Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10841 |
| ensemblid | ENSG00000160282.15 |
| hgncid | 3974 |
| symbol | FTCD |
| name | formimidoyltransferase cyclodeaminase |
| refseq_nuc | NM_206965.2 |
| refseq_prot | NP_996848.1 |
| ensembl_nuc | ENST00000397746.8 |
| ensembl_prot | ENSP00000380854.3 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 46136779 |
| end | 46155579 |
| strand | - |
| ver | v1.2 |
| region | chr21:46136779-46155579 |
| region5000 | chr21:46131779-46160579 |
| regionname0 | FTCD_chr21_46136779_46155579 |
| regionname5000 | FTCD_chr21_46131779_46160579 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 541 | 181 | 57 | 41 | 46 | 12 | 23 | 32 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0002 | 0/0 | 541 | 20 | 2 | 3 | 12 | 0 | 3 | 7 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0003 | 0/0 | 541 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0004 | 0/0 | 541 | 4 | 1 | 1 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0005 | 0/0 | 541 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0006 | 0/0 | 541 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0007 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0008 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0009 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(525): Show |
chr21 | 46131779 | 46160579 |
| a0010 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0011 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0012 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0013 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0014 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0015 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| a0016 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(404): Show |
chr21 | 46131779 | 46160579 |
| a0017 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | MSQLV others(536): Show |
chr21 | 46131779 | 46160579 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1623 | 88 | 25 | 15 | 28 | 6 | 13 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0002 | 0/1 | 1623 | 76 | 27 | 25 | 12 | 4 | 7 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0003 | 0/0 | 1623 | 11 | 1 | 1 | 5 | 2 | 2 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0010 | 0/0 | 1623 | 2 | 1 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0020 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0026 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0027 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0001c0030 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0002c0004 | 0/0 | 1623 | 9 | 1 | 1 | 7 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0002c0005 | 0/0 | 1623 | 8 | 1 | 2 | 4 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0002c0008 | 0/0 | 1623 | 2 | 0 | 0 | 0 | 0 | 2 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0002c0014 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0003c0006 | 0/0 | 1623 | 5 | 4 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0003c0012 | 0/0 | 1623 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0003c0013 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0003c0029 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0004c0007 | 0/0 | 1623 | 4 | 1 | 1 | 0 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0005c0009 | 0/0 | 1623 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0005c0015 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0006c0011 | 0/0 | 1623 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0007c0021 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0008c0016 | 0/0 | 1623 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0009c0023 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1585): Show |
chr21 | 46131779 | 46160579 | ||
| a0010c0017 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0011c0018 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0012c0025 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0013c0019 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0014c0031 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0015c0028 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 | ||
| a0016c0022 | 0/0 | 1670 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1665): Show |
chr21 | 46131779 | 46160579 | ||
| a0017c0024 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ATGTC others(1618): Show |
chr21 | 46131779 | 46160579 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1890 | 23 | 6 | 9 | 4 | 1 | 3 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0002 | 1/0 | 1890 | 30 | 12 | 4 | 3 | 4 | 6 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0003 | 0/0 | 1890 | 16 | 3 | 2 | 8 | 0 | 3 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0004 | 0/0 | 1890 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0005 | 0/0 | 1890 | 8 | 0 | 0 | 8 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0006 | 0/0 | 1890 | 4 | 4 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0008 | 0/0 | 1890 | 3 | 0 | 0 | 2 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0001t0009 | 0/0 | 1890 | 2 | 0 | 0 | 1 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0001 | 0/1 | 1890 | 55 | 15 | 22 | 9 | 2 | 6 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0002 | 0/0 | 1890 | 5 | 4 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0003 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0004 | 0/0 | 1890 | 6 | 0 | 3 | 2 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0006 | 0/0 | 1890 | 3 | 3 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0007 | 0/0 | 1890 | 4 | 4 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0008 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0002t0009 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0003t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0003t0002 | 0/0 | 1890 | 9 | 1 | 1 | 3 | 2 | 2 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0003t0008 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0010t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0010t0003 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0020t0002 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0026t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0027t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0001c0030t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0004t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0004t0002 | 0/0 | 1890 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0004t0003 | 0/0 | 1890 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0004t0004 | 0/0 | 1890 | 3 | 0 | 0 | 3 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0004t0005 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0005t0001 | 0/0 | 1890 | 7 | 0 | 2 | 4 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0005t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0008t0002 | 0/0 | 1890 | 2 | 0 | 0 | 0 | 0 | 2 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0002c0014t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0003c0006t0002 | 0/0 | 1890 | 5 | 4 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0003c0012t0001 | 0/0 | 1890 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0003c0013t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0003c0029t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0004c0007t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0004c0007t0007 | 0/0 | 1890 | 3 | 0 | 1 | 0 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0005c0009t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0005c0009t0009 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0005c0015t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0006c0011t0001 | 0/0 | 1890 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0007c0021t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0008c0016t0001 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0009c0023t0001 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1852): Show |
chr21 | 46131779 | 46160579 |
| a0010c0017t0003 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0011c0018t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0012c0025t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0013c0019t0001 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0014c0031t0001 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0015c0028t0002 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| a0016c0022t0002 | 0/0 | 1937 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1932): Show |
chr21 | 46131779 | 46160579 |
| a0017c0024t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | ACTGG others(1885): Show |
chr21 | 46131779 | 46160579 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0002t0009g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0003t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0010t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0010t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0020t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0026t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0027t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0001c0030t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0004t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0008t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0008t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0002c0014t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0006t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0006t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0006t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0006t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0006t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0012t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0012t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0013t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0003c0029t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0004c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0004c0007t0007g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0004c0007t0007g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0004c0007t0007g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0005c0009t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0005c0009t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0005c0015t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0006c0011t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0007c0021t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0008c0016t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0009c0023t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0010c0017t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0011c0018t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0012c0025t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0013c0019t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0014c0031t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0015c0028t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0016c0022t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| a0017c0024t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0167 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00140 | hp2 | a0004 | c0007 | t0007 | g0079 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0069 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00280 | hp2 | a0001 | c0002 | t0004 | g0204 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0148 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00423 | hp1 | a0005 | c0009 | t0009 | g0016 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00438 | hp2 | a0002 | c0004 | t0001 | g0099 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0149 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00544 | hp2 | a0002 | c0004 | t0003 | g0088 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00558 | hp1 | a0007 | c0021 | t0001 | g0035 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00558 | hp2 | a0002 | c0005 | t0001 | g0066 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00609 | hp1 | a0005 | c0009 | t0001 | g0029 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0176 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00673 | hp1 | a0002 | c0004 | t0005 | g0203 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0208 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00733 | hp1 | a0002 | c0005 | t0001 | g0146 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00738 | hp1 | a0004 | c0007 | t0007 | g0063 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01069 | hp1 | a0002 | c0005 | t0001 | g0192 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01069 | hp2 | a0006 | c0011 | t0001 | g0004 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01071 | hp1 | a0006 | c0011 | t0001 | g0004 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01081 | hp1 | a0002 | c0004 | t0002 | g0031 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01167 | hp2 | a0003 | c0012 | t0001 | g0118 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01517 | hp1 | a0004 | c0007 | t0007 | g0017 | EUR | IBS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01517 | hp2 | a0001 | c0002 | t0009 | g0094 | EUR | IBS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01884 | hp2 | a0003 | c0006 | t0002 | g0136 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01943 | hp2 | a0008 | c0016 | t0001 | g0057 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01978 | hp1 | a0003 | c0006 | t0002 | g0138 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01993 | hp1 | a0001 | c0002 | t0004 | g0207 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02027 | hp2 | a0002 | c0004 | t0004 | g0199 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0018 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02135 | hp1 | a0009 | c0023 | t0001 | g0011 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02135 | hp2 | a0001 | c0002 | t0008 | g0209 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CDX | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CDX | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0169 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02258 | hp1 | a0003 | c0006 | t0002 | g0135 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02280 | hp1 | a0001 | c0027 | t0001 | g0180 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02451 | hp1 | a0001 | c0026 | t0001 | g0182 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02622 | hp2 | a0001 | c0002 | t0007 | g0021 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02647 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02717 | hp1 | a0003 | c0006 | t0002 | g0077 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0181 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0141 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0124 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02965 | hp1 | a0003 | c0013 | t0002 | g0009 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02965 | hp2 | a0001 | c0002 | t0006 | g0126 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02970 | hp1 | a0001 | c0030 | t0002 | g0189 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0032 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03130 | hp2 | a0003 | c0012 | t0001 | g0137 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03453 | hp2 | a0002 | c0005 | t0002 | g0129 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03486 | hp1 | a0010 | c0017 | t0003 | g0130 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03516 | hp1 | a0011 | c0018 | t0002 | g0177 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03516 | hp2 | a0001 | c0002 | t0007 | g0024 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0114 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03579 | hp1 | a0012 | c0025 | t0001 | g0170 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03654 | hp1 | a0013 | c0019 | t0001 | g0150 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0215 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03688 | hp1 | a0002 | c0005 | t0001 | g0013 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03942 | hp1 | a0014 | c0031 | t0001 | g0026 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG03942 | hp2 | a0002 | c0008 | t0002 | g0098 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04115 | hp1 | a0015 | c0028 | t0002 | g0162 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04184 | hp1 | a0001 | c0010 | t0003 | g0191 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04184 | hp2 | a0016 | c0022 | t0002 | g0073 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0100 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04228 | hp1 | a0002 | c0008 | t0002 | g0062 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | CHB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18612 | hp2 | a0017 | c0024 | t0001 | g0089 | EAS | CHB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18943 | hp2 | a0002 | c0004 | t0004 | g0200 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18944 | hp2 | a0001 | c0001 | t0009 | g0048 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18945 | hp1 | a0002 | c0005 | t0001 | g0067 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18947 | hp2 | a0001 | c0001 | t0008 | g0216 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18952 | hp1 | a0002 | c0005 | t0001 | g0028 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0206 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18966 | hp2 | a0002 | c0004 | t0003 | g0068 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18984 | hp2 | a0005 | c0015 | t0001 | g0060 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18990 | hp1 | a0002 | c0005 | t0001 | g0030 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA18990 | hp2 | a0002 | c0014 | t0001 | g0027 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0198 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19064 | hp1 | a0001 | c0003 | t0008 | g0218 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19064 | hp2 | a0001 | c0020 | t0002 | g0034 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19066 | hp1 | a0002 | c0004 | t0004 | g0201 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0219 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20129 | hp1 | a0004 | c0007 | t0001 | g0166 | AFR | ASW | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0168 | AFR | ASW | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0154 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | GIH | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | GIH | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02109 | hp1 | a0003 | c0029 | t0002 | g0117 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02109 | hp2 | a0001 | c0010 | t0001 | g0178 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG06807 | hp1 | a0003 | c0006 | t0002 | g0078 | AFR | USA | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | USA | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0160 | REF | REF | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0080 | REF | REF | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:46137283 | GCACGTTG others(26): Show |
G | 1 | a0009 | 1 | HG02135.hp1 | conservative_inframe_deletion | MODERATE | c.1462_1494delGAGATG others(27): Show |
p.Glu488_Val498del | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/14 | 1550/1890 | 1462/1626 | 488/541 | chr21 | 46137283 | |||
| chr21:46138542 | C | T | 1 | a0006 | 2 | HG01069.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.1409G>A | p.Arg470Gln | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1465/1890 | 1409/1626 | 470/541 | chr21 | 46138542 | |||
| chr21:46138587 | G | A | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1364C>T | p.Ala455Val | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1420/1890 | 1364/1626 | 455/541 | chr21 | 46138587 | |||
| chr21:46138614 | C | T | 3 | a0005 a0009 a0017 |
5 | HG00423.hp1 HG00609.hp1 HG02135.hp1 others(2): Show |
missense_variant | MODERATE | c.1337G>A | p.Arg446Gln | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1393/1890 | 1337/1626 | 446/541 | chr21 | 46138614 | |||
| chr21:46138638 | G | A | 1 | a0004 | 4 | HG00140.hp2 HG00738.hp1 HG01517.hp1 others(1): Show |
missense_variant | MODERATE | c.1313C>T | p.Ala438Val | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1369/1890 | 1313/1626 | 438/541 | chr21 | 46138638 | |||
| chr21:46145471 | C | CGAAGCCT others(40): Show |
1 | a0016 | 1 | HG04184.hp2 | frameshift_variant&stop_gained | HIGH | c.1159_1205dupCTGGAC others(41): Show |
p.Ala403fs | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/14 | 1261/1890 | 1205/1626 | 402/541 | chr21 | 46145471 | |||
| chr21:46150186 | T | A | 1 | a0011 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.839A>T | p.Asp280Val | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/14 | 895/1890 | 839/1626 | 280/541 | chr21 | 46150186 | |||
| chr21:46151562 | T | C | 1 | a0015 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.632A>G | p.Asp211Gly | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 688/1890 | 632/1626 | 211/541 | chr21 | 46151562 | |||
| chr21:46151571 | C | T | 1 | a0007 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.623G>A | p.Arg208His | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 679/1890 | 623/1626 | 208/541 | chr21 | 46151571 | |||
| chr21:46151725 | C | A | 1 | a0013 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.469G>T | p.Asp157Tyr | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 525/1890 | 469/1626 | 157/541 | chr21 | 46151725 | |||
| chr21:46151896 | T | A | 1 | a0003 | 9 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(6): Show |
missense_variant | MODERATE | c.452A>T | p.Lys151Met | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 508/1890 | 452/1626 | 151/541 | chr21 | 46151896 | |||
| chr21:46151941 | C | T | 1 | a0010 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.407G>A | p.Arg136Gln | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 463/1890 | 407/1626 | 136/541 | chr21 | 46151941 | |||
| chr21:46151944 | C | T | 1 | a0008 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.404G>A | p.Arg135His | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 460/1890 | 404/1626 | 135/541 | chr21 | 46151944 | |||
| chr21:46152973 | C | T | 2 | a0002 a0005 |
23 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
missense_variant | MODERATE | c.301G>A | p.Val101Met | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/14 | 357/1890 | 301/1626 | 101/541 | chr21 | 46152973 | |||
| chr21:46154293 | C | A | 1 | a0014 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.94G>T | p.Gly32Cys | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/14 | 150/1890 | 94/1626 | 32/541 | chr21 | 46154293 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:46137308 | G | A | 8 | a0001c0001 a0001c0002 a0001c0010 others(5): Show |
43 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(40): Show |
synonymous_variant | LOW | c.1470C>T | p.Gly490Gly | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/14 | 1526/1890 | 1470/1626 | 490/541 | chr21 | 46137308 | |||
| chr21:46138559 | G | C | 18 | a0001c0002 a0001c0010 a0001c0026 others(15): Show |
106 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
synonymous_variant | LOW | c.1392C>G | p.Ala464Ala | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1448/1890 | 1392/1626 | 464/541 | chr21 | 46138559 | |||
| chr21:46145866 | G | C | 4 | a0001c0026 a0003c0006 a0003c0012 others(1): Show |
9 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(6): Show |
synonymous_variant | LOW | c.1050C>G | p.Arg350Arg | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/14 | 1106/1890 | 1050/1626 | 350/541 | chr21 | 46145866 | |||
| chr21:46145929 | G | C | 1 | a0001c0027 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.987C>G | p.Arg329Arg | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/14 | 1043/1890 | 987/1626 | 329/541 | chr21 | 46145929 | |||
| chr21:46146315 | G | A | 1 | a0003c0012 | 2 | HG01167.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.919C>T | p.Leu307Leu | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/14 | 975/1890 | 919/1626 | 307/541 | chr21 | 46146315 | |||
| chr21:46151714 | G | T | 1 | a0001c0020 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.480C>A | p.Pro160Pro | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 536/1890 | 480/1626 | 160/541 | chr21 | 46151714 | |||
| chr21:46151931 | C | T | 6 | a0001c0003 a0001c0010 a0002c0008 others(3): Show |
18 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(15): Show |
synonymous_variant | LOW | c.417G>A | p.Pro139Pro | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 473/1890 | 417/1626 | 139/541 | chr21 | 46151931 | |||
| chr21:46154168 | G | A | 1 | a0001c0030 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.219C>T | p.Ile73Ile | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/14 | 275/1890 | 219/1626 | 73/541 | chr21 | 46154168 | |||
| chr21:46155488 | C | T | 1 | a0003c0013 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.36G>A | p.Ser12Ser | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/14 | 92/1890 | 36/1626 | 12/541 | chr21 | 46155488 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:46136855 | G | A | 2 | a0001c0001t0006 a0001c0002t0006 |
7 | HG02257.hp2 HG02559.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*132C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 132 | chr21 | 46136855 | ||||||
| chr21:46136879 | C | T | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(26): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*108G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 108 | chr21 | 46136879 | ||||||
| chr21:46136895 | C | T | 10 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(7): Show |
34 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*92G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 92 | chr21 | 46136895 | ||||||
| chr21:46136968 | G | A | 2 | a0001c0002t0007 a0004c0007t0007 |
7 | HG00140.hp2 HG00738.hp1 HG01517.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*19C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 19 | chr21 | 46136968 | ||||||
| chr21:46155556 | G | A | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(5): Show |
25 | HG00280.hp2 HG00423.hp2 HG00673.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/14 | 33 | chr21 | 46155556 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:46137152 | C | A | 2 | a0001c0002t0001g0164 a0014c0031t0001g0026 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1540-79G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/13 | chr21 | 46137152 | |||||||
| chr21:46137160 | A | G | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(211): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1539+79T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/13 | chr21 | 46137160 | |||||||
| chr21:46137204 | G | A | 3 | a0004c0007t0007g0017 a0004c0007t0007g0063 a0004c0007t0007g0079 |
3 | HG00140.hp2 HG00738.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1539+35C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/13 | chr21 | 46137204 | |||||||
| chr21:46137466 | C | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0186 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1444-132G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137466 | |||||||
| chr21:46137499 | C | T | 4 | a0001c0001t0002g0113 a0001c0001t0002g0147 a0003c0013t0002g0009 others(1): Show |
4 | HG02965.hp1 HG03516.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444-165G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137499 | |||||||
| chr21:46137554 | G | A | 10 | a0001c0001t0006g0082 a0001c0001t0006g0083 a0001c0001t0006g0111 others(7): Show |
10 | HG02257.hp2 HG02559.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444-220C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137554 | |||||||
| chr21:46137585 | G | A | 2 | a0004c0007t0007g0063 a0004c0007t0007g0079 |
2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1444-251C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137585 | |||||||
| chr21:46137614 | A | C | 2 | a0001c0001t0002g0091 a0001c0003t0002g0033 |
2 | HG00438.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1444-280T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137614 | |||||||
| chr21:46137619 | CAA | C | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(119): Show |
131 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1444-287_1444-286d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137619 | |||||||
| chr21:46137737 | G | A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1444-403C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137737 | |||||||
| chr21:46137739 | G | A | 1 | a0005c0009t0009g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1444-405C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137739 | |||||||
| chr21:46137741 | C | CTTTCCTA others(23): Show |
1 | a0001c0001t0002g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1444-437_1444-408d others(32): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137741 | |||||||
| chr21:46137741 | C | T | 1 | a0004c0007t0007g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1444-407G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137741 | |||||||
| chr21:46137808 | A | G | 1 | a0002c0005t0001g0192 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1444-474T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137808 | |||||||
| chr21:46137849 | CCT | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(132): Show |
145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1444-517_1444-516d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137849 | |||||||
| chr21:46137936 | A | T | 1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1443+572T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137936 | |||||||
| chr21:46137937 | C | G | 1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1443+571G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137937 | |||||||
| chr21:46137966 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0045 others(33): Show |
39 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1443+542C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137966 | |||||||
| chr21:46137980 | T | C | 3 | a0004c0007t0007g0017 a0004c0007t0007g0063 a0004c0007t0007g0079 |
3 | HG00140.hp2 HG00738.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1443+528A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137980 | |||||||
| chr21:46138059 | A | G | 1 | a0001c0001t0008g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1443+449T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138059 | |||||||
| chr21:46138071 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1443+437A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138071 | |||||||
| chr21:46138083 | G | A | 2 | a0001c0002t0002g0197 a0001c0002t0002g0198 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1443+425C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138083 | |||||||
| chr21:46138111 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1443+397C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138111 | |||||||
| chr21:46138137 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1443+371G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138137 | |||||||
| chr21:46138214 | A | C | 13 | a0001c0001t0002g0113 a0001c0001t0002g0121 a0001c0001t0002g0139 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1443+294T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138214 | |||||||
| chr21:46138235 | G | A | 5 | a0001c0001t0001g0175 a0001c0002t0001g0093 a0001c0002t0001g0132 others(2): Show |
5 | HG02109.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1443+273C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138235 | |||||||
| chr21:46138266 | G | C | 1 | a0011c0018t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1443+242C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138266 | |||||||
| chr21:46138316 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0188 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1443+192C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138316 | |||||||
| chr21:46138349 | G | A | 1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1443+159C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138349 | |||||||
| chr21:46138372 | C | G | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1443+136G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138372 | |||||||
| chr21:46138375 | C | T | 1 | a0001c0003t0008g0218 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1443+133G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138375 | |||||||
| chr21:46138430 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1443+78C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138430 | |||||||
| chr21:46138672 | A | G | 80 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0076 others(77): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1305-26T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138672 | |||||||
| chr21:46138675 | A | G | 19 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0172 others(16): Show |
19 | HG00438.hp2 HG00639.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1305-29T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138675 | |||||||
| chr21:46138677 | A | G | 66 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0076 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.1305-31T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138677 | |||||||
| chr21:46138800 | C | T | 1 | a0001c0001t0005g0214 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1304+80G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138800 | |||||||
| chr21:46138801 | A | G | 1 | a0001c0002t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1304+79T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138801 | |||||||
| chr21:46138854 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1304+26G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138854 | |||||||
| chr21:46138855 | G | A | 1 | a0001c0002t0004g0206 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1304+25C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138855 | |||||||
| chr21:46138983 | T | C | 1 | a0001c0002t0004g0206 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1261-60A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46138983 | |||||||
| chr21:46138990 | C | T | 2 | a0001c0001t0002g0147 a0002c0004t0001g0099 |
2 | HG00438.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1261-67G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46138990 | |||||||
| chr21:46139080 | A | G | 94 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0076 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1261-157T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139080 | |||||||
| chr21:46139148 | G | A | 6 | a0001c0001t0006g0123 a0001c0002t0002g0197 a0001c0002t0002g0198 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1261-225C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139148 | |||||||
| chr21:46139287 | G | A | 1 | a0001c0030t0002g0189 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1261-364C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139287 | |||||||
| chr21:46139417 | G | A | 1 | a0001c0001t0004g0202 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1261-494C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139417 | |||||||
| chr21:46139434 | G | A | 2 | a0001c0001t0009g0154 a0001c0002t0009g0094 |
2 | HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1261-511C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139434 | |||||||
| chr21:46139466 | C | T | 203 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(200): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1261-543G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139466 | |||||||
| chr21:46139480 | C | T | 1 | a0003c0013t0002g0009 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1261-557G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139480 | |||||||
| chr21:46139505 | G | A | 38 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(35): Show |
39 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1261-582C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139505 | |||||||
| chr21:46139664 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1261-741G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139664 | |||||||
| chr21:46139696 | G | A | 33 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0157 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1261-773C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139696 | |||||||
| chr21:46139827 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1261-904G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139827 | |||||||
| chr21:46139833 | C | A | 14 | a0001c0001t0001g0045 a0001c0001t0002g0046 a0001c0001t0002g0072 others(11): Show |
14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-910G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139833 | |||||||
| chr21:46139856 | G | A | 2 | a0001c0001t0009g0154 a0001c0002t0009g0094 |
2 | HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1261-933C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139856 | |||||||
| chr21:46139861 | G | A | 33 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0157 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1261-938C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139861 | |||||||
| chr21:46139932 | G | A | 2 | a0001c0001t0003g0070 a0002c0004t0005g0203 |
2 | HG00673.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1261-1009C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139932 | |||||||
| chr21:46140029 | G | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(162): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1261-1106C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140029 | |||||||
| chr21:46140031 | G | A | 3 | a0001c0003t0002g0032 a0001c0003t0002g0069 a0001c0003t0002g0148 |
3 | HG00280.hp1 HG00323.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1261-1108C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140031 | |||||||
| chr21:46140084 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0006g0123 a0001c0002t0002g0197 others(4): Show |
8 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1261-1161C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140084 | |||||||
| chr21:46140116 | C | T | 2 | a0002c0004t0004g0200 a0002c0004t0004g0201 |
2 | NA18943.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1261-1193G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140116 | |||||||
| chr21:46140148 | C | G | 1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1261-1225G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140148 | |||||||
| chr21:46140264 | G | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(133): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1261-1341C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140264 | |||||||
| chr21:46140283 | A | G | 4 | a0001c0001t0006g0123 a0001c0002t0006g0124 a0001c0002t0006g0126 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1360T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140283 | |||||||
| chr21:46140283 | ACAGGGAA others(194): Show |
A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-1561_1261-136 others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140283 | |||||||
| chr21:46140296 | A | G | 32 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0157 others(29): Show |
33 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1261-1373T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140296 | |||||||
| chr21:46140359 | TC | T | 5 | a0001c0001t0006g0123 a0001c0002t0002g0140 a0001c0002t0006g0124 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-1437delG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140359 | |||||||
| chr21:46140360 | C | CCCCCGTC others(43): Show |
194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(191): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1261-1487_1261-143 others(54): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140360 | |||||||
| chr21:46140408 | A | ACTCCCCG others(143): Show |
1 | a0001c0003t0002g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1261-1486_1261-148 others(154): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140408 | |||||||
| chr21:46140410 | T | TC | 5 | a0001c0001t0006g0123 a0001c0002t0002g0140 a0001c0002t0006g0124 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-1488dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140410 | |||||||
| chr21:46140415 | G | A | 1 | a0001c0002t0006g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1261-1492C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140415 | |||||||
| chr21:46140425 | G | A | 7 | a0001c0001t0006g0123 a0001c0002t0002g0140 a0001c0002t0006g0124 others(4): Show |
7 | HG01978.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1261-1502C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140425 | |||||||
| chr21:46140435 | CAGGGAGT others(93): Show |
C | 4 | a0001c0001t0006g0123 a0001c0002t0006g0124 a0001c0002t0006g0126 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1612_1261-151 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140435 | |||||||
| chr21:46140442 | T | TGTAAACC others(93): Show |
1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1261-1520_1261-151 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140442 | |||||||
| chr21:46140442 | T | TGTAAACC others(143): Show |
1 | a0003c0006t0002g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1261-1520_1261-151 others(154): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140442 | |||||||
| chr21:46140484 | G | A | 1 | a0001c0003t0002g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1261-1561C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140484 | |||||||
| chr21:46140525 | G | A | 11 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1602C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140525 | |||||||
| chr21:46140527 | A | G | 11 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1604T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140527 | |||||||
| chr21:46140529 | T | G | 11 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1606A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140529 | |||||||
| chr21:46140535 | G | C | 11 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1612C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140535 | |||||||
| chr21:46140610 | TC | T | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1688delG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140610 | |||||||
| chr21:46140619 | C | T | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1696G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140619 | |||||||
| chr21:46140620 | A | G | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1697T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140620 | |||||||
| chr21:46140628 | G | A | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1705C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140628 | |||||||
| chr21:46140630 | G | T | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1707C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140630 | |||||||
| chr21:46140636 | C | CAGGGAGT others(193): Show |
1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1261-1714_1261-171 others(204): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140636 | |||||||
| chr21:46140636 | C | CAGGGAGT others(193): Show |
90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0152 others(87): Show |
98 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1261-1714_1261-171 others(204): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140636 | |||||||
| chr21:46140643 | T | C | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1720A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140643 | |||||||
| chr21:46140651 | C | A | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(149): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1261-1728G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140651 | |||||||
| chr21:46140661 | T | TCCTCGTC others(194): Show |
7 | a0001c0001t0001g0084 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
7 | HG00140.hp2 HG00738.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-1739_1261-173 others(205): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140661 | |||||||
| chr21:46140664 | C | T | 2 | a0001c0002t0001g0167 a0002c0004t0004g0199 |
2 | HG00140.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1261-1741G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140664 | |||||||
| chr21:46140677 | C | T | 4 | a0001c0001t0006g0123 a0001c0002t0006g0124 a0001c0002t0006g0126 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1754G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140677 | |||||||
| chr21:46140693 | T | C | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1770A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140693 | |||||||
| chr21:46140703 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1780A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140703 | |||||||
| chr21:46140719 | T | A | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1796A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140719 | |||||||
| chr21:46140719 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1796A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140719 | |||||||
| chr21:46140720 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1797C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140720 | |||||||
| chr21:46140728 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1805T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140728 | |||||||
| chr21:46140730 | T | G | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1807A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140730 | |||||||
| chr21:46140743 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1820G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140743 | |||||||
| chr21:46140753 | C | CCCAGCAC others(343): Show |
1 | a0002c0004t0004g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1261-1831_1261-183 others(354): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140753 | |||||||
| chr21:46140753 | C | T | 17 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(14): Show |
17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1261-1830G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140753 | |||||||
| chr21:46140764 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1841G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140764 | |||||||
| chr21:46140769 | C | T | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1846G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140769 | |||||||
| chr21:46140770 | A | G | 18 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(15): Show |
18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1261-1847T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140770 | |||||||
| chr21:46140770 | ACCTTCAC others(43): Show |
A | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1897_1261-184 others(54): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140770 | |||||||
| chr21:46140777 | C | T | 3 | a0001c0001t0002g0002 a0001c0002t0002g0197 a0001c0002t0002g0198 |
4 | HG02630.hp2 HG02723.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-1854G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140777 | |||||||
| chr21:46140778 | G | A | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1855C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140778 | |||||||
| chr21:46140780 | G | T | 16 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1857C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140780 | |||||||
| chr21:46140793 | C | T | 2 | a0001c0002t0001g0142 a0002c0004t0004g0199 |
2 | HG02027.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1261-1870G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140793 | |||||||
| chr21:46140803 | T | C | 9 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(6): Show |
9 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-1880A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140803 | |||||||
| chr21:46140811 | T | TCCCCGTC others(345): Show |
1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1889_1261-188 others(356): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140811 | |||||||
| chr21:46140819 | A | C | 26 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(23): Show |
26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1896T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140819 | |||||||
| chr21:46140819 | A | T | 1 | a0002c0004t0004g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1261-1896T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140819 | |||||||
| chr21:46140819 | AGCCTTCA others(43): Show |
A | 1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1261-1946_1261-189 others(54): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140819 | |||||||
| chr21:46140820 | G | A | 26 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(23): Show |
26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1897C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140820 | |||||||
| chr21:46140828 | A | G | 26 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(23): Show |
26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1905T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140828 | |||||||
| chr21:46140830 | T | G | 26 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(23): Show |
26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1907A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140830 | |||||||
| chr21:46140832 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1909G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140832 | |||||||
| chr21:46140835 | A | G | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1912T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140835 | |||||||
| chr21:46140842 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1919C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140842 | |||||||
| chr21:46140843 | C | CGTAAACC others(93): Show |
132 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(129): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1261-1921_1261-192 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140843 | |||||||
| chr21:46140843 | C | T | 17 | a0001c0001t0001g0175 a0001c0001t0002g0102 a0001c0001t0002g0158 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1261-1920G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140843 | |||||||
| chr21:46140849 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1926G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140849 | |||||||
| chr21:46140853 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1930A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140853 | |||||||
| chr21:46140859 | A | C | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1936T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140859 | |||||||
| chr21:46140866 | G | GTCTGCCT others(93): Show |
1 | a0001c0026t0001g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1261-1944_1261-194 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140866 | |||||||
| chr21:46140869 | T | A | 10 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(7): Show |
10 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1261-1946A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140869 | |||||||
| chr21:46140869 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1946A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140869 | |||||||
| chr21:46140870 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1947C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140870 | |||||||
| chr21:46140876 | A | G | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1953T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140876 | |||||||
| chr21:46140886 | C | G | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1963G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140886 | |||||||
| chr21:46140893 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1970G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140893 | |||||||
| chr21:46140903 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1980A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140903 | |||||||
| chr21:46140915 | C | T | 36 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(33): Show |
37 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1261-1992G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140915 | |||||||
| chr21:46140916 | G | GTCCACCT others(93): Show |
1 | a0001c0002t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1261-1994_1261-199 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140916 | |||||||
| chr21:46141021 | C | T | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-2098G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141021 | |||||||
| chr21:46141031 | C | T | 1 | a0001c0002t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1261-2108G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141031 | |||||||
| chr21:46141032 | C | T | 135 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0051 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1261-2109G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141032 | |||||||
| chr21:46141091 | T | G | 65 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(62): Show |
66 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1261-2168A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141091 | |||||||
| chr21:46141112 | A | AACATAAA others(5): Show |
1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1261-2201_1261-219 others(16): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141112 | |||||||
| chr21:46141124 | TTCC | T | 14 | a0001c0001t0001g0045 a0001c0001t0002g0046 a0001c0001t0002g0072 others(11): Show |
14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-2204_1261-220 others(7): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141124 | |||||||
| chr21:46141127 | C | T | 103 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0076 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1261-2204G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141127 | |||||||
| chr21:46141225 | ACTCCTGG others(7): Show |
A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-2316_1261-230 others(18): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141225 | |||||||
| chr21:46141258 | C | T | 1 | a0003c0006t0002g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1261-2335G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141258 | |||||||
| chr21:46141270 | G | A | 1 | a0001c0002t0004g0219 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1261-2347C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141270 | |||||||
| chr21:46141303 | A | AT | 8 | a0001c0001t0001g0175 a0001c0001t0002g0002 a0001c0002t0001g0133 others(5): Show |
9 | HG00738.hp1 HG01517.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-2381dupA | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141303 | |||||||
| chr21:46141303 | AT | A | 64 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(61): Show |
65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1261-2381delA | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141303 | |||||||
| chr21:46141356 | A | T | 1 | a0002c0005t0002g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1261-2433T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141356 | |||||||
| chr21:46141357 | G | C | 14 | a0001c0001t0001g0045 a0001c0001t0002g0046 a0001c0001t0002g0072 others(11): Show |
14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-2434C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141357 | |||||||
| chr21:46141403 | T | C | 65 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(62): Show |
66 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1261-2480A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141403 | |||||||
| chr21:46141405 | C | A | 1 | a0001c0002t0002g0050 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1261-2482G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141405 | |||||||
| chr21:46141615 | C | G | 1 | a0002c0004t0001g0099 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1261-2692G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141615 | |||||||
| chr21:46141625 | A | G | 6 | a0001c0001t0002g0102 a0001c0001t0002g0158 a0001c0001t0002g0159 others(3): Show |
6 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-2702T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141625 | |||||||
| chr21:46141653 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1261-2730T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141653 | |||||||
| chr21:46141716 | T | TAA | 14 | a0001c0001t0001g0045 a0001c0001t0002g0046 a0001c0001t0002g0072 others(11): Show |
14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-2795_1261-279 others(6): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141716 | |||||||
| chr21:46141802 | T | C | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-2879A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141802 | |||||||
| chr21:46141812 | G | A | 47 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(44): Show |
48 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1261-2889C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141812 | |||||||
| chr21:46141886 | T | C | 30 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0002g0046 others(27): Show |
30 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1261-2963A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141886 | |||||||
| chr21:46141914 | G | C | 10 | a0001c0001t0002g0081 a0001c0026t0001g0182 a0003c0006t0002g0077 others(7): Show |
10 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-2991C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141914 | |||||||
| chr21:46141957 | G | T | 47 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(44): Show |
49 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1261-3034C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141957 | |||||||
| chr21:46142039 | G | C | 1 | a0001c0002t0009g0094 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1261-3116C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142039 | |||||||
| chr21:46142059 | G | A | 1 | a0002c0005t0002g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1261-3136C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142059 | |||||||
| chr21:46142091 | A | G | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1261-3168T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142091 | |||||||
| chr21:46142094 | GTAAA | G | 2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-3175_1261-317 others(8): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142094 | |||||||
| chr21:46142276 | G | GAGCTCTT others(66): Show |
9 | a0001c0001t0001g0122 a0001c0002t0001g0142 a0001c0002t0001g0179 others(6): Show |
9 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+3140_1260+314 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | |||||||
| chr21:46142276 | G | GAGCTCTT others(139): Show |
1 | a0001c0001t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1260+3140_1260+314 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | |||||||
| chr21:46142276 | G | GAGCTCTT others(139): Show |
1 | a0001c0002t0002g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1260+3140_1260+314 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | |||||||
| chr21:46142276 | GAGCTCTT others(66): Show |
G | 6 | a0001c0001t0002g0061 a0001c0001t0005g0211 a0001c0001t0005g0212 others(3): Show |
6 | HG00323.hp1 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+3068_1260+314 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | |||||||
| chr21:46142292 | C | CGCGTCGG others(212): Show |
3 | a0001c0002t0006g0124 a0001c0002t0006g0126 a0001c0002t0006g0169 |
3 | HG02257.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1260+3124_1260+312 others(223): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142292 | |||||||
| chr21:46142292 | C | CGCGTCGG others(285): Show |
1 | a0001c0001t0006g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1260+3124_1260+312 others(296): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142292 | |||||||
| chr21:46142305 | G | A | 1 | a0001c0002t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1260+3112C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142305 | |||||||
| chr21:46142318 | G | C | 60 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(57): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1260+3099C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142318 | |||||||
| chr21:46142319 | G | A | 32 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(29): Show |
33 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1260+3098C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142319 | |||||||
| chr21:46142319 | G | C | 4 | a0001c0001t0006g0123 a0001c0002t0006g0124 a0001c0002t0006g0126 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+3098C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142319 | |||||||
| chr21:46142319 | G | GTGAGGCC others(67): Show |
2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1260+3097_1260+309 others(78): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142319 | |||||||
| chr21:46142329 | A | AGACCTTC others(140): Show |
1 | a0001c0001t0008g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(151): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142329 | A | AGACCTTC others(139): Show |
1 | a0001c0001t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142329 | A | AGACCTTC others(139): Show |
1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142329 | A | AGACCTTC others(66): Show |
2 | a0001c0002t0001g0133 a0012c0025t0001g0170 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+3015_1260+308 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142329 | A | AGACCTTC others(285): Show |
1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(296): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142329 | A | AGACCTTC others(67): Show |
2 | a0001c0002t0001g0093 a0001c0002t0001g0132 |
2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1260+3087_1260+308 others(78): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142329 | A | C | 61 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(58): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+3088T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | |||||||
| chr21:46142346 | C | G | 34 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(31): Show |
35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+3071G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142346 | |||||||
| chr21:46142347 | A | ATAAGCTC others(212): Show |
2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG00733.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1260+3069_1260+307 others(223): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | |||||||
| chr21:46142347 | A | ATAAGCTC others(139): Show |
2 | a0002c0004t0002g0181 a0002c0005t0002g0129 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+3069_1260+307 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | |||||||
| chr21:46142347 | A | ATAAGCTC others(66): Show |
1 | a0006c0011t0001g0004 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1260+2997_1260+306 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | |||||||
| chr21:46142347 | A | T | 34 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(31): Show |
35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+3070T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | |||||||
| chr21:46142347 | ATAAGCTC others(66): Show |
A | 1 | a0001c0001t0005g0210 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1260+2997_1260+306 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | |||||||
| chr21:46142391 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0139 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1260+3026G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142391 | |||||||
| chr21:46142392 | G | A | 4 | a0001c0001t0005g0211 a0001c0001t0005g0212 a0001c0001t0009g0048 others(1): Show |
4 | NA18943.hp1 NA18944.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+3025C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142392 | |||||||
| chr21:46142398 | C | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0139 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1260+3019G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142398 | |||||||
| chr21:46142419 | G | C | 34 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(31): Show |
35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+2998C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142419 | |||||||
| chr21:46142420 | T | A | 34 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(31): Show |
35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+2997A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142420 | |||||||
| chr21:46142420 | T | TTAAGCTC others(66): Show |
2 | a0001c0002t0001g0164 a0014c0031t0001g0026 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1260+2996_1260+299 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142420 | |||||||
| chr21:46142464 | C | CGTGAGGC others(66): Show |
6 | a0001c0001t0001g0116 a0001c0002t0001g0194 a0001c0003t0002g0032 others(3): Show |
6 | HG00140.hp2 HG00738.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+2952_1260+295 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142464 | |||||||
| chr21:46142464 | C | G | 60 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(57): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1260+2953G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142464 | |||||||
| chr21:46142465 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1260+2952C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142465 | |||||||
| chr21:46142475 | C | A | 10 | a0001c0001t0001g0175 a0001c0026t0001g0182 a0002c0005t0002g0129 others(7): Show |
10 | HG01167.hp2 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260+2942G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142475 | |||||||
| chr21:46142483 | G | A | 9 | a0001c0001t0001g0175 a0001c0026t0001g0182 a0003c0006t0002g0077 others(6): Show |
9 | HG01167.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+2934C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142483 | |||||||
| chr21:46142503 | T | C | 36 | a0001c0001t0001g0045 a0001c0001t0001g0195 a0001c0001t0002g0012 others(33): Show |
36 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1260+2914A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142503 | |||||||
| chr21:46142503 | T | TACAGGTG others(67): Show |
1 | a0001c0001t0001g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1260+2913_1260+291 others(78): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142503 | |||||||
| chr21:46142523 | G | C | 2 | a0001c0001t0004g0202 a0002c0004t0004g0199 |
2 | HG02027.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1260+2894C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142523 | |||||||
| chr21:46142531 | C | T | 1 | a0001c0003t0002g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1260+2886G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142531 | |||||||
| chr21:46142538 | C | G | 17 | a0001c0001t0001g0175 a0001c0001t0002g0003 a0001c0001t0002g0019 others(14): Show |
18 | HG00099.hp2 HG00639.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1260+2879G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142538 | |||||||
| chr21:46142567 | G | A | 2 | a0002c0004t0002g0181 a0002c0005t0002g0129 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+2850C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142567 | |||||||
| chr21:46142640 | G | A | 1 | a0003c0012t0001g0118 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260+2777C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142640 | |||||||
| chr21:46142646 | T | C | 70 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(67): Show |
71 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1260+2771A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142646 | |||||||
| chr21:46142651 | T | C | 1 | a0001c0002t0002g0050 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1260+2766A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142651 | |||||||
| chr21:46142670 | A | T | 81 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(78): Show |
83 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1260+2747T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142670 | |||||||
| chr21:46142680 | A | G | 66 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(63): Show |
67 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1260+2737T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142680 | |||||||
| chr21:46142691 | G | A | 1 | a0001c0001t0008g0208 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1260+2726C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142691 | |||||||
| chr21:46142692 | A | G | 70 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(67): Show |
71 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1260+2725T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142692 | |||||||
| chr21:46142718 | T | C | 81 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(78): Show |
82 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1260+2699A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142718 | |||||||
| chr21:46142721 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0002g0121 a0001c0001t0002g0139 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+2696G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142721 | |||||||
| chr21:46142722 | G | C | 7 | a0001c0002t0001g0101 a0001c0002t0001g0179 a0001c0002t0001g0183 others(4): Show |
7 | HG01433.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+2695C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142722 | |||||||
| chr21:46142753 | C | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0051 others(48): Show |
54 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1260+2664G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142753 | |||||||
| chr21:46142800 | C | CG | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+2616_1260+261 others(5): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142800 | |||||||
| chr21:46142801 | A | T | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+2616T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142801 | |||||||
| chr21:46142807 | C | A | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+2610G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142807 | |||||||
| chr21:46142877 | G | C | 70 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(67): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1260+2540C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142877 | |||||||
| chr21:46142891 | G | A | 1 | a0001c0010t0003g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1260+2526C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142891 | |||||||
| chr21:46142911 | A | T | 1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+2506T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142911 | |||||||
| chr21:46143070 | G | C | 7 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0002t0002g0140 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+2347C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143070 | |||||||
| chr21:46143152 | G | T | 1 | a0001c0001t0008g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1260+2265C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143152 | |||||||
| chr21:46143252 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1260+2165C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143252 | |||||||
| chr21:46143431 | C | G | 23 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0122 others(20): Show |
23 | HG01433.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1260+1986G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143431 | |||||||
| chr21:46143446 | C | T | 68 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(65): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1260+1971G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143446 | |||||||
| chr21:46143449 | T | C | 68 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0096 others(65): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1260+1968A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143449 | |||||||
| chr21:46143675 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1260+1742G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143675 | |||||||
| chr21:46143710 | C | A | 1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+1707G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143710 | |||||||
| chr21:46143723 | G | C | 11 | a0001c0001t0001g0122 a0001c0001t0006g0123 a0001c0002t0001g0101 others(8): Show |
11 | HG01433.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+1694C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143723 | |||||||
| chr21:46143756 | T | G | 1 | a0001c0001t0005g0217 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1260+1661A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143756 | |||||||
| chr21:46143779 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1260+1638G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143779 | |||||||
| chr21:46143853 | C | A | 1 | a0014c0031t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1260+1564G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143853 | |||||||
| chr21:46144033 | T | A | 1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+1384A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144033 | |||||||
| chr21:46144044 | A | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0139 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1260+1373T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144044 | |||||||
| chr21:46144048 | G | A | 18 | a0001c0001t0001g0045 a0001c0001t0002g0046 a0001c0001t0002g0072 others(15): Show |
18 | HG00099.hp1 HG00438.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1260+1369C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144048 | |||||||
| chr21:46144196 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1260+1221G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144196 | |||||||
| chr21:46144277 | T | A | 1 | a0001c0002t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1260+1140A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144277 | |||||||
| chr21:46144408 | A | C | 1 | a0001c0001t0003g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260+1009T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144408 | |||||||
| chr21:46144444 | CT | C | 5 | a0001c0001t0002g0102 a0001c0001t0008g0215 a0001c0002t0001g0144 others(2): Show |
5 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+972delA | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144444 | |||||||
| chr21:46144447 | T | C | 1 | a0001c0002t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1260+970A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144447 | |||||||
| chr21:46144451 | T | C | 1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+966A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144451 | |||||||
| chr21:46144453 | T | TCCCCCTC others(703): Show |
1 | a0001c0002t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1260+963_1260+964i others(712): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144453 | |||||||
| chr21:46144466 | C | CCCCTCTC others(740): Show |
1 | a0005c0009t0009g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1260+950_1260+951i others(749): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144466 | |||||||
| chr21:46144472 | C | CTCCCCCC others(714): Show |
1 | a0001c0002t0001g0193 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1260+944_1260+945i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | |||||||
| chr21:46144472 | C | CTCCCCCC others(712): Show |
1 | a0001c0002t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1260+944_1260+945i others(721): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | |||||||
| chr21:46144472 | C | CTCCCCCC others(711): Show |
4 | a0001c0002t0001g0085 a0002c0005t0001g0192 a0004c0007t0007g0017 others(1): Show |
4 | HG00140.hp2 HG01069.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+944_1260+945i others(720): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | |||||||
| chr21:46144472 | C | CTCCCCCC others(714): Show |
1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260+944_1260+945i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | |||||||
| chr21:46144472 | C | CTCCCCCC others(713): Show |
5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0009g0154 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+944_1260+945i others(722): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | |||||||
| chr21:46144472 | C | CTCCCCCC others(716): Show |
1 | a0001c0002t0001g0064 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1260+944_1260+945i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | |||||||
| chr21:46144473 | T | TC | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(144): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1260+943dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144473 | |||||||
| chr21:46144477 | C | T | 1 | a0005c0009t0009g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1260+940G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144477 | |||||||
| chr21:46144478 | C | CA | 37 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(34): Show |
38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1260+938_1260+939i others(3): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144478 | |||||||
| chr21:46144478 | C | G | 1 | a0005c0009t0009g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1260+939G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144478 | |||||||
| chr21:46144483 | C | CTCCCCTT others(721): Show |
1 | a0001c0001t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1260+933_1260+934i others(730): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144483 | |||||||
| chr21:46144485 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1260+932A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCCTT others(737): Show |
1 | a0001c0002t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(746): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTCC others(663): Show |
1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(672): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
1 | a0001c0002t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(730): Show |
1 | a0002c0008t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(739): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(698): Show |
1 | a0001c0002t0008g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(707): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(734): Show |
1 | a0002c0004t0004g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(743): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(727): Show |
1 | a0001c0002t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
1 | a0002c0005t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(735): Show |
1 | a0001c0002t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(744): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(687): Show |
1 | a0001c0002t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(696): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(716): Show |
1 | a0001c0001t0001g0005 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(751): Show |
1 | a0001c0002t0001g0015 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(760): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(723): Show |
2 | a0001c0001t0001g0006 a0001c0001t0002g0061 |
3 | HG00323.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(722): Show |
1 | a0004c0007t0001g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(731): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(723): Show |
1 | a0001c0002t0001g0001 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
1 | a0001c0002t0001g0001 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
1 | a0002c0004t0004g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
1 | a0001c0002t0004g0219 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(727): Show |
1 | a0001c0002t0007g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
1 | a0001c0002t0004g0207 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
2 | a0002c0005t0001g0030 a0002c0014t0001g0027 |
2 | NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
37 | a0001c0001t0001g0084 a0001c0001t0001g0195 a0001c0001t0002g0052 others(34): Show |
39 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(723): Show |
3 | a0001c0001t0001g0152 a0001c0002t0001g0058 a0001c0002t0004g0007 |
4 | HG01433.hp2 HG01496.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(714): Show |
1 | a0001c0002t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(716): Show |
1 | a0001c0030t0002g0189 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(715): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0172 a0001c0001t0001g0174 others(1): Show |
4 | HG01256.hp1 HG01975.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(724): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(716): Show |
1 | a0012c0025t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(699): Show |
1 | a0001c0002t0001g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(708): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(727): Show |
1 | a0001c0002t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(723): Show |
1 | a0001c0002t0001g0041 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(738): Show |
1 | a0001c0002t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(747): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0001c0002t0001g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
3 | a0001c0002t0001g0104 a0001c0002t0001g0127 a0001c0002t0001g0131 |
3 | HG00642.hp2 HG01258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(714): Show |
2 | a0001c0001t0002g0107 a0003c0029t0002g0117 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(734): Show |
1 | a0001c0001t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(743): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(716): Show |
1 | a0003c0006t0002g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(714): Show |
1 | a0003c0013t0002g0009 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(713): Show |
5 | a0001c0026t0001g0182 a0003c0006t0002g0078 a0003c0006t0002g0135 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(722): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(716): Show |
1 | a0003c0006t0002g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(712): Show |
1 | a0003c0006t0002g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(721): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(705): Show |
1 | a0001c0001t0002g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(714): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(738): Show |
1 | a0001c0001t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(747): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(740): Show |
2 | a0001c0002t0001g0125 a0001c0002t0001g0184 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(749): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0001c0001t0002g0012 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(699): Show |
1 | a0001c0002t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(708): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(766): Show |
1 | a0009c0023t0001g0011 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(775): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(733): Show |
1 | a0001c0020t0002g0034 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(742): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(732): Show |
1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(741): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(732): Show |
7 | a0001c0001t0001g0045 a0001c0001t0002g0046 a0001c0001t0002g0072 others(4): Show |
7 | HG01081.hp1 HG01081.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(741): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(732): Show |
1 | a0001c0001t0002g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(741): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0001c0001t0003g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0001c0001t0005g0008 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0001c0001t0001g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
1 | a0001c0001t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(723): Show |
1 | a0001c0001t0005g0213 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0010c0017t0003g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(725): Show |
1 | a0002c0004t0003g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
20 | a0001c0001t0001g0096 a0001c0001t0002g0113 a0001c0001t0003g0010 others(17): Show |
20 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(744): Show |
1 | a0001c0001t0006g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(753): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
1 | a0001c0001t0002g0155 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(722): Show |
4 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0003g0110 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(731): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(679): Show |
1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(688): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(677): Show |
4 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0003t0002g0141 others(1): Show |
4 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(686): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(713): Show |
1 | a0001c0003t0002g0018 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(722): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(729): Show |
2 | a0001c0001t0001g0051 a0015c0028t0002g0162 |
2 | HG00639.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(738): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(729): Show |
1 | a0002c0008t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(738): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(728): Show |
14 | a0001c0001t0001g0044 a0001c0001t0001g0157 a0001c0001t0001g0175 others(11): Show |
15 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(737): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(726): Show |
1 | a0001c0003t0008g0218 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(729): Show |
1 | a0001c0003t0002g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(738): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(684): Show |
1 | a0011c0018t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(693): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(753): Show |
1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(762): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(751): Show |
5 | a0001c0001t0001g0122 a0001c0001t0006g0123 a0001c0002t0006g0124 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(760): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(717): Show |
5 | a0001c0002t0001g0179 a0001c0002t0001g0183 a0001c0002t0001g0185 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(726): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(719): Show |
1 | a0001c0001t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(728): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(697): Show |
1 | a0001c0010t0003g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(706): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(706): Show |
1 | a0002c0004t0001g0099 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(715): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(696): Show |
4 | a0001c0001t0005g0210 a0001c0001t0008g0216 a0001c0002t0009g0094 others(1): Show |
4 | HG00738.hp1 HG01517.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(705): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(716): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0188 |
4 | HG00099.hp2 HG02809.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(765): Show |
1 | a0002c0005t0002g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(774): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(765): Show |
1 | a0002c0004t0002g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(774): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(762): Show |
2 | a0001c0001t0002g0102 a0001c0001t0008g0215 |
2 | HG00099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(771): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(763): Show |
1 | a0001c0002t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(772): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(727): Show |
2 | a0001c0002t0002g0197 a0001c0002t0002g0198 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
1 | a0001c0002t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(721): Show |
1 | a0001c0002t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(730): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(743): Show |
1 | a0001c0001t0006g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(752): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(719): Show |
1 | a0001c0002t0001g0151 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(728): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(714): Show |
1 | a0001c0001t0001g0171 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(720): Show |
1 | a0001c0001t0004g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(729): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(722): Show |
1 | a0001c0002t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(731): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(717): Show |
1 | a0001c0001t0002g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(726): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TCCCCTTT others(724): Show |
1 | a0001c0001t0002g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144485 | T | TGTCTCC | 14 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0087 others(11): Show |
15 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(8): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | |||||||
| chr21:46144492 | T | TCCCCCCT others(728): Show |
1 | a0002c0005t0001g0028 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1260+924_1260+925i others(737): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144492 | |||||||
| chr21:46144493 | C | CCCCCCTC others(741): Show |
1 | a0001c0001t0006g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1260+923_1260+924i others(750): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144493 | |||||||
| chr21:46144528 | C | T | 4 | a0001c0003t0002g0100 a0002c0008t0002g0062 a0002c0008t0002g0098 others(1): Show |
4 | HG03942.hp2 HG04115.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+889G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144528 | |||||||
| chr21:46144528 | CCT | C | 6 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0002t0002g0140 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+887_1260+888d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144528 | |||||||
| chr21:46144536 | C | T | 24 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0081 others(21): Show |
25 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1260+881G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144536 | |||||||
| chr21:46144550 | CCT | C | 25 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0157 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1260+865_1260+866d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144550 | |||||||
| chr21:46144600 | CCT | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0051 others(90): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1260+815_1260+816d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144600 | |||||||
| chr21:46144600 | CCTCT | C | 5 | a0001c0001t0002g0102 a0001c0001t0008g0215 a0001c0002t0001g0144 others(2): Show |
5 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+813_1260+816d others(6): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144600 | |||||||
| chr21:46144606 | T | C | 1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+811A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144606 | |||||||
| chr21:46144611 | G | C | 1 | a0001c0002t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+806C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144611 | |||||||
| chr21:46144611 | G | T | 6 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0003t0002g0141 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+806C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144611 | |||||||
| chr21:46144630 | T | TC | 6 | a0001c0001t0002g0012 a0001c0001t0002g0145 a0001c0002t0001g0054 others(3): Show |
6 | HG00544.hp1 HG00642.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+786dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144630 | |||||||
| chr21:46144644 | TCCTCCCC others(12): Show |
T | 1 | a0002c0005t0001g0013 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1260+754_1260+772d others(21): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144644 | |||||||
| chr21:46144657 | T | C | 1 | a0001c0002t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1260+760A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144657 | |||||||
| chr21:46144658 | C | T | 1 | a0001c0002t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1260+759G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144658 | |||||||
| chr21:46144751 | C | G | 10 | a0001c0001t0002g0081 a0001c0026t0001g0182 a0003c0006t0002g0077 others(7): Show |
10 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260+666G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144751 | |||||||
| chr21:46144782 | GAACTGCT others(46): Show |
G | 1 | a0002c0014t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+582_1260+634d others(55): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144782 | |||||||
| chr21:46144818 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1260+599A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144818 | |||||||
| chr21:46144856 | A | C | 1 | a0002c0014t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+561T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144856 | |||||||
| chr21:46144857 | C | T | 1 | a0002c0014t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+560G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144857 | |||||||
| chr21:46144859 | C | A | 1 | a0002c0014t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+558G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144859 | |||||||
| chr21:46144998 | G | C | 127 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0051 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1260+419C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144998 | |||||||
| chr21:46145072 | GC | G | 5 | a0001c0001t0002g0102 a0001c0001t0008g0215 a0001c0002t0001g0144 others(2): Show |
5 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+344delG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46145072 | |||||||
| chr21:46145279 | G | C | 1 | a0001c0002t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1260+138C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46145279 | |||||||
| chr21:46145631 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0092 a0001c0001t0003g0095 |
3 | HG03491.hp2 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1099-53C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145631 | |||||||
| chr21:46145733 | C | CCGTGCCC others(513): Show |
1 | a0001c0002t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1098+84_1098+85ins others(520): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145733 | |||||||
| chr21:46145735 | T | C | 1 | a0001c0002t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1098+83A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(197): Show |
1 | a0011c0018t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(204): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(510): Show |
3 | a0001c0002t0001g0183 a0001c0002t0001g0186 a0001c0002t0001g0187 |
3 | HG03130.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(517): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(214): Show |
4 | a0001c0001t0002g0121 a0001c0002t0002g0140 a0001c0003t0002g0141 others(1): Show |
4 | HG00639.hp2 HG01884.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(221): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(513): Show |
1 | a0001c0002t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(520): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(511): Show |
1 | a0001c0002t0001g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(518): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(196): Show |
1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(203): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(224): Show |
3 | a0001c0002t0001g0125 a0001c0002t0001g0142 a0001c0002t0001g0184 |
3 | HG02280.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(231): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(249): Show |
1 | a0001c0001t0002g0158 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(256): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCC others(250): Show |
4 | a0001c0001t0002g0159 a0001c0003t0002g0032 a0001c0003t0002g0069 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(257): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145735 | T | TGCCCTCG others(423): Show |
1 | a0001c0001t0002g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(430): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | |||||||
| chr21:46145753 | G | GCCCTTCC others(250): Show |
2 | a0003c0012t0001g0118 a0003c0012t0001g0137 |
2 | HG01167.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1098+64_1098+65ins others(257): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145753 | |||||||
| chr21:46145756 | C | CTTCCCCC others(265): Show |
1 | a0001c0002t0001g0064 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(272): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(247): Show |
1 | a0006c0011t0001g0004 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(254): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(264): Show |
4 | a0001c0002t0001g0085 a0002c0005t0001g0192 a0004c0007t0007g0017 others(1): Show |
4 | HG00140.hp2 HG01069.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(271): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(265): Show |
2 | a0001c0002t0001g0065 a0001c0002t0001g0193 |
2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(272): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(248): Show |
1 | a0001c0001t0009g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(255): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(240): Show |
4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0087 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(247): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(248): Show |
1 | a0001c0002t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(255): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0001c0002t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(270): Show |
1 | a0001c0002t0007g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(277): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(266): Show |
1 | a0001c0001t0002g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(273): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(312): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0172 others(7): Show |
11 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(319): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(270): Show |
1 | a0001c0001t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(277): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(265): Show |
1 | a0001c0002t0001g0151 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(272): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(250): Show |
3 | a0001c0002t0001g0071 a0001c0002t0001g0104 a0016c0022t0002g0073 |
3 | HG00642.hp2 HG04184.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(257): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(267): Show |
54 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0084 others(51): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(392): Show |
1 | a0002c0005t0001g0013 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(399): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0001c0002t0004g0219 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(405): Show |
1 | a0001c0001t0002g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(412): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0001c0002t0001g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0001c0002t0001g0131 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0002c0014t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0014c0031t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(285): Show |
1 | a0001c0002t0004g0207 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(292): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(269): Show |
1 | a0001c0002t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(276): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(192): Show |
1 | a0001c0001t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(199): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(269): Show |
1 | a0001c0002t0001g0043 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(276): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(268): Show |
1 | a0005c0009t0009g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(351): Show |
5 | a0001c0001t0001g0122 a0001c0001t0006g0123 a0001c0002t0006g0124 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(358): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | CTTCCCCC others(408): Show |
1 | a0001c0001t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(415): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145756 | C | G | 7 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0002t0002g0140 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+62G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | |||||||
| chr21:46145757 | T | TTCCCCCC others(300): Show |
1 | a0001c0001t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1098+60_1098+61ins others(307): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | |||||||
| chr21:46145757 | T | TTCCCCCT others(225): Show |
1 | a0003c0006t0002g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1098+60_1098+61ins others(232): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | |||||||
| chr21:46145757 | T | TTCCCCCT others(298): Show |
1 | a0001c0001t0002g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1098+60_1098+61ins others(305): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | |||||||
| chr21:46145757 | T | TTCCCCCT others(224): Show |
6 | a0001c0001t0002g0081 a0001c0026t0001g0182 a0003c0006t0002g0078 others(3): Show |
6 | HG01978.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+60_1098+61ins others(231): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | |||||||
| chr21:46145757 | T | TTCCCCCT others(241): Show |
13 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0107 others(10): Show |
14 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+60_1098+61ins others(248): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | |||||||
| chr21:46145758 | T | C | 9 | a0001c0002t0001g0125 a0001c0002t0001g0142 a0001c0002t0001g0179 others(6): Show |
9 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+60A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145758 | T | TCCCCCTC others(264): Show |
1 | a0001c0002t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(271): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145758 | T | TCCCCCTC others(408): Show |
2 | a0002c0004t0002g0181 a0002c0005t0002g0129 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+59_1098+60ins others(415): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145758 | T | TCCCCCTC others(441): Show |
1 | a0001c0002t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(448): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145758 | T | TCCCCCTC others(424): Show |
1 | a0001c0001t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(431): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145758 | T | TCCCCCTC others(226): Show |
1 | a0003c0006t0002g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(233): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145758 | T | TCCCCCTC others(427): Show |
1 | a0001c0001t0008g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(434): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | |||||||
| chr21:46145763 | C | CCTCCCCG others(247): Show |
1 | a0001c0002t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1098+54_1098+55ins others(254): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145763 | |||||||
| chr21:46145764 | T | C | 1 | a0001c0002t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1098+54A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145764 | |||||||
| chr21:46145764 | T | TCCCCGCC others(266): Show |
1 | a0001c0002t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1098+53_1098+54ins others(273): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145764 | |||||||
| chr21:46145767 | C | CCCGCCCT others(287): Show |
1 | a0001c0003t0002g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(294): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(285): Show |
1 | a0002c0008t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(292): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(365): Show |
1 | a0001c0001t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(372): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(367): Show |
1 | a0002c0004t0003g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(374): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(365): Show |
1 | a0001c0001t0004g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(372): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(184): Show |
2 | a0001c0002t0002g0197 a0001c0002t0002g0198 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(191): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(366): Show |
26 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0109 others(23): Show |
27 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(373): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(308): Show |
1 | a0001c0001t0005g0213 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(315): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(367): Show |
1 | a0001c0001t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(374): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(234): Show |
1 | a0001c0001t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(241): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(267): Show |
1 | a0001c0001t0002g0002 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(308): Show |
3 | a0001c0001t0003g0070 a0001c0001t0005g0217 a0001c0003t0001g0163 |
3 | HG00423.hp2 HG01168.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(315): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(176): Show |
1 | a0002c0004t0004g0201 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(183): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(287): Show |
1 | a0001c0001t0001g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(294): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(234): Show |
2 | a0001c0001t0001g0175 a0001c0002t0001g0133 |
2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(241): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(267): Show |
6 | a0001c0001t0001g0157 a0001c0002t0002g0050 a0001c0003t0002g0018 others(3): Show |
6 | HG02040.hp2 HG02132.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(267): Show |
1 | a0001c0001t0001g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(284): Show |
1 | a0002c0008t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(291): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(177): Show |
1 | a0002c0004t0004g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(184): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(286): Show |
1 | a0015c0028t0002g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(293): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(268): Show |
1 | a0001c0003t0002g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(367): Show |
1 | a0001c0001t0003g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(374): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145767 | C | CCGCCCTC others(369): Show |
1 | a0010c0017t0003g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(376): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | |||||||
| chr21:46145773 | T | TCCCCCCA others(252): Show |
1 | a0002c0005t0001g0030 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1098+44_1098+45ins others(259): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145773 | |||||||
| chr21:46145773 | T | TCCCCCCC others(368): Show |
1 | a0001c0001t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1098+44_1098+45ins others(375): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145773 | |||||||
| chr21:46145803 | T | TC | 6 | a0001c0001t0002g0052 a0001c0001t0002g0120 a0001c0002t0001g0038 others(3): Show |
6 | HG00544.hp2 HG01517.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+14dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145803 | |||||||
| chr21:46145961 | G | A | 2 | a0002c0004t0002g0181 a0002c0005t0002g0129 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.969-14C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46145961 | |||||||
| chr21:46145962 | C | A | 2 | a0002c0004t0002g0181 a0002c0005t0002g0129 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.969-15G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46145962 | |||||||
| chr21:46146046 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG00733.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.969-99C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146046 | |||||||
| chr21:46146080 | A | AC | 3 | a0001c0001t0002g0120 a0001c0001t0005g0210 a0001c0002t0001g0193 |
3 | HG02451.hp2 NA18971.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.969-134dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146080 | |||||||
| chr21:46146122 | G | T | 23 | a0001c0001t0002g0003 a0001c0001t0002g0107 a0001c0001t0002g0147 others(20): Show |
24 | HG00438.hp2 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.968+144C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146122 | |||||||
| chr21:46146172 | A | T | 1 | a0002c0004t0005g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.968+94T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146172 | |||||||
| chr21:46146176 | G | A | 16 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0019 others(13): Show |
17 | HG00099.hp2 HG00738.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.968+90C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146176 | |||||||
| chr21:46146373 | C | T | 1 | a0001c0010t0003g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.907-46G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146373 | |||||||
| chr21:46146404 | A | C | 2 | a0001c0001t0002g0120 a0001c0010t0001g0178 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.907-77T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146404 | |||||||
| chr21:46146405 | C | A | 1 | a0001c0010t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.907-78G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146405 | |||||||
| chr21:46146406 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.907-79G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146406 | |||||||
| chr21:46146418 | C | T | 2 | a0001c0001t0003g0106 a0001c0001t0003g0110 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.907-91G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146418 | |||||||
| chr21:46146431 | G | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0107 others(19): Show |
23 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.907-104C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146431 | |||||||
| chr21:46146476 | G | C | 1 | a0001c0002t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-149C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146476 | |||||||
| chr21:46146477 | C | A | 1 | a0001c0002t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-150G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146477 | |||||||
| chr21:46146478 | A | AC | 12 | a0001c0001t0002g0087 a0001c0001t0003g0010 a0001c0001t0003g0095 others(9): Show |
12 | HG00609.hp1 HG01109.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.907-152dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146478 | |||||||
| chr21:46146478 | A | C | 1 | a0001c0002t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-151T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146478 | |||||||
| chr21:46146488 | T | G | 38 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(35): Show |
39 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.907-161A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146488 | |||||||
| chr21:46146529 | A | C | 1 | a0001c0001t0002g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.907-202T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146529 | |||||||
| chr21:46146556 | A | G | 1 | a0001c0002t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.907-229T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146556 | |||||||
| chr21:46146754 | C | G | 3 | a0001c0026t0001g0182 a0003c0006t0002g0077 a0003c0006t0002g0078 |
3 | HG02451.hp1 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.907-427G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146754 | |||||||
| chr21:46146881 | A | C | 1 | a0001c0002t0001g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.907-554T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146881 | |||||||
| chr21:46146912 | G | C | 1 | a0004c0007t0007g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.907-585C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146912 | |||||||
| chr21:46146914 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0107 others(18): Show |
22 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.907-587C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146914 | |||||||
| chr21:46147037 | T | TCATTCGA others(67): Show |
1 | a0001c0003t0002g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.907-784_907-711dup others(74): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147037 | |||||||
| chr21:46147231 | C | G | 1 | a0009c0023t0001g0011 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.907-904G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147231 | |||||||
| chr21:46147265 | C | T | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0087 others(3): Show |
6 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-938G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147265 | |||||||
| chr21:46147289 | G | GA | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(135): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.907-963dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147289 | |||||||
| chr21:46147289 | G | GAA | 16 | a0001c0001t0001g0051 a0001c0001t0001g0115 a0001c0001t0001g0116 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.907-964_907-963dup others(2): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147289 | |||||||
| chr21:46147296 | A | C | 1 | a0001c0001t0005g0211 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.907-969T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147296 | |||||||
| chr21:46147354 | C | T | 2 | a0001c0002t0002g0197 a0001c0002t0002g0198 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.907-1027G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147354 | |||||||
| chr21:46147407 | G | C | 1 | a0001c0003t0002g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.907-1080C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147407 | |||||||
| chr21:46147412 | AG | A | 5 | a0001c0001t0002g0049 a0001c0001t0002g0061 a0001c0002t0001g0064 others(2): Show |
5 | HG00323.hp1 HG00558.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-1086delC | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147412 | |||||||
| chr21:46147446 | G | C | 22 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0157 others(19): Show |
23 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.907-1119C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147446 | |||||||
| chr21:46147534 | C | A | 1 | a0001c0001t0004g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.907-1207G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147534 | |||||||
| chr21:46147574 | G | T | 1 | a0001c0001t0004g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.907-1247C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147574 | |||||||
| chr21:46147619 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.907-1292G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147619 | |||||||
| chr21:46147714 | G | A | 45 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(42): Show |
47 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.907-1387C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147714 | |||||||
| chr21:46147734 | C | CAAGACCA others(4): Show |
1 | a0001c0020t0002g0034 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.907-1418_907-1408d others(13): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147734 | |||||||
| chr21:46147774 | T | TA | 8 | a0001c0001t0001g0051 a0001c0001t0001g0076 a0001c0001t0002g0091 others(5): Show |
8 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-1448dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147774 | |||||||
| chr21:46147933 | G | A | 210 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(207): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.907-1606C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147933 | |||||||
| chr21:46147942 | C | CA | 6 | a0001c0001t0002g0012 a0001c0001t0002g0087 a0001c0001t0005g0214 others(3): Show |
6 | HG01109.hp2 HG02132.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-1616dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147942 | |||||||
| chr21:46147942 | CA | C | 49 | a0001c0001t0001g0045 a0001c0001t0001g0084 a0001c0001t0001g0122 others(46): Show |
50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.907-1616delT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147942 | |||||||
| chr21:46147942 | CAA | C | 9 | a0001c0002t0001g0142 a0001c0026t0001g0182 a0003c0006t0002g0077 others(6): Show |
9 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.907-1617_907-1616d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147942 | |||||||
| chr21:46147958 | A | G | 6 | a0001c0002t0001g0179 a0001c0002t0001g0183 a0001c0002t0001g0185 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-1631T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147958 | |||||||
| chr21:46148239 | C | T | 7 | a0001c0001t0002g0081 a0001c0001t0002g0102 a0001c0001t0008g0215 others(4): Show |
7 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+1880G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148239 | |||||||
| chr21:46148381 | T | C | 4 | a0001c0002t0007g0020 a0001c0002t0007g0021 a0001c0002t0007g0024 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1738A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148381 | |||||||
| chr21:46148618 | C | G | 1 | a0012c0025t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.906+1501G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148618 | |||||||
| chr21:46148623 | G | C | 3 | a0001c0002t0001g0131 a0002c0004t0002g0181 a0002c0005t0002g0129 |
3 | HG02818.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.906+1496C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148623 | |||||||
| chr21:46148722 | T | C | 1 | a0016c0022t0002g0073 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.906+1397A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148722 | |||||||
| chr21:46148728 | T | G | 1 | a0001c0001t0006g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.906+1391A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148728 | |||||||
| chr21:46148761 | G | GAACAGTT others(6): Show |
1 | a0001c0001t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.906+1345_906+1357d others(15): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148761 | |||||||
| chr21:46149048 | GA | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0147 a0001c0002t0001g0133 others(1): Show |
4 | HG00438.hp1 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+1070delT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149048 | |||||||
| chr21:46149083 | G | A | 11 | a0001c0001t0001g0045 a0001c0001t0002g0019 a0001c0001t0002g0046 others(8): Show |
11 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+1036C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149083 | |||||||
| chr21:46149117 | G | A | 58 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0002g0002 others(55): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.906+1002C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149117 | |||||||
| chr21:46149157 | A | G | 13 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0002t0001g0179 others(10): Show |
13 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+962T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149157 | |||||||
| chr21:46149227 | G | A | 43 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0002g0002 others(40): Show |
45 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.906+892C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149227 | |||||||
| chr21:46149393 | A | C | 1 | a0001c0002t0001g0037 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.906+726T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149393 | |||||||
| chr21:46149453 | CACAA | C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0139 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.906+662_906+665del others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149453 | |||||||
| chr21:46149457 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.906+662T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149457 | |||||||
| chr21:46149507 | C | T | 13 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0002t0001g0179 others(10): Show |
13 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+612G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149507 | |||||||
| chr21:46149728 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.906+391G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149728 | |||||||
| chr21:46149813 | TGGAGGTG others(6): Show |
T | 1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906+293_906+305del others(13): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149813 | |||||||
| chr21:46149938 | C | CA | 6 | a0001c0001t0002g0047 a0001c0002t0001g0055 a0001c0002t0001g0065 others(3): Show |
6 | HG01261.hp2 HG02027.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+180dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149938 | |||||||
| chr21:46150104 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0006g0123 a0001c0002t0006g0124 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+15C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46150104 | |||||||
| chr21:46150106 | C | T | 1 | a0002c0005t0001g0013 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.906+13G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46150106 | |||||||
| chr21:46150270 | G | A | 1 | a0001c0002t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.775-20C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150270 | |||||||
| chr21:46150272 | C | T | 2 | a0001c0002t0002g0197 a0001c0002t0002g0198 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.775-22G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150272 | |||||||
| chr21:46150273 | A | AC | 5 | a0001c0001t0002g0049 a0001c0001t0003g0092 a0001c0002t0001g0185 others(2): Show |
5 | HG00280.hp1 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-24dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150273 | |||||||
| chr21:46150352 | G | A | 22 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0107 others(19): Show |
24 | HG00438.hp2 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.774+36C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150352 | |||||||
| chr21:46150553 | G | T | 1 | a0002c0004t0005g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.637-28C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150553 | |||||||
| chr21:46150631 | G | A | 1 | a0001c0001t0009g0048 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.637-106C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150631 | |||||||
| chr21:46150638 | G | C | 13 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0002t0001g0179 others(10): Show |
13 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.637-113C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150638 | |||||||
| chr21:46150718 | G | A | 1 | a0001c0002t0009g0094 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.637-193C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150718 | |||||||
| chr21:46150738 | A | G | 62 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0122 others(59): Show |
64 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.637-213T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150738 | |||||||
| chr21:46150751 | C | CCCG | 11 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0122 others(8): Show |
11 | HG01109.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-229_637-227dup others(3): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150751 | |||||||
| chr21:46150856 | T | TC | 4 | a0001c0001t0002g0012 a0001c0001t0002g0087 a0001c0027t0001g0180 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-332dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150856 | |||||||
| chr21:46150859 | C | A | 1 | a0011c0018t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637-334G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150859 | |||||||
| chr21:46150860 | A | C | 1 | a0011c0018t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637-335T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150860 | |||||||
| chr21:46150927 | G | T | 1 | a0001c0003t0002g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.637-402C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150927 | |||||||
| chr21:46150954 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.637-429G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150954 | |||||||
| chr21:46151060 | G | C | 2 | a0001c0001t0002g0147 a0002c0004t0001g0099 |
2 | HG00438.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.636+498C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151060 | |||||||
| chr21:46151090 | C | T | 1 | a0002c0005t0001g0192 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.636+468G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151090 | |||||||
| chr21:46151248 | G | A | 33 | a0001c0001t0001g0051 a0001c0001t0001g0115 a0001c0001t0001g0116 others(30): Show |
33 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.636+310C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151248 | |||||||
| chr21:46151261 | C | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0107 others(10): Show |
15 | HG00438.hp2 HG00738.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+297G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151261 | |||||||
| chr21:46151262 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0139 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.636+296C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151262 | |||||||
| chr21:46151295 | T | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0107 others(19): Show |
24 | HG00438.hp2 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.636+263A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151295 | |||||||
| chr21:46151307 | G | C | 4 | a0001c0003t0002g0141 a0001c0003t0002g0176 a0001c0010t0001g0178 others(1): Show |
4 | HG00639.hp2 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+251C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151307 | |||||||
| chr21:46151392 | T | TC | 7 | a0001c0001t0002g0052 a0001c0002t0001g0054 a0001c0002t0001g0056 others(4): Show |
7 | HG00642.hp1 HG01978.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.636+165dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151392 | |||||||
| chr21:46151454 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.636+104C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151454 | |||||||
| chr21:46151475 | G | A | 1 | a0001c0002t0007g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.636+83C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151475 | |||||||
| chr21:46151508 | C | G | 6 | a0001c0002t0001g0179 a0001c0002t0001g0183 a0001c0002t0001g0185 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+50G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151508 | |||||||
| chr21:46151515 | G | A | 37 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(34): Show |
38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.636+43C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151515 | |||||||
| chr21:46151753 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.457-16G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/13 | chr21 | 46151753 | |||||||
| chr21:46151787 | G | GC | 6 | a0001c0001t0002g0087 a0001c0001t0002g0091 a0001c0001t0003g0070 others(3): Show |
6 | HG00438.hp1 HG00642.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-51dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/13 | chr21 | 46151787 | |||||||
| chr21:46151871 | G | A | 5 | a0001c0002t0001g0179 a0001c0002t0001g0185 a0001c0002t0001g0186 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+21C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/13 | chr21 | 46151871 | |||||||
| chr21:46151997 | C | T | 1 | a0001c0001t0002g0002 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.368-17G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46151997 | |||||||
| chr21:46152013 | G | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.368-33C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152013 | |||||||
| chr21:46152029 | C | G | 1 | a0002c0005t0001g0013 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.368-49G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152029 | |||||||
| chr21:46152068 | G | GTCCCCCC others(8): Show |
1 | a0001c0001t0003g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.368-89_368-88insGT others(13): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152068 | |||||||
| chr21:46152119 | T | G | 7 | a0001c0001t0002g0121 a0001c0001t0002g0139 a0001c0002t0002g0140 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-139A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152119 | |||||||
| chr21:46152330 | G | A | 210 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.368-350C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152330 | |||||||
| chr21:46152342 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.368-362C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152342 | |||||||
| chr21:46152349 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.368-369G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152349 | |||||||
| chr21:46152382 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0087 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-402C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152382 | |||||||
| chr21:46152409 | ATGACCGT others(32): Show |
A | 2 | a0001c0003t0001g0163 a0003c0029t0002g0117 |
2 | HG02109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.367+459_368-430del others(39): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152409 | |||||||
| chr21:46152480 | C | T | 1 | a0001c0026t0001g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367+427G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152480 | |||||||
| chr21:46152486 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.367+421G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152486 | |||||||
| chr21:46152531 | C | T | 1 | a0001c0026t0001g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367+376G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152531 | |||||||
| chr21:46152755 | T | C | 1 | a0004c0007t0007g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.367+152A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152755 | |||||||
| chr21:46152879 | A | G | 4 | a0001c0003t0002g0176 a0001c0010t0001g0178 a0003c0013t0002g0009 others(1): Show |
4 | HG00639.hp2 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+28T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152879 | |||||||
| chr21:46153048 | G | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0188 a0001c0002t0001g0142 others(1): Show |
5 | HG02280.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-13C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153048 | |||||||
| chr21:46153104 | C | T | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0003c0013t0002g0009 |
3 | HG02451.hp2 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.239-69G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153104 | |||||||
| chr21:46153176 | A | G | 203 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(200): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.239-141T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153176 | |||||||
| chr21:46153209 | T | C | 7 | a0001c0001t0002g0188 a0001c0002t0001g0142 a0001c0002t0002g0198 others(4): Show |
7 | HG00639.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-174A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153209 | |||||||
| chr21:46153314 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.239-279G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153314 | |||||||
| chr21:46153315 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.239-280C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153315 | |||||||
| chr21:46153374 | T | G | 22 | a0001c0001t0002g0003 a0001c0001t0002g0139 a0001c0001t0002g0188 others(19): Show |
23 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.239-339A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153374 | |||||||
| chr21:46153424 | G | C | 29 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0122 others(26): Show |
30 | HG01109.hp2 HG01167.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.239-389C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153424 | |||||||
| chr21:46153526 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0006g0123 a0001c0002t0001g0125 others(3): Show |
6 | HG01258.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-491C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153526 | |||||||
| chr21:46153545 | G | A | 1 | a0001c0001t0008g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.239-510C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153545 | |||||||
| chr21:46153555 | G | A | 111 | a0001c0001t0001g0076 a0001c0001t0001g0084 a0001c0001t0001g0096 others(108): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.239-520C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153555 | |||||||
| chr21:46153596 | A | AC | 4 | a0001c0001t0002g0119 a0001c0001t0003g0092 a0001c0002t0001g0179 others(1): Show |
4 | HG02027.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+552dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153596 | |||||||
| chr21:46153636 | A | G | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(144): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.238+513T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153636 | |||||||
| chr21:46153782 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(87): Show |
97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.238+367G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153782 | |||||||
| chr21:46153784 | A | G | 8 | a0001c0001t0001g0084 a0001c0001t0003g0070 a0001c0001t0006g0082 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.238+365T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153784 | |||||||
| chr21:46153793 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.238+356A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153793 | |||||||
| chr21:46153795 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.238+354G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153795 | |||||||
| chr21:46153930 | G | A | 20 | a0001c0001t0002g0003 a0001c0001t0002g0128 a0001c0001t0002g0139 others(17): Show |
21 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.238+219C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153930 | |||||||
| chr21:46153941 | G | A | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | HG01884.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.238+208C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153941 | |||||||
| chr21:46153949 | C | G | 3 | a0001c0001t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 |
3 | HG01167.hp1 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.238+200G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153949 | |||||||
| chr21:46153973 | A | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(179): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.238+176T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153973 | |||||||
| chr21:46154392 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-60G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154392 | |||||||
| chr21:46154393 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-61A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154393 | |||||||
| chr21:46154407 | A | G | 3 | a0002c0004t0003g0068 a0002c0005t0001g0066 a0002c0005t0001g0067 |
3 | HG00558.hp2 NA18945.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.55-75T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154407 | |||||||
| chr21:46154411 | C | T | 3 | a0001c0001t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 |
3 | HG01167.hp1 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.55-79G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154411 | |||||||
| chr21:46154501 | G | GC | 5 | a0001c0001t0005g0217 a0001c0001t0008g0216 a0001c0002t0001g0190 others(2): Show |
5 | HG00423.hp2 HG02257.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-170dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154501 | |||||||
| chr21:46154512 | A | C | 1 | a0001c0001t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-180T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154512 | |||||||
| chr21:46154538 | A | AG | 47 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0051 others(44): Show |
51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.55-207dupC | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154538 | |||||||
| chr21:46154549 | A | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.55-217T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154549 | |||||||
| chr21:46154593 | C | T | 3 | a0001c0001t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 |
3 | HG01167.hp1 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.55-261G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154593 | |||||||
| chr21:46154594 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.55-262C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154594 | |||||||
| chr21:46154625 | C | T | 1 | a0002c0005t0001g0013 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.55-293G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154625 | |||||||
| chr21:46154657 | C | T | 3 | a0001c0001t0002g0081 a0001c0001t0006g0082 a0001c0001t0006g0083 |
3 | HG02897.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.55-325G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154657 | |||||||
| chr21:46154679 | A | AC | 7 | a0001c0001t0002g0012 a0001c0001t0003g0025 a0001c0002t0001g0165 others(4): Show |
7 | HG01261.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-348dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154679 | |||||||
| chr21:46154858 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55-526G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154858 | |||||||
| chr21:46154885 | G | C | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(162): Show |
174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.55-553C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154885 | |||||||
| chr21:46154922 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0152 others(19): Show |
25 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.54+548C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154922 | |||||||
| chr21:46155046 | G | A | 67 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0051 others(64): Show |
71 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.54+424C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155046 | |||||||
| chr21:46155115 | G | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(162): Show |
174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.54+355C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155115 | |||||||
| chr21:46155284 | C | T | 1 | a0002c0008t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.54+186G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155284 | |||||||
| chr21:46155323 | T | C | 8 | a0001c0001t0001g0195 a0001c0002t0001g0193 a0001c0002t0001g0194 others(5): Show |
8 | HG01069.hp1 HG01361.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+147A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155323 | |||||||
| chr21:46155346 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54+124C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155346 | |||||||
| chr21:46155373 | C | T | 1 | a0001c0001t0003g0010 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.54+97G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155373 | |||||||
| chr21:46155458 | C | T | 76 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0051 others(73): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.54+12G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155458 |