Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26502 |
| ensemblid | ENSG00000141562.19 |
| hgncid | 29916 |
| symbol | NARF |
| name | nuclear prelamin A recognition factor |
| refseq_nuc | NM_012336.4 |
| refseq_prot | NP_036468.1 |
| ensembl_nuc | ENST00000309794.16 |
| ensembl_prot | ENSP00000309899.10 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 82458741 |
| end | 82490537 |
| strand | + |
| ver | v1.2 |
| region | chr17:82458741-82490537 |
| region5000 | chr17:82453741-82495537 |
| regionname0 | NARF_chr17_82458741_82490537 |
| regionname5000 | NARF_chr17_82453741_82495537 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 456 | 350 | 93 | 72 | 128 | 13 | 42 | 91 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(451): Show |
chr17 | 82453741 | 82495537 |
| a0002 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(451): Show |
chr17 | 82453741 | 82495537 |
| a0003 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(451): Show |
chr17 | 82453741 | 82495537 |
| a0004 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(451): Show |
chr17 | 82453741 | 82495537 |
| a0005 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(451): Show |
chr17 | 82453741 | 82495537 |
| a0006 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(451): Show |
chr17 | 82453741 | 82495537 |
| a0007 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | MKCEH others(354): Show |
chr17 | 82453741 | 82495537 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1368 | 296 | 53 | 63 | 126 | 13 | 39 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0001c0002 | 0/0 | 1368 | 49 | 35 | 9 | 2 | 0 | 3 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0001c0003 | 0/0 | 1368 | 3 | 3 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0001c0010 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0001c0011 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0002c0009 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0003c0006 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0004c0005 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0005c0004 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0006c0007 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1363): Show |
chr17 | 82453741 | 82495537 | ||
| a0007c0008 | 0/0 | 1412 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | ATGAA others(1407): Show |
chr17 | 82453741 | 82495537 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3814 | 173 | 22 | 33 | 99 | 2 | 17 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0002 | 1/1 | 3814 | 73 | 21 | 13 | 12 | 9 | 16 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0005 | 0/0 | 3815 | 9 | 1 | 1 | 6 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0006 | 0/0 | 3815 | 9 | 0 | 3 | 3 | 0 | 3 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0007 | 0/0 | 3815 | 2 | 0 | 1 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0008 | 0/0 | 3815 | 5 | 0 | 4 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0009 | 0/0 | 3815 | 5 | 0 | 3 | 2 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0010 | 0/0 | 3814 | 4 | 1 | 3 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0013 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0014 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3811): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0016 | 0/0 | 3814 | 2 | 0 | 1 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0017 | 0/0 | 3815 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0019 | 0/0 | 3816 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3811): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0021 | 0/0 | 3815 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0026 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0027 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0028 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0029 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0032 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0033 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0034 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0001t0035 | 0/0 | 3815 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0001 | 0/0 | 3814 | 8 | 7 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0003 | 0/0 | 3814 | 11 | 11 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0004 | 0/0 | 3733 | 10 | 5 | 1 | 2 | 0 | 2 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3728): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0007 | 0/0 | 3815 | 6 | 0 | 6 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0008 | 0/0 | 3815 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0011 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0012 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0014 | 0/0 | 3816 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3811): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0018 | 0/0 | 3815 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3810): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0022 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3728): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0023 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3728): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0024 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3728): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0025 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0030 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0002t0031 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0003t0015 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0003t0020 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0010t0001 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0001c0011t0001 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0002c0009t0001 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0003c0006t0004 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3728): Show |
chr17 | 82453741 | 82495537 |
| a0004c0005t0001 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0005c0004t0001 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0006c0007t0001 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3809): Show |
chr17 | 82453741 | 82495537 |
| a0007c0008t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | GTCCC others(3853): Show |
chr17 | 82453741 | 82495537 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 1 | 3 | 0 | 4 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0002 | 0/0 | 7 | 1 | 2 | 1 | 1 | 2 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0015 | 0/1 | 4 | 0 | 1 | 0 | 0 | 2 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0006g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0008g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0009g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0010g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0013g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0014g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0016g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0016g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0019g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0021g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0026g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0027g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0028g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0029g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0032g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0033g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0034g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0001t0035g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0003g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0007g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0011g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0012g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0014g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0018g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0022g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0023g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0024g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0025g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0030g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0002t0031g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0003t0015g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0003t0015g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0003t0020g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0001c0011t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0002c0009t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0003c0006t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0004c0005t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0005c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0006c0007t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| a0007c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | GBR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00140 | hp1 | a0002 | c0009 | t0001 | g0170 | EUR | GBR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | FIN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | FIN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0102 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00738 | hp1 | a0001 | c0002 | t0014 | g0112 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01081 | hp2 | a0001 | c0002 | t0007 | g0017 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01167 | hp1 | a0001 | c0001 | t0016 | g0212 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0047 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0060 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0067 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01256 | hp1 | a0001 | c0002 | t0007 | g0113 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01257 | hp1 | a0001 | c0002 | t0007 | g0017 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01258 | hp2 | a0001 | c0002 | t0007 | g0017 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0211 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | IBS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0208 | EUR | IBS | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01928 | hp2 | a0001 | c0002 | t0007 | g0115 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01952 | hp1 | a0001 | c0002 | t0007 | g0114 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01993 | hp2 | a0001 | c0001 | t0019 | g0043 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0023 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02055 | hp1 | a0001 | c0002 | t0018 | g0236 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0172 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02145 | hp1 | a0001 | c0002 | t0012 | g0013 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02257 | hp1 | a0001 | c0001 | t0026 | g0051 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0023 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02451 | hp1 | a0001 | c0001 | t0034 | g0064 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0233 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02572 | hp2 | a0001 | c0003 | t0015 | g0229 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02622 | hp1 | a0001 | c0002 | t0011 | g0025 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02630 | hp2 | a0001 | c0002 | t0030 | g0152 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02647 | hp2 | a0001 | c0003 | t0015 | g0228 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02698 | hp2 | a0001 | c0001 | t0021 | g0048 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02717 | hp1 | a0001 | c0001 | t0028 | g0040 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02738 | hp2 | a0001 | c0002 | t0004 | g0136 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02809 | hp1 | a0001 | c0002 | t0031 | g0153 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02809 | hp2 | a0001 | c0001 | t0035 | g0016 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02818 | hp2 | a0001 | c0011 | t0001 | g0150 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02895 | hp1 | a0001 | c0002 | t0011 | g0025 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02896 | hp2 | a0001 | c0002 | t0011 | g0025 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0234 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02965 | hp1 | a0001 | c0002 | t0012 | g0013 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02976 | hp2 | a0001 | c0001 | t0027 | g0198 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0145 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03130 | hp2 | a0001 | c0002 | t0008 | g0235 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03139 | hp1 | a0003 | c0006 | t0004 | g0111 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03209 | hp1 | a0001 | c0010 | t0001 | g0227 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0146 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03453 | hp1 | a0001 | c0002 | t0024 | g0140 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0058 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0232 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0069 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0019 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0141 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03942 | hp2 | a0001 | c0002 | t0004 | g0138 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | STU | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | STU | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04184 | hp2 | a0001 | c0002 | t0022 | g0023 | SAS | BEB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18612 | hp2 | a0004 | c0005 | t0001 | g0009 | EAS | CHB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | YRI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | YRI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0033 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18950 | hp2 | a0005 | c0004 | t0001 | g0026 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18969 | hp1 | a0001 | c0001 | t0029 | g0192 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18979 | hp1 | a0006 | c0007 | t0001 | g0006 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18985 | hp1 | a0001 | c0001 | t0009 | g0056 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0224 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19003 | hp1 | a0001 | c0001 | t0014 | g0006 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19043 | hp1 | a0001 | c0003 | t0020 | g0230 | AFR | LWK | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19062 | hp2 | a0007 | c0008 | t0001 | g0120 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0132 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0038 | AFR | YRI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | ASW | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ASW | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0043 | EUR | TSI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | TSI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20905 | hp2 | a0001 | c0001 | t0033 | g0030 | SAS | GIH | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0203 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0059 | AMR | CLM | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02109 | hp2 | a0001 | c0002 | t0023 | g0147 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0038 | AFR | USA | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | LWK | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| NA21309 | hp2 | a0001 | c0002 | t0025 | g0149 | AFR | LWK | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0015 | REF | REF | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0082 | REF | REF | NARF_chr17_82453741_82495537 | NARF | chr17 | 82453741 | 82495537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82460037 | G | A | 1 | a0005 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.73G>A | p.Ala25Thr | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/11 | 136/3814 | 73/1371 | 25/456 | chr17 | 82460037 | |||
| chr17:82472638 | C | A | 1 | a0004 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.460C>A | p.Arg154Ser | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/11 | 523/3814 | 460/1371 | 154/456 | chr17 | 82472638 | |||
| chr17:82478814 | G | A | 1 | a0003 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.535G>A | p.Ala179Thr | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/11 | 598/3814 | 535/1371 | 179/456 | chr17 | 82478814 | |||
| chr17:82481128 | A | G | 1 | a0002 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.686A>G | p.Tyr229Cys | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/11 | 749/3814 | 686/1371 | 229/456 | chr17 | 82481128 | |||
| chr17:82481132 | C | A | 1 | a0006 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.690C>A | p.Asp230Glu | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/11 | 753/3814 | 690/1371 | 230/456 | chr17 | 82481132 | |||
| chr17:82485576 | A | AACATCCA others(37): Show |
1 | a0007 | 1 | NA19062.hp2 | frameshift_variant&stop_gained | HIGH | c.1061_1062insACATGA others(38): Show |
p.Asn354fs | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/11 | 1125/3814 | 1062/1371 | 354/456 | INFO_REALIGN_3_PRIME | chr17 | 82485576 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82464376 | C | G | 1 | a0001c0011 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.198C>G | p.Val66Val | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/11 | 261/3814 | 198/1371 | 66/456 | chr17 | 82464376 | |||
| chr17:82478819 | G | A | 1 | a0001c0003 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.540G>A | p.Glu180Glu | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/11 | 603/3814 | 540/1371 | 180/456 | chr17 | 82478819 | |||
| chr17:82481108 | C | T | 1 | a0001c0010 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.666C>T | p.His222His | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/11 | 729/3814 | 666/1371 | 222/456 | chr17 | 82481108 | |||
| chr17:82484846 | T | C | 4 | a0001c0002 a0001c0003 a0001c0010 others(1): Show |
54 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(51): Show |
synonymous_variant | LOW | c.867T>C | p.Arg289Arg | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/11 | 930/3814 | 867/1371 | 289/456 | chr17 | 82484846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82488288 | G | A | 2 | a0001c0002t0003 a0001c0002t0012 |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*131G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 131 | chr17 | 82488288 | ||||||
| chr17:82488300 | A | AC | 7 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0014 others(4): Show |
19 | HG00438.hp2 HG00735.hp2 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*147dupC | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 148 | INFO_REALIGN_3_PRIME | chr17 | 82488300 | |||||
| chr17:82488304 | C | A | 1 | a0001c0001t0013 | 2 | NA19240.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*147C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 147 | chr17 | 82488304 | ||||||
| chr17:82488380 | C | CT | 4 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0035 others(1): Show |
8 | HG01099.hp1 HG01123.hp1 HG01361.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*236dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 237 | INFO_REALIGN_3_PRIME | chr17 | 82488380 | |||||
| chr17:82488461 | T | C | 1 | a0001c0002t0011 | 3 | HG02622.hp1 HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 304 | chr17 | 82488461 | ||||||
| chr17:82488468 | C | T | 1 | a0001c0001t0034 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*311C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 311 | chr17 | 82488468 | ||||||
| chr17:82488587 | C | A | 1 | a0001c0003t0020 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*430C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 430 | chr17 | 82488587 | ||||||
| chr17:82488613 | T | C | 2 | a0001c0001t0010 a0001c0001t0021 |
5 | HG00642.hp2 HG01192.hp2 HG01496.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*456T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 456 | chr17 | 82488613 | ||||||
| chr17:82488617 | C | T | 1 | a0001c0001t0016 | 2 | HG01167.hp1 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*460C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 460 | chr17 | 82488617 | ||||||
| chr17:82488753 | G | A | 1 | a0001c0002t0001 | 2 | HG01884.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*596G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 596 | chr17 | 82488753 | ||||||
| chr17:82488889 | G | C | 1 | a0001c0001t0017 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 732 | chr17 | 82488889 | ||||||
| chr17:82489062 | A | G | 1 | a0001c0001t0033 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*905A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 905 | chr17 | 82489062 | ||||||
| chr17:82489119 | CCCATTCC others(74): Show |
C | 5 | a0001c0002t0004 a0001c0002t0022 a0001c0002t0023 others(2): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1030_*1110delTACT others(77): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1030 | INFO_REALIGN_3_PRIME | chr17 | 82489119 | |||||
| chr17:82489176 | C | T | 1 | a0001c0001t0001 | 4 | HG01074.hp2 HG01891.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1019C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1019 | chr17 | 82489176 | ||||||
| chr17:82489193 | G | C | 2 | a0001c0001t0001 a0001c0001t0005 |
6 | HG00438.hp2 NA18961.hp2 NA18997.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1036G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1036 | chr17 | 82489193 | ||||||
| chr17:82489272 | C | T | 1 | a0001c0001t0032 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1115C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1115 | chr17 | 82489272 | ||||||
| chr17:82489491 | C | T | 1 | a0001c0002t0012 | 2 | HG02145.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1334C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1334 | chr17 | 82489491 | ||||||
| chr17:82489530 | T | C | 1 | a0001c0002t0022 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1373 | chr17 | 82489530 | ||||||
| chr17:82489556 | C | T | 1 | a0001c0002t0031 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1399C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1399 | chr17 | 82489556 | ||||||
| chr17:82489709 | A | G | 2 | a0001c0002t0030 a0001c0002t0031 |
2 | HG02630.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1552A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1552 | chr17 | 82489709 | ||||||
| chr17:82489795 | A | C | 1 | a0001c0001t0029 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1638 | chr17 | 82489795 | ||||||
| chr17:82489818 | T | C | 5 | a0001c0002t0004 a0001c0002t0022 a0001c0002t0023 others(2): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1661T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1661 | chr17 | 82489818 | ||||||
| chr17:82489829 | A | AT | 6 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0014 others(3): Show |
20 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1688dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1689 | INFO_REALIGN_3_PRIME | chr17 | 82489829 | |||||
| chr17:82489859 | A | T | 1 | a0001c0001t0028 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1702A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1702 | chr17 | 82489859 | ||||||
| chr17:82489983 | G | A | 1 | a0001c0002t0025 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1826G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1826 | chr17 | 82489983 | ||||||
| chr17:82490033 | G | A | 5 | a0001c0002t0003 a0001c0002t0011 a0001c0002t0012 others(2): Show |
18 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1876G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1876 | chr17 | 82490033 | ||||||
| chr17:82490045 | C | T | 1 | a0001c0002t0018 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1888 | chr17 | 82490045 | ||||||
| chr17:82490076 | C | A | 1 | a0001c0002t0023 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1919 | chr17 | 82490076 | ||||||
| chr17:82490103 | C | T | 31 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(28): Show |
244 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1946C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1946 | chr17 | 82490103 | ||||||
| chr17:82490140 | T | A | 2 | a0001c0002t0003 a0001c0002t0012 |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1983T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1983 | chr17 | 82490140 | ||||||
| chr17:82490141 | T | A | 36 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(33): Show |
258 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1984T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1984 | chr17 | 82490141 | ||||||
| chr17:82490154 | G | T | 1 | a0001c0001t0026 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1997G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 1997 | chr17 | 82490154 | ||||||
| chr17:82490259 | G | T | 1 | a0001c0001t0027 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2102G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 2102 | chr17 | 82490259 | ||||||
| chr17:82490324 | G | C | 1 | a0001c0002t0024 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2167G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 2167 | chr17 | 82490324 | ||||||
| chr17:82490484 | C | T | 1 | a0001c0003t0015 | 2 | HG02572.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2327C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 11/11 | 2327 | chr17 | 82490484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82458892 | C | G | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+62C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82458892 | |||||||
| chr17:82458901 | C | T | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.27+71C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82458901 | |||||||
| chr17:82458907 | G | A | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.27+77G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82458907 | |||||||
| chr17:82459250 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.27+420C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459250 | |||||||
| chr17:82459274 | G | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
244 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.27+444G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459274 | |||||||
| chr17:82459300 | C | T | 1 | a0001c0003t0020g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+470C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459300 | |||||||
| chr17:82459329 | G | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0105 a0001c0001t0002g0106 |
4 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+499G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459329 | |||||||
| chr17:82459331 | A | G | 1 | a0001c0002t0001g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+501A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459331 | |||||||
| chr17:82459454 | C | T | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.28-538C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459454 | |||||||
| chr17:82459483 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
242 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.28-509T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459483 | |||||||
| chr17:82459546 | C | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
243 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.28-446C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459546 | |||||||
| chr17:82459567 | G | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
85 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.28-425G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459567 | |||||||
| chr17:82459656 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0107 others(4): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-336G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459656 | |||||||
| chr17:82459690 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
131 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.28-302C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459690 | |||||||
| chr17:82459784 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.28-208G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459784 | |||||||
| chr17:82459842 | C | T | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-150C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459842 | |||||||
| chr17:82459853 | C | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
85 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.28-139C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459853 | |||||||
| chr17:82459865 | TA | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
247 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.28-120delA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 82459865 | ||||||
| chr17:82459919 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18963.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.28-73G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 1/10 | chr17 | 82459919 | |||||||
| chr17:82460202 | C | A | 1 | a0003c0006t0004g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108+130C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460202 | |||||||
| chr17:82460305 | A | C | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+233A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460305 | |||||||
| chr17:82460326 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.108+254A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460326 | |||||||
| chr17:82460345 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.108+273A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460345 | |||||||
| chr17:82460523 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.108+451G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460523 | |||||||
| chr17:82460557 | G | T | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.108+485G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460557 | |||||||
| chr17:82460578 | C | G | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.108+506C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460578 | |||||||
| chr17:82460610 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.108+538A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460610 | |||||||
| chr17:82460673 | A | G | 4 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 others(1): Show |
6 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+601A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460673 | |||||||
| chr17:82460720 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.108+648C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460720 | |||||||
| chr17:82460722 | C | T | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.108+650C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460722 | |||||||
| chr17:82460723 | C | A | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.108+651C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460723 | |||||||
| chr17:82460818 | C | T | 2 | a0001c0001t0002g0223 a0001c0001t0009g0224 |
2 | NA18997.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.108+746C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460818 | |||||||
| chr17:82460828 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.108+756A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460828 | |||||||
| chr17:82460867 | G | T | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+795G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460867 | |||||||
| chr17:82460899 | T | TGGATTTC others(160): Show |
1 | a0001c0002t0030g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.108+841_108+842ins others(167): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 82460899 | ||||||
| chr17:82460899 | T | TGGATTTC others(162): Show |
1 | a0001c0002t0031g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.108+841_108+842ins others(169): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 82460899 | ||||||
| chr17:82460915 | A | AT | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.108+853dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 82460915 | ||||||
| chr17:82460925 | T | C | 1 | a0001c0002t0014g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.108+853T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82460925 | |||||||
| chr17:82461064 | A | G | 2 | a0001c0002t0030g0152 a0001c0002t0031g0153 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.108+992A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461064 | |||||||
| chr17:82461154 | G | A | 1 | a0001c0002t0008g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.108+1082G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461154 | |||||||
| chr17:82461227 | C | T | 1 | a0001c0002t0023g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.108+1155C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461227 | |||||||
| chr17:82461407 | T | C | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+1335T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461407 | |||||||
| chr17:82461560 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.108+1488G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461560 | |||||||
| chr17:82461567 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.108+1495C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461567 | |||||||
| chr17:82461616 | A | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
237 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.108+1544A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461616 | |||||||
| chr17:82461701 | G | A | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.108+1629G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461701 | |||||||
| chr17:82461732 | C | T | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+1660C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461732 | |||||||
| chr17:82461848 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
240 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.108+1776C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82461848 | |||||||
| chr17:82462138 | C | T | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | HG02615.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.108+2066C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462138 | |||||||
| chr17:82462161 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.108+2089C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462161 | |||||||
| chr17:82462322 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0005g0141 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.109-1965A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462322 | |||||||
| chr17:82462420 | G | A | 1 | a0001c0002t0008g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109-1867G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462420 | |||||||
| chr17:82462597 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109-1690G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462597 | |||||||
| chr17:82462597 | G | T | 2 | a0001c0003t0015g0228 a0001c0003t0015g0229 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.109-1690G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462597 | |||||||
| chr17:82462598 | G | A | 4 | a0001c0001t0010g0027 a0001c0001t0010g0046 a0001c0001t0010g0047 others(1): Show |
5 | HG00642.hp2 HG01192.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-1689G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462598 | |||||||
| chr17:82462717 | C | CA | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.109-1569dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 82462717 | ||||||
| chr17:82462801 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.109-1486G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462801 | |||||||
| chr17:82462865 | C | T | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109-1422C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462865 | |||||||
| chr17:82462895 | G | A | 2 | a0001c0003t0015g0228 a0001c0003t0015g0229 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.109-1392G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82462895 | |||||||
| chr17:82463090 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0050 |
3 | HG01074.hp1 HG01978.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.109-1197G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463090 | |||||||
| chr17:82463140 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.109-1147G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463140 | |||||||
| chr17:82463234 | C | T | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
80 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.109-1053C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463234 | |||||||
| chr17:82463263 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
125 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.109-1024A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463263 | |||||||
| chr17:82463343 | C | G | 2 | a0001c0002t0030g0152 a0001c0002t0031g0153 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.109-944C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463343 | |||||||
| chr17:82463614 | G | A | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.109-673G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463614 | |||||||
| chr17:82463666 | G | A | 1 | a0001c0002t0025g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-621G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463666 | |||||||
| chr17:82463963 | G | A | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109-324G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463963 | |||||||
| chr17:82463994 | A | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
147 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.109-293A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463994 | |||||||
| chr17:82463994 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.109-293A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82463994 | |||||||
| chr17:82464238 | A | G | 1 | a0001c0002t0008g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109-49A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 2/10 | chr17 | 82464238 | |||||||
| chr17:82464447 | A | T | 14 | a0001c0002t0001g0037 a0001c0002t0003g0012 a0001c0002t0003g0013 others(11): Show |
26 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.252+17A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464447 | |||||||
| chr17:82464592 | A | G | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+162A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464592 | |||||||
| chr17:82464593 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.252+163T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464593 | |||||||
| chr17:82464720 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.252+290C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464720 | |||||||
| chr17:82464739 | G | A | 1 | a0001c0001t0026g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.252+309G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464739 | |||||||
| chr17:82464817 | C | G | 1 | a0001c0002t0025g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.252+387C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464817 | |||||||
| chr17:82464949 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.252+519T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82464949 | |||||||
| chr17:82465034 | C | G | 2 | a0001c0001t0001g0142 a0001c0001t0005g0141 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.252+604C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465034 | |||||||
| chr17:82465040 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.252+610C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465040 | |||||||
| chr17:82465523 | G | A | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.252+1093G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465523 | |||||||
| chr17:82465580 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.252+1150A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465580 | |||||||
| chr17:82465582 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0002g0091 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.252+1152A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465582 | |||||||
| chr17:82465606 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.252+1176C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465606 | |||||||
| chr17:82465670 | G | A | 1 | a0001c0002t0023g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.252+1240G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465670 | |||||||
| chr17:82465677 | C | G | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1247C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465677 | |||||||
| chr17:82465709 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.252+1279A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465709 | |||||||
| chr17:82465836 | G | T | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
80 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.252+1406G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465836 | |||||||
| chr17:82465954 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.252+1524C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82465954 | |||||||
| chr17:82466260 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.252+1830C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466260 | |||||||
| chr17:82466280 | G | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02083.hp1 NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.252+1850G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466280 | |||||||
| chr17:82466281 | T | C | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.252+1851T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466281 | |||||||
| chr17:82466391 | T | C | 1 | a0001c0002t0008g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+1961T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466391 | |||||||
| chr17:82466510 | T | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
85 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.252+2080T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466510 | |||||||
| chr17:82466649 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.253-2115C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466649 | |||||||
| chr17:82466672 | C | T | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.253-2092C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466672 | |||||||
| chr17:82466705 | G | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 |
3 | HG01934.hp1 HG02738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.253-2059G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466705 | |||||||
| chr17:82466747 | C | G | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.253-2017C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466747 | |||||||
| chr17:82466748 | C | T | 1 | a0001c0001t0026g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.253-2016C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466748 | |||||||
| chr17:82466836 | CTCTCTTA others(72): Show |
C | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.253-1926_253-1848d others(81): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82466836 | ||||||
| chr17:82466845 | A | G | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-1919A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466845 | |||||||
| chr17:82466882 | C | T | 1 | a0001c0001t0027g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.253-1882C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82466882 | |||||||
| chr17:82466995 | C | CT | 7 | a0001c0001t0001g0139 a0001c0001t0001g0214 a0001c0001t0002g0087 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-1755dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82466995 | ||||||
| chr17:82467086 | G | A | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.253-1678G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82467086 | |||||||
| chr17:82467391 | TCTAGTTT others(3): Show |
T | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.253-1361_253-1352d others(12): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82467391 | ||||||
| chr17:82467497 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.253-1267T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82467497 | |||||||
| chr17:82467664 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.253-1100C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82467664 | |||||||
| chr17:82467785 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.253-979T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82467785 | |||||||
| chr17:82468003 | G | A | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.253-761G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468003 | |||||||
| chr17:82468084 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.253-680G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468084 | |||||||
| chr17:82468206 | G | A | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.253-558G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468206 | |||||||
| chr17:82468236 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.253-528G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468236 | |||||||
| chr17:82468245 | A | G | 1 | a0001c0001t0016g0212 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.253-519A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468245 | |||||||
| chr17:82468274 | GTACTGTA others(41): Show |
G | 1 | a0001c0001t0001g0044 | 2 | NA18961.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.253-457_253-410del others(48): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82468274 | ||||||
| chr17:82468276 | A | G | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-488A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468276 | |||||||
| chr17:82468307 | G | GT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0022 others(13): Show |
21 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.253-441dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82468307 | ||||||
| chr17:82468307 | GT | G | 7 | a0001c0001t0029g0192 a0001c0002t0003g0012 a0001c0002t0003g0013 others(4): Show |
14 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.253-441delT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82468307 | ||||||
| chr17:82468332 | C | G | 1 | a0001c0001t0002g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.253-432C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468332 | |||||||
| chr17:82468350 | ACT | A | 3 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 |
5 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-411_253-410del others(2): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82468350 | ||||||
| chr17:82468399 | G | A | 1 | a0001c0001t0005g0168 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.253-365G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468399 | |||||||
| chr17:82468408 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.253-356A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468408 | |||||||
| chr17:82468487 | T | G | 1 | a0001c0002t0011g0025 | 3 | HG02622.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.253-277T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468487 | |||||||
| chr17:82468555 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.253-209T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468555 | |||||||
| chr17:82468674 | TA | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
239 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.253-88delA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 82468674 | ||||||
| chr17:82468759 | T | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0164 others(15): Show |
28 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.253-5T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 3/10 | chr17 | 82468759 | |||||||
| chr17:82469021 | C | T | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.385+125C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469021 | |||||||
| chr17:82469070 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.385+174G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469070 | |||||||
| chr17:82469112 | G | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
126 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.385+216G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469112 | |||||||
| chr17:82469114 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
101 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.385+218G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469114 | |||||||
| chr17:82469126 | A | G | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385+230A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469126 | |||||||
| chr17:82469262 | T | C | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+366T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469262 | |||||||
| chr17:82469277 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.385+381T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469277 | |||||||
| chr17:82469410 | G | A | 1 | a0001c0001t0013g0038 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.385+514G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469410 | |||||||
| chr17:82469464 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
239 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.385+568G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469464 | |||||||
| chr17:82469532 | G | A | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+636G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469532 | |||||||
| chr17:82469634 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385+738C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469634 | |||||||
| chr17:82469643 | T | G | 3 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 |
5 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+747T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469643 | |||||||
| chr17:82469698 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.385+802C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469698 | |||||||
| chr17:82469701 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.385+805G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469701 | |||||||
| chr17:82469722 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.385+826C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469722 | |||||||
| chr17:82469750 | T | G | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.385+854T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469750 | |||||||
| chr17:82469754 | C | T | 3 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 |
5 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+858C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469754 | |||||||
| chr17:82469861 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
126 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.385+965C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469861 | |||||||
| chr17:82469862 | C | T | 1 | a0001c0002t0008g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.385+966C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469862 | |||||||
| chr17:82469927 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.385+1031G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469927 | |||||||
| chr17:82469941 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
239 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.385+1045A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82469941 | |||||||
| chr17:82470099 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
109 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.385+1203G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470099 | |||||||
| chr17:82470138 | C | T | 1 | a0001c0002t0031g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.385+1242C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470138 | |||||||
| chr17:82470223 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
120 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.385+1327G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470223 | |||||||
| chr17:82470322 | G | C | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.385+1426G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470322 | |||||||
| chr17:82470358 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.385+1462A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470358 | |||||||
| chr17:82470374 | C | T | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.385+1478C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470374 | |||||||
| chr17:82470403 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.385+1507C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470403 | |||||||
| chr17:82470404 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.385+1508T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470404 | |||||||
| chr17:82470423 | T | C | 1 | a0001c0001t0009g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.385+1527T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470423 | |||||||
| chr17:82470435 | A | C | 3 | a0001c0001t0008g0043 a0001c0001t0008g0211 a0001c0001t0019g0043 |
3 | HG01361.hp2 HG01993.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.385+1539A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470435 | |||||||
| chr17:82470435 | A | G | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+1539A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470435 | |||||||
| chr17:82470459 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385+1563G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470459 | |||||||
| chr17:82470587 | C | T | 1 | a0001c0001t0026g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.385+1691C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470587 | |||||||
| chr17:82470595 | C | T | 2 | a0001c0002t0030g0152 a0001c0002t0031g0153 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.385+1699C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470595 | |||||||
| chr17:82470656 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
85 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.385+1760G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470656 | |||||||
| chr17:82470702 | G | T | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.385+1806G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470702 | |||||||
| chr17:82470756 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.386-1808A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470756 | |||||||
| chr17:82470774 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.386-1790G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470774 | |||||||
| chr17:82470846 | G | A | 1 | a0001c0001t0032g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.386-1718G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470846 | |||||||
| chr17:82470864 | T | C | 2 | a0001c0001t0006g0029 a0001c0001t0006g0059 |
3 | HG01106.hp2 HG01123.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.386-1700T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470864 | |||||||
| chr17:82470912 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.386-1652C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470912 | |||||||
| chr17:82470928 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.386-1636C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82470928 | |||||||
| chr17:82471055 | C | T | 7 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0049 others(4): Show |
9 | HG00408.hp1 HG02135.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-1509C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471055 | |||||||
| chr17:82471080 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.386-1484T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471080 | |||||||
| chr17:82471081 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.386-1483C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471081 | |||||||
| chr17:82471105 | G | A | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1459G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471105 | |||||||
| chr17:82471152 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.386-1412T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471152 | |||||||
| chr17:82471160 | T | TC | 3 | a0001c0001t0001g0117 a0001c0001t0001g0155 a0001c0001t0005g0182 |
3 | NA18963.hp1 NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.386-1404_386-1403i others(3): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471160 | |||||||
| chr17:82471161 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0155 a0001c0001t0005g0182 |
3 | NA18963.hp1 NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.386-1403G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471161 | |||||||
| chr17:82471161 | G | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
234 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.386-1403G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471161 | |||||||
| chr17:82471190 | TC | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
109 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.386-1373delC | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471190 | |||||||
| chr17:82471200 | A | C | 1 | a0001c0002t0030g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.386-1364A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471200 | |||||||
| chr17:82471208 | C | G | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-1356C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471208 | |||||||
| chr17:82471230 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.386-1334C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471230 | |||||||
| chr17:82471251 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
241 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.386-1313T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471251 | |||||||
| chr17:82471269 | C | A | 1 | a0001c0001t0005g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-1295C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471269 | |||||||
| chr17:82471312 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-1252G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471312 | |||||||
| chr17:82471315 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.386-1249C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471315 | |||||||
| chr17:82471316 | G | A | 1 | a0001c0002t0018g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.386-1248G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471316 | |||||||
| chr17:82471327 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.386-1237C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471327 | |||||||
| chr17:82471328 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.386-1236G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471328 | |||||||
| chr17:82471450 | G | C | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-1114G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471450 | |||||||
| chr17:82471454 | C | CA | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
115 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.386-1093dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471454 | ||||||
| chr17:82471474 | C | A | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-1090C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471474 | |||||||
| chr17:82471510 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.386-1054T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471510 | |||||||
| chr17:82471558 | C | A | 3 | a0001c0001t0002g0034 a0001c0001t0002g0105 a0001c0001t0002g0106 |
4 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1006C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471558 | |||||||
| chr17:82471589 | G | A | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.386-975G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471589 | |||||||
| chr17:82471620 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
242 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.386-944A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471620 | |||||||
| chr17:82471742 | G | A | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-822G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471742 | |||||||
| chr17:82471748 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.386-816C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471748 | |||||||
| chr17:82471749 | G | A | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.386-815G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471749 | |||||||
| chr17:82471768 | C | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
236 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.386-796C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471768 | |||||||
| chr17:82471791 | C | CAAAAAAA others(1): Show |
21 | a0001c0001t0001g0009 a0001c0001t0001g0134 a0001c0001t0001g0206 others(18): Show |
35 | HG01099.hp1 HG01884.hp2 HG01928.hp1 others(32): Show |
intron_variant | MODIFIER | c.386-764_386-757dup others(8): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(2): Show |
42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
62 | HG00621.hp1 HG00639.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.386-765_386-757dup others(9): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(3): Show |
15 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0107 others(12): Show |
21 | HG00423.hp2 HG00597.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.386-766_386-757dup others(10): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(5): Show |
6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-768_386-757dup others(12): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(6): Show |
1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-769_386-757dup others(13): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0100 a0001c0002t0001g0104 |
2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.386-770_386-757dup others(14): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0202 a0001c0002t0001g0099 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.386-771_386-757dup others(15): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0225 others(1): Show |
4 | HG02818.hp2 NA18960.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-757_386-756ins others(20): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(14): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(15): Show |
32 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.386-757_386-756ins others(21): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(15): Show |
23 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0042 others(20): Show |
31 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.386-757_386-756ins others(22): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(16): Show |
16 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0041 others(13): Show |
22 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.386-757_386-756ins others(23): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(17): Show |
6 | a0001c0001t0001g0040 a0001c0001t0001g0184 a0001c0001t0001g0210 others(3): Show |
7 | HG01496.hp1 HG02717.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-757_386-756ins others(24): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0005g0168 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.386-757_386-756ins others(25): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(19): Show |
1 | a0002c0009t0001g0170 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.386-757_386-756ins others(26): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471791 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.386-757_386-756ins others(36): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471791 | ||||||
| chr17:82471805 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-757_386-756ins others(21): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82471805 | ||||||
| chr17:82471839 | C | T | 1 | a0001c0001t0013g0038 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.386-725C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471839 | |||||||
| chr17:82471977 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
77 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.386-587G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471977 | |||||||
| chr17:82471999 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.386-565A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82471999 | |||||||
| chr17:82472266 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.386-298T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82472266 | |||||||
| chr17:82472483 | C | CA | 7 | a0001c0001t0001g0119 a0001c0002t0001g0099 a0001c0002t0001g0100 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.386-66dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82472483 | ||||||
| chr17:82472483 | CA | C | 8 | a0001c0001t0001g0080 a0001c0001t0001g0110 a0001c0001t0001g0121 others(5): Show |
9 | HG00323.hp2 HG01943.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-66delA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 82472483 | ||||||
| chr17:82472560 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp1 | splice_region_variant&intron_variant | LOW | c.386-4G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 4/10 | chr17 | 82472560 | |||||||
| chr17:82472928 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
240 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.520+230A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82472928 | |||||||
| chr17:82472944 | T | A | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520+246T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82472944 | |||||||
| chr17:82472948 | A | AT | 7 | a0001c0001t0009g0056 a0001c0002t0003g0012 a0001c0002t0003g0013 others(4): Show |
14 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.520+260dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82472948 | ||||||
| chr17:82472948 | A | T | 1 | a0001c0002t0025g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.520+250A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82472948 | |||||||
| chr17:82473080 | A | G | 1 | a0001c0002t0004g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.520+382A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473080 | |||||||
| chr17:82473122 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.520+424G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473122 | |||||||
| chr17:82473295 | A | AT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
219 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.520+613dupT | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82473295 | ||||||
| chr17:82473295 | A | ATT | 8 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(5): Show |
15 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.520+612_520+613dup others(2): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82473295 | ||||||
| chr17:82473295 | A | C | 1 | a0001c0001t0006g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.520+597A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473295 | |||||||
| chr17:82473315 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.520+617G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473315 | |||||||
| chr17:82473410 | T | G | 4 | a0001c0001t0001g0200 a0001c0001t0002g0062 a0001c0001t0002g0090 others(1): Show |
4 | HG00323.hp2 HG01255.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.520+712T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473410 | |||||||
| chr17:82473494 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0226 |
2 | HG01358.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.520+796G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473494 | |||||||
| chr17:82473543 | G | A | 1 | a0001c0002t0008g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.520+845G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473543 | |||||||
| chr17:82473553 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
101 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.520+855G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473553 | |||||||
| chr17:82473626 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.520+928C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473626 | |||||||
| chr17:82473631 | G | A | 23 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(20): Show |
27 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.520+933G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473631 | |||||||
| chr17:82473827 | G | A | 1 | a0001c0001t0009g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.520+1129G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473827 | |||||||
| chr17:82473842 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
124 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.520+1144G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473842 | |||||||
| chr17:82473993 | C | T | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.520+1295C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473993 | |||||||
| chr17:82473994 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.520+1296G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82473994 | |||||||
| chr17:82474006 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.520+1308A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474006 | |||||||
| chr17:82474020 | C | CA | 5 | a0001c0001t0001g0122 a0001c0001t0001g0137 a0001c0001t0001g0217 others(2): Show |
5 | HG03516.hp1 NA18947.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.520+1331dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82474020 | ||||||
| chr17:82474030 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.520+1332C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474030 | |||||||
| chr17:82474031 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.520+1333A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474031 | |||||||
| chr17:82474135 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.520+1437T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474135 | |||||||
| chr17:82474163 | A | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0049 a0001c0001t0002g0083 others(1): Show |
6 | HG00408.hp1 NA18943.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+1465A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474163 | |||||||
| chr17:82474191 | C | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0186 others(3): Show |
10 | HG00741.hp2 HG01175.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.520+1493C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474191 | |||||||
| chr17:82474348 | C | A | 1 | a0001c0003t0020g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.520+1650C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474348 | |||||||
| chr17:82474421 | TAG | T | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.520+1728_520+1729d others(4): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82474421 | ||||||
| chr17:82474446 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18963.hp2 NA18966.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.520+1748C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474446 | |||||||
| chr17:82474487 | C | T | 1 | a0001c0002t0023g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.520+1789C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474487 | |||||||
| chr17:82474591 | C | G | 1 | a0001c0001t0001g0041 | 2 | NA18959.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.520+1893C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474591 | |||||||
| chr17:82474859 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.520+2161T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474859 | |||||||
| chr17:82474883 | C | A | 1 | a0001c0002t0025g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.520+2185C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82474883 | |||||||
| chr17:82475187 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.520+2489A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475187 | |||||||
| chr17:82475338 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.520+2640C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475338 | |||||||
| chr17:82475366 | C | A | 1 | a0001c0001t0002g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.520+2668C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475366 | |||||||
| chr17:82475578 | CAG | C | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.520+2883_520+2884d others(4): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82475578 | ||||||
| chr17:82475640 | A | G | 1 | a0001c0001t0021g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.520+2942A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475640 | |||||||
| chr17:82475656 | G | A | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.520+2958G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475656 | |||||||
| chr17:82475681 | G | A | 2 | a0001c0002t0003g0012 a0001c0002t0003g0234 |
6 | HG02258.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.520+2983G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475681 | |||||||
| chr17:82475721 | G | GA | 14 | a0001c0001t0002g0014 a0001c0001t0002g0021 a0001c0001t0002g0033 others(11): Show |
18 | HG00408.hp1 HG01099.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.520+3024dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 82475721 | ||||||
| chr17:82475804 | A | G | 8 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0077 others(5): Show |
11 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.521-2996A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475804 | |||||||
| chr17:82475814 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.521-2986G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475814 | |||||||
| chr17:82475908 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.521-2892G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82475908 | |||||||
| chr17:82476182 | A | G | 1 | a0001c0002t0007g0115 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.521-2618A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476182 | |||||||
| chr17:82476231 | C | G | 1 | a0001c0001t0002g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.521-2569C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476231 | |||||||
| chr17:82476256 | C | T | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-2544C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476256 | |||||||
| chr17:82476281 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.521-2519A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476281 | |||||||
| chr17:82476353 | G | T | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-2447G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476353 | |||||||
| chr17:82476417 | C | T | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.521-2383C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476417 | |||||||
| chr17:82476418 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.521-2382A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82476418 | |||||||
| chr17:82477131 | C | T | 1 | a0001c0001t0026g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.521-1669C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477131 | |||||||
| chr17:82477242 | G | C | 1 | a0001c0002t0030g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.521-1558G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477242 | |||||||
| chr17:82477274 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.521-1526C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477274 | |||||||
| chr17:82477530 | C | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0061 a0001c0001t0002g0074 others(2): Show |
7 | HG00099.hp1 HG00280.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.521-1270C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477530 | |||||||
| chr17:82477531 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0073 others(2): Show |
13 | HG01167.hp2 HG01261.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.521-1269A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477531 | |||||||
| chr17:82477740 | C | G | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-1060C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477740 | |||||||
| chr17:82477810 | G | A | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-990G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477810 | |||||||
| chr17:82477868 | A | G | 1 | a0001c0001t0034g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.521-932A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477868 | |||||||
| chr17:82477873 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.521-927C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477873 | |||||||
| chr17:82477936 | T | C | 5 | a0001c0001t0006g0019 a0001c0001t0006g0029 a0001c0001t0006g0059 others(2): Show |
8 | HG01106.hp2 HG01123.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.521-864T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477936 | |||||||
| chr17:82477965 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.521-835T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82477965 | |||||||
| chr17:82478032 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.521-768C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478032 | |||||||
| chr17:82478148 | G | A | 1 | a0001c0002t0025g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.521-652G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478148 | |||||||
| chr17:82478165 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.521-635G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478165 | |||||||
| chr17:82478368 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.521-432C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478368 | |||||||
| chr17:82478421 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0074 a0001c0001t0002g0090 |
3 | HG01255.hp2 HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.521-379G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478421 | |||||||
| chr17:82478452 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.521-348C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478452 | |||||||
| chr17:82478453 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.521-347A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478453 | |||||||
| chr17:82478501 | A | G | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.521-299A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478501 | |||||||
| chr17:82478563 | C | T | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-237C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 5/10 | chr17 | 82478563 | |||||||
| chr17:82478978 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.639+60C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82478978 | |||||||
| chr17:82479089 | C | T | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.639+171C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479089 | |||||||
| chr17:82479175 | G | A | 1 | a0001c0001t0002g0032 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.639+257G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479175 | |||||||
| chr17:82479223 | C | A | 1 | a0001c0001t0001g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.639+305C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479223 | |||||||
| chr17:82479244 | G | A | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.639+326G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479244 | |||||||
| chr17:82479363 | G | A | 3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.639+445G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479363 | |||||||
| chr17:82479407 | T | C | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.639+489T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479407 | |||||||
| chr17:82479539 | A | G | 1 | a0001c0001t0009g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.639+621A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479539 | |||||||
| chr17:82479605 | C | G | 1 | a0001c0001t0027g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.639+687C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479605 | |||||||
| chr17:82479734 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.639+816C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479734 | |||||||
| chr17:82479735 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.639+817G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479735 | |||||||
| chr17:82479813 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.639+895A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479813 | |||||||
| chr17:82479902 | C | T | 1 | a0001c0002t0011g0025 | 3 | HG02622.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.639+984C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479902 | |||||||
| chr17:82479947 | G | A | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+1029G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479947 | |||||||
| chr17:82479966 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.639+1048A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82479966 | |||||||
| chr17:82480079 | T | C | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-1003T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480079 | |||||||
| chr17:82480258 | G | T | 3 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 |
5 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-824G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480258 | |||||||
| chr17:82480283 | G | C | 1 | a0001c0002t0001g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.640-799G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480283 | |||||||
| chr17:82480287 | G | GCA | 14 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0001c0001t0001g0215 others(11): Show |
23 | HG01074.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.640-794_640-793ins others(2): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480287 | ||||||
| chr17:82480287 | G | GCACACAC others(3): Show |
1 | a0001c0003t0015g0229 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.640-794_640-793ins others(10): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480287 | ||||||
| chr17:82480287 | G | GCACACAC others(5): Show |
1 | a0001c0002t0025g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.640-794_640-793ins others(12): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480287 | ||||||
| chr17:82480287 | G | GCACACAC others(7): Show |
2 | a0001c0003t0015g0228 a0001c0003t0020g0230 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.640-794_640-793ins others(14): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480287 | ||||||
| chr17:82480289 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.640-793G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480289 | |||||||
| chr17:82480289 | G | GCA | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
66 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.640-771_640-770dup others(2): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480289 | ||||||
| chr17:82480289 | G | GCACA | 15 | a0001c0001t0001g0125 a0001c0002t0001g0017 a0001c0002t0004g0023 others(12): Show |
20 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.640-773_640-770dup others(4): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480289 | ||||||
| chr17:82480291 | A | G | 5 | a0001c0001t0002g0068 a0001c0001t0002g0072 a0001c0001t0002g0079 others(2): Show |
5 | HG01123.hp2 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-791A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480291 | |||||||
| chr17:82480370 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(19): Show |
39 | HG00597.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.640-712G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480370 | |||||||
| chr17:82480374 | T | C | 1 | a0001c0002t0004g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.640-708T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480374 | |||||||
| chr17:82480397 | A | T | 1 | a0001c0001t0005g0185 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.640-685A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480397 | |||||||
| chr17:82480582 | C | T | 1 | a0001c0002t0004g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.640-500C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480582 | |||||||
| chr17:82480622 | A | C | 1 | a0001c0002t0030g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.640-460A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480622 | |||||||
| chr17:82480652 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.640-430G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480652 | |||||||
| chr17:82480685 | T | C | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-397T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480685 | |||||||
| chr17:82480702 | C | T | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-380C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480702 | |||||||
| chr17:82480840 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.640-242G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480840 | |||||||
| chr17:82480856 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18963.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.640-226C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480856 | |||||||
| chr17:82480857 | G | A | 4 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-225G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480857 | |||||||
| chr17:82480930 | C | CA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(122): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.640-133dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480930 | ||||||
| chr17:82480930 | C | CAA | 6 | a0001c0001t0001g0171 a0001c0001t0001g0180 a0001c0001t0001g0187 others(3): Show |
6 | HG00558.hp1 HG03710.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-134_640-133dup others(2): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480930 | ||||||
| chr17:82480940 | AAAAAAAA others(3): Show |
A | 3 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 |
5 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-140_640-131del others(10): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480940 | ||||||
| chr17:82480948 | AAG | A | 8 | a0001c0001t0001g0110 a0001c0002t0001g0017 a0001c0002t0007g0017 others(5): Show |
10 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-131_640-130del others(2): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82480948 | ||||||
| chr17:82480949 | AG | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(37): Show |
63 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.640-132delG | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480949 | |||||||
| chr17:82480950 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0122 a0001c0001t0001g0125 others(4): Show |
7 | HG02148.hp1 HG02738.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.640-132G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480950 | |||||||
| chr17:82480986 | G | T | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.640-96G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82480986 | |||||||
| chr17:82481007 | T | G | 1 | a0001c0001t0001g0020 | 3 | HG01167.hp2 HG01261.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.640-75T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82481007 | |||||||
| chr17:82481010 | T | C | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-72T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82481010 | |||||||
| chr17:82481026 | C | T | 2 | a0001c0003t0015g0228 a0001c0003t0015g0229 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.640-56C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82481026 | |||||||
| chr17:82481069 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.640-13C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | chr17 | 82481069 | |||||||
| chr17:82481072 | T | TCCTTCCC others(3): Show |
1 | a0007c0008t0001g0120 | 1 | NA19062.hp2 | splice_region_variant&intron_variant | LOW | c.640-9_640-8insCTTC others(6): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 82481072 | ||||||
| chr17:82481241 | G | A | 1 | a0001c0001t0010g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.769+30G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481241 | |||||||
| chr17:82481260 | G | A | 2 | a0001c0002t0030g0152 a0001c0002t0031g0153 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.769+49G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481260 | |||||||
| chr17:82481318 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.769+107A>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481318 | |||||||
| chr17:82481322 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.769+111T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481322 | |||||||
| chr17:82481526 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.769+315C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481526 | |||||||
| chr17:82481537 | T | G | 1 | a0001c0001t0002g0071 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.769+326T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481537 | |||||||
| chr17:82481594 | G | A | 10 | a0001c0002t0001g0037 a0001c0002t0003g0012 a0001c0002t0003g0013 others(7): Show |
20 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+383G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481594 | |||||||
| chr17:82481623 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.769+412G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481623 | |||||||
| chr17:82481684 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0194 |
2 | HG00735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.769+473C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481684 | |||||||
| chr17:82481730 | CA | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
108 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.769+535delA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82481730 | ||||||
| chr17:82481744 | A | T | 2 | a0001c0002t0030g0152 a0001c0002t0031g0153 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.769+533A>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481744 | |||||||
| chr17:82481774 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.769+563T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481774 | |||||||
| chr17:82481857 | C | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
77 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.769+646C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481857 | |||||||
| chr17:82481954 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.769+743T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481954 | |||||||
| chr17:82481966 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.769+755C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82481966 | |||||||
| chr17:82482031 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
85 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.769+820A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482031 | |||||||
| chr17:82482049 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
107 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.769+838T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482049 | |||||||
| chr17:82482058 | C | T | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.769+847C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482058 | |||||||
| chr17:82482139 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.769+928T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482139 | |||||||
| chr17:82482192 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG00621.hp1 NA18953.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+981G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482192 | |||||||
| chr17:82482224 | A | G | 7 | a0001c0002t0001g0045 a0001c0002t0001g0099 a0001c0002t0001g0100 others(4): Show |
8 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+1013A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482224 | |||||||
| chr17:82482281 | T | C | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.769+1070T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482281 | |||||||
| chr17:82482326 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.769+1115G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482326 | |||||||
| chr17:82482375 | C | G | 11 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 others(8): Show |
20 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+1164C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482375 | |||||||
| chr17:82482385 | A | G | 3 | a0001c0002t0025g0149 a0001c0002t0030g0152 a0001c0002t0031g0153 |
3 | HG02630.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.769+1174A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482385 | |||||||
| chr17:82482408 | A | ATGTTGAC others(173): Show |
1 | a0001c0002t0011g0025 | 3 | HG02622.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.769+1197_769+1198i others(182): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482408 | |||||||
| chr17:82482408 | A | ATGTTGAC others(144): Show |
2 | a0001c0002t0030g0152 a0001c0002t0031g0153 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.769+1197_769+1198i others(153): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482408 | |||||||
| chr17:82482409 | C | CGTTGACA others(23): Show |
2 | a0001c0003t0015g0228 a0001c0003t0015g0229 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.769+1201_769+1230d others(32): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82482409 | ||||||
| chr17:82482409 | C | CGTTGACA others(53): Show |
7 | a0001c0002t0001g0037 a0001c0002t0001g0045 a0001c0002t0008g0235 others(4): Show |
9 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+1230_769+1231i others(62): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82482409 | ||||||
| chr17:82482409 | C | T | 9 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(6): Show |
18 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.769+1198C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482409 | |||||||
| chr17:82482411 | T | TTGACAAA others(23): Show |
3 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0104 |
3 | HG02145.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.769+1229_769+1230i others(32): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82482411 | ||||||
| chr17:82482420 | T | TAAAACAT others(24): Show |
138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
193 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.769+1230_769+1231i others(33): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82482420 | ||||||
| chr17:82482420 | T | TAAAACAT others(205): Show |
6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.769+1230_769+1231i others(214): Show |
NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82482420 | ||||||
| chr17:82482674 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.770-1042A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482674 | |||||||
| chr17:82482726 | G | A | 3 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 |
5 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-990G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482726 | |||||||
| chr17:82482992 | G | A | 3 | a0001c0003t0015g0228 a0001c0003t0015g0229 a0001c0003t0020g0230 |
3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.770-724G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82482992 | |||||||
| chr17:82483030 | A | G | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.770-686A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483030 | |||||||
| chr17:82483054 | A | G | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.770-662A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483054 | |||||||
| chr17:82483296 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.770-420G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483296 | |||||||
| chr17:82483301 | G | A | 9 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(6): Show |
11 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-415G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483301 | |||||||
| chr17:82483319 | CA | C | 7 | a0001c0001t0001g0129 a0001c0001t0002g0068 a0001c0001t0002g0084 others(4): Show |
7 | HG00735.hp2 HG02055.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-384delA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 82483319 | ||||||
| chr17:82483338 | C | G | 5 | a0001c0002t0001g0037 a0001c0002t0025g0149 a0001c0003t0015g0228 others(2): Show |
6 | HG01884.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-378C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483338 | |||||||
| chr17:82483379 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0054 |
2 | HG02738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.770-337A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483379 | |||||||
| chr17:82483533 | C | T | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.770-183C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483533 | |||||||
| chr17:82483571 | C | A | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.770-145C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 7/10 | chr17 | 82483571 | |||||||
| chr17:82484114 | C | T | 1 | a0001c0002t0004g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.833+335C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484114 | |||||||
| chr17:82484210 | C | T | 6 | a0001c0002t0004g0023 a0001c0002t0004g0132 a0001c0002t0004g0136 others(3): Show |
7 | HG02040.hp1 HG02273.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.833+431C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484210 | |||||||
| chr17:82484227 | A | G | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.833+448A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484227 | |||||||
| chr17:82484239 | G | A | 1 | a0001c0001t0009g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.833+460G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484239 | |||||||
| chr17:82484241 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.833+462C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484241 | |||||||
| chr17:82484392 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.834-421G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484392 | |||||||
| chr17:82484396 | G | T | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.834-417G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484396 | |||||||
| chr17:82484592 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.834-221G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484592 | |||||||
| chr17:82484634 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.834-179C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484634 | |||||||
| chr17:82484689 | G | C | 6 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0003g0232 others(3): Show |
13 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.834-124G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484689 | |||||||
| chr17:82484715 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0005g0141 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.834-98G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484715 | |||||||
| chr17:82484771 | G | A | 2 | a0001c0002t0001g0045 a0001c0002t0018g0236 |
3 | HG02055.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.834-42G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484771 | |||||||
| chr17:82484807 | T | G | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.834-6T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 8/10 | chr17 | 82484807 | |||||||
| chr17:82485077 | T | G | 3 | a0001c0002t0001g0045 a0001c0002t0008g0235 a0001c0002t0018g0236 |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+127T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485077 | |||||||
| chr17:82485158 | G | A | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971+208G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485158 | |||||||
| chr17:82485187 | C | T | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.971+237C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485187 | |||||||
| chr17:82485238 | A | G | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.972-259A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485238 | |||||||
| chr17:82485249 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0139 |
2 | HG01070.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.972-248A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485249 | |||||||
| chr17:82485274 | T | A | 38 | a0001c0002t0001g0017 a0001c0002t0001g0037 a0001c0002t0001g0045 others(35): Show |
54 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(51): Show |
intron_variant | MODIFIER | c.972-223T>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485274 | |||||||
| chr17:82485277 | C | T | 31 | a0001c0002t0001g0017 a0001c0002t0001g0037 a0001c0002t0003g0012 others(28): Show |
46 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.972-220C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485277 | |||||||
| chr17:82485291 | A | G | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.972-206A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485291 | |||||||
| chr17:82485323 | A | G | 3 | a0001c0002t0004g0024 a0001c0002t0004g0145 a0001c0002t0004g0146 |
5 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.972-174A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485323 | |||||||
| chr17:82485361 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.972-136C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485361 | |||||||
| chr17:82485419 | T | G | 1 | a0001c0001t0001g0036 | 2 | NA19004.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.972-78T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485419 | |||||||
| chr17:82485420 | C | CA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
183 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.972-66dupA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 82485420 | ||||||
| chr17:82485420 | C | CAA | 24 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0148 others(21): Show |
34 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.972-67_972-66dupAA | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 82485420 | ||||||
| chr17:82485433 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
237 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.972-64G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 9/10 | chr17 | 82485433 | |||||||
| chr17:82485679 | G | T | 11 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0132 others(8): Show |
14 | HG01884.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1129+25G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82485679 | |||||||
| chr17:82485850 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1129+196C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82485850 | |||||||
| chr17:82486132 | T | G | 1 | a0001c0002t0007g0114 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1129+478T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486132 | |||||||
| chr17:82486229 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1129+575G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486229 | |||||||
| chr17:82486261 | G | C | 1 | a0001c0002t0004g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1129+607G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486261 | |||||||
| chr17:82486299 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1129+645G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486299 | |||||||
| chr17:82486329 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0176 |
2 | NA18943.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1129+675C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486329 | |||||||
| chr17:82486340 | C | CG | 13 | a0001c0001t0002g0089 a0001c0001t0002g0094 a0001c0001t0002g0095 others(10): Show |
20 | HG00741.hp1 HG01192.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1129+694dupG | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr17 | 82486340 | ||||||
| chr17:82486343 | G | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0080 others(4): Show |
16 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1129+689G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486343 | |||||||
| chr17:82486346 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1129+692G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486346 | |||||||
| chr17:82486399 | C | T | 1 | a0001c0002t0011g0025 | 3 | HG02622.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1129+745C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486399 | |||||||
| chr17:82486431 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0009g0060 |
3 | HG01243.hp1 HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1129+777G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486431 | |||||||
| chr17:82486433 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1129+779G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486433 | |||||||
| chr17:82486452 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129+798G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486452 | |||||||
| chr17:82486462 | G | T | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129+808G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486462 | |||||||
| chr17:82486506 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1129+852G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486506 | |||||||
| chr17:82486567 | C | A | 20 | a0001c0002t0001g0017 a0001c0002t0001g0037 a0001c0002t0003g0012 others(17): Show |
32 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.1129+913C>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486567 | |||||||
| chr17:82486605 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129+951C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486605 | |||||||
| chr17:82486955 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1130-961C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82486955 | |||||||
| chr17:82487009 | G | C | 1 | a0001c0001t0008g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1130-907G>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487009 | |||||||
| chr17:82487249 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0005g0141 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1130-667C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487249 | |||||||
| chr17:82487318 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1130-598T>C | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487318 | |||||||
| chr17:82487433 | G | T | 1 | a0001c0010t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1130-483G>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487433 | |||||||
| chr17:82487471 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1130-445G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487471 | |||||||
| chr17:82487563 | C | T | 1 | a0001c0002t0003g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1130-353C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487563 | |||||||
| chr17:82487574 | T | G | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1130-342T>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487574 | |||||||
| chr17:82487611 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1130-305G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487611 | |||||||
| chr17:82487639 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1130-277C>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487639 | |||||||
| chr17:82487677 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1130-239G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487677 | |||||||
| chr17:82487686 | C | T | 1 | a0001c0002t0001g0037 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1130-230C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487686 | |||||||
| chr17:82487700 | A | G | 2 | a0001c0001t0001g0151 a0001c0011t0001g0150 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1130-216A>G | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487700 | |||||||
| chr17:82487776 | G | A | 1 | a0001c0002t0024g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1130-140G>A | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487776 | |||||||
| chr17:82487778 | C | T | 6 | a0001c0002t0001g0017 a0001c0002t0007g0017 a0001c0002t0007g0113 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1130-138C>T | NARF | ENSG00000141562.19 | transcript | ENST00000309794.16 | protein_coding | 10/10 | chr17 | 82487778 |