t0024 a0001c0011t0015 |
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 | a0001c0002t0052 | 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 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0018 others(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 | a0001c0005t0019 a0001c0005t0033 |
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 | a0001c0001t0015 a0001c0002t0047 a0001c0003t0024 others(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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(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 | a0001c0002t0046 | 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 | 98 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(95): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): 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 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0032 others(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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0027 others(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 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0052 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(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 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0032 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:204871352 | G | A | 11 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0002t0001g0261 a0001c0006t0003g0260 |
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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0001t0001g0258 a0001c0001t0006g0257 a0001c0002t0001g0256 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0249 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0002g0131 a0001c0004t0038g0132 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0021g0219 a0001c0003t0035g0220 |
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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0001t0001g0141 a0001c0001t0023g0144 a0001c0002t0001g0142 others(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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0002t0001g0261 a0001c0006t0003g0260 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0002g0128 a0001c0002t0006g0129 |
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 | a0002c0025t0013g0148 | 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 | a0001c0001t0005g0139 a0001c0001t0009g0009 a0001c0002t0001g0013 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0002g0027 others(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 | a0001c0001t0001g0016 a0001c0001t0002g0017 a0001c0001t0002g0131 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0005g0139 a0001c0001t0009g0009 a0001c0001t0053g0209 others(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 | a0001c0002t0004g0214 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0040g0019 a0001c0002t0001g0018 |
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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0001t0005g0139 a0001c0002t0004g0133 a0001c0002t0043g0182 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0021g0219 a0001c0003t0035g0220 a0001c0011t0030g0015 |
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 | a0001c0001t0007g0048 a0001c0002t0002g0047 a0001c0002t0004g0034 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0002g0122 others(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 | a0001c0001t0001g0123 a0001c0002t0002g0250 a0001c0002t0005g0254 others(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 | 46 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0068 others(43): Show |
46 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(43): 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 | a0001c0001t0002g0027 a0001c0001t0003g0045 a0001c0001t0007g0032 others(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 | a0001c0001t0006g0024 a0001c0001t0007g0048 a0001c0002t0001g0018 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0002t0002g0055 | 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 | a0002c0025t0013g0148 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0186 a0001c0001t0036g0203 others(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 | a0001c0001t0012g0165 a0001c0002t0005g0213 a0001c0008t0001g0143 others(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 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0002t0001g0149 |
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 | a0001c0001t0001g0194 a0001c0001t0001g0258 a0001c0001t0006g0257 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0158 a0001c0001t0001g0173 others(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 | a0001c0001t0011g0168 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0193 others(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 | a0001c0003t0024g0221 a0001c0005t0003g0218 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0170 a0001c0001t0012g0166 others(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 | a0001c0001t0002g0153 a0001c0002t0001g0142 a0001c0002t0001g0169 |
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 | a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0002t0001g0199 others(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 | a0001c0001t0009g0009 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | a0001c0001t0001g0154 a0001c0001t0002g0163 a0001c0002t0001g0174 others(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 | a0001c0002t0004g0230 a0001c0002t0004g0248 a0001c0002t0005g0140 |
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 | a0001c0002t0002g0071 | 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 | a0001c0006t0017g0134 a0001c0006t0017g0135 a0001c0007t0026g0094 others(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 | a0001c0027t0004g0011 | 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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0023g0144 a0001c0002t0001g0152 a0001c0002t0001g0171 others(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 | a0001c0002t0008g0222 | 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 | a0001c0002t0008g0222 | 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 | a0001c0001t0005g0226 a0001c0002t0008g0222 a0001c0006t0017g0134 others(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 | a0001c0001t0005g0226 a0001c0002t0008g0222 |
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 | a0001c0020t0016g0157 | 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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0022t0031g0136 |
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 | a0001c0001t0005g0139 a0001c0006t0017g0134 a0001c0006t0017g0135 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0155 a0001c0001t0001g0158 others(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 | a0001c0002t0003g0227 a0001c0014t0004g0228 a0004c0019t0001g0229 |
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 | a0001c0001t0015g0239 a0001c0002t0005g0140 a0001c0002t0008g0222 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0086 a0001c0002t0002g0151 |
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 | a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
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 | a0001c0002t0003g0227 a0001c0002t0009g0255 a0001c0014t0004g0228 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0005g0139 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0003g0175 a0001c0011t0015g0176 a0006c0026t0003g0177 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0015g0025 a0001c0002t0005g0026 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0114 | 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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0004g0214 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | 64 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0068 others(61): Show |
65 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(62): 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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0002t0014g0216 | 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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0003g0175 a0001c0011t0015g0176 a0006c0026t0003g0177 |
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 | a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0005g0254 a0001c0002t0008g0252 a0001c0002t0008g0253 others(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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0001t0001g0057 a0001c0002t0020g0056 |
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 | a0001c0001t0005g0139 a0001c0002t0004g0133 a0001c0002t0008g0222 others(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 | a0001c0003t0001g0120 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0042g0115 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0053g0209 a0001c0002t0001g0207 a0001c0002t0001g0208 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0002t0004g0217 | 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 | a0001c0002t0004g0214 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0001t0015g0239 a0001c0002t0009g0245 a0001c0005t0003g0246 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0041g0188 |
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 | a0001c0001t0005g0139 a0001c0002t0004g0133 a0001c0002t0043g0182 others(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 | a0001c0001t0001g0202 a0001c0001t0036g0203 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0001g0152 | 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 | a0001c0002t0014g0216 | 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 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0007g0048 a0001c0002t0002g0047 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | 1 | a0001c0004t0001g0058 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-91+13806G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204884876 | |||||||
| chr1:204884932 | A | T | 3 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0002t0004g0214 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0001t0001g0016 a0001c0001t0002g0017 |
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 | a0001c0009t0001g0002 a0001c0009t0001g0119 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0003g0190 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0214 a0001c0002t0004g0217 others(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 | a0001c0002t0004g0217 | 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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0002t0002g0204 a0001c0002t0002g0205 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0083 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0170 others(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 | a0001c0002t0001g0147 a0001c0002t0001g0152 a0001c0002t0001g0174 others(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 | a0001c0001t0001g0123 a0001c0001t0009g0009 a0001c0001t0027g0087 others(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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0009c0018t0001g0191 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0003t0001g0137 a0001c0003t0003g0138 a0001c0006t0017g0134 others(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 | a0001c0001t0009g0009 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0007g0048 a0001c0002t0002g0047 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0002t0001g0106 others(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 | a0001c0001t0027g0087 a0001c0001t0042g0115 |
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 | a0001c0001t0003g0045 a0001c0002t0008g0043 a0001c0002t0008g0222 others(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 | a0008c0023t0012g0192 | 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 | a0001c0001t0003g0045 a0001c0002t0008g0043 a0001c0002t0008g0222 others(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 | a0001c0001t0001g0114 a0001c0007t0016g0104 |
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 | a0008c0023t0012g0192 | 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 | a0001c0002t0003g0190 | 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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0001t0007g0048 a0001c0002t0002g0047 a0001c0002t0004g0034 others(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 | a0001c0001t0001g0126 a0001c0001t0002g0122 |
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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0002g0027 a0001c0001t0010g0028 a0001c0002t0001g0023 others(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 | a0001c0001t0028g0183 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0001t0028g0183 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0020t0016g0157 | 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 | a0001c0001t0001g0173 | 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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0006t0017g0134 a0001c0006t0017g0135 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0013g0121 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0002t0004g0217 | 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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0007g0048 a0001c0002t0002g0047 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0057 a0001c0002t0020g0056 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0002t0002g0204 a0001c0002t0002g0205 |
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 | a0001c0001t0028g0183 a0001c0002t0004g0217 a0001c0002t0005g0213 others(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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0002t0004g0217 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0002t0004g0217 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0003t0003g0138 a0001c0006t0017g0134 a0001c0006t0017g0135 others(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 | a0001c0006t0017g0134 a0001c0006t0017g0135 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0141 a0001c0001t0001g0154 others(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 | a0001c0001t0005g0139 a0001c0001t0028g0183 a0001c0002t0004g0217 others(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 | a0001c0003t0003g0138 a0001c0006t0017g0134 a0001c0006t0017g0135 others(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 | a0001c0007t0016g0097 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0003t0003g0138 a0001c0006t0017g0134 a0001c0006t0017g0135 others(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 | a0001c0002t0008g0222 a0001c0003t0024g0221 |
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 | a0001c0020t0016g0157 | 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 | a0001c0001t0005g0139 a0001c0001t0028g0183 a0001c0002t0014g0216 others(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 | a0001c0001t0002g0241 a0001c0001t0002g0249 a0001c0001t0005g0226 others(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 | a0001c0001t0002g0241 a0001c0001t0002g0249 a0001c0001t0006g0243 others(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 | a0001c0001t0003g0045 a0001c0001t0015g0239 a0001c0003t0001g0070 |
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 | a0001c0001t0001g0194 | 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 | a0001c0002t0014g0216 | 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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0002t0002g0077 a0001c0003t0001g0127 |
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 | a0001c0001t0007g0032 a0001c0001t0010g0029 a0001c0002t0002g0031 |
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 | a0002c0025t0013g0148 | 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 | a0001c0002t0004g0133 a0001c0005t0003g0218 |
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 | a0001c0001t0006g0243 a0001c0001t0011g0242 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0141 others(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 | a0001c0002t0002g0236 a0001c0002t0003g0234 a0001c0002t0008g0238 others(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 | a0001c0002t0046g0172 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0201 a0001c0001t0053g0209 a0001c0002t0001g0207 others(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 | a0001c0002t0003g0190 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0141 others(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 | a0001c0002t0008g0043 a0001c0003t0007g0042 a0001c0003t0007g0044 |
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 | a0001c0001t0005g0139 a0001c0001t0028g0183 a0001c0002t0004g0217 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0141 others(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 | a0001c0001t0003g0045 a0001c0002t0008g0043 a0001c0002t0009g0037 others(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 | a0001c0002t0004g0217 | 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 | a0001c0001t0002g0027 a0001c0001t0002g0061 a0001c0001t0007g0032 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-91+30860C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204901930 | |||||||
| chr1:204902018 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(126): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): 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 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0155 others(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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0001c0002t0001g0169 | 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 | a0001c0001t0003g0045 a0001c0002t0009g0037 a0001c0003t0003g0035 others(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 | a0001c0001t0005g0226 a0001c0001t0007g0048 a0001c0001t0010g0112 others(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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-91+31632T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | chr1 | 204902702 | |||||||
| chr1:204902853 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0057 others(55): Show |
61 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(58): 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 | a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | a0001c0001t0003g0045 a0001c0001t0005g0226 a0001c0001t0007g0048 others(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 | a0001c0001t0011g0242 | 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 | a0001c0001t0002g0131 a0001c0002t0001g0062 a0001c0002t0002g0077 others(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 | a0001c0001t0015g0025 a0001c0002t0005g0026 a0001c0006t0034g0030 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0110 a0001c0001t0001g0154 others(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 | a0001c0002t0003g0190 a0001c0003t0010g0040 |
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 | a0002c0013t0012g0185 | 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 | a0001c0007t0016g0097 | 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 | a0001c0001t0011g0168 a0001c0017t0001g0167 |
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 | a0001c0001t0002g0241 | 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 | a0001c0001t0002g0131 a0001c0001t0010g0112 a0001c0001t0014g0064 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0086 others(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 | a0001c0001t0007g0048 a0001c0001t0009g0009 a0001c0002t0001g0013 others(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 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0002t0001g0152 others(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 | 52 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0075 others(49): Show |
52 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(49): 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 | a0001c0005t0010g0212 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0001g0113 others(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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0003t0007g0012 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0110 a0001c0001t0001g0154 others(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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0003t0007g0012 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0001g0113 others(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 | a0001c0001t0042g0115 | 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 | a0002c0013t0012g0185 | 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 | a0001c0001t0002g0131 a0001c0002t0002g0077 a0001c0004t0001g0078 others(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 | a0001c0001t0002g0131 a0001c0001t0010g0112 a0001c0001t0014g0064 others(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 | a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | a0001c0001t0001g0196 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | 94 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0057 others(91): Show |
96 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(93): 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 | a0001c0002t0003g0190 a0001c0003t0010g0040 |
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 | a0001c0001t0005g0139 a0001c0002t0003g0227 a0001c0002t0009g0255 others(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 | 98 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0083 others(95): Show |
99 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(96): 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 | a0001c0001t0005g0139 a0001c0002t0003g0227 a0001c0002t0009g0255 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0105 others(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 | a0001c0002t0001g0065 | 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 | a0001c0001t0001g0193 a0001c0002t0005g0140 |
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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0015g0025 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | a0001c0001t0003g0045 a0001c0001t0009g0009 a0001c0001t0009g0111 others(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 | a0001c0001t0044g0233 | 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 | a0001c0001t0001g0159 a0001c0001t0005g0139 a0001c0001t0044g0233 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0110 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0114 a0001c0002t0001g0206 |
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 | a0001c0001t0001g0114 | 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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0003t0007g0012 others(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 | 32 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0155 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(29): 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 | a0001c0002t0003g0175 a0001c0014t0004g0228 |
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 | a0001c0001t0053g0209 | 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 | a0001c0001t0001g0123 a0001c0001t0002g0122 a0001c0001t0002g0131 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0005g0139 a0001c0002t0001g0013 a0001c0002t0002g0006 others(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 | a0001c0001t0015g0025 a0001c0002t0047g0237 a0001c0006t0034g0030 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0015g0025 a0001c0006t0034g0030 |
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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0008g0238 | 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 | a0001c0002t0046g0172 | 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 | a0002c0013t0012g0185 | 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 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0005g0139 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0001g0013 a0001c0002t0003g0175 a0001c0014t0004g0228 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0020t0016g0157 | 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 | a0001c0002t0002g0071 | 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 | a0001c0002t0005g0140 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | a0001c0002t0008g0238 | 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 | a0001c0001t0003g0045 a0001c0002t0003g0234 a0001c0002t0008g0043 others(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 | a0001c0002t0005g0140 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0005g0254 a0001c0002t0008g0252 a0001c0002t0008g0253 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0047g0237 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0005g0140 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0005g0139 others(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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0020t0016g0157 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0015g0025 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0015g0025 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | a0001c0002t0005g0140 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0003t0007g0181 |
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 | a0002c0013t0012g0185 | 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 | a0001c0002t0047g0237 | 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 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0005g0139 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0003g0175 a0001c0014t0004g0228 a0001c0022t0031g0136 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0005g0139 others(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 | a0002c0013t0012g0185 | 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 | a0001c0002t0046g0172 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0002g0027 a0001c0001t0010g0028 |
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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0005g0140 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | a0001c0002t0021g0219 a0001c0003t0035g0220 |
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 | a0007c0028t0022g0089 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0002g0071 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0037g0225 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0005g0254 a0001c0002t0008g0252 a0001c0002t0008g0253 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0003g0227 a0001c0002t0009g0255 a0001c0005t0003g0218 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0015g0025 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0003g0045 a0001c0002t0009g0037 |
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 | a0001c0001t0007g0032 a0001c0002t0002g0031 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0012g0165 | 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 | a0001c0002t0001g0197 | 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(222): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0118 a0001c0001t0054g0164 |
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 | a0001c0002t0003g0175 a0001c0014t0004g0228 |
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 | a0002c0013t0012g0185 | 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 | a0001c0002t0047g0237 | 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 | a0002c0013t0012g0185 | 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 | a0001c0001t0007g0032 a0001c0002t0002g0031 |
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 | a0001c0002t0004g0034 a0001c0002t0005g0140 a0001c0002t0009g0245 others(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 | a0001c0001t0002g0061 a0001c0016t0002g0066 |
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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0124 a0001c0001t0013g0121 a0001c0001t0041g0188 others(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 | a0001c0002t0001g0152 a0001c0002t0002g0071 |
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 | a0001c0002t0004g0034 a0001c0002t0005g0140 a0001c0002t0009g0245 others(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 | a0001c0002t0052g0235 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0011g0168 a0001c0017t0001g0167 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | 54 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0110 others(51): Show |
54 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(51): 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 | a0001c0001t0005g0139 a0001c0001t0009g0009 a0001c0002t0008g0238 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0014g0064 others(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 | a0001c0006t0017g0134 a0001c0006t0017g0135 a0001c0011t0015g0176 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0001c0002t0002g0006 | 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 | a0001c0001t0001g0189 a0001c0001t0041g0188 |
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 | a0001c0001t0001g0110 a0001c0001t0040g0019 a0001c0001t0045g0072 others(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 | a0001c0001t0023g0144 | 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 | a0002c0013t0012g0185 | 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 | a0001c0002t0001g0013 a0001c0002t0003g0175 a0001c0014t0004g0228 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0083 others(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 | a0002c0013t0012g0185 | 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 | a0001c0002t0003g0175 a0001c0014t0004g0228 |
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 | a0001c0002t0001g0147 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0002t0002g0116 |
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 | a0001c0002t0001g0174 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0114 a0001c0001t0001g0170 others(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 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
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 | a0001c0001t0001g0095 a0001c0001t0002g0061 a0001c0016t0002g0066 |
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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(222): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): 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 | a0001c0002t0003g0175 a0001c0014t0004g0228 |
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 | a0002c0013t0012g0185 | 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 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0037g0225 |
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 | a0001c0001t0025g0088 a0001c0010t0026g0022 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0013g0100 others(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 | a0001c0001t0048g0195 | 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 | a0001c0002t0001g0013 a0001c0002t0003g0175 a0001c0002t0004g0034 others(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 | a0001c0001t0028g0183 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0002t0009g0245 a0001c0003t0003g0138 a0001c0003t0024g0221 |
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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0001c0002t0003g0190 | 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 | a0001c0001t0013g0121 | 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 | a0001c0002t0001g0208 | 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 | a0001c0001t0001g0095 | 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 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0037g0225 |
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 | 42 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0123 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): 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 | a0001c0001t0001g0155 a0001c0001t0001g0258 a0001c0001t0006g0257 others(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 | a0001c0001t0007g0032 a0001c0001t0009g0111 a0001c0001t0010g0029 others(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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0001c0002t0003g0175 a0001c0014t0004g0228 |
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 | a0001c0001t0002g0153 | 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 | a0001c0001t0007g0032 a0001c0001t0009g0111 a0001c0001t0010g0029 others(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 | a0001c0002t0047g0237 | 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 | a0002c0013t0012g0185 | 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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0105 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0155 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0258 a0001c0001t0006g0069 others(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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0005t0033g0244 | 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 | a0001c0001t0001g0110 a0001c0001t0040g0019 a0001c0001t0045g0072 others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0002g0122 a0001c0001t0005g0139 a0001c0002t0043g0182 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0001c0001t0002g0131 a0001c0001t0014g0064 a0001c0001t0025g0088 others(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 | a0001c0001t0001g0068 a0001c0001t0002g0103 a0001c0001t0011g0099 others(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 | a0001c0002t0008g0238 a0001c0002t0009g0037 |
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 | a0002c0013t0012g0185 | 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 | a0001c0005t0003g0246 | 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 | a0001c0005t0014g0005 | 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 | a0001c0002t0003g0190 | 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 | a0001c0002t0046g0172 | 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 | a0001c0001t0001g0075 a0001c0001t0001g0123 a0001c0001t0011g0242 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0187 a0001c0002t0001g0142 others(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 | 8 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0003t0003g0035 others(5): Show |
8 | HG00639.hp2 HG01192.hp1 HG02451.hp1 others(5): 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 | a0001c0001t0002g0081 a0001c0001t0015g0239 a0001c0002t0002g0047 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0259 a0001c0001t0036g0203 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0223 others(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 | a0001c0001t0009g0111 | 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 | a0001c0001t0010g0029 a0001c0003t0010g0040 |
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 | a0001c0005t0007g0247 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0126 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0201 a0001c0001t0027g0087 others(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 | a0001c0001t0009g0111 a0001c0003t0007g0012 a0001c0005t0007g0247 |
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 | a0001c0001t0054g0164 | 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 | a0001c0006t0017g0134 a0001c0006t0017g0135 |
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 | a0001c0002t0001g0013 a0001c0002t0003g0190 a0001c0002t0005g0140 others(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 | a0001c0002t0046g0172 | 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 | a0001c0002t0046g0172 | 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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0002c0013t0012g0185 | 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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0001c0001t0001g0107 | 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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0010g0112 | 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 | a0001c0001t0007g0032 a0001c0001t0009g0111 a0001c0001t0010g0029 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0034 a0001c0003t0010g0040 others(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 | a0001c0001t0007g0048 a0001c0002t0017g0215 a0001c0005t0010g0212 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(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 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0037g0225 |
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 | a0001c0003t0001g0070 a0001c0004t0001g0051 a0001c0004t0001g0053 |
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 | a0001c0002t0003g0227 a0001c0002t0009g0255 a0004c0019t0001g0229 |
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 | a0001c0002t0008g0238 | 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 | a0001c0001t0002g0122 | 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 | a0001c0003t0003g0035 a0001c0003t0003g0036 a0001c0003t0037g0225 |
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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0002t0047g0237 | 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 | a0001c0002t0001g0142 | 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 | a0002c0013t0012g0185 | 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 | a0001c0002t0003g0190 a0001c0002t0005g0254 a0001c0002t0008g0252 others(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 | a0001c0001t0001g0189 a0001c0001t0041g0188 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0002t0021g0219 a0001c0014t0004g0228 |
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 | a0001c0001t0010g0029 a0001c0002t0005g0140 a0001c0002t0009g0037 others(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 | a0001c0001t0002g0163 | 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 | a0001c0001t0001g0123 | 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 | a0001c0002t0009g0255 a0001c0005t0003g0218 a0001c0022t0031g0136 |
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 | a0001c0001t0015g0239 a0001c0002t0004g0214 |
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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0002t0009g0255 a0001c0005t0003g0218 a0002c0013t0001g0084 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | a0001c0002t0009g0255 a0001c0005t0003g0218 |
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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0075 others(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 | a0001c0002t0020g0056 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0075 others(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 | 81 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0110 others(78): Show |
83 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(80): 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 | a0001c0001t0002g0081 a0001c0001t0028g0183 a0001c0001t0040g0019 others(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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): 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 | a0001c0002t0009g0255 a0001c0005t0003g0218 |
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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(87): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): 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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0110 a0001c0001t0028g0183 a0001c0001t0040g0019 others(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 | a0001c0002t0008g0238 a0001c0002t0009g0255 a0001c0005t0003g0218 others(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 | a0001c0002t0009g0037 a0001c0002t0009g0245 a0001c0003t0003g0138 others(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 | a0001c0003t0004g0004 | 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 | 62 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(59): Show |
64 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(61): 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 | a0001c0001t0001g0187 a0001c0002t0001g0174 a0001c0002t0002g0116 others(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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0002t0001g0206 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(77): Show |
82 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(79): 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 | a0001c0002t0047g0237 | 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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0110 others(86): Show |
91 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(88): 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 | a0001c0001t0001g0258 a0001c0001t0006g0257 a0001c0001t0020g0085 others(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 | a0001c0001t0011g0242 | 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 | a0001c0001t0010g0029 a0001c0002t0003g0175 a0001c0002t0003g0234 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0154 a0001c0001t0025g0088 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(50): Show |
55 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0001g0223 a0001c0002t0001g0199 a0001c0002t0001g0231 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0201 a0001c0001t0001g0202 others(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 | a0001c0001t0010g0029 a0001c0002t0003g0175 a0001c0002t0008g0043 others(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 | a0001c0001t0007g0048 a0001c0002t0003g0190 a0001c0002t0004g0034 others(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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0003t0035g0220 others(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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): 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 | a0001c0005t0007g0247 a0001c0005t0014g0005 a0001c0005t0019g0210 others(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 | a0001c0001t0015g0239 a0001c0002t0004g0214 |
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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0001t0010g0029 others(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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0002t0008g0238 | 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 | a0001c0003t0001g0137 a0006c0026t0003g0177 |
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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0002t0003g0175 a0001c0020t0016g0157 a0004c0019t0001g0229 |
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 | a0001c0005t0019g0210 a0001c0005t0019g0211 |
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 | 188 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(185): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(50): Show |
55 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(52): 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0001t0010g0029 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0028g0183 a0001c0001t0040g0019 others(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 | a0001c0001t0010g0029 a0001c0002t0003g0175 a0001c0002t0003g0234 others(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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0001t0010g0029 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0007t0026g0094 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0028g0183 a0001c0001t0040g0019 others(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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0002t0001g0206 others(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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0110 others(116): Show |
121 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(118): 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 | a0001c0001t0010g0029 a0001c0003t0003g0035 a0001c0003t0003g0036 others(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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0040g0019 a0001c0001t0045g0072 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0001 a0001c0001t0002g0027 a0001c0001t0010g0028 others(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 | a0001c0001t0002g0080 a0001c0001t0013g0100 a0001c0002t0047g0237 others(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 | 15 | a0001c0001t0003g0045 a0001c0001t0010g0029 a0001c0002t0001g0023 others(12): Show |
15 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(12): 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 | a0001c0001t0001g0170 a0001c0001t0001g0223 a0001c0001t0002g0103 others(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 | a0001c0002t0001g0050 a0001c0002t0001g0208 a0001c0002t0001g0232 others(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 | a0001c0002t0001g0108 a0001c0002t0002g0071 a0001c0002t0013g0125 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0173 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0068 a0001c0002t0004g0217 a0001c0002t0008g0222 others(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 | a0001c0001t0014g0064 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0124 a0001c0003t0001g0137 |
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 | a0001c0001t0001g0101 a0001c0001t0002g0081 a0001c0001t0002g0249 others(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 | a0001c0002t0043g0182 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0020t0016g0157 a0005c0024t0001g0052 |
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 | a0001c0002t0003g0234 a0001c0002t0008g0043 a0001c0002t0022g0039 others(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 | a0001c0001t0028g0183 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0020t0016g0157 a0005c0024t0001g0052 |
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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0002t0014g0216 | 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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0002t0001g0206 others(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 | a0001c0002t0047g0237 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0015g0025 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | 58 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(55): Show |
60 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(57): 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 | a0001c0011t0015g0176 a0001c0011t0030g0015 |
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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0002t0002g0071 a0001c0002t0002g0151 |
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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0001g0110 a0001c0001t0010g0029 a0001c0001t0028g0183 others(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 | a0001c0001t0015g0025 a0001c0002t0002g0006 a0001c0002t0002g0007 others(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 | a0001c0002t0039g0160 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0110 others(118): Show |
123 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(120): 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 | a0001c0001t0001g0110 a0001c0001t0007g0048 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0101 | 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 | a0001c0002t0047g0237 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0005g0139 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0005g0139 others(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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0002t0004g0217 | 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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(44): Show |
49 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(46): 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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(120): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): 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 | a0001c0002t0002g0047 a0001c0002t0002g0236 |
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 | a0001c0010t0001g0091 a0002c0025t0013g0148 |
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 | a0001c0002t0003g0234 a0001c0002t0008g0043 a0001c0002t0009g0037 others(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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(114): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(183): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): 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 | a0001c0002t0002g0055 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0002t0003g0234 a0001c0002t0008g0043 a0001c0002t0009g0245 others(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 | 57 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(54): Show |
59 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(56): 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(48): Show |
53 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(50): 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 | a0001c0001t0001g0083 a0001c0001t0002g0082 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(183): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.91+118A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204944524 | |||||||
| chr1:204944624 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0110 others(85): Show |
90 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(87): 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 | a0001c0001t0010g0029 a0001c0003t0003g0035 a0001c0003t0003g0036 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0095 a0001c0001t0002g0061 a0001c0016t0002g0066 |
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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0002t0047g0237 others(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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0004t0001g0051 a0001c0004t0001g0053 a0001c0004t0001g0078 |
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 | a0001c0006t0003g0260 a0001c0020t0016g0157 a0004c0019t0001g0229 |
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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0001t0042g0115 | 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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): 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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0001t0007g0032 a0001c0002t0002g0031 |
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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0005t0019g0210 | 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 | a0001c0001t0001g0110 a0001c0001t0007g0048 a0001c0001t0028g0183 others(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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0002t0047g0237 others(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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.91+2370A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204946776 | |||||||
| chr1:204946792 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0020t0016g0157 | 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 | a0001c0002t0008g0238 | 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 | a0001c0002t0003g0234 a0001c0002t0008g0043 a0001c0002t0009g0037 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0001g0196 | 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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0009g0255 others(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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0006g0243 | 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 | a0001c0002t0001g0062 | 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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0001t0015g0239 a0001c0002t0004g0214 |
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 | 59 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(56): Show |
61 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.91+3438A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 2/27 | chr1 | 204947844 | |||||||
| chr1:204947980 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(248): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): 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 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0075 others(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 | a0001c0002t0005g0254 a0001c0002t0008g0252 a0001c0002t0008g0253 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0002t0003g0175 others(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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0002t0003g0175 others(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 | a0001c0001t0001g0110 a0001c0001t0015g0025 a0001c0001t0028g0183 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0010g0029 others(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 | a0002c0025t0013g0148 | 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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0010g0029 others(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 | a0001c0001t0002g0163 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(114): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): 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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0001t0001g0110 a0001c0001t0015g0025 a0001c0001t0028g0183 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0010g0029 a0001c0003t0003g0035 a0001c0003t0003g0036 others(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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0258 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0170 a0001c0001t0001g0223 others(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 | AT | A | 47 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0002g0081 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0180 others(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 | 59 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(56): Show |
61 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(58): 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0010g0029 others(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 | a0001c0001t0001g0189 a0001c0001t0041g0188 |
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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0001t0010g0029 a0001c0003t0003g0035 a0001c0003t0003g0036 others(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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0002t0003g0234 others(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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0110 others(94): Show |
99 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(96): 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 | a0001c0001t0007g0048 a0001c0002t0005g0140 a0001c0003t0010g0040 others(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 | a0001c0001t0001g0113 | 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 | a0001c0002t0001g0013 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0002t0009g0245 a0001c0003t0003g0138 a0001c0003t0024g0221 |
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 | a0001c0005t0003g0246 a0001c0005t0007g0247 a0001c0005t0014g0005 others(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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(52): Show |
57 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(54): 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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0002t0008g0238 | 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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(52): Show |
57 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(54): 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 | a0001c0005t0003g0246 a0001c0005t0007g0247 a0001c0005t0014g0005 others(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 | 46 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(43): Show |
48 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(45): 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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0002t0003g0234 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0224 a0001c0017t0001g0167 |
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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(67): Show |
72 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(69): 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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0010g0029 others(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 | a0002c0013t0001g0084 a0002c0013t0012g0185 a0005c0024t0001g0052 |
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 | a0001c0001t0048g0195 a0001c0002t0001g0013 a0001c0002t0002g0047 others(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 | a0001c0002t0003g0234 a0001c0002t0008g0043 a0001c0002t0009g0245 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0007g0048 others(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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0002t0003g0234 others(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 | a0001c0002t0001g0013 a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0002g0081 a0001c0002t0001g0206 a0001c0002t0003g0234 others(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 | a0001c0001t0005g0139 a0001c0002t0043g0182 a0001c0002t0047g0237 others(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 | a0001c0002t0002g0047 a0001c0002t0002g0236 a0001c0002t0004g0217 |
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 | a0001c0001t0048g0195 a0001c0003t0007g0012 a0001c0003t0007g0181 others(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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0001t0007g0048 a0001c0002t0005g0140 a0001c0003t0010g0040 others(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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0170 others(40): Show |
45 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(42): 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 | a0001c0001t0002g0081 a0001c0001t0007g0048 a0001c0001t0010g0029 others(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 | a0001c0002t0001g0013 a0001c0011t0015g0176 a0001c0011t0030g0015 others(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 | a0001c0001t0036g0203 | 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 | a0001c0001t0007g0048 a0001c0002t0005g0140 a0001c0003t0010g0040 others(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 | a0001c0001t0007g0048 a0001c0002t0005g0140 a0001c0003t0010g0040 others(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 | a0001c0011t0015g0176 a0001c0011t0030g0015 a0001c0014t0004g0228 |
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 | a0001c0002t0003g0175 a0001c0006t0003g0260 a0001c0020t0016g0157 others(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 | a0001c0001t0007g0048 a0001c0002t0005g0140 a0001c0003t0010g0040 others(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 | a0001c0001t0002g0122 | 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 | 65 | a0001c0001t0001g0170 a0001c0001t0002g0081 a0001c0001t0002g0103 others(62): Show |
67 | HG00323.hp1 HG00558.hp2 HG00741.hp1 others(64): 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 | a0001c0001t0007g0048 a0001c0002t0005g0140 a0001c0003t0010g0040 others(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 | a0001c0001t0007g0048 a0001c0005t0003g0246 a0001c0005t0007g0247 others(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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0001t0042g0115 | 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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0002t0009g0245 a0001c0003t0003g0138 a0001c0003t0024g0221 |
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 | a0001c0002t0002g0007 | 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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0002t0003g0227 a0001c0002t0046g0172 |
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 | a0001c0001t0048g0195 a0002c0013t0001g0084 a0002c0013t0012g0185 others(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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0002t0001g0106 a0001c0002t0001g0142 a0001c0002t0001g0171 others(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 | a0001c0001t0048g0195 a0002c0013t0001g0084 a0002c0013t0012g0185 |
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 | a0001c0002t0008g0238 | 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 | 51 | a0001c0001t0001g0170 a0001c0001t0002g0081 a0001c0001t0002g0103 others(48): Show |
53 | HG00323.hp1 HG00558.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.688+1201A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 6/27 | chr1 | 204959027 | |||||||
| chr1:204959061 | G | GT | 87 | a0001c0001t0001g0170 a0001c0001t0001g0196 a0001c0001t0002g0081 others(84): Show |
89 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(86): 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 | a0001c0002t0008g0238 | 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 | a0001c0001t0025g0088 a0001c0007t0016g0104 |
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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0062 | 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 | 77 | a0001c0001t0001g0170 a0001c0001t0001g0196 a0001c0001t0002g0081 others(74): Show |
79 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(76): 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0002t0008g0238 | 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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0006g0024 others(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 | a0001c0002t0001g0050 a0001c0002t0001g0108 a0001c0002t0001g0261 |
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 | a0001c0001t0001g0196 | 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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): 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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0075 others(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 | a0001c0002t0003g0175 a0004c0019t0001g0229 |
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 | a0001c0001t0015g0239 a0001c0002t0004g0214 |
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 | a0001c0001t0023g0144 | 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0107 others(104): Show |
110 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(107): 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0154 others(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 | a0001c0002t0001g0108 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0095 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0196 a0001c0001t0002g0131 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0154 others(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 | a0001c0002t0043g0182 a0001c0002t0047g0237 a0001c0003t0003g0036 others(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 | a0001c0001t0050g0021 | 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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0011g0099 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0012t0001g0067 a0001c0012t0001g0117 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0001t0003g0045 a0001c0001t0010g0029 |
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 | a0001c0001t0001g0189 | 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 | a0001c0003t0001g0070 | 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 | a0001c0002t0001g0106 a0001c0002t0001g0142 a0001c0002t0001g0147 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0001g0154 a0001c0001t0006g0069 a0001c0001t0018g0161 others(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 | a0001c0002t0003g0234 a0001c0002t0008g0043 a0001c0002t0052g0235 |
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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0008g0222 | 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0003g0045 a0001c0001t0010g0029 |
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 | a0001c0002t0001g0169 | 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 | a0001c0002t0001g0169 | 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 | a0001c0002t0001g0178 a0009c0018t0001g0191 |
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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0008g0222 | 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0027t0004g0011 | 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0054g0164 | 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 | a0001c0002t0005g0026 a0001c0002t0005g0046 |
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 | a0001c0001t0048g0195 a0002c0013t0001g0084 a0002c0013t0012g0185 |
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 | a0001c0002t0001g0013 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0131 a0001c0002t0001g0065 others(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 | a0001c0003t0024g0221 | 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 | a0001c0001t0001g0110 a0001c0001t0002g0131 a0001c0002t0001g0065 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0096 | 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 | a0001c0001t0014g0064 | 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 | a0001c0001t0001g0114 | 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0002g0027 a0001c0001t0010g0028 |
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 | a0001c0002t0001g0013 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0002t0003g0227 a0001c0002t0004g0034 a0001c0002t0046g0172 |
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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0001g0092 a0001c0002t0001g0106 a0001c0002t0001g0142 others(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 | a0001c0011t0015g0176 a0001c0011t0030g0015 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0041g0188 |
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 | a0001c0001t0001g0259 a0009c0018t0001g0191 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0042g0115 |
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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0002t0004g0217 | 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 | a0001c0001t0042g0115 a0001c0002t0004g0214 a0001c0002t0009g0245 others(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 | 151 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0060 others(148): Show |
153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): 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 | a0001c0001t0001g0196 a0001c0001t0005g0139 a0001c0001t0006g0069 others(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 | 42 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(39): Show |
44 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(41): 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0005t0051g0033 | 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0002c0025t0013g0148 | 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 | a0001c0001t0048g0195 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0002t0039g0160 | 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 | a0001c0002t0021g0219 a0001c0003t0007g0012 a0001c0003t0007g0181 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0046 |
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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0048g0195 a0001c0002t0001g0206 a0001c0002t0021g0219 others(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 | a0001c0002t0004g0217 | 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0001g0193 | 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0001t0015g0025 a0001c0001t0015g0239 a0001c0002t0003g0234 others(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 | a0005c0024t0001g0052 | 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 | a0005c0024t0001g0052 | 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | 41 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(38): Show |
42 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(39): 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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0002t0003g0190 a0001c0002t0003g0234 a0001c0002t0004g0133 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0003g0190 a0001c0002t0003g0234 a0001c0002t0004g0133 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0001t0036g0203 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0173 a0001c0001t0001g0193 others(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 | 258 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(255): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): 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 | a0001c0002t0004g0034 a0001c0002t0005g0140 |
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 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
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 | 43 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(40): Show |
44 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(41): 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 | a0001c0006t0017g0134 a0001c0006t0017g0135 |
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 | a0001c0001t0014g0064 | 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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0002g0081 a0001c0001t0002g0103 |
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 | a0001c0011t0015g0176 a0001c0011t0030g0015 |
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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0092 a0001c0002t0001g0106 a0001c0002t0001g0142 others(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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1313-379C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973800 | |||||||
| chr1:204973826 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1313-353G>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973826 | |||||||
| chr1:204973851 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1313-328G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 11/27 | chr1 | 204973851 | |||||||
| chr1:204973905 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): 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 | a0009c0018t0001g0191 | 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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): 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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0008t0001g0143 a0001c0008t0001g0145 a0001c0008t0001g0146 |
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 | a0001c0003t0024g0221 | 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 | a0001c0002t0003g0190 a0001c0002t0003g0234 a0001c0002t0004g0217 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(223): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0003g0227 a0001c0002t0005g0213 a0001c0002t0046g0172 others(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 | a0001c0001t0011g0099 | 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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0003g0227 a0001c0002t0005g0026 a0001c0002t0005g0046 others(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 | a0001c0001t0001g0201 a0001c0001t0002g0240 a0001c0001t0002g0241 |
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 | a0001c0006t0003g0260 a0001c0006t0004g0184 a0001c0006t0005g0054 others(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 | a0001c0002t0004g0034 a0001c0002t0005g0140 |
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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0046 a0001c0002t0005g0254 others(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 | a0001c0002t0001g0206 a0001c0002t0004g0034 a0001c0002t0005g0140 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0002t0001g0013 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0002t0004g0034 a0001c0002t0005g0140 |
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 | a0001c0002t0001g0206 a0001c0003t0001g0070 a0001c0003t0001g0120 others(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 | a0001c0002t0001g0206 a0001c0002t0004g0034 a0001c0002t0005g0140 others(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 | a0001c0001t0028g0183 a0001c0014t0004g0228 |
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 | 43 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(40): Show |
44 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(41): 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 | a0001c0006t0003g0260 a0001c0006t0004g0184 a0001c0006t0005g0054 others(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 | a0001c0002t0001g0206 a0001c0002t0004g0034 a0001c0002t0005g0140 others(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 | a0001c0002t0001g0206 a0001c0002t0004g0034 a0001c0002t0005g0140 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0217 a0001c0002t0004g0230 others(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 | a0001c0002t0001g0206 a0001c0002t0004g0034 a0001c0002t0005g0140 others(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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0020t0016g0157 | 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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0013 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0005c0024t0001g0052 | 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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0002t0004g0034 a0001c0002t0005g0140 a0001c0003t0001g0070 others(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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0001t0002g0061 | 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | 44 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(41): Show |
45 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(42): 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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0217 a0001c0002t0008g0043 others(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 | a0001c0002t0003g0190 | 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 | a0001c0002t0004g0034 a0001c0002t0005g0140 |
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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0013 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0046 a0001c0002t0005g0254 others(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 | 97 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(94): Show |
99 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(96): 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0001g0013 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0046 a0001c0002t0005g0254 others(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 | a0001c0001t0010g0112 a0001c0002t0002g0077 |
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 | a0001c0003t0003g0035 | 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 | |||||||
| chr1:204981602 | C | T | 1 | a0007c0028t0022g0089 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0005c0024t0001g0052 | 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 | a0001c0003t0001g0070 a0001c0003t0001g0127 a0001c0009t0001g0002 others(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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | 44 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(41): Show |
45 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(42): 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 | a0001c0002t0003g0227 a0001c0002t0046g0172 |
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 | 74 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(71): Show |
76 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(73): 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 | a0001c0002t0002g0007 | 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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | 247 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): 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 | a0001c0002t0005g0026 a0001c0002t0005g0046 a0001c0002t0005g0254 others(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 | a0005c0024t0001g0052 | 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 | a0005c0024t0001g0052 | 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 | a0005c0024t0001g0052 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | 79 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(76): Show |
81 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(78): 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 | a0001c0001t0001g0170 | 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 | 74 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(71): Show |
76 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(73): 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 | a0001c0002t0003g0227 a0001c0002t0005g0026 a0001c0002t0005g0046 others(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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0002t0001g0065 a0001c0002t0013g0125 a0001c0003t0004g0004 others(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 | a0001c0006t0004g0184 a0001c0006t0017g0134 a0001c0006t0017g0135 others(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 | 70 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(67): Show |
71 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(68): 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 | a0001c0001t0014g0064 a0001c0002t0001g0013 a0001c0002t0003g0190 others(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 | a0001c0002t0008g0222 a0001c0005t0003g0246 a0001c0005t0007g0247 others(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 | 78 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(75): Show |
79 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(76): 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 | a0001c0002t0001g0065 a0001c0002t0013g0125 a0001c0003t0001g0070 others(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 | a0001c0001t0053g0209 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0101 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0110 a0001c0002t0001g0197 a0001c0002t0002g0047 others(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 | a0001c0001t0025g0088 a0001c0002t0005g0026 a0001c0002t0005g0046 others(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 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0008 others(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 | a0001c0002t0005g0254 a0001c0002t0008g0252 a0001c0002t0008g0253 others(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 | a0001c0002t0003g0227 a0001c0002t0004g0133 a0001c0002t0004g0214 others(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 | a0001c0002t0046g0172 a0001c0002t0047g0237 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0123 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0095 a0001c0001t0002g0061 a0001c0002t0001g0079 others(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 | 65 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(62): Show |
67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): 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 | a0005c0024t0001g0052 | 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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | 54 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(51): Show |
55 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2619+457C>T | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204984599 | |||||||
| chr1:204984649 | GA | G | 58 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(55): Show |
59 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(56): 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 | a0001c0001t0015g0025 a0001c0001t0015g0239 |
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 | a0005c0024t0001g0052 | 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 | a0001c0002t0003g0227 a0001c0002t0005g0213 a0001c0002t0046g0172 |
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 | a0001c0003t0024g0221 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0006t0004g0184 a0001c0006t0034g0030 |
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 | a0001c0001t0053g0209 | 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 | a0007c0028t0022g0089 | 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 | a0001c0001t0012g0166 a0008c0023t0012g0192 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0187 |
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 | 104 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(101): Show |
106 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.2620-45A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 21/27 | chr1 | 204985865 | |||||||
| chr1:204986191 | G | A | 58 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(55): Show |
59 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2824+77G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 22/27 | chr1 | 204986191 | |||||||
| chr1:204986201 | A | G | 58 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(55): Show |
59 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(56): 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 | a0001c0001t0002g0131 a0001c0001t0027g0087 |
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 | 58 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(55): Show |
59 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(56): 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 | a0001c0001t0006g0243 a0001c0001t0036g0203 |
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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0003g0234 a0001c0002t0004g0217 a0001c0002t0004g0230 others(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 | a0001c0003t0001g0070 a0001c0003t0001g0120 a0001c0003t0001g0127 others(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 | a0001c0002t0001g0208 | 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 | a0001c0001t0028g0183 a0001c0014t0004g0228 |
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 | 55 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(52): Show |
55 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(52): 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 | a0001c0003t0004g0004 a0001c0027t0004g0011 |
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 | 116 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0095 others(113): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): 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 | a0001c0002t0001g0013 a0001c0003t0004g0004 a0001c0003t0004g0038 others(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 | a0001c0002t0003g0227 a0001c0002t0005g0213 a0001c0002t0046g0172 |
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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0002t0002g0205 | 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 | a0001c0001t0028g0183 a0001c0002t0005g0026 a0001c0002t0005g0046 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0092 a0001c0002t0001g0179 |
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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0003t0010g0040 a0001c0006t0003g0260 a0001c0006t0004g0184 others(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 | a0001c0003t0010g0040 a0001c0006t0003g0260 a0001c0006t0004g0184 others(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 | a0001c0003t0024g0221 a0005c0024t0001g0052 |
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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0004g0230 a0001c0002t0004g0248 a0001c0002t0014g0216 others(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 | a0001c0002t0001g0197 | 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 | a0001c0003t0024g0221 | 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 | a0001c0001t0011g0168 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0002t0047g0237 a0001c0003t0001g0120 a0001c0003t0003g0035 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0003g0227 a0001c0002t0046g0172 |
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 | a0001c0001t0001g0107 | 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 | a0001c0002t0003g0190 a0001c0003t0010g0040 a0001c0006t0003g0260 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0001t0001g0101 others(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 | a0001c0003t0001g0070 | 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 | a0001c0001t0028g0183 a0001c0002t0005g0026 a0001c0002t0005g0046 others(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 | a0001c0003t0024g0221 | 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 | a0001c0002t0003g0234 a0001c0002t0004g0217 a0001c0002t0008g0043 others(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 | a0001c0005t0003g0246 a0001c0005t0007g0247 a0001c0005t0010g0212 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): 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 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0009g0009 others(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 | a0001c0003t0024g0221 | 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 | a0001c0003t0024g0221 | 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 | a0005c0024t0001g0052 | 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 | a0005c0024t0001g0052 | 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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0095 others(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 | a0005c0024t0001g0052 | 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 | a0001c0003t0024g0221 | 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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0001t0014g0064 | 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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0005c0024t0001g0052 | 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 | a0001c0002t0001g0207 | 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 | a0005c0024t0001g0052 | 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 | a0001c0005t0003g0246 a0001c0005t0007g0247 a0001c0005t0010g0212 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0028g0183 a0001c0002t0003g0227 a0001c0002t0005g0026 others(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 | a0001c0002t0004g0230 a0001c0002t0004g0248 a0001c0002t0014g0216 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0002g0027 others(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 | a0001c0001t0001g0110 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(254): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3136+1937T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204993243 | |||||||
| chr1:204993277 | A | G | 42 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(39): Show |
43 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(40): 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 | a0009c0018t0001g0191 | 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0009g0009 | 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 | a0001c0001t0001g0105 | 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 | 43 | a0001c0001t0002g0081 a0001c0001t0002g0103 a0001c0002t0001g0018 others(40): Show |
44 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(41): 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 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0075 others(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 | a0005c0024t0001g0052 | 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 | 258 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(255): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): 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 | a0001c0001t0001g0083 a0001c0001t0002g0082 a0001c0003t0004g0004 others(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 | a0001c0003t0024g0221 | 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 | a0001c0005t0003g0246 a0001c0005t0007g0247 a0001c0005t0010g0212 others(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 | a0001c0001t0013g0100 a0001c0001t0027g0087 |
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 | 83 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0095 others(80): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): 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 | a0001c0002t0001g0232 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0095 others(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 | a0001c0003t0024g0221 | 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 | a0001c0001t0006g0024 a0001c0001t0048g0195 |
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 | a0001c0002t0002g0077 a0001c0002t0003g0175 a0001c0002t0009g0037 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0016 a0001c0001t0044g0233 a0001c0001t0048g0195 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0001t0001g0083 a0001c0001t0028g0183 a0001c0001t0054g0164 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0057 others(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 | 14 | a0001c0001t0003g0045 a0001c0001t0005g0139 a0001c0001t0005g0226 others(11): Show |
14 | HG01109.hp1 HG01192.hp1 HG02109.hp1 others(11): 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 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0027 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0110 | 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 | a0001c0003t0024g0221 | 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 | a0001c0003t0024g0221 | 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 | a0001c0003t0024g0221 | 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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0001c0003t0004g0004 a0001c0003t0004g0038 a0001c0003t0007g0042 others(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 | a0005c0024t0001g0052 | 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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3136+5090T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204996396 | |||||||
| chr1:204996529 | A | G | 154 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0075 others(151): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 |
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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0006 others(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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0201 a0001c0002t0001g0106 a0001c0002t0001g0142 others(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 | 56 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0126 others(53): Show |
58 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(55): 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 | a0001c0001t0001g0124 a0001c0006t0005g0054 |
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 | a0001c0002t0046g0172 | 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 | a0001c0001t0028g0183 a0001c0002t0003g0175 a0001c0002t0004g0034 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0068 others(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 | a0001c0002t0023g0098 | 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 | a0001c0009t0001g0002 a0001c0009t0001g0119 |
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 | a0001c0001t0001g0196 | 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 | a0001c0002t0004g0034 a0001c0005t0051g0033 |
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 | 221 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.3136+6256G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204997562 | |||||||
| chr1:204997621 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(222): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0002t0004g0133 a0001c0002t0004g0214 a0001c0002t0043g0182 |
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 | a0001c0003t0001g0127 a0004c0019t0001g0229 |
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 | a0001c0001t0009g0009 a0001c0002t0003g0190 a0001c0002t0004g0230 others(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 | a0001c0001t0028g0183 a0001c0006t0034g0030 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0002g0047 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 a0005c0024t0001g0052 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0015g0025 a0001c0001t0015g0239 |
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 | a0001c0011t0015g0176 a0001c0011t0030g0015 |
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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(254): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): 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 | a0005c0024t0001g0052 | 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 | a0001c0001t0001g0001 a0001c0017t0001g0167 |
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 | a0001c0001t0018g0161 a0001c0001t0018g0162 a0005c0024t0001g0052 |
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 | a0001c0002t0001g0079 a0001c0003t0010g0040 a0001c0006t0003g0260 others(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 | 52 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(49): Show |
52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3136+7824C>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 204999130 | |||||||
| chr1:204999211 | C | T | 49 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(46): Show |
49 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(46): 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0002t0001g0079 a0001c0003t0010g0040 a0001c0006t0003g0260 others(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 | a0001c0001t0001g0126 a0001c0001t0003g0045 a0001c0001t0005g0139 others(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 | a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | 50 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(47): Show |
50 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(47): 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 | a0001c0009t0001g0002 a0001c0009t0001g0119 |
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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0005g0140 others(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 | 50 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(47): Show |
50 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(47): 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 | a0001c0001t0010g0112 | 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 | 50 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(47): Show |
50 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(47): 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 | a0001c0002t0001g0065 a0001c0002t0001g0197 a0001c0002t0003g0175 others(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 | a0001c0001t0006g0243 | 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 | a0001c0001t0001g0170 | 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 | a0001c0002t0004g0230 a0001c0002t0004g0248 |
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 | 50 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(47): Show |
50 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(47): 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 | a0001c0002t0003g0190 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0187 |
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 | 47 | a0001c0001t0001g0180 a0001c0001t0002g0080 a0001c0001t0002g0081 others(44): Show |
47 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(44): 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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | a0001c0001t0009g0111 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 a0005c0024t0001g0052 |
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 | a0001c0001t0009g0111 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | 52 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(49): Show |
52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): 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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | a0004c0019t0001g0229 | 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 | a0001c0005t0051g0033 | 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 | 48 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(45): Show |
48 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(45): 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 | 51 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(48): Show |
51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.3137-8442A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001115 | |||||||
| chr1:205001174 | T | C | 51 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(48): Show |
51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): 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 | a0001c0002t0001g0174 | 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 | a0001c0002t0001g0106 | 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 | 51 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(48): Show |
51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): 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 | 48 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(45): Show |
48 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.3137-7977G>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001580 | |||||||
| chr1:205001649 | T | A | 51 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(48): Show |
51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.3137-7908T>A | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205001649 | |||||||
| chr1:205001716 | C | A | 48 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(45): Show |
48 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(45): 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 | a0001c0001t0013g0100 a0001c0001t0013g0121 a0001c0001t0027g0087 |
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 | a0001c0001t0018g0161 a0001c0001t0018g0162 a0005c0024t0001g0052 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | 52 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0017 others(49): Show |
52 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(49): 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 | a0001c0002t0001g0197 | 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 | 53 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(50): Show |
53 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(50): 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 | a0001c0003t0024g0221 | 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 | 51 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0080 others(48): Show |
51 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(48): 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 | a0001c0001t0009g0111 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0005t0051g0033 a0001c0006t0017g0134 a0001c0006t0017g0135 |
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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0009g0111 others(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 | 54 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0002g0017 others(51): Show |
54 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(51): 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 | a0001c0002t0003g0175 a0001c0002t0004g0214 a0001c0002t0043g0182 others(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 | a0001c0001t0015g0025 a0001c0003t0037g0225 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0018g0161 a0001c0001t0018g0162 a0001c0002t0004g0217 others(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 | a0001c0001t0007g0032 a0001c0001t0007g0048 a0001c0002t0047g0237 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.3137-6042C>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205003515 | |||||||
| chr1:205003528 | A | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): 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 | a0001c0001t0009g0111 a0001c0002t0004g0217 a0001c0002t0004g0230 others(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 | a0001c0002t0004g0217 a0001c0002t0004g0230 a0001c0002t0004g0248 others(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 | a0001c0001t0009g0111 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | 157 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.3137-5547A>G | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | chr1 | 205004010 | |||||||
| chr1:205004046 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0001c0001t0012g0166 a0008c0023t0012g0192 |
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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0007g0032 others(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 | a0001c0002t0001g0231 | 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 | a0001c0002t0046g0172 | 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 | a0001c0001t0009g0009 a0001c0002t0004g0217 a0001c0002t0004g0230 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0110 others(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 | a0001c0001t0054g0164 | 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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0001t0007g0032 a0001c0001t0007g0048 a0001c0002t0001g0013 others(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 | a0001c0001t0007g0032 a0001c0001t0007g0048 a0001c0002t0001g0013 others(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 | a0001c0002t0001g0018 a0001c0002t0001g0065 a0001c0012t0001g0067 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0003t0003g0036 | 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 | a0001c0001t0001g0086 a0001c0001t0001g0186 a0001c0001t0001g0202 others(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 | a0001c0003t0024g0221 | 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 | a0001c0001t0001g0110 | 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 | a0001c0002t0008g0222 | 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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0007g0032 others(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 | a0001c0002t0001g0149 a0001c0002t0002g0116 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0002t0002g0236 | 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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0001t0003g0045 a0001c0002t0003g0190 a0001c0002t0003g0234 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0001t0009g0009 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0002g0163 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0007t0026g0094 | 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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0010g0028 others(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 | a0001c0001t0007g0032 a0001c0001t0007g0048 a0001c0001t0010g0029 others(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 | a0001c0002t0023g0098 | 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 | a0001c0001t0001g0068 a0001c0001t0002g0249 a0001c0001t0011g0099 others(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 | a0001c0001t0002g0131 a0001c0001t0003g0045 a0001c0001t0005g0139 others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0010g0028 others(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 | a0001c0001t0048g0195 | 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 | a0001c0001t0010g0112 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0009g0009 others(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 | a0001c0001t0003g0045 a0001c0002t0003g0190 a0001c0002t0003g0234 others(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 | a0001c0002t0001g0018 a0001c0002t0001g0065 a0001c0012t0001g0067 others(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 | a0001c0001t0011g0242 | 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 | a0001c0002t0001g0232 | 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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0009g0009 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0010t0001g0091 a0001c0010t0025g0049 a0001c0010t0026g0022 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0006g0024 a0001c0001t0006g0069 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0001t0009g0111 a0001c0002t0009g0037 a0001c0002t0009g0245 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0002t0003g0175 a0001c0006t0004g0184 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0003t0024g0221 | 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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0110 a0001c0001t0009g0009 a0001c0002t0004g0133 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0013g0100 others(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 | a0001c0001t0001g0083 a0001c0001t0002g0082 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0113 others(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 | a0001c0003t0024g0221 | 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 | a0001c0001t0015g0025 a0001c0001t0015g0239 a0001c0002t0003g0175 others(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 | a0001c0001t0014g0064 | 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 | a0001c0001t0014g0064 | 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 | a0001c0002t0001g0231 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0010g0028 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0002t0003g0175 a0001c0003t0024g0221 |
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 | a0001c0001t0050g0021 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0041g0188 others(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 | a0001c0003t0035g0220 a0001c0007t0016g0097 a0001c0007t0016g0104 others(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 | a0001c0001t0003g0045 a0001c0001t0007g0032 a0001c0001t0007g0048 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0002t0013g0125 | 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 | a0001c0003t0035g0220 a0001c0007t0016g0097 a0001c0007t0016g0104 others(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 | a0001c0002t0004g0034 a0001c0002t0017g0215 a0001c0003t0010g0040 others(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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0003t0035g0220 a0001c0007t0016g0097 a0001c0007t0016g0104 others(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 | a0001c0003t0004g0004 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0083 others(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 | a0001c0002t0005g0140 a0001c0003t0003g0035 |
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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0002t0021g0156 | 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 | a0001c0001t0003g0045 a0001c0001t0028g0183 a0001c0002t0003g0190 others(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 | a0001c0001t0003g0045 a0006c0026t0003g0177 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0002t0023g0098 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0095 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0007t0016g0097 a0001c0007t0016g0104 |
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 | a0001c0001t0010g0029 a0001c0001t0015g0025 a0001c0001t0015g0239 others(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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0009g0009 a0001c0001t0009g0111 a0001c0001t0010g0029 others(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 | a0001c0002t0004g0034 a0001c0002t0017g0215 a0001c0003t0010g0040 others(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 | a0001c0001t0001g0068 | 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 | a0001c0002t0001g0096 | 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 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
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 | a0001c0001t0007g0032 a0001c0001t0007g0048 a0001c0002t0003g0175 others(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 | a0001c0001t0009g0009 a0001c0001t0009g0111 a0001c0002t0009g0037 others(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 | a0001c0001t0050g0021 | 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 | a0001c0001t0001g0057 a0001c0001t0002g0027 a0001c0001t0007g0032 others(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 | 65 | a0001c0001t0001g0083 a0001c0001t0001g0105 a0001c0001t0001g0110 others(62): Show |
67 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(64): 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 | a0001c0001t0009g0009 a0001c0001t0009g0111 a0001c0002t0009g0037 others(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 | a0001c0001t0003g0045 a0001c0001t0007g0032 a0001c0001t0007g0048 others(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 | a0001c0003t0024g0221 | 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 | a0001c0002t0017g0215 a0001c0005t0051g0033 a0001c0006t0017g0134 others(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 | a0001c0001t0002g0131 a0001c0001t0005g0139 a0001c0001t0005g0226 others(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 | a0001c0001t0001g0114 | 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 | 49 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0057 others(46): Show |
52 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(49): 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 | a0001c0005t0019g0210 a0001c0005t0019g0211 a0001c0005t0033g0244 |
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 | a0001c0002t0047g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3339-13T>C | NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 27/27 | chr1 | 205016295 |