Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25794 |
| ensemblid | ENSG00000186765.12 |
| hgncid | 3960 |
| symbol | FSCN2 |
| name | fascin actin-bundling protein 2, retinal |
| refseq_nuc | NM_012418.4 |
| refseq_prot | NP_036550.1 |
| ensembl_nuc | ENST00000417245.7 |
| ensembl_prot | ENSP00000388716.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 81528377 |
| end | 81537130 |
| strand | + |
| ver | v1.2 |
| region | chr17:81528377-81537130 |
| region5000 | chr17:81523377-81542130 |
| regionname0 | FSCN2_chr17_81528377_81537130 |
| regionname5000 | FSCN2_chr17_81523377_81542130 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 492 | 418 | 95 | 82 | 175 | 17 | 47 | 132 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| a0002 | 0/0 | 143 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(138): Show |
chr17 | 81523377 | 81542130 |
| a0003 | 0/0 | 492 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| a0004 | 0/0 | 492 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| a0005 | 0/0 | 492 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| a0006 | 0/0 | 492 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| a0007 | 0/0 | 492 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| a0008 | 0/0 | 502 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(497): Show |
chr17 | 81523377 | 81542130 |
| a0009 | 0/0 | 492 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | MPTNG others(487): Show |
chr17 | 81523377 | 81542130 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1476 | 316 | 58 | 65 | 133 | 15 | 43 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0002 | 0/0 | 1476 | 36 | 26 | 4 | 4 | 0 | 2 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0003 | 0/0 | 1476 | 26 | 0 | 8 | 18 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0004 | 0/0 | 1476 | 20 | 0 | 0 | 20 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0006 | 0/0 | 1476 | 5 | 0 | 4 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0007 | 0/0 | 1476 | 4 | 4 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0009 | 0/0 | 1476 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0010 | 0/0 | 1476 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0011 | 0/0 | 1476 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0012 | 0/0 | 1476 | 2 | 0 | 1 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0017 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0001c0018 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0002c0005 | 0/0 | 1475 | 5 | 0 | 0 | 5 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1470): Show |
chr17 | 81523377 | 81542130 | ||
| a0003c0008 | 0/0 | 1476 | 3 | 0 | 2 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0004c0015 | 0/0 | 1476 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0005c0013 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0006c0016 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0007c0014 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 | ||
| a0008c0020 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1501): Show |
chr17 | 81523377 | 81542130 | ||
| a0009c0019 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | ATGCC others(1471): Show |
chr17 | 81523377 | 81542130 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1684 | 243 | 46 | 50 | 96 | 11 | 39 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0001t0002 | 1/0 | 1684 | 66 | 12 | 8 | 37 | 4 | 4 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0001t0003 | 0/0 | 1684 | 6 | 0 | 6 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0001t0004 | 0/0 | 1684 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0002t0002 | 0/0 | 1684 | 35 | 25 | 4 | 4 | 0 | 2 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0002t0005 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0003t0001 | 0/0 | 1684 | 26 | 0 | 8 | 18 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0004t0001 | 0/0 | 1684 | 20 | 0 | 0 | 20 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0006t0001 | 0/0 | 1684 | 5 | 0 | 4 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0007t0001 | 0/0 | 1684 | 4 | 4 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0009t0001 | 0/0 | 1684 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0010t0002 | 0/0 | 1684 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0011t0002 | 0/0 | 1684 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0012t0001 | 0/0 | 1684 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0012t0002 | 0/0 | 1684 | 1 | 0 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0017t0001 | 0/0 | 1684 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0001c0018t0001 | 0/0 | 1684 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0002c0005t0002 | 0/0 | 1683 | 5 | 0 | 0 | 5 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1678): Show |
chr17 | 81523377 | 81542130 |
| a0003c0008t0001 | 0/0 | 1684 | 3 | 0 | 2 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0004c0015t0002 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0005c0013t0001 | 0/0 | 1684 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0006c0016t0001 | 0/0 | 1684 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0007c0014t0002 | 0/0 | 1684 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| a0008c0020t0001 | 0/0 | 1714 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1709): Show |
chr17 | 81523377 | 81542130 |
| a0009c0019t0002 | 0/0 | 1684 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | AGAGG others(1679): Show |
chr17 | 81523377 | 81542130 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 65 | 0 | 2 | 45 | 3 | 15 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0002 | 0/0 | 24 | 0 | 9 | 4 | 3 | 8 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 2 | 0 | 3 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0006 | 0/0 | 8 | 5 | 1 | 1 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0010 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0017 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0018 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0019 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0023 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0034 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0003 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0009 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0014 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0015 | 0/0 | 5 | 0 | 1 | 0 | 4 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0024 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0003g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0005 | 0/0 | 10 | 5 | 3 | 1 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0003t0001g0001 | 0/0 | 23 | 0 | 7 | 16 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0004t0001g0001 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0004t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0006t0001g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0007t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0007t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0009t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0010t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0011t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0012t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0012t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0017t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0001c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0002c0005t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0002c0005t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0003c0008t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0004c0015t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0005c0013t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0006c0016t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0007c0014t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0008c0020t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| a0009c0019t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00099 | hp2 | a0003 | c0008 | t0001 | g0025 | EUR | GBR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00733 | hp2 | a0003 | c0008 | t0001 | g0025 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00735 | hp1 | a0001 | c0012 | t0001 | g0006 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01358 | hp1 | a0001 | c0006 | t0001 | g0004 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01496 | hp2 | a0003 | c0008 | t0001 | g0025 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01515 | hp1 | a0001 | c0012 | t0002 | g0084 | EUR | IBS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01993 | hp1 | a0001 | c0006 | t0001 | g0004 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02055 | hp2 | a0004 | c0015 | t0002 | g0057 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02074 | hp2 | a0002 | c0005 | t0002 | g0007 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02257 | hp2 | a0001 | c0009 | t0001 | g0030 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02273 | hp2 | a0001 | c0006 | t0001 | g0004 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02280 | hp1 | a0001 | c0009 | t0001 | g0030 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02738 | hp1 | a0005 | c0013 | t0001 | g0137 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03041 | hp2 | a0001 | c0010 | t0002 | g0020 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03195 | hp1 | a0001 | c0011 | t0002 | g0020 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0033 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03453 | hp2 | a0001 | c0007 | t0001 | g0033 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03491 | hp1 | a0006 | c0016 | t0001 | g0002 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | GWD | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0067 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03831 | hp1 | a0001 | c0018 | t0001 | g0001 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03834 | hp1 | a0001 | c0017 | t0001 | g0002 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04199 | hp2 | a0007 | c0014 | t0002 | g0068 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18906 | hp2 | a0001 | c0011 | t0002 | g0020 | AFR | YRI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18940 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18945 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18947 | hp2 | a0002 | c0005 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18953 | hp2 | a0002 | c0005 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18962 | hp1 | a0002 | c0005 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18970 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18974 | hp2 | a0008 | c0020 | t0001 | g0002 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19007 | hp2 | a0009 | c0019 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0053 | AFR | LWK | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | LWK | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19064 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19067 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0113 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19079 | hp2 | a0002 | c0005 | t0002 | g0090 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA19240 | hp2 | a0001 | c0007 | t0001 | g0033 | AFR | YRI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20129 | hp2 | a0001 | c0009 | t0001 | g0030 | AFR | ASW | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20805 | hp2 | a0001 | c0006 | t0001 | g0004 | EUR | TSI | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG01123 | hp2 | a0001 | c0006 | t0001 | g0004 | AMR | CLM | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02486 | hp2 | a0001 | c0010 | t0002 | g0020 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03471 | hp1 | a0001 | c0007 | t0001 | g0143 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA21309 | hp1 | a0001 | c0002 | t0005 | g0063 | AFR | LWK | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0092 | REF | REF | FSCN2_chr17_81523377_81542130 | FSCN2 | chr17 | 81523377 | 81542130 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81528573 | T | TGGCCTCG others(23): Show |
1 | a0008 | 1 | NA18974.hp2 | conservative_inframe_insertion | MODERATE | c.43_72dupGGCCTCGTCA others(20): Show |
p.Gly15_Leu24dup | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 228/1684 | 73/1479 | 25/492 | INFO_REALIGN_3_PRIME | chr17 | 81528573 | ||
| chr17:81528602 | TG | T | 1 | a0002 | 5 | HG02074.hp2 NA18947.hp2 NA18953.hp2 others(2): Show |
frameshift_variant | HIGH | c.72delG | p.Thr25fs | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 227/1684 | 72/1479 | 24/492 | chr17 | 81528602 | |||
| chr17:81528677 | A | C | 1 | a0009 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.146A>C | p.Glu49Ala | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 301/1684 | 146/1479 | 49/492 | chr17 | 81528677 | |||
| chr17:81529042 | G | A | 1 | a0005 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.511G>A | p.Val171Met | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 666/1684 | 511/1479 | 171/492 | chr17 | 81529042 | |||
| chr17:81535123 | A | G | 1 | a0006 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.898A>G | p.Thr300Ala | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/5 | 1053/1684 | 898/1479 | 300/492 | chr17 | 81535123 | |||
| chr17:81535192 | G | A | 1 | a0003 | 3 | HG00099.hp2 HG00733.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.967G>A | p.Ala323Thr | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/5 | 1122/1684 | 967/1479 | 323/492 | chr17 | 81535192 | |||
| chr17:81536640 | C | G | 1 | a0004 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1124C>G | p.Thr375Ser | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 4/5 | 1279/1684 | 1124/1479 | 375/492 | chr17 | 81536640 | |||
| chr17:81536968 | G | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1367G>A | p.Arg456His | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 5/5 | 1522/1684 | 1367/1479 | 456/492 | chr17 | 81536968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81528753 | C | T | 1 | a0001c0018 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.222C>T | p.Asp74Asp | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 377/1684 | 222/1479 | 74/492 | chr17 | 81528753 | |||
| chr17:81528840 | G | A | 1 | a0001c0010 | 2 | HG02486.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.309G>A | p.Arg103Arg | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 464/1684 | 309/1479 | 103/492 | chr17 | 81528840 | |||
| chr17:81528864 | C | T | 1 | a0001c0009 | 3 | HG02257.hp2 HG02280.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.333C>T | p.Phe111Phe | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 488/1684 | 333/1479 | 111/492 | chr17 | 81528864 | |||
| chr17:81528912 | G | A | 2 | a0001c0010 a0001c0011 |
4 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.381G>A | p.Pro127Pro | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 536/1684 | 381/1479 | 127/492 | chr17 | 81528912 | |||
| chr17:81528984 | C | T | 2 | a0001c0007 a0001c0017 |
5 | HG03225.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
synonymous_variant | LOW | c.453C>T | p.Tyr151Tyr | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 608/1684 | 453/1479 | 151/492 | chr17 | 81528984 | |||
| chr17:81529164 | G | A | 1 | a0001c0004 | 20 | NA18940.hp1 NA18941.hp1 NA18945.hp2 others(17): Show |
synonymous_variant | LOW | c.633G>A | p.Thr211Thr | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 788/1684 | 633/1479 | 211/492 | chr17 | 81529164 | |||
| chr17:81529263 | G | A | 1 | a0001c0003 | 26 | HG00423.hp1 HG00423.hp2 HG01070.hp1 others(23): Show |
synonymous_variant | LOW | c.732G>A | p.Thr244Thr | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 887/1684 | 732/1479 | 244/492 | chr17 | 81529263 | |||
| chr17:81529269 | T | C | 5 | a0001c0002 a0001c0010 a0001c0011 others(2): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
synonymous_variant | LOW | c.738T>C | p.Pro246Pro | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 893/1684 | 738/1479 | 246/492 | chr17 | 81529269 | |||
| chr17:81535191 | C | T | 1 | a0001c0012 | 2 | HG00735.hp1 HG01515.hp1 |
synonymous_variant | LOW | c.966C>T | p.His322His | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/5 | 1121/1684 | 966/1479 | 322/492 | chr17 | 81535191 | |||
| chr17:81536209 | C | T | 1 | a0001c0007 | 4 | HG03225.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.1047C>T | p.Asn349Asn | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/5 | 1202/1684 | 1047/1479 | 349/492 | chr17 | 81536209 | |||
| chr17:81537047 | C | T | 1 | a0001c0006 | 5 | HG01123.hp2 HG01358.hp1 HG01993.hp1 others(2): Show |
synonymous_variant | LOW | c.1446C>T | p.Asp482Asp | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 5/5 | 1601/1684 | 1446/1479 | 482/492 | chr17 | 81537047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81528401 | G | C | 1 | a0001c0001t0003 | 6 | HG01106.hp2 HG01975.hp1 HG01975.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-131G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 131 | chr17 | 81528401 | ||||||
| chr17:81528442 | G | A | 1 | a0001c0001t0004 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-90G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 90 | chr17 | 81528442 | ||||||
| chr17:81528493 | C | T | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0003t0001 others(11): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 39 | chr17 | 81528493 | ||||||
| chr17:81528494 | G | C | 1 | a0001c0002t0005 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/5 | 38 | chr17 | 81528494 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81529443 | T | C | 3 | a0001c0002t0002g0035 a0001c0002t0002g0053 a0001c0002t0002g0054 |
4 | HG02109.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+86T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81529443 | |||||||
| chr17:81529452 | G | C | 1 | a0001c0001t0004g0055 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.826+95G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81529452 | |||||||
| chr17:81529543 | C | G | 1 | a0001c0007t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.826+186C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81529543 | |||||||
| chr17:81529733 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.826+376T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81529733 | |||||||
| chr17:81529785 | T | C | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+428T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81529785 | |||||||
| chr17:81529971 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.826+614G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81529971 | |||||||
| chr17:81530010 | C | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(7): Show |
30 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.826+653C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530010 | |||||||
| chr17:81530011 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0002g0037 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.826+654T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530011 | |||||||
| chr17:81530229 | G | C | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+872G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530229 | |||||||
| chr17:81530286 | C | CGGGGCCT others(9): Show |
1 | a0001c0001t0001g0079 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.826+931_826+946dup others(16): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81530286 | ||||||
| chr17:81530395 | G | A | 1 | a0001c0004t0001g0013 | 5 | NA18950.hp1 NA18957.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+1038G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530395 | |||||||
| chr17:81530409 | C | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.826+1052C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530409 | |||||||
| chr17:81530515 | C | T | 1 | a0001c0001t0002g0024 | 4 | HG00639.hp2 HG01175.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+1158C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530515 | |||||||
| chr17:81530516 | G | A | 1 | a0004c0015t0002g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.826+1159G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530516 | |||||||
| chr17:81530530 | A | G | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+1173A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530530 | |||||||
| chr17:81530580 | GTCCTTCC others(47): Show |
G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.826+1227_826+1280d others(56): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81530580 | ||||||
| chr17:81530601 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.826+1244C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530601 | |||||||
| chr17:81530665 | C | T | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+1308C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530665 | |||||||
| chr17:81530782 | A | G | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+1425A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530782 | |||||||
| chr17:81530788 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.826+1431G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530788 | |||||||
| chr17:81530910 | G | C | 1 | a0001c0012t0002g0084 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.826+1553G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530910 | |||||||
| chr17:81530912 | C | CG | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.826+1558dupG | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81530912 | ||||||
| chr17:81530912 | C | G | 1 | a0001c0012t0002g0084 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.826+1555C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530912 | |||||||
| chr17:81530918 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.826+1561T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530918 | |||||||
| chr17:81530965 | T | C | 2 | a0001c0002t0002g0058 a0004c0015t0002g0057 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.826+1608T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81530965 | |||||||
| chr17:81531006 | T | A | 1 | a0001c0001t0002g0080 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.826+1649T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531006 | |||||||
| chr17:81531038 | G | T | 22 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(19): Show |
39 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.826+1681G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531038 | |||||||
| chr17:81531084 | T | G | 23 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(20): Show |
40 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.826+1727T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531084 | |||||||
| chr17:81531089 | A | G | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+1732A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531089 | |||||||
| chr17:81531102 | A | G | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+1745A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531102 | |||||||
| chr17:81531150 | ATGGTGAT others(11): Show |
A | 3 | a0001c0001t0001g0142 a0001c0001t0002g0021 a0001c0002t0002g0062 |
6 | HG02257.hp1 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+1823_826+1840d others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531150 | ||||||
| chr17:81531165 | ATGG | A | 11 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0080 others(8): Show |
28 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.826+1814_826+1816d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531165 | ||||||
| chr17:81531167 | G | C | 1 | a0001c0003t0001g0001 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.826+1810G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531167 | |||||||
| chr17:81531171 | GTGATGGT others(2): Show |
G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0078 a0001c0001t0001g0141 |
5 | HG01891.hp1 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+1823_826+1831d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531171 | ||||||
| chr17:81531180 | A | ATGATGGT others(11): Show |
1 | a0001c0001t0002g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.826+1850_826+1867d others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531180 | ||||||
| chr17:81531180 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1823A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531180 | |||||||
| chr17:81531180 | ATGATGGT others(2): Show |
A | 24 | a0001c0001t0001g0001 a0001c0001t0003g0093 a0001c0002t0002g0005 others(21): Show |
43 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(40): Show |
intron_variant | MODIFIER | c.826+1859_826+1867d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531180 | ||||||
| chr17:81531186 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1829G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531186 | |||||||
| chr17:81531189 | G | A | 2 | a0001c0001t0001g0094 a0001c0002t0002g0062 |
2 | HG02129.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.826+1832G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531189 | |||||||
| chr17:81531197 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.826+1840G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531197 | |||||||
| chr17:81531204 | G | A | 1 | a0004c0015t0002g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.826+1847G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531204 | |||||||
| chr17:81531213 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.826+1856G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531213 | |||||||
| chr17:81531225 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1868A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531225 | |||||||
| chr17:81531227 | A | G | 2 | a0001c0002t0002g0058 a0004c0015t0002g0057 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.826+1870A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531227 | |||||||
| chr17:81531234 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1877A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531234 | |||||||
| chr17:81531240 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1883G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531240 | |||||||
| chr17:81531243 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1886A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531243 | |||||||
| chr17:81531246 | A | G | 1 | a0004c0015t0002g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.826+1889A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531246 | |||||||
| chr17:81531249 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1892G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531249 | |||||||
| chr17:81531252 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1895A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531252 | |||||||
| chr17:81531258 | A | G | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+1901A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531258 | |||||||
| chr17:81531261 | A | ATGGTGGT others(65): Show |
1 | a0001c0002t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+1912_826+1913i others(74): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531261 | ||||||
| chr17:81531261 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+1904A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531261 | |||||||
| chr17:81531262 | TGGTGGTG others(5): Show |
T | 2 | a0001c0007t0001g0033 a0001c0007t0001g0143 |
4 | HG03225.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+1917_826+1928d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531262 | ||||||
| chr17:81531264 | G | GTGGTGGT others(32): Show |
1 | a0001c0002t0005g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826+1912_826+1913i others(41): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531264 | ||||||
| chr17:81531270 | A | G | 20 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(17): Show |
37 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.826+1913A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531270 | |||||||
| chr17:81531273 | G | A | 19 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(16): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.826+1916G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531273 | |||||||
| chr17:81531274 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.826+1917C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531274 | |||||||
| chr17:81531276 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.826+1919G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531276 | |||||||
| chr17:81531279 | G | A | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+1922G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531279 | |||||||
| chr17:81531282 | A | G | 2 | a0001c0001t0001g0140 a0001c0002t0002g0054 |
2 | HG02109.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.826+1925A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531282 | |||||||
| chr17:81531285 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+1928G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531285 | |||||||
| chr17:81531288 | A | G | 22 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0002t0002g0005 others(19): Show |
39 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.826+1931A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531288 | |||||||
| chr17:81531291 | G | A | 21 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0002t0002g0005 others(18): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+1934G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531291 | |||||||
| chr17:81531297 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(33): Show |
89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.826+1940A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531297 | |||||||
| chr17:81531303 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0002t0002g0054 |
3 | HG02109.hp1 NA18954.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.826+1946A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531303 | |||||||
| chr17:81531312 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0002t0002g0054 others(1): Show |
4 | HG02109.hp1 HG03130.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+1955G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531312 | |||||||
| chr17:81531315 | GTGA | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0141 a0001c0001t0001g0142 |
5 | HG01891.hp1 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+1964_826+1966d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531315 | ||||||
| chr17:81531318 | A | ATGATGGT others(41): Show |
17 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(14): Show |
33 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.826+1969_826+1970i others(50): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531318 | ||||||
| chr17:81531318 | A | ATGATGGT others(56): Show |
2 | a0001c0002t0002g0035 a0001c0002t0002g0053 |
3 | HG02451.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.826+1969_826+1970i others(65): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531318 | ||||||
| chr17:81531318 | A | ATGGTGGT others(17): Show |
1 | a0004c0015t0002g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.826+1963_826+1964i others(26): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531318 | ||||||
| chr17:81531318 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0002t0002g0054 |
3 | HG02109.hp1 NA18954.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.826+1961A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531318 | |||||||
| chr17:81531318 | ATGATGGT others(2): Show |
A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(12): Show |
51 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.826+1964_826+1972d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531318 | ||||||
| chr17:81531321 | A | ATGGTGGT others(23): Show |
1 | a0001c0002t0002g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.826+1978_826+1979i others(32): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531321 | ||||||
| chr17:81531321 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(69): Show |
227 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.826+1964A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531321 | |||||||
| chr17:81531324 | G | GTGGTGGT others(26): Show |
1 | a0001c0002t0002g0060 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.826+1978_826+1979i others(35): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531324 | ||||||
| chr17:81531327 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0096 |
2 | NA18954.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.826+1970G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531327 | |||||||
| chr17:81531327 | G | GTGGGTGA | 1 | a0001c0001t0001g0016 | 5 | HG02258.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+1973_826+1974i others(9): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531327 | ||||||
| chr17:81531327 | G | GTGGTGA | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(61): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.826+1975_826+1976i others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531327 | ||||||
| chr17:81531327 | G | GTGGTGAT others(35): Show |
1 | a0001c0001t0001g0040 | 2 | NA18955.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.826+1975_826+1976i others(44): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531327 | ||||||
| chr17:81531327 | G | GTGGTGGT others(2): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(19): Show |
59 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.826+1979_826+1987d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531327 | ||||||
| chr17:81531333 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0132 a0001c0002t0005g0063 |
3 | HG02965.hp1 NA18961.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.826+1976G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531333 | |||||||
| chr17:81531336 | A | ATGG | 20 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(17): Show |
33 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.826+1988_826+1990d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531336 | ||||||
| chr17:81531336 | A | ATGGTGGT others(188): Show |
1 | a0001c0001t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.826+1999_826+2000i others(197): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531336 | ||||||
| chr17:81531336 | A | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | HG02809.hp1 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+1979A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531336 | |||||||
| chr17:81531339 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.826+1982G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531339 | |||||||
| chr17:81531345 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+1988G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531345 | |||||||
| chr17:81531348 | A | G | 5 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0001g0142 others(2): Show |
9 | HG02622.hp2 HG02809.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.826+1991A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531348 | |||||||
| chr17:81531351 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+1994A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531351 | |||||||
| chr17:81531354 | G | A | 2 | a0001c0002t0002g0012 a0001c0002t0002g0072 |
6 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+1997G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531354 | |||||||
| chr17:81531357 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(72): Show |
246 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.826+2000A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531357 | |||||||
| chr17:81531360 | G | A | 3 | a0001c0001t0001g0142 a0001c0002t0002g0012 a0001c0002t0002g0072 |
7 | HG02622.hp2 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+2003G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531360 | |||||||
| chr17:81531363 | A | G | 3 | a0001c0001t0001g0142 a0001c0002t0002g0012 a0001c0002t0002g0072 |
7 | HG02622.hp2 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+2006A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531363 | |||||||
| chr17:81531366 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+2009A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531366 | |||||||
| chr17:81531372 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+2015G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531372 | |||||||
| chr17:81531375 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+2018G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531375 | |||||||
| chr17:81531378 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+2021A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531378 | |||||||
| chr17:81531381 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2024G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531381 | |||||||
| chr17:81531387 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2030A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531387 | |||||||
| chr17:81531393 | ATGATGG | A | 12 | a0001c0001t0001g0138 a0001c0001t0002g0003 a0001c0001t0002g0039 others(9): Show |
29 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.826+2051_826+2056d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531393 | ||||||
| chr17:81531396 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2039A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531396 | |||||||
| chr17:81531406 | TGATGGTG others(20): Show |
T | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.826+2060_826+2086d others(29): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531406 | ||||||
| chr17:81531414 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2057G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531414 | |||||||
| chr17:81531422 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2065A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531422 | |||||||
| chr17:81531429 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2072A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531429 | |||||||
| chr17:81531435 | ATGGTGGT others(5): Show |
A | 1 | a0001c0001t0001g0029 | 3 | HG00621.hp2 HG00673.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.826+2093_826+2104d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531435 | ||||||
| chr17:81531441 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2084G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531441 | |||||||
| chr17:81531443 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2086G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531443 | |||||||
| chr17:81531444 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2087A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531444 | |||||||
| chr17:81531447 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2090G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531447 | |||||||
| chr17:81531450 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+2093G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531450 | |||||||
| chr17:81531465 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0002g0100 a0001c0001t0003g0093 |
5 | HG00140.hp1 HG00558.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+2108A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531465 | |||||||
| chr17:81531474 | G | GTGATGGT others(5): Show |
1 | a0001c0001t0003g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.826+2119_826+2120i others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531474 | ||||||
| chr17:81531474 | GTGGTGAT others(8): Show |
G | 1 | a0001c0001t0001g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.826+2132_826+2146d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531474 | ||||||
| chr17:81531477 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.826+2120G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531477 | |||||||
| chr17:81531486 | A | G | 1 | a0005c0013t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.826+2129A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531486 | |||||||
| chr17:81531486 | ATGATGG | A | 3 | a0001c0001t0001g0076 a0001c0001t0002g0099 a0001c0012t0002g0084 |
3 | HG01515.hp1 HG02723.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.826+2144_826+2149d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531486 | ||||||
| chr17:81531489 | A | ATGGTGAT others(2): Show |
8 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0080 others(5): Show |
25 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.826+2135_826+2143d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531489 | ||||||
| chr17:81531489 | A | ATGGTGAT others(8): Show |
17 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(14): Show |
43 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.826+2157_826+2171d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531489 | ||||||
| chr17:81531489 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0093 a0005c0013t0001g0137 |
3 | HG00558.hp1 HG02300.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.826+2132A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531489 | |||||||
| chr17:81531495 | A | ATGGTGAT others(32): Show |
1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+2146_826+2147i others(41): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531495 | ||||||
| chr17:81531497 | G | GATGATGA others(5): Show |
1 | a0001c0002t0002g0064 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.826+2140_826+2141i others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531497 | |||||||
| chr17:81531497 | G | GGTGATGA others(8): Show |
21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+2146_826+2147i others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531497 | ||||||
| chr17:81531505 | T | C | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+2148T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531505 | |||||||
| chr17:81531507 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+2150G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531507 | |||||||
| chr17:81531514 | T | C | 2 | a0001c0002t0002g0065 a0001c0002t0002g0072 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.826+2157T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531514 | |||||||
| chr17:81531519 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+2162G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531519 | |||||||
| chr17:81531534 | G | A | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+2177G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531534 | |||||||
| chr17:81531543 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.826+2186A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531543 | |||||||
| chr17:81531545 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.826+2188G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531545 | |||||||
| chr17:81531561 | GTGA | G | 18 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(15): Show |
47 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.826+2209_826+2211d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531561 | ||||||
| chr17:81531597 | GTGA | G | 3 | a0001c0001t0001g0105 a0001c0002t0002g0060 a0001c0002t0002g0061 |
3 | HG02559.hp2 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.826+2245_826+2247d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531597 | ||||||
| chr17:81531609 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.826+2252G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531609 | |||||||
| chr17:81531621 | ATGGTGGT others(11): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826+2273_826+2290d others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531621 | ||||||
| chr17:81531636 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826+2279G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531636 | |||||||
| chr17:81531638 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826+2281G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531638 | |||||||
| chr17:81531642 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826+2285G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531642 | |||||||
| chr17:81531678 | A | ATGG | 1 | a0001c0002t0002g0012 | 5 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+2323_826+2324i others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531678 | ||||||
| chr17:81531678 | A | G | 1 | a0001c0002t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826+2321A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531678 | |||||||
| chr17:81531681 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0131 |
5 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+2324A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531681 | |||||||
| chr17:81531684 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0131 a0001c0002t0002g0071 |
6 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+2327G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531684 | |||||||
| chr17:81531687 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0131 |
5 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+2330A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531687 | |||||||
| chr17:81531690 | A | G | 21 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(18): Show |
34 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.826+2333A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531690 | |||||||
| chr17:81531692 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826+2335G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531692 | |||||||
| chr17:81531693 | G | A | 24 | a0001c0001t0001g0022 a0001c0001t0001g0131 a0001c0002t0002g0005 others(21): Show |
44 | HG00733.hp1 HG01069.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.826+2336G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531693 | |||||||
| chr17:81531698 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0131 a0001c0002t0002g0012 |
10 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+2341G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531698 | |||||||
| chr17:81531699 | G | A | 21 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(18): Show |
34 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.826+2342G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531699 | |||||||
| chr17:81531702 | A | ATAG | 21 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(18): Show |
34 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.826+2346_826+2347i others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531702 | ||||||
| chr17:81531702 | A | G | 1 | a0001c0002t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826+2345A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531702 | |||||||
| chr17:81531705 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0131 a0001c0002t0002g0012 |
10 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+2348A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531705 | |||||||
| chr17:81531707 | GATA | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0131 a0001c0002t0002g0012 |
10 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+2351_826+2353d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531707 | |||||||
| chr17:81531708 | A | G | 22 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(19): Show |
35 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.826+2351A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531708 | |||||||
| chr17:81531710 | A | G | 22 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(19): Show |
35 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.826+2353A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531710 | |||||||
| chr17:81531717 | GTGGTGA | G | 1 | a0001c0001t0001g0010 | 7 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+2375_826+2380d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531717 | ||||||
| chr17:81531720 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0022 others(12): Show |
38 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+2363G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531720 | |||||||
| chr17:81531723 | A | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0022 others(12): Show |
38 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+2366A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531723 | |||||||
| chr17:81531726 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(13): Show |
45 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.826+2369G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531726 | |||||||
| chr17:81531726 | G | GTGA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
10 | HG01261.hp1 HG01358.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.826+2372_826+2374d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531726 | ||||||
| chr17:81531726 | G | GTGATGAT others(5): Show |
1 | a0001c0001t0001g0045 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.826+2374_826+2375i others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531726 | ||||||
| chr17:81531726 | G | GTGATGGT others(2): Show |
67 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(64): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.826+2383_826+2391d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531726 | ||||||
| chr17:81531726 | G | GTGATGGT others(3): Show |
1 | a0001c0001t0001g0136 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.826+2377_826+2378i others(12): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531726 | ||||||
| chr17:81531733 | TGATGATG others(17): Show |
T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0082 a0001c0001t0002g0091 others(2): Show |
11 | HG02074.hp2 NA18942.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+2400_826+2423d others(26): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531733 | ||||||
| chr17:81531735 | A | ATGATGG | 1 | a0001c0002t0002g0012 | 5 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+2384_826+2389d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531735 | ||||||
| chr17:81531742 | TGATGATA others(8): Show |
T | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.826+2392_826+2406d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531742 | ||||||
| chr17:81531744 | ATGATAG | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(36): Show |
162 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.826+2392_826+2397d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531744 | ||||||
| chr17:81531749 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.826+2392A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531749 | |||||||
| chr17:81531757 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(36): Show |
162 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.826+2400C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531757 | |||||||
| chr17:81531761 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.826+2404G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531761 | |||||||
| chr17:81531762 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.826+2405A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531762 | |||||||
| chr17:81531764 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(36): Show |
162 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.826+2407G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531764 | |||||||
| chr17:81531771 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(37): Show |
163 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.826+2414A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531771 | |||||||
| chr17:81531772 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(37): Show |
163 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.826+2415T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531772 | |||||||
| chr17:81531773 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(38): Show |
164 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.826+2416A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531773 | |||||||
| chr17:81531774 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(37): Show |
163 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.826+2417G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531774 | |||||||
| chr17:81531780 | GTGATGAT others(5): Show |
G | 1 | a0001c0002t0002g0060 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.826+2431_826+2442d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531780 | ||||||
| chr17:81531781 | T | C | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.826+2424T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531781 | |||||||
| chr17:81531785 | GATGGTGA others(8): Show |
G | 1 | a0001c0004t0001g0107 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.826+2441_826+2455d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531785 | ||||||
| chr17:81531788 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(37): Show |
163 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.826+2431G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531788 | |||||||
| chr17:81531789 | GTGA | G | 1 | a0001c0001t0001g0022 | 4 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+2440_826+2442d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531789 | ||||||
| chr17:81531791 | GATGATGA others(2): Show |
G | 20 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(17): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.826+2438_826+2446d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531791 | ||||||
| chr17:81531793 | T | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0056 |
9 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+2436T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531793 | |||||||
| chr17:81531795 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(40): Show |
167 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.826+2438A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531795 | |||||||
| chr17:81531798 | A | G | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.826+2441A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531798 | |||||||
| chr17:81531800 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(38): Show |
164 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.826+2443A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531800 | |||||||
| chr17:81531810 | ATGG | A | 4 | a0001c0002t0002g0035 a0001c0002t0002g0053 a0001c0002t0002g0054 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+2462_826+2464d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531810 | ||||||
| chr17:81531812 | G | A | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(18): Show |
37 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.826+2455G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531812 | |||||||
| chr17:81531813 | G | A | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(18): Show |
37 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.826+2456G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531813 | |||||||
| chr17:81531819 | G | A | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(18): Show |
37 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.826+2462G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531819 | |||||||
| chr17:81531831 | G | A | 20 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(17): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.826+2474G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531831 | |||||||
| chr17:81531831 | GTGGTGAT others(8): Show |
G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0106 |
7 | HG01261.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+2493_826+2507d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531831 | ||||||
| chr17:81531837 | A | G | 20 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(17): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.826+2480A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531837 | |||||||
| chr17:81531837 | ATGGTGGT others(11): Show |
A | 1 | a0001c0002t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+2486_826+2503d others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531837 | ||||||
| chr17:81531840 | GTGGTGAT others(5): Show |
G | 2 | a0001c0002t0002g0035 a0001c0002t0002g0053 |
3 | HG02451.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.826+2489_826+2500d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531840 | ||||||
| chr17:81531852 | ATGG | A | 18 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0036 others(15): Show |
34 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.826+2501_826+2503d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531852 | ||||||
| chr17:81531855 | G | A | 2 | a0001c0002t0002g0035 a0001c0002t0002g0053 |
3 | HG02451.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.826+2498G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531855 | |||||||
| chr17:81531855 | G | GTGGTGAT others(8): Show |
1 | a0001c0001t0001g0019 | 5 | HG01074.hp1 HG01099.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+2507_826+2521d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531855 | ||||||
| chr17:81531865 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.826+2508C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531865 | |||||||
| chr17:81531965 | A | G | 3 | a0001c0002t0002g0035 a0001c0002t0002g0053 a0001c0002t0002g0054 |
4 | HG02109.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+2608A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531965 | |||||||
| chr17:81531974 | A | G | 3 | a0001c0002t0002g0035 a0001c0002t0002g0053 a0001c0002t0002g0054 |
4 | HG02109.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+2617A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81531974 | |||||||
| chr17:81531987 | ATGGTGAT others(5): Show |
A | 1 | a0001c0002t0002g0012 | 5 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+2641_826+2652d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81531987 | ||||||
| chr17:81532020 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2663A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532020 | |||||||
| chr17:81532026 | GTGATGGT others(5): Show |
G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0108 |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+2684_826+2695d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532026 | ||||||
| chr17:81532032 | GTGA | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(85): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.826+2684_826+2686d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532032 | ||||||
| chr17:81532041 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2684A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532041 | |||||||
| chr17:81532052 | GGTGATGG others(8): Show |
G | 1 | a0001c0001t0002g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.826+2705_826+2719d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532052 | ||||||
| chr17:81532056 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2699A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532056 | |||||||
| chr17:81532062 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2705A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532062 | |||||||
| chr17:81532065 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2708A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532065 | |||||||
| chr17:81532067 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2710A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532067 | |||||||
| chr17:81532071 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2714A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532071 | |||||||
| chr17:81532080 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2723A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532080 | |||||||
| chr17:81532090 | TGATGATG others(17): Show |
T | 1 | a0001c0001t0002g0080 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.826+2757_826+2780d others(26): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532090 | ||||||
| chr17:81532095 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2738A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532095 | |||||||
| chr17:81532116 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2759A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532116 | |||||||
| chr17:81532116 | ATGATGGT others(8): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.826+2773_826+2787d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532116 | ||||||
| chr17:81532119 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2762A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532119 | |||||||
| chr17:81532128 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2771A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532128 | |||||||
| chr17:81532140 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2783A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532140 | |||||||
| chr17:81532143 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2786A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532143 | |||||||
| chr17:81532143 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.826+2786A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532143 | |||||||
| chr17:81532143 | ATGGTGAT others(2): Show |
A | 2 | a0001c0010t0002g0020 a0001c0011t0002g0020 |
4 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+2789_826+2797d others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532143 | ||||||
| chr17:81532146 | G | A | 9 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0080 others(6): Show |
26 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.826+2789G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532146 | |||||||
| chr17:81532149 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2792A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532149 | |||||||
| chr17:81532158 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2801A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532158 | |||||||
| chr17:81532158 | ATGATGGT others(5): Show |
A | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.826+2804_826+2815d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532158 | ||||||
| chr17:81532161 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2804A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532161 | |||||||
| chr17:81532161 | ATGGTGAT others(5): Show |
A | 20 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(17): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.826+2834_826+2845d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532161 | ||||||
| chr17:81532170 | G | A | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+2813G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532170 | |||||||
| chr17:81532170 | G | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.826+2813G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532170 | |||||||
| chr17:81532179 | ATGGTGGT others(8): Show |
A | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+2837_827-2844d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532179 | ||||||
| chr17:81532182 | G | A | 22 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(19): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.826+2825G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532182 | |||||||
| chr17:81532208 | G | C | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-2844G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532208 | |||||||
| chr17:81532209 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2843A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532209 | |||||||
| chr17:81532210 | T | C | 23 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(20): Show |
40 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.827-2842T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532210 | |||||||
| chr17:81532215 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2837A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532215 | |||||||
| chr17:81532218 | GTGA | G | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-2826_827-2824d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532218 | ||||||
| chr17:81532227 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2825A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532227 | |||||||
| chr17:81532227 | A | G | 1 | a0001c0001t0002g0015 | 5 | HG01255.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-2825A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532227 | |||||||
| chr17:81532229 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2823A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532229 | |||||||
| chr17:81532229 | A | G | 1 | a0001c0001t0002g0015 | 5 | HG01255.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-2823A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532229 | |||||||
| chr17:81532248 | GTGA | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0002t0002g0066 |
9 | HG01943.hp1 HG01978.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.827-2790_827-2788d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532248 | ||||||
| chr17:81532254 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2798A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532254 | |||||||
| chr17:81532255 | T | A | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2797T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532255 | |||||||
| chr17:81532257 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2795A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532257 | |||||||
| chr17:81532260 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2792A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532260 | |||||||
| chr17:81532265 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2787A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532265 | |||||||
| chr17:81532269 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2783A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532269 | |||||||
| chr17:81532270 | T | A | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2782T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532270 | |||||||
| chr17:81532272 | G | A | 1 | a0001c0001t0001g0028 | 3 | HG00639.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.827-2780G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532272 | |||||||
| chr17:81532284 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2768A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532284 | |||||||
| chr17:81532287 | GTGGTGAT others(38): Show |
G | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.827-2740_827-2696d others(47): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532287 | ||||||
| chr17:81532290 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2762G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532290 | |||||||
| chr17:81532293 | A | ATAGTGAT others(68): Show |
1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2758_827-2757i others(77): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532293 | ||||||
| chr17:81532293 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2759A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532293 | |||||||
| chr17:81532296 | A | ATGATGAT others(2): Show |
23 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(20): Show |
40 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.827-2749_827-2748i others(11): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532296 | ||||||
| chr17:81532296 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2756A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532296 | |||||||
| chr17:81532299 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2753A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532299 | |||||||
| chr17:81532299 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2753A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532299 | |||||||
| chr17:81532302 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2750A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532302 | |||||||
| chr17:81532302 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2750A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532302 | |||||||
| chr17:81532304 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2748A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532304 | |||||||
| chr17:81532308 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2744A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532308 | |||||||
| chr17:81532312 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2740C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532312 | |||||||
| chr17:81532313 | G | A | 1 | a0001c0002t0002g0059 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.827-2739G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532313 | |||||||
| chr17:81532314 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2738A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532314 | |||||||
| chr17:81532314 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2738A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532314 | |||||||
| chr17:81532317 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.827-2735A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532317 | |||||||
| chr17:81532323 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2729A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532323 | |||||||
| chr17:81532326 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2726A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532326 | |||||||
| chr17:81532338 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2714A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532338 | |||||||
| chr17:81532338 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.827-2714A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532338 | |||||||
| chr17:81532341 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2711A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532341 | |||||||
| chr17:81532344 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2708A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532344 | |||||||
| chr17:81532347 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2705A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532347 | |||||||
| chr17:81532353 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2699A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532353 | |||||||
| chr17:81532362 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2690A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532362 | |||||||
| chr17:81532365 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2687G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532365 | |||||||
| chr17:81532367 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2685G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532367 | |||||||
| chr17:81532368 | A | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2684A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532368 | |||||||
| chr17:81532371 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2681G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532371 | |||||||
| chr17:81532374 | A | ATGATGG | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.827-2674_827-2673i others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532374 | ||||||
| chr17:81532377 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2675A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532377 | |||||||
| chr17:81532384 | T | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2668T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532384 | |||||||
| chr17:81532385 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2667G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532385 | |||||||
| chr17:81532386 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2666G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532386 | |||||||
| chr17:81532387 | C | A | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-2665C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532387 | |||||||
| chr17:81532389 | A | ATGATGAT others(5): Show |
2 | a0001c0002t0002g0058 a0004c0015t0002g0057 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.827-2658_827-2657i others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532389 | ||||||
| chr17:81532392 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2660A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532392 | |||||||
| chr17:81532401 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2651A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532401 | |||||||
| chr17:81532403 | A | AGTGATGG others(8): Show |
21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-2634_827-2620d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532403 | ||||||
| chr17:81532403 | A | G | 3 | a0001c0001t0002g0082 a0001c0002t0002g0058 a0004c0015t0002g0057 |
3 | HG02055.hp2 HG03130.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2649A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532403 | |||||||
| chr17:81532404 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.827-2648G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532404 | |||||||
| chr17:81532407 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2645A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532407 | |||||||
| chr17:81532408 | T | A | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2644T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532408 | |||||||
| chr17:81532416 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-2636A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532416 | |||||||
| chr17:81532420 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2632T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532420 | |||||||
| chr17:81532424 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2628G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532424 | |||||||
| chr17:81532426 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2626T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532426 | |||||||
| chr17:81532430 | G | A | 1 | a0001c0001t0002g0039 | 2 | NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.827-2622G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532430 | |||||||
| chr17:81532431 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2621A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532431 | |||||||
| chr17:81532433 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2619A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532433 | |||||||
| chr17:81532433 | A | G | 2 | a0001c0001t0002g0039 a0001c0002t0002g0073 |
3 | HG03516.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.827-2619A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532433 | |||||||
| chr17:81532433 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-2619A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532433 | |||||||
| chr17:81532434 | A | G | 1 | a0001c0001t0002g0039 | 2 | NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.827-2618A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532434 | |||||||
| chr17:81532437 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0082 |
3 | NA18983.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.827-2615G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532437 | |||||||
| chr17:81532437 | G | GTGA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.827-2606_827-2604d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532437 | ||||||
| chr17:81532442 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2610G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532442 | |||||||
| chr17:81532443 | A | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2609A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532443 | |||||||
| chr17:81532445 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2607G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532445 | |||||||
| chr17:81532445 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2607G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532445 | |||||||
| chr17:81532446 | ATGG | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0022 others(9): Show |
31 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.827-2603_827-2601d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532446 | ||||||
| chr17:81532449 | G | A | 2 | a0001c0001t0001g0052 a0001c0003t0001g0125 |
3 | HG01109.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.827-2603G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532449 | |||||||
| chr17:81532452 | A | G | 1 | a0001c0001t0001g0052 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.827-2600A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532452 | |||||||
| chr17:81532454 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2598G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532454 | |||||||
| chr17:81532455 | G | A | 2 | a0001c0001t0001g0052 a0001c0002t0002g0073 |
3 | HG02886.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.827-2597G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532455 | |||||||
| chr17:81532458 | G | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0022 others(11): Show |
33 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.827-2594G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532458 | |||||||
| chr17:81532461 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2591G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532461 | |||||||
| chr17:81532461 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2591G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532461 | |||||||
| chr17:81532464 | A | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0022 others(12): Show |
35 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.827-2588A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532464 | |||||||
| chr17:81532466 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2586G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532466 | |||||||
| chr17:81532467 | G | A | 2 | a0001c0001t0001g0052 a0001c0002t0002g0073 |
3 | HG02886.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.827-2585G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532467 | |||||||
| chr17:81532472 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2580G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532472 | |||||||
| chr17:81532473 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2579G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532473 | |||||||
| chr17:81532475 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2577G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532475 | |||||||
| chr17:81532476 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2576G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532476 | |||||||
| chr17:81532476 | GTGA | G | 2 | a0001c0001t0002g0037 a0001c0002t0002g0012 |
6 | HG02622.hp2 HG02965.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-2571_827-2569d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532476 | ||||||
| chr17:81532477 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2575T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532477 | |||||||
| chr17:81532479 | A | G | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2573A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532479 | |||||||
| chr17:81532482 | A | G | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2570A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532482 | |||||||
| chr17:81532484 | A | G | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2568A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532484 | |||||||
| chr17:81532484 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-2568A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532484 | |||||||
| chr17:81532488 | A | G | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2564A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532488 | |||||||
| chr17:81532491 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2561G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532491 | |||||||
| chr17:81532496 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2556G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532496 | |||||||
| chr17:81532499 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2553G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532499 | |||||||
| chr17:81532500 | G | A | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2552G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532500 | |||||||
| chr17:81532500 | G | GTGA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.827-2547_827-2545d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532500 | ||||||
| chr17:81532505 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2547G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532505 | |||||||
| chr17:81532507 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2545T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532507 | |||||||
| chr17:81532508 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2544A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532508 | |||||||
| chr17:81532512 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2540G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532512 | |||||||
| chr17:81532515 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2537A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532515 | |||||||
| chr17:81532516 | C | T | 2 | a0001c0001t0001g0051 a0001c0002t0002g0073 |
3 | HG01346.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.827-2536C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532516 | |||||||
| chr17:81532516 | CGATGGT | C | 21 | a0001c0002t0002g0005 a0001c0002t0002g0035 a0001c0002t0002g0036 others(18): Show |
34 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.827-2531_827-2526d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532516 | ||||||
| chr17:81532518 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2534A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532518 | |||||||
| chr17:81532518 | ATGG | A | 2 | a0001c0002t0002g0012 a0001c0002t0002g0060 |
6 | HG02622.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-2531_827-2529d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532518 | ||||||
| chr17:81532521 | G | A | 2 | a0001c0001t0002g0082 a0001c0002t0002g0061 |
2 | NA18983.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-2531G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532521 | |||||||
| chr17:81532521 | G | GTGA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.827-2520_827-2518d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532521 | ||||||
| chr17:81532527 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2525A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532527 | |||||||
| chr17:81532529 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2523G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532529 | |||||||
| chr17:81532530 | A | ATAGTGAT others(5): Show |
1 | a0001c0002t0002g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.827-2521_827-2520i others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532530 | ||||||
| chr17:81532532 | G | A | 2 | a0001c0001t0002g0082 a0001c0002t0002g0073 |
2 | HG03516.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2520G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532532 | |||||||
| chr17:81532533 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2519A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532533 | |||||||
| chr17:81532535 | A | G | 3 | a0001c0001t0002g0091 a0001c0002t0002g0061 a0001c0002t0002g0073 |
3 | HG03516.hp1 NA18980.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-2517A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532535 | |||||||
| chr17:81532542 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2510G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532542 | |||||||
| chr17:81532544 | G | T | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2508G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532544 | |||||||
| chr17:81532545 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2507G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532545 | |||||||
| chr17:81532550 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-2502G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532550 | |||||||
| chr17:81532557 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2495G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532557 | |||||||
| chr17:81532560 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2492G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532560 | |||||||
| chr17:81532565 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2487G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532565 | |||||||
| chr17:81532568 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2484G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532568 | |||||||
| chr17:81532571 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2481G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532571 | |||||||
| chr17:81532572 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2480G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532572 | |||||||
| chr17:81532574 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2478G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532574 | |||||||
| chr17:81532575 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2477G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532575 | |||||||
| chr17:81532576 | T | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2476T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532576 | |||||||
| chr17:81532578 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2474A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532578 | |||||||
| chr17:81532581 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2471A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532581 | |||||||
| chr17:81532581 | A | G | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2471A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532581 | |||||||
| chr17:81532587 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.827-2465A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532587 | |||||||
| chr17:81532591 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2461T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532591 | |||||||
| chr17:81532591 | T | C | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.827-2461T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532591 | |||||||
| chr17:81532593 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2459A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532593 | |||||||
| chr17:81532606 | T | A | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2446T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532606 | |||||||
| chr17:81532608 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2444A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532608 | |||||||
| chr17:81532609 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2443T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532609 | |||||||
| chr17:81532616 | GATA | G | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-2433_827-2431d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532616 | ||||||
| chr17:81532617 | A | ATGG | 2 | a0001c0010t0002g0020 a0001c0011t0002g0020 |
4 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-2434_827-2433i others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532617 | ||||||
| chr17:81532617 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2435A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532617 | |||||||
| chr17:81532617 | ATAATGGT others(8): Show |
A | 1 | a0001c0001t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.827-2433_827-2419d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532617 | ||||||
| chr17:81532619 | A | G | 2 | a0001c0010t0002g0020 a0001c0011t0002g0020 |
4 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-2433A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532619 | |||||||
| chr17:81532626 | A | G | 2 | a0001c0002t0002g0058 a0004c0015t0002g0057 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.827-2426A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532626 | |||||||
| chr17:81532629 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2423A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532629 | |||||||
| chr17:81532629 | A | G | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-2423A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532629 | |||||||
| chr17:81532629 | ATGGTGAT others(11): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.827-2404_827-2387d others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532629 | ||||||
| chr17:81532630 | T | A | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2422T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532630 | |||||||
| chr17:81532632 | G | A | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
36 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-2420G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532632 | |||||||
| chr17:81532632 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2420G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532632 | |||||||
| chr17:81532635 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2417A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532635 | |||||||
| chr17:81532638 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2414G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532638 | |||||||
| chr17:81532639 | T | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2413T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532639 | |||||||
| chr17:81532640 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2412G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532640 | |||||||
| chr17:81532641 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2411A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532641 | |||||||
| chr17:81532641 | A | G | 23 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(20): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-2411A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532641 | |||||||
| chr17:81532644 | ATGG | A | 23 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(20): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-2402_827-2400d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532644 | ||||||
| chr17:81532647 | G | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2405G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532647 | |||||||
| chr17:81532647 | G | GTGGTGA | 2 | a0001c0010t0002g0020 a0001c0011t0002g0020 |
4 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-2396_827-2391d others(8): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532647 | ||||||
| chr17:81532650 | G | T | 1 | a0001c0001t0001g0022 | 4 | HG00733.hp1 HG01106.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-2402G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532650 | |||||||
| chr17:81532651 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2401T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532651 | |||||||
| chr17:81532658 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2394G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532658 | |||||||
| chr17:81532659 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2393A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532659 | |||||||
| chr17:81532660 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2392T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532660 | |||||||
| chr17:81532666 | A | T | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.827-2386A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532666 | |||||||
| chr17:81532670 | AATGGTGA others(8): Show |
A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0121 others(1): Show |
8 | HG00741.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-2372_827-2358d others(17): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532670 | ||||||
| chr17:81532677 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2375A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532677 | |||||||
| chr17:81532680 | A | T | 1 | a0002c0005t0002g0007 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.827-2372A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532680 | |||||||
| chr17:81532682 | A | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2370A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532682 | |||||||
| chr17:81532685 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2367G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532685 | |||||||
| chr17:81532686 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2366A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532686 | |||||||
| chr17:81532691 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2361G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532691 | |||||||
| chr17:81532692 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2360A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532692 | |||||||
| chr17:81532696 | C | T | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-2356C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532696 | |||||||
| chr17:81532698 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2354A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532698 | |||||||
| chr17:81532698 | ATAGTGAT others(11): Show |
A | 1 | a0004c0015t0002g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.827-2352_827-2335d others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532698 | ||||||
| chr17:81532704 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2348A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532704 | |||||||
| chr17:81532706 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2346A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532706 | |||||||
| chr17:81532710 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2342A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532710 | |||||||
| chr17:81532710 | ATGG | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(32): Show |
72 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.827-2333_827-2331d others(5): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532710 | ||||||
| chr17:81532715 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2337G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532715 | |||||||
| chr17:81532719 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2333G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532719 | |||||||
| chr17:81532722 | A | C | 2 | a0001c0001t0002g0082 a0001c0003t0001g0125 |
2 | HG01109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.827-2330A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532722 | |||||||
| chr17:81532724 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2328A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532724 | |||||||
| chr17:81532728 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2324A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532728 | |||||||
| chr17:81532730 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2322G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532730 | |||||||
| chr17:81532731 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2321G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532731 | |||||||
| chr17:81532732 | T | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2320T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532732 | |||||||
| chr17:81532733 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2319G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532733 | |||||||
| chr17:81532736 | GGTGATGA others(5): Show |
G | 1 | a0001c0002t0002g0012 | 5 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-2306_827-2295d others(14): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532736 | ||||||
| chr17:81532745 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2307G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532745 | |||||||
| chr17:81532746 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2306A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532746 | |||||||
| chr17:81532749 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2303G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532749 | |||||||
| chr17:81532750 | T | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2302T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532750 | |||||||
| chr17:81532751 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2301G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532751 | |||||||
| chr17:81532752 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2300A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532752 | |||||||
| chr17:81532752 | A | T | 1 | a0001c0002t0002g0012 | 5 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-2300A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532752 | |||||||
| chr17:81532755 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2297A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532755 | |||||||
| chr17:81532757 | G | A | 1 | a0001c0002t0002g0012 | 5 | HG02622.hp2 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-2295G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532757 | |||||||
| chr17:81532758 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2294G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532758 | |||||||
| chr17:81532759 | T | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2293T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532759 | |||||||
| chr17:81532760 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2292G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532760 | |||||||
| chr17:81532764 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2288G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532764 | |||||||
| chr17:81532768 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2284T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532768 | |||||||
| chr17:81532770 | A | C | 1 | a0001c0003t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827-2282A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532770 | |||||||
| chr17:81532770 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2282A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532770 | |||||||
| chr17:81532773 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2279G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532773 | |||||||
| chr17:81532785 | C | CAGTA | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.827-2265_827-2264i others(6): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81532785 | ||||||
| chr17:81532795 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2257G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532795 | |||||||
| chr17:81532796 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2256A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532796 | |||||||
| chr17:81532799 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827-2253G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532799 | |||||||
| chr17:81532841 | A | G | 11 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0080 others(8): Show |
28 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.827-2211A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532841 | |||||||
| chr17:81532858 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.827-2194C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532858 | |||||||
| chr17:81532859 | C | G | 1 | a0001c0001t0003g0086 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.827-2193C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532859 | |||||||
| chr17:81532893 | A | G | 1 | a0001c0009t0001g0030 | 3 | HG02257.hp2 HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.827-2159A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532893 | |||||||
| chr17:81532967 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.827-2085G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532967 | |||||||
| chr17:81532989 | G | A | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.827-2063G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81532989 | |||||||
| chr17:81533027 | C | T | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-2025C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533027 | |||||||
| chr17:81533076 | G | T | 1 | a0001c0001t0001g0044 | 2 | HG01099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.827-1976G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533076 | |||||||
| chr17:81533175 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827-1877G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533175 | |||||||
| chr17:81533197 | C | G | 1 | a0001c0001t0001g0052 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.827-1855C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533197 | |||||||
| chr17:81533238 | C | A | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.827-1814C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533238 | |||||||
| chr17:81533373 | G | A | 11 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0080 others(8): Show |
28 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.827-1679G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533373 | |||||||
| chr17:81533414 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0041 others(6): Show |
21 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.827-1638C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533414 | |||||||
| chr17:81533440 | C | T | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-1612C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533440 | |||||||
| chr17:81533596 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
412 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.827-1456T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533596 | |||||||
| chr17:81533647 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.827-1405C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533647 | |||||||
| chr17:81533694 | G | T | 1 | a0001c0001t0001g0049 | 2 | NA18939.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.827-1358G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533694 | |||||||
| chr17:81533727 | G | A | 20 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(17): Show |
37 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.827-1325G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533727 | |||||||
| chr17:81533768 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.827-1284G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533768 | |||||||
| chr17:81533778 | G | A | 1 | a0001c0004t0001g0113 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.827-1274G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533778 | |||||||
| chr17:81533866 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.827-1186C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533866 | |||||||
| chr17:81533867 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0126 others(1): Show |
7 | HG00741.hp2 HG01070.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-1185G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533867 | |||||||
| chr17:81533914 | G | A | 2 | a0001c0002t0002g0058 a0004c0015t0002g0057 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.827-1138G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533914 | |||||||
| chr17:81533920 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.827-1132C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533920 | |||||||
| chr17:81533963 | C | T | 21 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(18): Show |
38 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-1089C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81533963 | |||||||
| chr17:81534024 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-1028G>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534024 | |||||||
| chr17:81534064 | A | G | 1 | a0001c0003t0001g0119 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.827-988A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534064 | |||||||
| chr17:81534093 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.827-959C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534093 | |||||||
| chr17:81534107 | C | T | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.827-945C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534107 | |||||||
| chr17:81534134 | G | C | 2 | a0001c0002t0002g0058 a0004c0015t0002g0057 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.827-918G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534134 | |||||||
| chr17:81534240 | G | A | 1 | a0007c0014t0002g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.827-812G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534240 | |||||||
| chr17:81534274 | TG | T | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.827-773delG | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 81534274 | ||||||
| chr17:81534448 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-604T>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534448 | |||||||
| chr17:81534449 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-603A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534449 | |||||||
| chr17:81534450 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-602G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534450 | |||||||
| chr17:81534644 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0002g0087 |
4 | HG01109.hp2 NA18960.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-408G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534644 | |||||||
| chr17:81534645 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.827-407C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534645 | |||||||
| chr17:81534868 | C | T | 25 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(22): Show |
42 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.827-184C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 1/4 | chr17 | 81534868 | |||||||
| chr17:81535255 | T | TCACCATC others(8): Show |
2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.983+61_983+62insCC others(13): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535255 | ||||||
| chr17:81535255 | T | TCACCATC others(152): Show |
1 | a0001c0001t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.983+81_983+82insCT others(157): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535255 | ||||||
| chr17:81535255 | T | TCACCATC others(152): Show |
1 | a0001c0001t0001g0052 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.983+81_983+82insCT others(157): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535255 | ||||||
| chr17:81535255 | T | TCACCATC others(146): Show |
1 | a0001c0001t0001g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.983+81_983+82insCT others(151): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535255 | ||||||
| chr17:81535257 | A | ACCATCCC others(122): Show |
1 | a0001c0001t0001g0048 | 2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.983+81_983+82insCT others(127): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535257 | ||||||
| chr17:81535257 | ACCATCCC others(224): Show |
A | 16 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(13): Show |
32 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.983+62_983+292del | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535257 | ||||||
| chr17:81535270 | T | C | 5 | a0001c0002t0002g0036 a0001c0002t0002g0066 a0001c0002t0002g0069 others(2): Show |
6 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.983+62T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535270 | |||||||
| chr17:81535278 | CCCACCAT others(245): Show |
C | 2 | a0001c0002t0002g0066 a0001c0002t0005g0063 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.983+74_983+325del | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535278 | ||||||
| chr17:81535278 | CCCACCAT others(266): Show |
C | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.983+74_983+346del | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535278 | ||||||
| chr17:81535287 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.983+79C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535287 | |||||||
| chr17:81535290 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(106): Show |
331 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.983+82A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535290 | |||||||
| chr17:81535306 | C | G | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.983+98C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535306 | |||||||
| chr17:81535320 | C | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(102): Show |
325 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.983+112C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535320 | |||||||
| chr17:81535371 | A | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0117 a0001c0001t0001g0121 others(1): Show |
5 | HG01361.hp1 HG01952.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.983+163A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535371 | |||||||
| chr17:81535380 | GCCATCCC others(3): Show |
G | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+175_983+184del others(10): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535380 | ||||||
| chr17:81535392 | C | T | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+184C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535392 | |||||||
| chr17:81535394 | C | A | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+186C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535394 | |||||||
| chr17:81535398 | A | C | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.983+190A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535398 | |||||||
| chr17:81535399 | T | C | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.983+191T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535399 | |||||||
| chr17:81535424 | C | T | 2 | a0001c0002t0002g0060 a0001c0002t0002g0061 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.983+216C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535424 | |||||||
| chr17:81535447 | G | C | 3 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0002c0005t0002g0090 |
3 | HG02809.hp1 NA19043.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.983+239G>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535447 | |||||||
| chr17:81535449 | A | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(82): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.983+241A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535449 | |||||||
| chr17:81535465 | C | T | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+257C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535465 | |||||||
| chr17:81535479 | A | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(82): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.983+271A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535479 | |||||||
| chr17:81535494 | CCCATCAC others(23): Show |
C | 1 | a0001c0002t0002g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.983+296_983+325del others(30): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535494 | ||||||
| chr17:81535499 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(82): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.983+291C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535499 | |||||||
| chr17:81535508 | C | T | 1 | a0001c0002t0002g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.983+300C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535508 | |||||||
| chr17:81535509 | CCCATCTC others(14): Show |
C | 16 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(13): Show |
32 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.983+307_983+327del others(21): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535509 | ||||||
| chr17:81535515 | TCCA | T | 32 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0075 others(29): Show |
79 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.983+311_983+313del others(3): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535515 | ||||||
| chr17:81535515 | TCCACCAT others(23): Show |
T | 1 | a0001c0001t0003g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.983+311_983+340del others(30): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535515 | ||||||
| chr17:81535518 | A | ACCATCTC others(149): Show |
83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(80): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.983+321_983+322ins others(156): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535518 | ||||||
| chr17:81535518 | A | ACCATCTC others(134): Show |
1 | a0001c0001t0001g0002 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.983+321_983+322ins others(141): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535518 | ||||||
| chr17:81535518 | A | ACCATCTC others(150): Show |
1 | a0001c0001t0001g0079 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.983+321_983+322ins others(157): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535518 | ||||||
| chr17:81535518 | A | ACCATCTC others(149): Show |
1 | a0001c0001t0001g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.983+321_983+322ins others(156): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535518 | ||||||
| chr17:81535518 | A | ACCATCTC others(155): Show |
1 | a0001c0001t0001g0001 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.983+321_983+322ins others(162): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535518 | ||||||
| chr17:81535530 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.983+322A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535530 | |||||||
| chr17:81535531 | CCAT | C | 1 | a0003c0008t0001g0025 | 3 | HG00099.hp2 HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.983+329_983+331del others(3): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535531 | ||||||
| chr17:81535534 | T | A | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+326T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535534 | |||||||
| chr17:81535537 | T | A | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+329T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535537 | |||||||
| chr17:81535539 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.983+331A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535539 | |||||||
| chr17:81535545 | C | CCCATCCC others(122): Show |
1 | a0001c0001t0001g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.983+342_983+343ins others(129): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535545 | ||||||
| chr17:81535557 | A | T | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+349A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535557 | |||||||
| chr17:81535558 | C | T | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.983+350C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535558 | |||||||
| chr17:81535561 | C | T | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+353C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535561 | |||||||
| chr17:81535563 | A | C | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+355A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535563 | |||||||
| chr17:81535564 | T | A | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+356T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535564 | |||||||
| chr17:81535572 | A | T | 3 | a0001c0002t0002g0036 a0001c0002t0002g0069 a0001c0002t0002g0073 |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.983+364A>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535572 | |||||||
| chr17:81535578 | C | T | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+370C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535578 | |||||||
| chr17:81535584 | T | C | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+376T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535584 | |||||||
| chr17:81535585 | C | A | 1 | a0002c0005t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.983+377C>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535585 | |||||||
| chr17:81535626 | TCCACCAT others(35): Show |
T | 1 | a0001c0002t0002g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.983+432_984-465del others(42): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535626 | ||||||
| chr17:81535647 | TCCACCAT others(14): Show |
T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(417): Show |
intron_variant | MODIFIER | c.983+464_984-454del others(21): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535647 | ||||||
| chr17:81535650 | ACCATCCC others(26): Show |
A | 2 | a0001c0001t0002g0014 a0001c0002t0005g0063 |
2 | HG02015.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.983+456_984-450del others(33): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535650 | ||||||
| chr17:81535651 | CCATCCCC others(13): Show |
C | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.983+445_983+464del others(20): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535651 | ||||||
| chr17:81535737 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.984-409C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535737 | |||||||
| chr17:81535770 | A | C | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.984-376A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535770 | |||||||
| chr17:81535771 | T | A | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.984-375T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535771 | |||||||
| chr17:81535772 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.984-374C>T | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535772 | |||||||
| chr17:81535786 | TCATCCCC others(8): Show |
T | 1 | a0001c0001t0001g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.984-345_984-331del others(15): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535786 | ||||||
| chr17:81535800 | A | ACCATCCC others(29): Show |
9 | a0001c0001t0002g0003 a0001c0001t0002g0039 a0001c0001t0002g0080 others(6): Show |
23 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.984-292_984-257dup others(36): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535800 | ||||||
| chr17:81535809 | A | C | 1 | a0001c0002t0002g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.984-337A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535809 | |||||||
| chr17:81535812 | TCCATCAC others(17): Show |
T | 1 | a0001c0002t0002g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.984-328_984-305del others(24): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535812 | ||||||
| chr17:81535818 | A | C | 1 | a0001c0001t0001g0010 | 7 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.984-328A>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535818 | |||||||
| chr17:81535827 | CTCTCCAT others(11): Show |
C | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.984-310_984-293del others(18): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535827 | ||||||
| chr17:81535842 | CCCATCT | C | 22 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(19): Show |
39 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.984-298_984-293del others(6): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535842 | ||||||
| chr17:81535848 | T | C | 1 | a0001c0002t0002g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.984-298T>C | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535848 | |||||||
| chr17:81535866 | TCCATCCC others(20): Show |
T | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.984-270_984-244del others(27): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 81535866 | ||||||
| chr17:81535979 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.984-167G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 2/4 | chr17 | 81535979 | |||||||
| chr17:81536269 | T | A | 1 | a0001c0003t0001g0114 | 1 | NA18954.hp1 | splice_donor_variant&intron_variant | HIGH | c.1105+2T>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | chr17 | 81536269 | |||||||
| chr17:81536328 | G | A | 17 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(14): Show |
33 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1105+61G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | chr17 | 81536328 | |||||||
| chr17:81536375 | G | A | 19 | a0001c0002t0002g0005 a0001c0002t0002g0012 a0001c0002t0002g0035 others(16): Show |
35 | HG01069.hp1 HG01074.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.1105+108G>A | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | chr17 | 81536375 | |||||||
| chr17:81536446 | A | G | 46 | a0001c0001t0001g0023 a0001c0001t0001g0075 a0001c0001t0001g0121 others(43): Show |
94 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(91): Show |
intron_variant | MODIFIER | c.1106-176A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | chr17 | 81536446 | |||||||
| chr17:81536454 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0109 |
3 | NA18951.hp1 NA19010.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1106-168A>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | chr17 | 81536454 | |||||||
| chr17:81536556 | C | CACCCCGC others(27): Show |
1 | a0001c0001t0001g0115 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1106-65_1106-32dup others(34): Show |
FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 81536556 | ||||||
| chr17:81536560 | C | G | 1 | a0001c0001t0002g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1106-62C>G | FSCN2 | ENSG00000186765.12 | transcript | ENST00000417245.7 | protein_coding | 3/4 | chr17 | 81536560 |