| geneid | 2175 |
|---|---|
| ensemblid | ENSG00000187741.16 |
| hgncid | 3582 |
| symbol | FANCA |
| name | FA complementation group A |
| refseq_nuc | NM_000135.4 |
| refseq_prot | NP_000126.2 |
| ensembl_nuc | ENST00000389301.8 |
| ensembl_prot | ENSP00000373952.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89737549 |
| end | 89816647 |
| strand | - |
| ver | v1.2 |
| region | chr16:89737549-89816647 |
| region5000 | chr16:89732549-89821647 |
| regionname0 | FANCA_chr16_89737549_89816647 |
| regionname5000 | FANCA_chr16_89732549_89821647 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1455 | 99 | 27 | 17 | 44 | 2 | 9 | 33 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002 | 0/1 | 1455 | 74 | 14 | 10 | 31 | 2 | 16 | 22 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0003 | 0/0 | 1455 | 32 | 9 | 11 | 2 | 2 | 8 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0004 | 1/0 | 1455 | 28 | 3 | 18 | 0 | 3 | 3 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0005 | 0/0 | 1455 | 21 | 0 | 0 | 19 | 0 | 2 | 10 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006 | 0/0 | 1455 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0007 | 0/0 | 1455 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0008 | 0/0 | 1455 | 7 | 0 | 1 | 5 | 1 | 0 | 4 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0009 | 0/0 | 1455 | 6 | 0 | 3 | 0 | 2 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0010 | 0/0 | 1455 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0011 | 0/0 | 1455 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0012 | 0/0 | 1455 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0013 | 0/0 | 1455 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0014 | 0/0 | 1455 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0015 | 0/0 | 1455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0016 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0017 | 0/0 | 1455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0018 | 0/0 | 1455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0019 | 0/0 | 1455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0020 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0021 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0022 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0023 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0024 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0025 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0026 | 0/0 | 1455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0027 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0028 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0029 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0030 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0031 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0032 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0033 | 0/0 | 524 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0034 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0035 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0036 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0037 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0038 | 0/0 | 1455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0039 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0040 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0041 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4368 | 93 | 25 | 17 | 42 | 2 | 7 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0002 | 0/1 | 4368 | 56 | 9 | 9 | 26 | 2 | 9 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0003 | 0/0 | 4368 | 31 | 9 | 10 | 2 | 2 | 8 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0004 | 1/0 | 4368 | 28 | 3 | 18 | 0 | 3 | 3 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0005 | 0/0 | 4368 | 21 | 0 | 0 | 19 | 0 | 2 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0006 | 0/0 | 4368 | 13 | 1 | 1 | 5 | 0 | 6 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0007 | 0/0 | 4368 | 10 | 8 | 2 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0008 | 0/0 | 4368 | 7 | 0 | 1 | 5 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0009 | 0/0 | 4368 | 7 | 7 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0010 | 0/0 | 4368 | 6 | 0 | 3 | 0 | 2 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0011 | 0/0 | 4368 | 4 | 0 | 2 | 0 | 1 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0012 | 0/0 | 4368 | 3 | 0 | 3 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0013 | 0/0 | 4368 | 3 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0014 | 0/0 | 4368 | 3 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0015 | 0/0 | 4368 | 2 | 0 | 1 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0016 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0017 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0018 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0019 | 0/0 | 4368 | 2 | 0 | 0 | 2 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0020 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0021 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0022 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0023 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0024 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0025 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0026 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0027 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0028 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0029 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0030 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0031 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0032 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0033 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0034 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0035 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0036 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0037 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0038 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0039 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0040 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0041 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0042 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0043 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0044 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0045 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0046 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0047 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0048 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0049 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0050 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0051 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0052 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0053 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0054 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0055 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0056 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| c0057 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1084 | 192 | 51 | 29 | 88 | 4 | 19 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0002 | 1/0 | 1085 | 81 | 16 | 37 | 3 | 9 | 15 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0003 | 0/0 | 1084 | 15 | 0 | 0 | 14 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0004 | 0/0 | 1084 | 10 | 9 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0005 | 0/0 | 1084 | 7 | 0 | 0 | 0 | 0 | 7 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0006 | 0/0 | 1084 | 6 | 6 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0007 | 0/0 | 1084 | 5 | 5 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0008 | 0/0 | 1084 | 5 | 0 | 0 | 5 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0009 | 0/0 | 1084 | 3 | 2 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0010 | 0/0 | 1084 | 3 | 0 | 0 | 0 | 0 | 3 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0011 | 0/0 | 1084 | 2 | 1 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0012 | 0/0 | 1084 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0013 | 0/0 | 1085 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0014 | 0/0 | 1084 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0015 | 0/0 | 1084 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| t0016 | 0/0 | 1084 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4368 | 93 | 25 | 17 | 42 | 2 | 7 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0026 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0029 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0030 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0033 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0034 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0052 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0002 | 0/1 | 4368 | 56 | 9 | 9 | 26 | 2 | 9 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0006 | 0/0 | 4368 | 13 | 1 | 1 | 5 | 0 | 6 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0035 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0038 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0041 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0047 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0051 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0003c0003 | 0/0 | 4368 | 31 | 9 | 10 | 2 | 2 | 8 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0003c0022 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0004c0004 | 1/0 | 4368 | 28 | 3 | 18 | 0 | 3 | 3 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0005c0005 | 0/0 | 4368 | 21 | 0 | 0 | 19 | 0 | 2 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0007 | 0/0 | 4368 | 10 | 8 | 2 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0055 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0056 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0007c0009 | 0/0 | 4368 | 7 | 7 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0007c0057 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0008c0008 | 0/0 | 4368 | 7 | 0 | 1 | 5 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0009c0010 | 0/0 | 4368 | 6 | 0 | 3 | 0 | 2 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0010c0011 | 0/0 | 4368 | 4 | 0 | 2 | 0 | 1 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0011c0012 | 0/0 | 4368 | 3 | 0 | 3 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0012c0013 | 0/0 | 4368 | 3 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0013c0014 | 0/0 | 4368 | 3 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0014c0015 | 0/0 | 4368 | 2 | 0 | 1 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0015c0020 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0016c0019 | 0/0 | 4368 | 2 | 0 | 0 | 2 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0017c0018 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0018c0017 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0019c0016 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0020c0021 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0021c0053 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0022c0054 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0023c0042 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0024c0040 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0025c0039 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0026c0036 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0027c0037 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0028c0043 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0029c0028 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0030c0027 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0031c0031 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0032c0032 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0033c0025 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0034c0046 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0035c0044 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0036c0045 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0037c0048 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0038c0023 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0039c0024 | 0/0 | 4368 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0040c0050 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0041c0049 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5451 | 68 | 20 | 16 | 27 | 1 | 4 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0001t0002 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0001t0003 | 0/0 | 5451 | 14 | 0 | 0 | 13 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0001t0006 | 0/0 | 5451 | 5 | 5 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0001t0010 | 0/0 | 5451 | 3 | 0 | 0 | 0 | 0 | 3 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0001t0012 | 0/0 | 5451 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0001t0016 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0026t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0029t0005 | 0/0 | 5451 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0030t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0033t0006 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0034t0001 | 0/0 | 5451 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0001c0052t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0002t0001 | 0/1 | 5451 | 56 | 9 | 9 | 26 | 2 | 9 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0006t0005 | 0/0 | 5451 | 6 | 0 | 0 | 0 | 0 | 6 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0006t0008 | 0/0 | 5451 | 5 | 0 | 0 | 5 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0006t0011 | 0/0 | 5451 | 2 | 1 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0035t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0038t0001 | 0/0 | 5451 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0041t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0047t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0002c0051t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0003c0003t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0003c0003t0002 | 0/0 | 5452 | 30 | 8 | 10 | 2 | 2 | 8 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0003c0022t0002 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0004c0004t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0004c0004t0002 | 1/0 | 5452 | 27 | 2 | 18 | 0 | 3 | 3 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0005c0005t0001 | 0/0 | 5451 | 20 | 0 | 0 | 18 | 0 | 2 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0005c0005t0014 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0007t0004 | 0/0 | 5451 | 8 | 7 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0007t0009 | 0/0 | 5451 | 2 | 1 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0055t0009 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0006c0056t0004 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0007c0009t0001 | 0/0 | 5451 | 7 | 7 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0007c0057t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0008c0008t0001 | 0/0 | 5451 | 7 | 0 | 1 | 5 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0009c0010t0002 | 0/0 | 5452 | 6 | 0 | 3 | 0 | 2 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0010c0011t0002 | 0/0 | 5452 | 4 | 0 | 2 | 0 | 1 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0011c0012t0001 | 0/0 | 5451 | 3 | 0 | 3 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0012c0013t0007 | 0/0 | 5451 | 3 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0013c0014t0002 | 0/0 | 5452 | 3 | 3 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0014c0015t0002 | 0/0 | 5452 | 2 | 0 | 1 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0015c0020t0001 | 0/0 | 5451 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0016c0019t0001 | 0/0 | 5451 | 2 | 0 | 0 | 2 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0017c0018t0002 | 0/0 | 5452 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0018c0017t0001 | 0/0 | 5451 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0019c0016t0007 | 0/0 | 5451 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0020c0021t0002 | 0/0 | 5452 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0021c0053t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0022c0054t0002 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0023c0042t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0024c0040t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0025c0039t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0026c0036t0002 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0027c0037t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0028c0043t0015 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0029c0028t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0030c0027t0001 | 0/0 | 5451 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0031c0031t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0032c0032t0001 | 0/0 | 5451 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0033c0025t0003 | 0/0 | 5450 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0034c0046t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0035c0044t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0036c0045t0001 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0037c0048t0001 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0038c0023t0002 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0039c0024t0002 | 0/0 | 5452 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0040c0050t0013 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| a0041c0049t0004 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | copy fasta | chr16 | 89732549 | 89821647 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0010g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0001t0016g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0026t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0029t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0030t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0033t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0034t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0001c0052t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0008g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0008g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0006t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0035t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0038t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0041t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0047t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0002c0051t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0003c0022t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0004c0004t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0005c0005t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0009g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0007t0009g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0055t0009g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0006c0056t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0009t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0007c0057t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0008c0008t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0009c0010t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0009c0010t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0009c0010t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0009c0010t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0009c0010t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0009c0010t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0010c0011t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0010c0011t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0010c0011t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0010c0011t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0011c0012t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0011c0012t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0011c0012t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0012c0013t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0012c0013t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0012c0013t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0013c0014t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0013c0014t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0013c0014t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0014c0015t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0014c0015t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0015c0020t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0016c0019t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0016c0019t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0017c0018t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0017c0018t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0018c0017t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0018c0017t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0019c0016t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0019c0016t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0020c0021t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0021c0053t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0022c0054t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0023c0042t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0024c0040t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0025c0039t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0026c0036t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0027c0037t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0028c0043t0015g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0029c0028t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0030c0027t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0031c0031t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0032c0032t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0033c0025t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0034c0046t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0035c0044t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0036c0045t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0037c0048t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0038c0023t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0039c0024t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0040c0050t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| a0041c0049t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0010 | t0002 | g0299 | EUR | GBR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00140 | hp1 | a0004 | c0004 | t0002 | g0269 | EUR | GBR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0274 | EUR | GBR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0029 | EUR | FIN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00280 | hp2 | a0003 | c0003 | t0002 | g0238 | EUR | FIN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00323 | hp1 | a0014 | c0015 | t0002 | g0011 | EUR | FIN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00323 | hp2 | a0008 | c0008 | t0001 | g0016 | EUR | FIN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00438 | hp1 | a0005 | c0005 | t0001 | g0064 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00558 | hp1 | a0035 | c0044 | t0001 | g0155 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00597 | hp2 | a0005 | c0005 | t0001 | g0194 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00621 | hp1 | a0005 | c0005 | t0001 | g0036 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0290 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00639 | hp2 | a0004 | c0004 | t0002 | g0243 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0261 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00642 | hp2 | a0004 | c0004 | t0002 | g0265 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00673 | hp1 | a0025 | c0039 | t0001 | g0184 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00733 | hp1 | a0004 | c0004 | t0002 | g0279 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00733 | hp2 | a0010 | c0011 | t0002 | g0005 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00735 | hp1 | a0009 | c0010 | t0002 | g0289 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00735 | hp2 | a0004 | c0004 | t0002 | g0266 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00738 | hp1 | a0004 | c0004 | t0002 | g0273 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00738 | hp2 | a0004 | c0004 | t0002 | g0254 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00741 | hp1 | a0004 | c0004 | t0002 | g0237 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG00741 | hp2 | a0003 | c0022 | t0002 | g0295 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01069 | hp1 | a0004 | c0004 | t0002 | g0249 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01070 | hp1 | a0004 | c0004 | t0002 | g0247 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01074 | hp1 | a0004 | c0004 | t0002 | g0258 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0260 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01081 | hp2 | a0004 | c0004 | t0002 | g0304 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01099 | hp1 | a0004 | c0004 | t0002 | g0251 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01099 | hp2 | a0010 | c0011 | t0002 | g0010 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01106 | hp1 | a0004 | c0004 | t0002 | g0230 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01109 | hp1 | a0006 | c0007 | t0009 | g0308 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01109 | hp2 | a0009 | c0010 | t0002 | g0287 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01167 | hp1 | a0002 | c0006 | t0011 | g0227 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0294 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01168 | hp1 | a0004 | c0004 | t0002 | g0232 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0293 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01175 | hp1 | a0004 | c0004 | t0002 | g0233 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01175 | hp2 | a0008 | c0008 | t0001 | g0021 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01192 | hp1 | a0006 | c0007 | t0004 | g0313 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0302 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01243 | hp2 | a0011 | c0012 | t0001 | g0006 | AMR | PUR | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01255 | hp2 | a0004 | c0004 | t0002 | g0264 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01261 | hp2 | a0026 | c0036 | t0002 | g0234 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01358 | hp2 | a0009 | c0010 | t0002 | g0288 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01361 | hp2 | a0004 | c0004 | t0002 | g0250 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0061 | EUR | IBS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01516 | hp2 | a0009 | c0010 | t0002 | g0296 | EUR | IBS | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01884 | hp1 | a0004 | c0004 | t0001 | g0231 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01891 | hp1 | a0012 | c0013 | t0007 | g0079 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01928 | hp1 | a0001 | c0001 | t0012 | g0125 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01934 | hp2 | a0003 | c0003 | t0002 | g0259 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0263 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01978 | hp2 | a0004 | c0004 | t0002 | g0300 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01993 | hp2 | a0038 | c0023 | t0002 | g0297 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02015 | hp1 | a0005 | c0005 | t0001 | g0187 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02027 | hp1 | a0001 | c0052 | t0001 | g0211 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02040 | hp1 | a0016 | c0019 | t0001 | g0108 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02040 | hp2 | a0029 | c0028 | t0001 | g0096 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02056 | hp1 | a0005 | c0005 | t0001 | g0190 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02056 | hp2 | a0023 | c0042 | t0001 | g0041 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02071 | hp2 | a0003 | c0003 | t0002 | g0285 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02074 | hp1 | a0005 | c0005 | t0014 | g0196 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02074 | hp2 | a0031 | c0031 | t0001 | g0055 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02080 | hp2 | a0036 | c0045 | t0001 | g0185 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02135 | hp1 | a0005 | c0005 | t0001 | g0197 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02145 | hp2 | a0006 | c0007 | t0004 | g0316 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02148 | hp1 | a0011 | c0012 | t0001 | g0003 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | CDX | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02165 | hp2 | a0008 | c0008 | t0001 | g0018 | EAS | CDX | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02257 | hp1 | a0003 | c0003 | t0002 | g0255 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02257 | hp2 | a0027 | c0037 | t0001 | g0301 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02258 | hp2 | a0007 | c0009 | t0001 | g0322 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02280 | hp1 | a0006 | c0007 | t0009 | g0314 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02280 | hp2 | a0007 | c0009 | t0001 | g0324 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02293 | hp1 | a0011 | c0012 | t0001 | g0007 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02300 | hp2 | a0014 | c0015 | t0002 | g0008 | AMR | PEL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02451 | hp1 | a0040 | c0050 | t0013 | g0206 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02523 | hp2 | a0005 | c0005 | t0001 | g0191 | EAS | KHV | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02572 | hp2 | a0041 | c0049 | t0004 | g0207 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02602 | hp1 | a0003 | c0003 | t0002 | g0284 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02615 | hp1 | a0002 | c0035 | t0001 | g0110 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02615 | hp2 | a0006 | c0007 | t0004 | g0317 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02630 | hp2 | a0022 | c0054 | t0002 | g0312 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02647 | hp2 | a0003 | c0003 | t0002 | g0242 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02698 | hp1 | a0039 | c0024 | t0002 | g0278 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0286 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02723 | hp1 | a0019 | c0016 | t0007 | g0276 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02723 | hp2 | a0006 | c0056 | t0004 | g0320 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02735 | hp2 | a0001 | c0034 | t0001 | g0104 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0178 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02738 | hp2 | a0003 | c0003 | t0002 | g0282 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02809 | hp2 | a0007 | c0057 | t0001 | g0328 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02818 | hp1 | a0006 | c0007 | t0004 | g0318 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02818 | hp2 | a0007 | c0009 | t0001 | g0329 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0280 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02895 | hp2 | a0001 | c0026 | t0001 | g0023 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02896 | hp1 | a0007 | c0009 | t0001 | g0327 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02896 | hp2 | a0017 | c0018 | t0002 | g0305 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0270 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02897 | hp2 | a0017 | c0018 | t0002 | g0306 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02965 | hp1 | a0018 | c0017 | t0001 | g0277 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02965 | hp2 | a0019 | c0016 | t0007 | g0291 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02970 | hp2 | a0002 | c0047 | t0001 | g0082 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0168 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03017 | hp2 | a0001 | c0001 | t0010 | g0035 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03041 | hp2 | a0002 | c0006 | t0011 | g0228 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03098 | hp2 | a0006 | c0007 | t0004 | g0310 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03130 | hp2 | a0006 | c0007 | t0004 | g0311 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03139 | hp1 | a0028 | c0043 | t0015 | g0307 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03195 | hp1 | a0015 | c0020 | t0001 | g0002 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03195 | hp2 | a0006 | c0007 | t0004 | g0319 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03209 | hp1 | a0037 | c0048 | t0001 | g0093 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03225 | hp2 | a0001 | c0033 | t0006 | g0171 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03239 | hp2 | a0002 | c0006 | t0005 | g0219 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03486 | hp1 | a0003 | c0003 | t0002 | g0281 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03491 | hp2 | a0005 | c0005 | t0001 | g0181 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03492 | hp2 | a0005 | c0005 | t0001 | g0192 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03516 | hp1 | a0012 | c0013 | t0007 | g0081 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03516 | hp2 | a0018 | c0017 | t0001 | g0244 | AFR | ESN | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03540 | hp1 | a0002 | c0041 | t0001 | g0221 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03579 | hp1 | a0007 | c0009 | t0001 | g0325 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0013 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03669 | hp1 | a0010 | c0011 | t0002 | g0004 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03669 | hp2 | a0002 | c0006 | t0005 | g0218 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03688 | hp1 | a0003 | c0003 | t0002 | g0292 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03688 | hp2 | a0032 | c0032 | t0001 | g0070 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03704 | hp1 | a0002 | c0006 | t0005 | g0223 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03704 | hp2 | a0004 | c0004 | t0002 | g0252 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0239 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03710 | hp2 | a0002 | c0038 | t0001 | g0077 | SAS | PJL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03831 | hp1 | a0002 | c0006 | t0005 | g0025 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03831 | hp2 | a0004 | c0004 | t0002 | g0256 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03834 | hp1 | a0009 | c0010 | t0002 | g0298 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03834 | hp2 | a0004 | c0004 | t0002 | g0248 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0026 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04115 | hp1 | a0002 | c0006 | t0005 | g0217 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04115 | hp2 | a0030 | c0027 | t0001 | g0200 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04184 | hp1 | a0003 | c0003 | t0002 | g0272 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0283 | SAS | BEB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0275 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04204 | hp2 | a0002 | c0006 | t0005 | g0229 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04228 | hp1 | a0020 | c0021 | t0002 | g0012 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | STU | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18522 | hp1 | a0007 | c0009 | t0001 | g0323 | AFR | YRI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18522 | hp2 | a0012 | c0013 | t0007 | g0095 | AFR | YRI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18612 | hp2 | a0005 | c0005 | t0001 | g0182 | EAS | CHB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18906 | hp1 | a0003 | c0003 | t0002 | g0267 | AFR | YRI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18906 | hp2 | a0015 | c0020 | t0001 | g0002 | AFR | YRI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18939 | hp1 | a0002 | c0006 | t0008 | g0224 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18940 | hp2 | a0005 | c0005 | t0001 | g0188 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18947 | hp1 | a0008 | c0008 | t0001 | g0020 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18950 | hp1 | a0033 | c0025 | t0003 | g0180 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18950 | hp2 | a0008 | c0008 | t0001 | g0015 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18951 | hp2 | a0002 | c0006 | t0008 | g0226 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18952 | hp1 | a0005 | c0005 | t0001 | g0066 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18952 | hp2 | a0001 | c0001 | t0016 | g0134 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18954 | hp1 | a0005 | c0005 | t0001 | g0195 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18967 | hp1 | a0001 | c0030 | t0001 | g0130 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18967 | hp2 | a0034 | c0046 | t0001 | g0094 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18968 | hp1 | a0005 | c0005 | t0001 | g0189 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18979 | hp2 | a0002 | c0006 | t0008 | g0220 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18984 | hp2 | a0008 | c0008 | t0001 | g0019 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0271 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18990 | hp2 | a0005 | c0005 | t0001 | g0065 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18994 | hp2 | a0005 | c0005 | t0001 | g0068 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19001 | hp2 | a0002 | c0006 | t0008 | g0215 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19002 | hp1 | a0008 | c0008 | t0001 | g0167 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19003 | hp2 | a0024 | c0040 | t0001 | g0017 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19030 | hp2 | a0002 | c0051 | t0001 | g0032 | AFR | LWK | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19043 | hp2 | a0003 | c0003 | t0002 | g0257 | AFR | LWK | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19057 | hp2 | a0002 | c0006 | t0008 | g0225 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19062 | hp2 | a0005 | c0005 | t0001 | g0067 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19070 | hp1 | a0005 | c0005 | t0001 | g0183 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19074 | hp1 | a0005 | c0005 | t0001 | g0186 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19087 | hp1 | a0016 | c0019 | t0001 | g0156 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | YRI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA19240 | hp2 | a0021 | c0053 | t0001 | g0321 | AFR | YRI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20129 | hp1 | a0013 | c0014 | t0002 | g0331 | AFR | ASW | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | ASW | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0151 | EUR | TSI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20752 | hp2 | a0004 | c0004 | t0002 | g0253 | EUR | TSI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20805 | hp1 | a0010 | c0011 | t0002 | g0009 | EUR | TSI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20805 | hp2 | a0004 | c0004 | t0002 | g0245 | EUR | TSI | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | GIH | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20905 | hp2 | a0001 | c0029 | t0005 | g0103 | SAS | GIH | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0262 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0240 | AMR | CLM | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02109 | hp1 | a0013 | c0014 | t0002 | g0330 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02486 | hp1 | a0004 | c0004 | t0002 | g0236 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02559 | hp1 | a0006 | c0007 | t0004 | g0315 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0303 | AFR | ACB | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03471 | hp1 | a0013 | c0014 | t0002 | g0332 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG06807 | hp1 | a0003 | c0003 | t0002 | g0268 | AFR | USA | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| HG06807 | hp2 | a0004 | c0004 | t0002 | g0235 | AFR | USA | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18955 | hp1 | a0005 | c0005 | t0001 | g0198 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | USA | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA21309 | hp1 | a0007 | c0009 | t0001 | g0326 | AFR | LWK | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| NA21309 | hp2 | a0006 | c0055 | t0009 | g0309 | AFR | LWK | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0089 | REF | REF | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| homoSapiens_grch38 | hp1 | a0004 | c0004 | t0002 | g0246 | REF | REF | FANCA_chr16_89732549_89821647 | FANCA | chr16 | 89732549 | 89821647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89738666
|
C | T | 1 | a0041 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.4303G>A | p.Ala1435Thr | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 4335/5452 | 4303/4368 | 1435/1455 | chr16 | 89738666 | ||
| chr16:89738910
|
G | A | 1 | a0034 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.4232C>T | p.Pro1411Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 42/43 | 4264/5452 | 4232/4368 | 1411/1455 | chr16 | 89738910 | ||
| chr16:89738917
|
G | A | 1 | a0031 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.4225C>T | p.Arg1409Trp | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 42/43 | 4257/5452 | 4225/4368 | 1409/1455 | chr16 | 89738917 | ||
| chr16:89739236
|
T | A | 1 | a0038 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.4064A>T | p.His1355Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 41/43 | 4096/5452 | 4064/4368 | 1355/1455 | chr16 | 89739236 | ||
| chr16:89739264
|
C | T | 2 | a0030a0032 | 2 | HG03688.hp2 HG04115.hp2 |
missense_variant | MODERATE | c.4036G>A | p.Ala1346Thr | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 41/43 | 4068/5452 | 4036/4368 | 1346/1455 | chr16 | 89739264 | ||
| chr16:89739506
|
T | C | 7 | a0005a0008a0016others(4): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
missense_variant | MODERATE | c.3982A>G | p.Thr1328Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 40/43 | 4014/5452 | 3982/4368 | 1328/1455 | chr16 | 89739506 | ||
| chr16:89740069
|
C | T | 2 | a0012a0019 | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.3859G>A | p.Val1287Ile | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/43 | 3891/5452 | 3859/4368 | 1287/1455 | chr16 | 89740069 | ||
| chr16:89742831
|
T | C | 1 | a0020 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.3734A>G | p.Gln1245Arg | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/43 | 3766/5452 | 3734/4368 | 1245/1455 | chr16 | 89742831 | ||
| chr16:89742869
|
A | C | 1 | a0036 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.3696T>G | p.Phe1232Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/43 | 3728/5452 | 3696/4368 | 1232/1455 | chr16 | 89742869 | ||
| chr16:89745001
|
C | T | 1 | a0028 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.3584G>A | p.Arg1195Gln | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/43 | 3616/5452 | 3584/4368 | 1195/1455 | chr16 | 89745001 | ||
| chr16:89748744
|
G | A | 2 | a0008a0024 | 8 | HG00323.hp2 HG01175.hp2 HG02165.hp2 others(5): Show |
missense_variant | MODERATE | c.3263C>T | p.Ser1088Phe | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/43 | 3295/5452 | 3263/4368 | 1088/1455 | chr16 | 89748744 | ||
| chr16:89748766
|
T | C | 1 | a0027 | 1 | HG02257.hp2 | missense_variant&splice_region_variant | MODERATE | c.3241A>G | p.Ile1081Val | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/43 | 3273/5452 | 3241/4368 | 1081/1455 | chr16 | 89748766 | ||
| chr16:89749892
|
G | A | 1 | a0031 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.3077C>T | p.Ala1026Val | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/43 | 3109/5452 | 3077/4368 | 1026/1455 | chr16 | 89749892 | ||
| chr16:89758581
|
G | T | 1 | a0028 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2977C>A | p.Gln993Lys | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/43 | 3009/5452 | 2977/4368 | 993/1455 | chr16 | 89758581 | ||
| chr16:89758699
|
G | C | 1 | a0039 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2859C>G | p.Asp953Glu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/43 | 2891/5452 | 2859/4368 | 953/1455 | chr16 | 89758699 | ||
| chr16:89767168
|
G | C | 2 | a0014a0020 | 3 | HG00323.hp1 HG02300.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.2574C>G | p.Ser858Arg | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/43 | 2606/5452 | 2574/4368 | 858/1455 | chr16 | 89767168 | ||
| chr16:89769915
|
C | T | 25 | a0001a0002a0005others(22): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
missense_variant | MODERATE | c.2426G>A | p.Gly809Asp | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/43 | 2458/5452 | 2426/4368 | 809/1455 | chr16 | 89769915 | ||
| chr16:89770570
|
G | A | 1 | a0040 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.2216C>T | p.Pro739Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/43 | 2248/5452 | 2216/4368 | 739/1455 | chr16 | 89770570 | ||
| chr16:89771678
|
C | A | 1 | a0009 | 6 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.2151G>T | p.Met717Ile | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/43 | 2183/5452 | 2151/4368 | 717/1455 | chr16 | 89771678 | ||
| chr16:89773357
|
G | C | 1 | a0013 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.1928C>G | p.Pro643Arg | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/43 | 1960/5452 | 1928/4368 | 643/1455 | chr16 | 89773357 | ||
| chr16:89773358
|
G | C | 8 | a0005a0008a0016others(5): Show | 35 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
missense_variant | MODERATE | c.1927C>G | p.Pro643Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/43 | 1959/5452 | 1927/4368 | 643/1455 | chr16 | 89773358 | ||
| chr16:89783072
|
C | T | 32 | a0001a0003a0005others(29): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
missense_variant | MODERATE | c.1501G>A | p.Gly501Ser | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 16/43 | 1533/5452 | 1501/4368 | 501/1455 | chr16 | 89783072 | ||
| chr16:89784926
|
G | C | 1 | a0023 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1398C>G | p.Ser466Arg | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/43 | 1430/5452 | 1398/4368 | 466/1455 | chr16 | 89784926 | ||
| chr16:89784963
|
GCCTGTGT others(58): Show |
G | 1 | a0033 | 1 | NA18950.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1360-64_1360delACA others(62): Show |
p.Ala454fs | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/43 | 1392/5452 | 1360/4368 | 454/1455 | chr16 | 89784963 | ||
| chr16:89791527
|
G | A | 5 | a0005a0008a0034others(2): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
missense_variant | MODERATE | c.1235C>T | p.Ala412Val | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/43 | 1267/5452 | 1235/4368 | 412/1455 | chr16 | 89791527 | ||
| chr16:89799202
|
T | C | 1 | a0037 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.857A>G | p.Gln286Arg | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/43 | 889/5452 | 857/4368 | 286/1455 | chr16 | 89799202 | ||
| chr16:89799635
|
T | C | 31 | a0001a0002a0005others(28): Show | 255 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(252): Show |
missense_variant | MODERATE | c.796A>G | p.Thr266Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 9/43 | 828/5452 | 796/4368 | 266/1455 | chr16 | 89799635 | ||
| chr16:89803296
|
T | C | 3 | a0007a0015a0021 | 11 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(8): Show |
missense_variant | MODERATE | c.755A>G | p.Asp252Gly | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/43 | 787/5452 | 755/4368 | 252/1455 | chr16 | 89803296 | ||
| chr16:89803297
|
C | T | 1 | a0015 | 2 | HG03195.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.754G>A | p.Asp252Asn | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/43 | 786/5452 | 754/4368 | 252/1455 | chr16 | 89803297 | ||
| chr16:89805366
|
G | A | 1 | a0040 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.623C>T | p.Ser208Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/43 | 655/5452 | 623/4368 | 208/1455 | chr16 | 89805366 | ||
| chr16:89808348
|
G | A | 6 | a0006a0007a0015others(3): Show | 25 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(22): Show |
missense_variant | MODERATE | c.542C>T | p.Ala181Val | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/43 | 574/5452 | 542/4368 | 181/1455 | chr16 | 89808348 | ||
| chr16:89816592
|
G | C | 5 | a0006a0007a0015others(2): Show | 24 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(21): Show |
missense_variant | MODERATE | c.24C>G | p.Asn8Lys | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/43 | 56/5452 | 24/4368 | 8/1455 | chr16 | 89816592 | ||
| chr16:89816599
|
A | T | 4 | a0010a0011a0014others(1): Show | 10 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(7): Show |
missense_variant | MODERATE | c.17T>A | p.Val6Asp | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/43 | 49/5452 | 17/4368 | 6/1455 | chr16 | 89816599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89740037
|
C | T | 1 | a0007c0057 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.3891G>A | p.Lys1297Lys | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/43 | 3923/5452 | 3891/4368 | 1297/1455 | chr16 | 89740037 | ||
| chr16:89740825
|
C | G | 13 | a0001c0029a0002c0006a0005c0005others(10): Show | 61 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(58): Show |
synonymous_variant | LOW | c.3807G>C | p.Leu1269Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/43 | 3839/5452 | 3807/4368 | 1269/1455 | chr16 | 89740825 | ||
| chr16:89742911
|
T | C | 16 | a0001c0029a0002c0006a0005c0005others(13): Show | 67 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(64): Show |
synonymous_variant | LOW | c.3654A>G | p.Pro1218Pro | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/43 | 3686/5452 | 3654/4368 | 1218/1455 | chr16 | 89742911 | ||
| chr16:89744994
|
C | T | 1 | a0040c0050 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3591G>A | p.Leu1197Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/43 | 3623/5452 | 3591/4368 | 1197/1455 | chr16 | 89744994 | ||
| chr16:89749771
|
A | G | 1 | a0028c0043 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.3198T>C | p.Ala1066Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/43 | 3230/5452 | 3198/4368 | 1066/1455 | chr16 | 89749771 | ||
| chr16:89749855
|
G | A | 1 | a0001c0030 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.3114C>T | p.Leu1038Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/43 | 3146/5452 | 3114/4368 | 1038/1455 | chr16 | 89749855 | ||
| chr16:89749876
|
C | T | 1 | a0001c0034 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.3093G>A | p.Gln1031Gln | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/43 | 3125/5452 | 3093/4368 | 1031/1455 | chr16 | 89749876 | ||
| chr16:89758657
|
G | A | 6 | a0005c0005a0008c0008a0016c0019others(3): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
synonymous_variant | LOW | c.2901C>T | p.Ser967Ser | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/43 | 2933/5452 | 2901/4368 | 967/1455 | chr16 | 89758657 | ||
| chr16:89769950
|
C | T | 1 | a0003c0022 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.2391G>A | p.Ala797Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/43 | 2423/5452 | 2391/4368 | 797/1455 | chr16 | 89769950 | ||
| chr16:89769970
|
G | A | 1 | a0001c0033 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.2371C>T | p.Leu791Leu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/43 | 2403/5452 | 2371/4368 | 791/1455 | chr16 | 89769970 | ||
| chr16:89769977
|
G | A | 2 | a0002c0038a0002c0051 | 2 | HG03710.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.2364C>T | p.Ala788Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/43 | 2396/5452 | 2364/4368 | 788/1455 | chr16 | 89769977 | ||
| chr16:89770016
|
G | A | 1 | a0001c0034 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.2325C>T | p.Ser775Ser | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/43 | 2357/5452 | 2325/4368 | 775/1455 | chr16 | 89770016 | ||
| chr16:89773344
|
C | T | 7 | a0001c0026a0006c0007a0006c0055others(4): Show | 16 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.1941G>A | p.Glu647Glu | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/43 | 1973/5452 | 1941/4368 | 647/1455 | chr16 | 89773344 | ||
| chr16:89778821
|
C | T | 1 | a0002c0035 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1806G>A | p.Ala602Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/43 | 1838/5452 | 1806/4368 | 602/1455 | chr16 | 89778821 | ||
| chr16:89778964
|
G | C | 1 | a0002c0041 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1755C>G | p.Pro585Pro | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 19/43 | 1787/5452 | 1755/4368 | 585/1455 | chr16 | 89778964 | ||
| chr16:89791472
|
C | T | 4 | a0006c0007a0006c0056a0022c0054others(1): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
synonymous_variant | LOW | c.1290G>A | p.Ala430Ala | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/43 | 1322/5452 | 1290/4368 | 430/1455 | chr16 | 89791472 | ||
| chr16:89791535
|
G | A | 1 | a0006c0056 | 1 | HG02723.hp2 | splice_region_variant&synonymous_variant | LOW | c.1227C>T | p.Asp409Asp | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/43 | 1259/5452 | 1227/4368 | 409/1455 | chr16 | 89791535 | ||
| chr16:89792009
|
C | A | 6 | a0005c0005a0008c0008a0028c0043others(3): Show | 32 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
synonymous_variant | LOW | c.1143G>T | p.Thr381Thr | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/43 | 1175/5452 | 1143/4368 | 381/1455 | chr16 | 89792009 | ||
| chr16:89796009
|
C | A | 1 | a0002c0047 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.903G>T | p.Val301Val | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/43 | 935/5452 | 903/4368 | 301/1455 | chr16 | 89796009 | ||
| chr16:89810956
|
G | A | 1 | a0002c0051 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.399C>T | p.His133His | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 4/43 | 431/5452 | 399/4368 | 133/1455 | chr16 | 89810956 | ||
| chr16:89815951
|
T | G | 1 | a0001c0052 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.115A>C | p.Arg39Arg | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/43 | 147/5452 | 115/4368 | 39/1455 | chr16 | 89815951 | ||
| chr16:89816595
|
C | A | 1 | a0013c0014 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.21G>T | p.Pro7Pro | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/43 | 53/5452 | 21/4368 | 7/1455 | chr16 | 89816595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89737590
|
G | A | 2 | a0001c0001t0006a0001c0033t0006 | 6 | HG02451.hp2 HG02976.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1011C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 1011 | chr16 | 89737590 | |||||
| chr16:89737615
|
C | T | 10 | a0001c0029t0005a0002c0006t0005a0002c0006t0008others(7): Show | 28 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*986G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 986 | chr16 | 89737615 | |||||
| chr16:89737664
|
T | A | 1 | a0002c0006t0008 | 5 | NA18939.hp1 NA18951.hp2 NA18979.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 937 | chr16 | 89737664 | |||||
| chr16:89737897
|
G | A | 1 | a0005c0005t0014 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 704 | chr16 | 89737897 | |||||
| chr16:89737921
|
GA | G | 6 | a0006c0007t0004a0006c0007t0009a0006c0055t0009others(3): Show | 14 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*679delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 679 | chr16 | 89737921 | |||||
| chr16:89737922
|
A | C | 4 | a0001c0029t0005a0002c0006t0005a0002c0006t0008others(1): Show | 13 | HG02451.hp1 HG03239.hp2 HG03669.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*679T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 679 | chr16 | 89737922 | |||||
| chr16:89737927
|
CT | C | 45 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(42): Show | 226 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*673delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 673 | chr16 | 89737927 | |||||
| chr16:89737928
|
T | C | 7 | a0006c0007t0004a0006c0007t0009a0006c0055t0009others(4): Show | 15 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*673A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 673 | chr16 | 89737928 | |||||
| chr16:89737928
|
TC | T | 3 | a0001c0029t0005a0002c0006t0005a0002c0006t0008 | 12 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*672delG | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 672 | chr16 | 89737928 | |||||
| chr16:89737931
|
C | A | 3 | a0006c0007t0004a0006c0056t0004a0041c0049t0004 | 10 | HG01192.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 670 | chr16 | 89737931 | |||||
| chr16:89738216
|
G | C | 2 | a0001c0001t0003a0033c0025t0003 | 15 | HG00558.hp2 HG00609.hp1 HG02071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*385C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 385 | chr16 | 89738216 | |||||
| chr16:89738314
|
C | T | 2 | a0012c0013t0007a0019c0016t0007 | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*287G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 287 | chr16 | 89738314 | |||||
| chr16:89738315
|
G | A | 1 | a0001c0001t0010 | 3 | HG02738.hp1 HG03017.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*286C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 286 | chr16 | 89738315 | |||||
| chr16:89738349
|
C | G | 6 | a0006c0007t0004a0006c0007t0009a0006c0055t0009others(3): Show | 14 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 252 | chr16 | 89738349 | |||||
| chr16:89738428
|
C | A | 1 | a0001c0001t0012 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 173 | chr16 | 89738428 | |||||
| chr16:89738429
|
C | T | 1 | a0001c0001t0012 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 172 | chr16 | 89738429 | |||||
| chr16:89738447
|
C | T | 55 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(52): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*154G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 154 | chr16 | 89738447 | |||||
| chr16:89738454
|
G | A | 1 | a0028c0043t0015 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 147 | chr16 | 89738454 | |||||
| chr16:89738498
|
G | C | 1 | a0001c0001t0016 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 43/43 | 103 | chr16 | 89738498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89738741
|
C | T | 1 | a0002c0002t0001g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4261-33G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 42/42 | chr16 | 89738741 | ||||||
| chr16:89738802
|
C | A | 1 | a0003c0003t0002g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4260+80G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 42/42 | chr16 | 89738802 | ||||||
| chr16:89738853
|
A | G | 298 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(295): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.4260+29T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 42/42 | chr16 | 89738853 | ||||||
| chr16:89739013
|
T | TA | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4168-40dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 41/42 | chr16 | 89739013 | ||||||
| chr16:89739060
|
G | A | 1 | a0004c0004t0002g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4167+73C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 41/42 | chr16 | 89739060 | ||||||
| chr16:89739311
|
C | G | 1 | a0013c0014t0002g0330 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4011-22G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 40/42 | chr16 | 89739311 | ||||||
| chr16:89739386
|
A | G | 62 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(59): Show | 62 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.4010+92T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 40/42 | chr16 | 89739386 | ||||||
| chr16:89739562
|
C | T | 2 | a0006c0007t0009g0308a0006c0007t0009g0314 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3935-9G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739562 | ||||||
| chr16:89739569
|
G | A | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3935-16C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739569 | ||||||
| chr16:89739655
|
G | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3935-102C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739655 | ||||||
| chr16:89739673
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3935-120C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739673 | ||||||
| chr16:89739698
|
C | G | 1 | a0006c0007t0004g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3935-145G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739698 | ||||||
| chr16:89739737
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3935-184C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739737 | ||||||
| chr16:89739819
|
C | T | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.3934+175G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739819 | ||||||
| chr16:89739935
|
C | A | 63 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(60): Show | 63 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3934+59G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739935 | ||||||
| chr16:89739939
|
A | T | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.3934+55T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 39/42 | chr16 | 89739939 | ||||||
| chr16:89740206
|
T | A | 63 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(60): Show | 63 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3829-107A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740206 | ||||||
| chr16:89740324
|
G | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3829-225C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740324 | ||||||
| chr16:89740397
|
T | C | 1 | a0008c0008t0001g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3829-298A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740397 | ||||||
| chr16:89740405
|
C | T | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3829-306G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740405 | ||||||
| chr16:89740553
|
T | C | 29 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.3828+251A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740553 | ||||||
| chr16:89740636
|
C | CA | 23 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0052others(20): Show | 23 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.3828+167dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740636 | ||||||
| chr16:89740636
|
C | CAAAAA | 27 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(24): Show | 27 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3828+163_3828+167d others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740636 | ||||||
| chr16:89740636
|
C | CAAAAAA | 6 | a0005c0005t0001g0189a0005c0005t0001g0190a0005c0005t0001g0194others(3): Show | 6 | HG00597.hp2 HG02056.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3828+162_3828+167d others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740636 | ||||||
| chr16:89740636
|
CA | C | 11 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(8): Show | 11 | HG01192.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3828+167delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740636 | ||||||
| chr16:89740723
|
C | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3828+81G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740723 | ||||||
| chr16:89740783
|
G | A | 1 | a0039c0024t0002g0278 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3828+21C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 38/42 | chr16 | 89740783 | ||||||
| chr16:89741008
|
A | G | 15 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(12): Show | 15 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.3766-142T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741008 | ||||||
| chr16:89741135
|
G | A | 35 | a0002c0002t0001g0165a0005c0005t0001g0036a0005c0005t0001g0064others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.3766-269C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741135 | ||||||
| chr16:89741297
|
T | C | 296 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.3766-431A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741297 | ||||||
| chr16:89741324
|
C | T | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3766-458G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741324 | ||||||
| chr16:89741371
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3766-505G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741371 | ||||||
| chr16:89741377
|
C | T | 86 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0219others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.3766-511G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741377 | ||||||
| chr16:89741400
|
C | A | 16 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(13): Show | 16 | HG01167.hp1 HG02451.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.3766-534G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741400 | ||||||
| chr16:89741420
|
C | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3766-554G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741420 | ||||||
| chr16:89741436
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3766-570C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741436 | ||||||
| chr16:89741442
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3766-576A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741442 | ||||||
| chr16:89741729
|
C | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3766-863G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741729 | ||||||
| chr16:89741833
|
T | C | 10 | a0002c0002t0001g0029a0002c0002t0001g0080a0002c0002t0001g0085others(7): Show | 10 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.3765+967A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741833 | ||||||
| chr16:89741867
|
A | C | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.3765+933T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741867 | ||||||
| chr16:89741910
|
C | T | 1 | a0008c0008t0001g0016 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3765+890G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741910 | ||||||
| chr16:89741969
|
C | A | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3765+831G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741969 | ||||||
| chr16:89741972
|
A | AT | 36 | a0001c0001t0001g0212a0001c0029t0005g0103a0002c0006t0005g0025others(33): Show | 36 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.3765+827dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89741972 | ||||||
| chr16:89742004
|
C | G | 15 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(12): Show | 15 | HG01167.hp1 HG02451.hp1 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.3765+796G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742004 | ||||||
| chr16:89742026
|
C | T | 19 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3765+774G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742026 | ||||||
| chr16:89742059
|
G | A | 3 | a0014c0015t0002g0008a0014c0015t0002g0011a0020c0021t0002g0012 | 3 | HG00323.hp1 HG02300.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3765+741C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742059 | ||||||
| chr16:89742123
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3765+677G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742123 | ||||||
| chr16:89742194
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3765+606G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742194 | ||||||
| chr16:89742244
|
T | C | 2 | a0004c0004t0002g0245a0004c0004t0002g0269 | 2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3765+556A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742244 | ||||||
| chr16:89742386
|
AGAGGCTG others(9): Show |
A | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3765+398_3765+413d others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742386 | ||||||
| chr16:89742423
|
G | C | 13 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3765+377C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742423 | ||||||
| chr16:89742435
|
G | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3765+365C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742435 | ||||||
| chr16:89742442
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3765+358G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742442 | ||||||
| chr16:89742463
|
C | G | 19 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3765+337G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742463 | ||||||
| chr16:89742531
|
T | C | 67 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3765+269A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742531 | ||||||
| chr16:89742592
|
G | A | 1 | a0007c0009t0001g0329 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3765+208C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742592 | ||||||
| chr16:89742653
|
C | CA | 32 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0057others(29): Show | 32 | HG00423.hp2 HG00642.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.3765+146dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
C | CAAAAAA | 15 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0218others(12): Show | 15 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.3765+141_3765+146d others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
C | CAAAAAAA others(7): Show |
1 | a0008c0008t0001g0016 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3765+133_3765+146d others(16): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
C | CAAAAAAA others(8): Show |
20 | a0005c0005t0001g0064a0005c0005t0001g0181a0005c0005t0001g0182others(17): Show | 20 | HG00438.hp1 HG01175.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.3765+132_3765+146d others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
C | CAAAAAAA others(9): Show |
9 | a0005c0005t0001g0036a0005c0005t0001g0065a0005c0005t0001g0066others(6): Show | 9 | HG00597.hp2 HG00621.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.3765+131_3765+146d others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
C | CAAAAAAA others(10): Show |
2 | a0005c0005t0001g0067a0005c0005t0001g0188 | 2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.3765+130_3765+146d others(19): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
CA | C | 18 | a0001c0001t0003g0101a0001c0001t0003g0159a0002c0002t0001g0022others(15): Show | 18 | HG00639.hp1 HG01167.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.3765+146delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742653
|
CAAAAAAA | C | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3765+140_3765+146d others(9): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742653 | ||||||
| chr16:89742720
|
T | C | 1 | a0001c0001t0003g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3765+80A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742720 | ||||||
| chr16:89742763
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3765+37G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742763 | ||||||
| chr16:89742764
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3765+36C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 37/42 | chr16 | 89742764 | ||||||
| chr16:89742990
|
G | A | 1 | a0002c0006t0005g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3627-52C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89742990 | ||||||
| chr16:89743057
|
G | A | 2 | a0003c0003t0002g0267a0003c0003t0002g0268 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3627-119C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743057 | ||||||
| chr16:89743109
|
A | G | 1 | a0002c0002t0001g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3627-171T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743109 | ||||||
| chr16:89743140
|
C | A | 34 | a0004c0004t0002g0233a0005c0005t0001g0036a0005c0005t0001g0064others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3627-202G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743140 | ||||||
| chr16:89743141
|
A | G | 69 | a0001c0001t0001g0222a0001c0029t0005g0103a0002c0006t0005g0025others(66): Show | 69 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.3627-203T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743141 | ||||||
| chr16:89743281
|
T | C | 1 | a0001c0001t0003g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3627-343A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743281 | ||||||
| chr16:89743285
|
G | T | 8 | a0001c0001t0001g0069a0007c0009t0001g0322a0007c0009t0001g0323others(5): Show | 9 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3627-347C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743285 | ||||||
| chr16:89743494
|
T | C | 52 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(49): Show | 52 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3627-556A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743494 | ||||||
| chr16:89743529
|
TAAAC | T | 34 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(31): Show | 34 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.3627-595_3627-592d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743529 | ||||||
| chr16:89743549
|
C | T | 2 | a0002c0006t0008g0224a0002c0006t0008g0225 | 2 | NA18939.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3627-611G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743549 | ||||||
| chr16:89743554
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3627-616A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743554 | ||||||
| chr16:89743556
|
G | C | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3627-618C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743556 | ||||||
| chr16:89743734
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3627-796C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743734 | ||||||
| chr16:89743778
|
G | A | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3627-840C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743778 | ||||||
| chr16:89743812
|
A | C | 75 | a0001c0001t0001g0024a0001c0001t0001g0048a0001c0001t0001g0049others(72): Show | 75 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.3627-874T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743812 | ||||||
| chr16:89743851
|
TCAGA | T | 4 | a0002c0006t0008g0220a0002c0006t0008g0224a0002c0006t0008g0225others(1): Show | 4 | NA18939.hp1 NA18951.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.3627-917_3627-914d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743851 | ||||||
| chr16:89743908
|
C | CTTT | 67 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3627-973_3627-971d others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743908 | ||||||
| chr16:89743909
|
T | C | 1 | a0004c0004t0002g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3627-971A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743909 | ||||||
| chr16:89743913
|
T | C | 1 | a0029c0028t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3627-975A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743913 | ||||||
| chr16:89743919
|
T | C | 67 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3627-981A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743919 | ||||||
| chr16:89743929
|
C | T | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3627-991G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89743929 | ||||||
| chr16:89744185
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0199others(1): Show | 4 | HG02040.hp2 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.3626+774C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744185 | ||||||
| chr16:89744190
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3626+769C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744190 | ||||||
| chr16:89744220
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3626+739G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744220 | ||||||
| chr16:89744245
|
C | T | 35 | a0001c0029t0005g0103a0002c0002t0001g0078a0002c0006t0005g0025others(32): Show | 35 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.3626+714G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744245 | ||||||
| chr16:89744309
|
G | T | 34 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(31): Show | 34 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.3626+650C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744309 | ||||||
| chr16:89744357
|
T | G | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3626+602A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744357 | ||||||
| chr16:89744366
|
G | A | 5 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3626+593C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744366 | ||||||
| chr16:89744415
|
T | C | 297 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.3626+544A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744415 | ||||||
| chr16:89744533
|
C | A | 67 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3626+426G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744533 | ||||||
| chr16:89744534
|
G | A | 2 | a0005c0005t0001g0191a0005c0005t0001g0197 | 2 | HG02135.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.3626+425C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744534 | ||||||
| chr16:89744629
|
G | A | 1 | a0003c0003t0002g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3626+330C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744629 | ||||||
| chr16:89744665
|
G | GT | 106 | a0001c0001t0001g0024a0001c0001t0001g0048a0001c0001t0001g0049others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.3626+293dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744665 | ||||||
| chr16:89744677
|
G | GT | 29 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.3626+281dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744677 | ||||||
| chr16:89744677
|
G | T | 3 | a0003c0003t0002g0238a0003c0003t0002g0274a0020c0021t0002g0012 | 3 | HG00140.hp2 HG00280.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3626+282C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744677 | ||||||
| chr16:89744743
|
A | G | 67 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3626+216T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744743 | ||||||
| chr16:89744788
|
T | C | 251 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.3626+171A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744788 | ||||||
| chr16:89744801
|
C | T | 53 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3626+158G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 36/42 | chr16 | 89744801 | ||||||
| chr16:89745100
|
A | C | 1 | a0007c0009t0001g0329 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3514-29T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745100 | ||||||
| chr16:89745138
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-67T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745138 | ||||||
| chr16:89745221
|
C | T | 13 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3514-150G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745221 | ||||||
| chr16:89745255
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-184A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745255 | ||||||
| chr16:89745313
|
G | C | 3 | a0001c0026t0001g0023a0002c0002t0001g0039a0004c0004t0002g0252 | 3 | HG02717.hp2 HG02895.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.3514-242C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745313 | ||||||
| chr16:89745343
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-272G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745343 | ||||||
| chr16:89745377
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3514-306A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745377 | ||||||
| chr16:89745388
|
T | C | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3514-317A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745388 | ||||||
| chr16:89745389
|
GAAACAGT others(297): Show |
G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-622_3514-319d others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745389 | ||||||
| chr16:89745389
|
GAAACAGT others(335): Show |
G | 33 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(30): Show | 33 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.3514-660_3514-319d others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745389 | ||||||
| chr16:89745411
|
C | G | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3514-340G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745411 | ||||||
| chr16:89745413
|
T | C | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3514-342A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745413 | ||||||
| chr16:89745414
|
C | G | 1 | a0002c0002t0001g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3514-343G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745414 | ||||||
| chr16:89745427
|
A | G | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3514-356T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745427 | ||||||
| chr16:89745465
|
AAAACAGT others(145): Show |
A | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3514-546_3514-395d others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745465 | ||||||
| chr16:89745489
|
TCTGAGCT others(107): Show |
T | 2 | a0007c0009t0001g0322a0007c0009t0001g0326 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3514-532_3514-419d others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745489 | ||||||
| chr16:89745489
|
TCTGAGCT others(183): Show |
T | 182 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.3514-608_3514-419d others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745489 | ||||||
| chr16:89745503
|
G | GAAACAGT others(69): Show |
2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3514-508_3514-433d others(78): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745503 | ||||||
| chr16:89745503
|
GAAACAGT others(69): Show |
G | 1 | a0003c0003t0002g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3514-508_3514-433d others(78): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745503 | ||||||
| chr16:89745540
|
C | T | 1 | a0004c0004t0002g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3514-469G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745540 | ||||||
| chr16:89745617
|
G | A | 2 | a0007c0009t0001g0322a0007c0009t0001g0326 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3514-546C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745617 | ||||||
| chr16:89745655
|
A | G | 2 | a0007c0009t0001g0322a0007c0009t0001g0326 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3514-584T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745655 | ||||||
| chr16:89745677
|
G | C | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3514-606C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745677 | ||||||
| chr16:89745679
|
C | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3514-608G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745679 | ||||||
| chr16:89745693
|
A | G | 3 | a0006c0055t0009g0309a0007c0009t0001g0322a0007c0009t0001g0326 | 3 | HG02258.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3514-622T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745693 | ||||||
| chr16:89745715
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-644G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745715 | ||||||
| chr16:89745717
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-646A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745717 | ||||||
| chr16:89745731
|
A | G | 218 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.3514-660T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745731 | ||||||
| chr16:89745743
|
G | A | 2 | a0007c0009t0001g0322a0007c0009t0001g0326 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3514-672C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745743 | ||||||
| chr16:89745747
|
C | T | 21 | a0001c0001t0001g0212a0002c0002t0001g0001a0002c0002t0001g0029others(18): Show | 22 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.3514-676G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745747 | ||||||
| chr16:89745751
|
C | A | 1 | a0002c0035t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3514-680G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745751 | ||||||
| chr16:89745751
|
C | G | 1 | a0016c0019t0001g0156 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3514-680G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745751 | ||||||
| chr16:89745791
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-720G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745791 | ||||||
| chr16:89745793
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3514-722A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745793 | ||||||
| chr16:89745807
|
G | A | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3514-736C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745807 | ||||||
| chr16:89745819
|
A | G | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3514-748T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745819 | ||||||
| chr16:89745875
|
G | A | 218 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.3513+709C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745875 | ||||||
| chr16:89745891
|
C | T | 27 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.3513+693G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745891 | ||||||
| chr16:89745921
|
A | G | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3513+663T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745921 | ||||||
| chr16:89745980
|
G | A | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+604C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745980 | ||||||
| chr16:89745981
|
T | C | 1 | a0002c0002t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3513+603A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745981 | ||||||
| chr16:89745982
|
G | A | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+602C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745982 | ||||||
| chr16:89745985
|
G | A | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+599C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745985 | ||||||
| chr16:89745986
|
C | G | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+598G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745986 | ||||||
| chr16:89745987
|
G | A | 1 | a0001c0030t0001g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3513+597C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745987 | ||||||
| chr16:89745987
|
G | T | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+597C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745987 | ||||||
| chr16:89745990
|
G | T | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+594C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745990 | ||||||
| chr16:89745991
|
A | G | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+593T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745991 | ||||||
| chr16:89745992
|
A | T | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+592T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745992 | ||||||
| chr16:89745993
|
A | T | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3513+591T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89745993 | ||||||
| chr16:89746174
|
C | T | 1 | a0004c0004t0002g0233 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3513+410G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746174 | ||||||
| chr16:89746209
|
C | T | 254 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(251): Show | 256 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.3513+375G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746209 | ||||||
| chr16:89746223
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0140 | 2 | HG01358.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3513+361C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746223 | ||||||
| chr16:89746253
|
G | T | 1 | a0010c0011t0002g0009 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3513+331C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746253 | ||||||
| chr16:89746353
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3513+231C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746353 | ||||||
| chr16:89746354
|
C | A | 254 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(251): Show | 256 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.3513+230G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746354 | ||||||
| chr16:89746370
|
G | A | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3513+214C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746370 | ||||||
| chr16:89746394
|
G | A | 1 | a0002c0006t0008g0215 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3513+190C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746394 | ||||||
| chr16:89746401
|
C | G | 9 | a0003c0003t0002g0240a0003c0003t0002g0282a0004c0004t0002g0300others(6): Show | 9 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3513+183G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746401 | ||||||
| chr16:89746422
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3513+162C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746422 | ||||||
| chr16:89746425
|
A | G | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3513+159T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746425 | ||||||
| chr16:89746443
|
CTG | C | 53 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3513+139_3513+140d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746443 | ||||||
| chr16:89746522
|
G | A | 2 | a0010c0011t0002g0005a0010c0011t0002g0010 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.3513+62C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746522 | ||||||
| chr16:89746527
|
C | T | 20 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3513+57G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 35/42 | chr16 | 89746527 | ||||||
| chr16:89746786
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3408+45G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 34/42 | chr16 | 89746786 | ||||||
| chr16:89746798
|
A | G | 5 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3408+33T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 34/42 | chr16 | 89746798 | ||||||
| chr16:89746953
|
G | C | 2 | a0002c0002t0001g0216a0002c0051t0001g0032 | 2 | HG01081.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3349-63C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89746953 | ||||||
| chr16:89746958
|
G | T | 1 | a0007c0057t0001g0328 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3349-68C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89746958 | ||||||
| chr16:89746980
|
G | A | 1 | a0021c0053t0001g0321 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3349-90C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89746980 | ||||||
| chr16:89747048
|
C | T | 5 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3349-158G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747048 | ||||||
| chr16:89747152
|
G | A | 1 | a0006c0007t0009g0308 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3349-262C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747152 | ||||||
| chr16:89747179
|
G | C | 1 | a0016c0019t0001g0156 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3349-289C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747179 | ||||||
| chr16:89747181
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3349-291G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747181 | ||||||
| chr16:89747255
|
A | C | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3349-365T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747255 | ||||||
| chr16:89747332
|
C | T | 1 | a0006c0007t0009g0308 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3349-442G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747332 | ||||||
| chr16:89747347
|
G | C | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3349-457C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747347 | ||||||
| chr16:89747351
|
C | T | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3349-461G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747351 | ||||||
| chr16:89747413
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3349-523C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747413 | ||||||
| chr16:89747474
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3349-584C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747474 | ||||||
| chr16:89747524
|
C | T | 15 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(12): Show | 15 | HG01167.hp1 HG02630.hp1 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.3349-634G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747524 | ||||||
| chr16:89747558
|
T | G | 99 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.3349-668A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747558 | ||||||
| chr16:89747564
|
C | T | 251 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(248): Show | 252 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.3349-674G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747564 | ||||||
| chr16:89747580
|
T | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3349-690A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747580 | ||||||
| chr16:89747656
|
T | G | 297 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.3349-766A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747656 | ||||||
| chr16:89747702
|
A | G | 5 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3349-812T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747702 | ||||||
| chr16:89747703
|
A | AAAAT | 3 | a0002c0002t0001g0164a0006c0007t0004g0316a0037c0048t0001g0093 | 3 | HG00621.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3349-817_3349-814d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747703 | ||||||
| chr16:89747780
|
A | G | 254 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(251): Show | 256 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.3348+879T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747780 | ||||||
| chr16:89747945
|
C | T | 1 | a0002c0002t0001g0034 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3348+714G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747945 | ||||||
| chr16:89747950
|
T | C | 1 | a0009c0010t0002g0296 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3348+709A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747950 | ||||||
| chr16:89747979
|
C | G | 1 | a0005c0005t0001g0036 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3348+680G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89747979 | ||||||
| chr16:89748117
|
G | A | 35 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(32): Show | 35 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.3348+542C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748117 | ||||||
| chr16:89748186
|
G | A | 13 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(10): Show | 13 | HG02630.hp1 HG03239.hp2 HG03669.hp2 others(10): Show |
intron_variant | MODIFIER | c.3348+473C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748186 | ||||||
| chr16:89748190
|
G | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3348+469C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748190 | ||||||
| chr16:89748196
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3348+463C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748196 | ||||||
| chr16:89748285
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3348+374G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748285 | ||||||
| chr16:89748307
|
C | CT | 10 | a0001c0001t0001g0069a0007c0009t0001g0322a0007c0009t0001g0323others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.3348+351dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748307 | ||||||
| chr16:89748307
|
CT | C | 68 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(65): Show | 68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3348+351delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748307 | ||||||
| chr16:89748399
|
T | C | 31 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.3348+260A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748399 | ||||||
| chr16:89748410
|
T | A | 13 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(10): Show | 13 | HG02630.hp1 HG03239.hp2 HG03669.hp2 others(10): Show |
intron_variant | MODIFIER | c.3348+249A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748410 | ||||||
| chr16:89748410
|
T | G | 186 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(183): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.3348+249A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748410 | ||||||
| chr16:89748478
|
G | A | 1 | a0002c0002t0001g0122 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3348+181C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748478 | ||||||
| chr16:89748481
|
G | A | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3348+178C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748481 | ||||||
| chr16:89748522
|
G | C | 1 | a0003c0003t0002g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3348+137C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748522 | ||||||
| chr16:89748630
|
G | A | 1 | a0003c0003t0002g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3348+29C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748630 | ||||||
| chr16:89748641
|
T | C | 2 | a0004c0004t0002g0247a0004c0004t0002g0258 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3348+18A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 33/42 | chr16 | 89748641 | ||||||
| chr16:89748802
|
C | T | 2 | a0019c0016t0007g0276a0019c0016t0007g0291 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3240-35G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89748802 | ||||||
| chr16:89748809
|
C | T | 183 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(180): Show | 185 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.3240-42G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89748809 | ||||||
| chr16:89748825
|
A | G | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3240-58T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89748825 | ||||||
| chr16:89748910
|
T | C | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.3240-143A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89748910 | ||||||
| chr16:89748913
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3240-146G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89748913 | ||||||
| chr16:89748989
|
AAAC | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3240-225_3240-223d others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89748989 | ||||||
| chr16:89749135
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3240-368C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749135 | ||||||
| chr16:89749158
|
T | G | 15 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(12): Show | 15 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3240-391A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749158 | ||||||
| chr16:89749160
|
C | G | 35 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(32): Show | 35 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.3240-393G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749160 | ||||||
| chr16:89749216
|
TTTGTTG | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3240-455_3240-450d others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749216 | ||||||
| chr16:89749248
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3240-481A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749248 | ||||||
| chr16:89749373
|
T | C | 254 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(251): Show | 256 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.3239+357A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749373 | ||||||
| chr16:89749391
|
T | C | 186 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(183): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.3239+339A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749391 | ||||||
| chr16:89749416
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3239+314C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749416 | ||||||
| chr16:89749466
|
A | G | 1 | a0003c0003t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3239+264T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749466 | ||||||
| chr16:89749575
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3239+155C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 32/42 | chr16 | 89749575 | ||||||
| chr16:89749906
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
splice_region_variant&intron_variant | LOW | c.3067-4T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89749906 | ||||||
| chr16:89749925
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-23G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89749925 | ||||||
| chr16:89749938
|
C | T | 1 | a0005c0005t0001g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3067-36G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89749938 | ||||||
| chr16:89749959
|
T | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-57A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89749959 | ||||||
| chr16:89749999
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-97T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89749999 | ||||||
| chr16:89750016
|
G | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-114C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750016 | ||||||
| chr16:89750104
|
T | G | 14 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(11): Show | 14 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3067-202A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750104 | ||||||
| chr16:89750161
|
C | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-259G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750161 | ||||||
| chr16:89750164
|
TACTACTT others(4): Show |
T | 1 | a0004c0004t0002g0304 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3067-273_3067-263d others(13): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750164 | ||||||
| chr16:89750184
|
T | C | 1 | a0002c0006t0005g0218 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3067-282A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750184 | ||||||
| chr16:89750337
|
G | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-435C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750337 | ||||||
| chr16:89750352
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3067-450C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750352 | ||||||
| chr16:89750407
|
C | T | 5 | a0010c0011t0002g0004a0010c0011t0002g0009a0014c0015t0002g0008others(2): Show | 5 | HG00323.hp1 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-505G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750407 | ||||||
| chr16:89750483
|
A | AAAAAAAA others(3): Show |
2 | a0002c0006t0005g0025a0002c0006t0008g0220 | 2 | HG03831.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3067-582_3067-581i others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750483 | ||||||
| chr16:89750484
|
A | AAAAAAAA others(2): Show |
27 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0217others(24): Show | 27 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.3067-583_3067-582i others(11): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750484 | ||||||
| chr16:89750488
|
A | C | 3 | a0002c0002t0001g0029a0003c0003t0001g0303a0003c0003t0002g0281 | 3 | HG00280.hp1 HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3067-586T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750488 | ||||||
| chr16:89750488
|
AAAAC | A | 30 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.3067-590_3067-587d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750488 | ||||||
| chr16:89750489
|
AAAC | A | 7 | a0001c0001t0001g0212a0006c0055t0009g0309a0012c0013t0007g0079others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3067-590_3067-588d others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750489 | ||||||
| chr16:89750492
|
C | A | 62 | a0001c0001t0001g0047a0001c0029t0005g0103a0002c0006t0005g0025others(59): Show | 62 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3067-590G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750492 | ||||||
| chr16:89750496
|
C | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-594G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750496 | ||||||
| chr16:89750501
|
A | AAAAAAAA others(2): Show |
10 | a0005c0005t0001g0064a0005c0005t0001g0065a0005c0005t0001g0182others(7): Show | 10 | HG00438.hp1 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.3067-600_3067-599i others(11): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750501 | ||||||
| chr16:89750501
|
A | AAAAAAAA others(1): Show |
21 | a0005c0005t0001g0036a0005c0005t0001g0066a0005c0005t0001g0067others(18): Show | 21 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.3067-600_3067-599i others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750501 | ||||||
| chr16:89750512
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-610C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750512 | ||||||
| chr16:89750537
|
C | T | 2 | a0001c0001t0001g0102a0001c0034t0001g0104 | 2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.3067-635G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750537 | ||||||
| chr16:89750609
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-707A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750609 | ||||||
| chr16:89750795
|
C | CA | 37 | a0001c0001t0003g0148a0005c0005t0001g0036a0005c0005t0001g0064others(34): Show | 37 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.3067-894dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750795 | ||||||
| chr16:89750798
|
A | C | 3 | a0001c0001t0001g0047a0002c0006t0011g0227a0002c0006t0011g0228 | 3 | HG01167.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3067-896T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750798 | ||||||
| chr16:89750891
|
TTTGTTG | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3067-995_3067-990d others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750891 | ||||||
| chr16:89750986
|
A | C | 1 | a0007c0009t0001g0329 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3067-1084T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89750986 | ||||||
| chr16:89751052
|
T | G | 1 | a0002c0002t0001g0166 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3066+1086A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751052 | ||||||
| chr16:89751141
|
C | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3066+997G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751141 | ||||||
| chr16:89751161
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3066+977C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751161 | ||||||
| chr16:89751171
|
G | C | 1 | a0030c0027t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3066+967C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751171 | ||||||
| chr16:89751266
|
G | A | 2 | a0005c0005t0001g0181a0005c0005t0001g0192 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3066+872C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751266 | ||||||
| chr16:89751369
|
G | T | 200 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(197): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3066+769C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751369 | ||||||
| chr16:89751464
|
C | A | 8 | a0003c0003t0002g0240a0003c0003t0002g0282a0009c0010t0002g0287others(5): Show | 8 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3066+674G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751464 | ||||||
| chr16:89751529
|
A | G | 329 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.3066+609T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751529 | ||||||
| chr16:89751574
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3066+564C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751574 | ||||||
| chr16:89751590
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3066+548G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751590 | ||||||
| chr16:89751681
|
A | G | 236 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(233): Show | 238 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.3066+457T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751681 | ||||||
| chr16:89751770
|
C | CT | 62 | a0001c0001t0012g0125a0003c0003t0002g0238a0003c0003t0002g0239others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.3066+367dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751770 | ||||||
| chr16:89751795
|
C | T | 5 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3066+343G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751795 | ||||||
| chr16:89751857
|
G | A | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3066+281C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751857 | ||||||
| chr16:89751902
|
G | C | 296 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.3066+236C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751902 | ||||||
| chr16:89751932
|
G | C | 198 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(195): Show | 200 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.3066+206C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751932 | ||||||
| chr16:89751972
|
G | T | 2 | a0002c0002t0001g0030a0002c0002t0001g0092 | 2 | NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.3066+166C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89751972 | ||||||
| chr16:89752013
|
G | A | 5 | a0002c0006t0008g0215a0002c0006t0008g0220a0002c0006t0008g0224others(2): Show | 5 | NA18939.hp1 NA18951.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.3066+125C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89752013 | ||||||
| chr16:89752021
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3066+117G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89752021 | ||||||
| chr16:89752049
|
C | T | 1 | a0001c0001t0003g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3066+89G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89752049 | ||||||
| chr16:89752083
|
T | C | 200 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(197): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3066+55A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 31/42 | chr16 | 89752083 | ||||||
| chr16:89752293
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2982-71C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752293 | ||||||
| chr16:89752324
|
C | G | 6 | a0002c0002t0001g0042a0002c0002t0001g0060a0002c0002t0001g0128others(3): Show | 6 | HG00423.hp2 HG00597.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2982-102G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752324 | ||||||
| chr16:89752500
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-278G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752500 | ||||||
| chr16:89752518
|
T | A | 1 | a0006c0007t0004g0317 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2982-296A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752518 | ||||||
| chr16:89752562
|
T | A | 6 | a0003c0003t0001g0303a0012c0013t0007g0079a0012c0013t0007g0081others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2982-340A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752562 | ||||||
| chr16:89752580
|
T | C | 3 | a0001c0001t0001g0241a0002c0002t0001g0027a0002c0002t0001g0028 | 3 | HG03041.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2982-358A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752580 | ||||||
| chr16:89752601
|
C | T | 3 | a0001c0001t0001g0047a0002c0006t0011g0227a0002c0006t0011g0228 | 3 | HG01167.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2982-379G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752601 | ||||||
| chr16:89752633
|
C | T | 1 | a0004c0004t0002g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2982-411G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752633 | ||||||
| chr16:89752652
|
C | T | 1 | a0008c0008t0001g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2982-430G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752652 | ||||||
| chr16:89752722
|
T | G | 1 | a0005c0005t0001g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2982-500A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752722 | ||||||
| chr16:89752776
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0150 | 2 | NA18998.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2982-554C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752776 | ||||||
| chr16:89752835
|
A | G | 30 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.2982-613T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752835 | ||||||
| chr16:89752873
|
C | T | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2982-651G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752873 | ||||||
| chr16:89752897
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-675G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89752897 | ||||||
| chr16:89753019
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-797A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753019 | ||||||
| chr16:89753170
|
A | G | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.2982-948T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753170 | ||||||
| chr16:89753186
|
C | T | 1 | a0011c0012t0001g0003 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2982-964G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753186 | ||||||
| chr16:89753208
|
T | C | 182 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.2982-986A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753208 | ||||||
| chr16:89753232
|
C | G | 22 | a0002c0002t0001g0001a0002c0002t0001g0029a0002c0002t0001g0030others(19): Show | 23 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.2982-1010G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753232 | ||||||
| chr16:89753294
|
G | A | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.2982-1072C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753294 | ||||||
| chr16:89753329
|
G | A | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2982-1107C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753329 | ||||||
| chr16:89753408
|
A | G | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2982-1186T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753408 | ||||||
| chr16:89753410
|
C | T | 1 | a0002c0006t0008g0215 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2982-1188G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753410 | ||||||
| chr16:89753411
|
G | A | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2982-1189C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753411 | ||||||
| chr16:89753428
|
A | G | 2 | a0018c0017t0001g0244a0018c0017t0001g0277 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2982-1206T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753428 | ||||||
| chr16:89753465
|
T | C | 1 | a0009c0010t0002g0298 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2982-1243A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753465 | ||||||
| chr16:89753473
|
G | C | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.2982-1251C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753473 | ||||||
| chr16:89753524
|
G | A | 71 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2982-1302C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753524 | ||||||
| chr16:89753662
|
G | A | 5 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2982-1440C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753662 | ||||||
| chr16:89753741
|
A | C | 182 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.2982-1519T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753741 | ||||||
| chr16:89753777
|
A | G | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2982-1555T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753777 | ||||||
| chr16:89753792
|
C | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2982-1570G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753792 | ||||||
| chr16:89753794
|
C | G | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2982-1572G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753794 | ||||||
| chr16:89753853
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2982-1631C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753853 | ||||||
| chr16:89753853
|
G | C | 1 | a0005c0005t0001g0188 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2982-1631C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753853 | ||||||
| chr16:89753915
|
C | T | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2982-1693G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89753915 | ||||||
| chr16:89754008
|
A | C | 198 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(195): Show | 200 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.2982-1786T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754008 | ||||||
| chr16:89754016
|
T | C | 1 | a0035c0044t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2982-1794A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754016 | ||||||
| chr16:89754033
|
C | G | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2982-1811G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754033 | ||||||
| chr16:89754047
|
C | A | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2982-1825G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754047 | ||||||
| chr16:89754208
|
C | T | 2 | a0018c0017t0001g0244a0018c0017t0001g0277 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2982-1986G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754208 | ||||||
| chr16:89754240
|
CAA | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.2982-2020_2982-201 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754240 | ||||||
| chr16:89754248
|
C | CA | 3 | a0005c0005t0001g0189a0005c0005t0001g0195a0008c0008t0001g0021 | 3 | HG01175.hp2 NA18954.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.2982-2027dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754248 | ||||||
| chr16:89754250
|
AC | A | 197 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.2982-2029delG | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754250 | ||||||
| chr16:89754251
|
C | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-2029G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754251 | ||||||
| chr16:89754258
|
A | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.2982-2036T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754258 | ||||||
| chr16:89754284
|
C | T | 2 | a0018c0017t0001g0244a0018c0017t0001g0277 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2982-2062G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754284 | ||||||
| chr16:89754285
|
G | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0169a0001c0001t0006g0062others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2982-2063C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754285 | ||||||
| chr16:89754297
|
CAAGAAA | C | 10 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(7): Show | 10 | HG01192.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2982-2081_2982-207 others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754297 | ||||||
| chr16:89754369
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2982-2147A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754369 | ||||||
| chr16:89754383
|
T | G | 3 | a0001c0001t0001g0142a0002c0002t0001g0083a0002c0002t0001g0098 | 3 | NA18961.hp2 NA19007.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2982-2161A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754383 | ||||||
| chr16:89754514
|
G | A | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2982-2292C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754514 | ||||||
| chr16:89754620
|
C | T | 8 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982-2398G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754620 | ||||||
| chr16:89754652
|
A | C | 1 | a0002c0002t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2982-2430T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754652 | ||||||
| chr16:89754672
|
C | T | 293 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.2982-2450G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754672 | ||||||
| chr16:89754723
|
G | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-2501C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754723 | ||||||
| chr16:89754802
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2982-2580C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754802 | ||||||
| chr16:89754844
|
A | G | 6 | a0001c0001t0001g0141a0003c0003t0002g0259a0003c0003t0002g0260others(3): Show | 6 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.2982-2622T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754844 | ||||||
| chr16:89754852
|
C | A | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2982-2630G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754852 | ||||||
| chr16:89754853
|
G | C | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2982-2631C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89754853 | ||||||
| chr16:89755081
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-2859G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755081 | ||||||
| chr16:89755101
|
G | C | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2982-2879C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755101 | ||||||
| chr16:89755120
|
T | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2982-2898A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755120 | ||||||
| chr16:89755212
|
ATT | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-2992_2982-299 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755212 | ||||||
| chr16:89755322
|
TGCC | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2982-3103_2982-310 others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755322 | ||||||
| chr16:89755338
|
C | G | 2 | a0006c0007t0009g0308a0006c0007t0009g0314 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2982-3116G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755338 | ||||||
| chr16:89755468
|
G | A | 1 | a0010c0011t0002g0009 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2981+3109C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755468 | ||||||
| chr16:89755552
|
A | G | 211 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(208): Show | 213 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.2981+3025T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755552 | ||||||
| chr16:89755555
|
C | G | 1 | a0004c0004t0002g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2981+3022G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755555 | ||||||
| chr16:89755691
|
A | G | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2981+2886T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755691 | ||||||
| chr16:89755694
|
A | T | 2 | a0006c0055t0009g0309a0040c0050t0013g0206 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2981+2883T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755694 | ||||||
| chr16:89755710
|
T | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.2981+2867A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755710 | ||||||
| chr16:89755742
|
T | G | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2981+2835A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755742 | ||||||
| chr16:89755831
|
CCCCGCAC others(48): Show |
C | 1 | a0005c0005t0001g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2981+2691_2981+274 others(59): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755831 | ||||||
| chr16:89755867
|
A | G | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2981+2710T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755867 | ||||||
| chr16:89755876
|
G | C | 1 | a0002c0002t0001g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2981+2701C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755876 | ||||||
| chr16:89755887
|
C | G | 1 | a0003c0003t0002g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2981+2690G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755887 | ||||||
| chr16:89755921
|
C | T | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2981+2656G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755921 | ||||||
| chr16:89755923
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+2654G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755923 | ||||||
| chr16:89755927
|
A | C | 1 | a0004c0004t0002g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2981+2650T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755927 | ||||||
| chr16:89755944
|
G | A | 1 | a0031c0031t0001g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2981+2633C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755944 | ||||||
| chr16:89755956
|
C | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+2621G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755956 | ||||||
| chr16:89755966
|
G | A | 2 | a0005c0005t0001g0186a0005c0005t0014g0196 | 2 | HG02074.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2981+2611C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89755966 | ||||||
| chr16:89756123
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2981+2454A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756123 | ||||||
| chr16:89756171
|
T | C | 1 | a0001c0001t0003g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2981+2406A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756171 | ||||||
| chr16:89756172
|
G | C | 1 | a0002c0002t0001g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2981+2405C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756172 | ||||||
| chr16:89756349
|
G | A | 30 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.2981+2228C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756349 | ||||||
| chr16:89756353
|
T | G | 1 | a0002c0006t0008g0220 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2981+2224A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756353 | ||||||
| chr16:89756385
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+2192A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756385 | ||||||
| chr16:89756601
|
CAAAG | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+1972_2981+197 others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756601 | ||||||
| chr16:89756749
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+1828G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756749 | ||||||
| chr16:89756762
|
AAGGCTGA others(4): Show |
A | 14 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(11): Show | 14 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2981+1804_2981+181 others(15): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756762 | ||||||
| chr16:89756935
|
G | C | 1 | a0011c0012t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2981+1642C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756935 | ||||||
| chr16:89756985
|
C | T | 276 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.2981+1592G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89756985 | ||||||
| chr16:89757031
|
T | C | 2 | a0006c0007t0009g0308a0006c0007t0009g0314 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2981+1546A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757031 | ||||||
| chr16:89757054
|
T | A | 1 | a0013c0014t0002g0330 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2981+1523A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757054 | ||||||
| chr16:89757101
|
G | A | 2 | a0003c0022t0002g0295a0038c0023t0002g0297 | 2 | HG00741.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2981+1476C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757101 | ||||||
| chr16:89757155
|
T | C | 1 | a0003c0003t0002g0290 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2981+1422A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757155 | ||||||
| chr16:89757280
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2981+1297C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757280 | ||||||
| chr16:89757286
|
G | T | 3 | a0002c0002t0001g0118a0002c0002t0001g0122a0002c0002t0001g0124 | 3 | NA18951.hp1 NA18968.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2981+1291C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757286 | ||||||
| chr16:89757372
|
G | A | 1 | a0002c0006t0005g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2981+1205C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757372 | ||||||
| chr16:89757536
|
C | G | 1 | a0003c0003t0002g0271 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2981+1041G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757536 | ||||||
| chr16:89757543
|
A | T | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.2981+1034T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757543 | ||||||
| chr16:89757664
|
C | T | 30 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.2981+913G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757664 | ||||||
| chr16:89757667
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2981+910C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757667 | ||||||
| chr16:89757692
|
A | G | 2 | a0006c0007t0009g0308a0006c0007t0009g0314 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2981+885T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757692 | ||||||
| chr16:89757697
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2981+880G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757697 | ||||||
| chr16:89757781
|
G | C | 12 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(9): Show | 12 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.2981+796C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757781 | ||||||
| chr16:89757793
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2981+784G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757793 | ||||||
| chr16:89757794
|
A | G | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2981+783T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757794 | ||||||
| chr16:89757795
|
G | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2981+782C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757795 | ||||||
| chr16:89757855
|
G | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+722C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757855 | ||||||
| chr16:89757940
|
C | A | 181 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(178): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.2981+637G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757940 | ||||||
| chr16:89757976
|
C | G | 200 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(197): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.2981+601G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89757976 | ||||||
| chr16:89758154
|
G | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2981+423C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89758154 | ||||||
| chr16:89758305
|
T | C | 2 | a0009c0010t0002g0289a0009c0010t0002g0299 | 2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2981+272A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89758305 | ||||||
| chr16:89758345
|
T | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.2981+232A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89758345 | ||||||
| chr16:89758424
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2981+153C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 30/42 | chr16 | 89758424 | ||||||
| chr16:89758749
|
G | A | 6 | a0005c0005t0001g0068a0005c0005t0001g0182a0005c0005t0001g0183others(3): Show | 6 | HG02015.hp1 HG02056.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.2853-44C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758749 | ||||||
| chr16:89758840
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-135A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758840 | ||||||
| chr16:89758928
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-223G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758928 | ||||||
| chr16:89758930
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-225T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758930 | ||||||
| chr16:89758969
|
C | T | 1 | a0002c0002t0001g0164 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2853-264G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758969 | ||||||
| chr16:89758973
|
G | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853-268C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758973 | ||||||
| chr16:89758997
|
G | T | 2 | a0002c0002t0001g0027a0002c0002t0001g0028 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2853-292C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89758997 | ||||||
| chr16:89759004
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2853-299C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759004 | ||||||
| chr16:89759056
|
C | T | 29 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2853-351G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759056 | ||||||
| chr16:89759087
|
C | G | 293 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.2853-382G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759087 | ||||||
| chr16:89759092
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2853-387C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759092 | ||||||
| chr16:89759111
|
G | A | 8 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2853-406C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759111 | ||||||
| chr16:89759130
|
G | A | 1 | a0009c0010t0002g0288 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2853-425C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759130 | ||||||
| chr16:89759195
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-490G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759195 | ||||||
| chr16:89759236
|
T | C | 1 | a0002c0002t0001g0091 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2853-531A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759236 | ||||||
| chr16:89759243
|
C | A | 8 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2853-538G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759243 | ||||||
| chr16:89759254
|
A | T | 15 | a0001c0001t0001g0179a0002c0002t0001g0022a0002c0002t0001g0042others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.2853-549T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759254 | ||||||
| chr16:89759264
|
G | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2853-559C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759264 | ||||||
| chr16:89759306
|
C | T | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2853-601G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759306 | ||||||
| chr16:89759315
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2853-610C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759315 | ||||||
| chr16:89759318
|
T | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-613A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(3): Show |
1 | a0004c0004t0001g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2853-623_2853-614d others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(7): Show |
1 | a0003c0003t0002g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2853-627_2853-614d others(16): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(10): Show |
1 | a0004c0004t0002g0233 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2853-630_2853-614d others(19): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(13): Show |
1 | a0004c0004t0002g0232 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2853-633_2853-614d others(22): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(14): Show |
2 | a0004c0004t0002g0245a0004c0004t0002g0269 | 2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2853-634_2853-614d others(23): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(15): Show |
1 | a0004c0004t0002g0256 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2853-635_2853-614d others(24): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(17): Show |
1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2853-637_2853-614d others(26): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(18): Show |
1 | a0004c0004t0002g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2853-638_2853-614d others(27): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(19): Show |
1 | a0004c0004t0002g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2853-639_2853-614d others(28): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(22): Show |
1 | a0004c0004t0002g0279 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2853-642_2853-614d others(31): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TAAAAAAA others(23): Show |
1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2853-643_2853-614d others(32): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TATAAAAA others(22): Show |
1 | a0003c0003t0002g0271 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2853-614_2853-613i others(31): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTA | 6 | a0003c0003t0002g0281a0005c0005t0001g0183a0005c0005t0001g0189others(3): Show | 6 | HG00323.hp2 HG02451.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAA | 23 | a0005c0005t0001g0036a0005c0005t0001g0065a0005c0005t0001g0066others(20): Show | 23 | HG00621.hp1 HG01175.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAA | 3 | a0005c0005t0001g0191a0005c0005t0001g0194a0005c0005t0001g0197 | 3 | HG00597.hp2 HG02135.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2853-614_2853-613i others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(1): Show |
8 | a0003c0003t0002g0240a0003c0003t0002g0274a0003c0003t0002g0292others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(2): Show |
11 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0283others(8): Show | 11 | HG00280.hp2 HG00741.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(11): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(3): Show |
6 | a0003c0003t0002g0282a0003c0003t0002g0293a0003c0003t0002g0294others(3): Show | 6 | HG00323.hp1 HG00733.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(4): Show |
5 | a0003c0003t0002g0275a0004c0004t0002g0264a0014c0015t0002g0008others(2): Show | 5 | HG01255.hp2 HG02300.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(13): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(5): Show |
2 | a0003c0003t0001g0303a0003c0003t0002g0285 | 2 | HG02071.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2853-614_2853-613i others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(10): Show |
3 | a0003c0003t0002g0270a0003c0003t0002g0280a0003c0003t0002g0290 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2853-614_2853-613i others(19): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(11): Show |
4 | a0003c0003t0002g0242a0003c0003t0002g0257a0003c0003t0002g0268others(1): Show | 4 | HG02647.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2853-614_2853-613i others(20): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(12): Show |
3 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2853-614_2853-613i others(21): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
T | TTAAAAAA others(18): Show |
1 | a0003c0003t0002g0255 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2853-614_2853-613i others(27): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
TA | T | 8 | a0004c0004t0002g0300a0006c0007t0004g0310a0006c0007t0004g0313others(5): Show | 8 | HG01192.hp1 HG01978.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2853-614delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
TAA | T | 32 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0057others(29): Show | 33 | HG00280.hp1 HG00558.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-615_2853-614d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
TAAA | T | 162 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(159): Show | 163 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.2853-616_2853-614d others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
TAAAA | T | 13 | a0001c0001t0001g0102a0001c0001t0001g0120a0001c0001t0001g0142others(10): Show | 13 | HG01255.hp1 HG01943.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.2853-617_2853-614d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0139 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2853-626_2853-614d others(15): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759318
|
TAAAAAAA others(7): Show |
T | 1 | a0004c0004t0002g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2853-627_2853-614d others(16): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759318 | ||||||
| chr16:89759319
|
A | T | 6 | a0005c0005t0001g0067a0006c0007t0004g0315a0006c0007t0004g0316others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2853-614T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759319 | ||||||
| chr16:89759320
|
A | T | 7 | a0006c0007t0004g0310a0006c0007t0004g0313a0006c0007t0004g0317others(4): Show | 7 | HG01192.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2853-615T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759320 | ||||||
| chr16:89759321
|
A | T | 30 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0057others(27): Show | 31 | HG00280.hp1 HG00558.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2853-616T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759321 | ||||||
| chr16:89759322
|
A | T | 157 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(154): Show | 158 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2853-617T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759322 | ||||||
| chr16:89759323
|
A | T | 13 | a0001c0001t0001g0102a0001c0001t0001g0120a0001c0001t0001g0142others(10): Show | 13 | HG01255.hp1 HG01943.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.2853-618T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759323 | ||||||
| chr16:89759326
|
A | T | 1 | a0003c0003t0002g0267 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2853-621T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759326 | ||||||
| chr16:89759332
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2853-627T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759332 | ||||||
| chr16:89759334
|
A | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-629T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759334 | ||||||
| chr16:89759350
|
G | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-645C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759350 | ||||||
| chr16:89759351
|
T | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-646A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759351 | ||||||
| chr16:89759358
|
G | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-653C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759358 | ||||||
| chr16:89759360
|
A | G | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-655T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759360 | ||||||
| chr16:89759367
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-662G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759367 | ||||||
| chr16:89759369
|
G | C | 1 | a0003c0003t0002g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2853-664C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759369 | ||||||
| chr16:89759428
|
A | G | 1 | a0024c0040t0001g0017 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2853-723T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759428 | ||||||
| chr16:89759436
|
G | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-731C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759436 | ||||||
| chr16:89759437
|
A | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-732T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759437 | ||||||
| chr16:89759449
|
C | T | 182 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.2853-744G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759449 | ||||||
| chr16:89759512
|
G | T | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-807C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759512 | ||||||
| chr16:89759562
|
A | G | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.2853-857T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759562 | ||||||
| chr16:89759611
|
A | T | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-906T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759611 | ||||||
| chr16:89759621
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-916G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759621 | ||||||
| chr16:89759669
|
G | C | 5 | a0002c0006t0008g0215a0002c0006t0008g0220a0002c0006t0008g0224others(2): Show | 5 | NA18939.hp1 NA18951.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2853-964C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759669 | ||||||
| chr16:89759710
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2853-1005C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759710 | ||||||
| chr16:89759737
|
G | T | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-1032C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759737 | ||||||
| chr16:89759739
|
C | T | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-1034G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759739 | ||||||
| chr16:89759740
|
A | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-1035T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759740 | ||||||
| chr16:89759845
|
C | G | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2853-1140G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759845 | ||||||
| chr16:89759870
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-1165G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759870 | ||||||
| chr16:89759907
|
G | GGGGTGCT others(22): Show |
1 | a0004c0004t0002g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2853-1231_2853-120 others(33): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759907 | ||||||
| chr16:89759907
|
G | T | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-1202C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759907 | ||||||
| chr16:89759928
|
G | C | 32 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(29): Show | 32 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.2853-1223C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759928 | ||||||
| chr16:89759930
|
G | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2853-1225C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759930 | ||||||
| chr16:89759934
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-1229G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759934 | ||||||
| chr16:89759936
|
T | TGGGTGCT others(22): Show |
1 | a0003c0003t0002g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2853-1260_2853-123 others(33): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759936 | ||||||
| chr16:89759955
|
G | C | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2853-1250C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759955 | ||||||
| chr16:89759957
|
G | GCGGGACC others(22): Show |
1 | a0001c0001t0001g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2853-1281_2853-125 others(33): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759957 | ||||||
| chr16:89759964
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-1259G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759964 | ||||||
| chr16:89759965
|
G | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-1260C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759965 | ||||||
| chr16:89759986
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-1281G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759986 | ||||||
| chr16:89759987
|
C | T | 1 | a0003c0003t0002g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2853-1282G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759987 | ||||||
| chr16:89759988
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2853-1283C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89759988 | ||||||
| chr16:89760168
|
C | T | 2 | a0002c0002t0001g0075a0002c0038t0001g0077 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2853-1463G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760168 | ||||||
| chr16:89760222
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2853-1517C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760222 | ||||||
| chr16:89760302
|
C | G | 1 | a0002c0002t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2853-1597G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760302 | ||||||
| chr16:89760315
|
G | A | 229 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2853-1610C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760315 | ||||||
| chr16:89760331
|
G | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2852+1618C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760331 | ||||||
| chr16:89760332
|
C | G | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2852+1617G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760332 | ||||||
| chr16:89760349
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2852+1600A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760349 | ||||||
| chr16:89760484
|
T | A | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2852+1465A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760484 | ||||||
| chr16:89760493
|
G | A | 199 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(196): Show | 201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2852+1456C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760493 | ||||||
| chr16:89760514
|
C | T | 278 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.2852+1435G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760514 | ||||||
| chr16:89760518
|
A | G | 278 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.2852+1431T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760518 | ||||||
| chr16:89760594
|
T | C | 277 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.2852+1355A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760594 | ||||||
| chr16:89760603
|
C | G | 293 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.2852+1346G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760603 | ||||||
| chr16:89760831
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+1118A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760831 | ||||||
| chr16:89760843
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+1106C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760843 | ||||||
| chr16:89760885
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2852+1064C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760885 | ||||||
| chr16:89760922
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+1027G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760922 | ||||||
| chr16:89760942
|
G | A | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2852+1007C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760942 | ||||||
| chr16:89760979
|
C | T | 1 | a0001c0001t0010g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2852+970G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89760979 | ||||||
| chr16:89761027
|
A | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+922T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761027 | ||||||
| chr16:89761033
|
C | T | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2852+916G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761033 | ||||||
| chr16:89761145
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2852+804G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761145 | ||||||
| chr16:89761148
|
G | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+801C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761148 | ||||||
| chr16:89761167
|
G | A | 1 | a0008c0008t0001g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2852+782C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761167 | ||||||
| chr16:89761202
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+747C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761202 | ||||||
| chr16:89761255
|
C | T | 329 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2852+694G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761255 | ||||||
| chr16:89761324
|
C | A | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2852+625G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761324 | ||||||
| chr16:89761325
|
A | G | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2852+624T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761325 | ||||||
| chr16:89761347
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+602T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761347 | ||||||
| chr16:89761360
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2852+589T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761360 | ||||||
| chr16:89761372
|
T | G | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2852+577A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761372 | ||||||
| chr16:89761420
|
G | GA | 162 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(159): Show | 164 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2852+528dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761420 | ||||||
| chr16:89761420
|
G | GAA | 33 | a0001c0001t0001g0057a0001c0001t0001g0123a0001c0001t0001g0179others(30): Show | 33 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+527_2852+528d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761420 | ||||||
| chr16:89761460
|
G | A | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2852+489C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761460 | ||||||
| chr16:89761470
|
T | A | 4 | a0001c0001t0001g0201a0001c0001t0001g0203a0030c0027t0001g0200others(1): Show | 4 | HG00099.hp2 HG03688.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2852+479A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761470 | ||||||
| chr16:89761477
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2852+472C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761477 | ||||||
| chr16:89761503
|
C | T | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2852+446G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761503 | ||||||
| chr16:89761616
|
T | C | 7 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0317others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2852+333A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761616 | ||||||
| chr16:89761635
|
T | A | 22 | a0001c0001t0001g0057a0001c0001t0001g0179a0002c0002t0001g0022others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2852+314A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761635 | ||||||
| chr16:89761812
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2852+137T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761812 | ||||||
| chr16:89761816
|
G | C | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2852+133C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | 89761816 | ||||||
| chr16:89762029
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
splice_region_variant&intron_variant | LOW | c.2779-7T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762029 | ||||||
| chr16:89762075
|
C | T | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2779-53G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762075 | ||||||
| chr16:89762076
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-54G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762076 | ||||||
| chr16:89762077
|
G | C | 22 | a0002c0002t0001g0001a0002c0002t0001g0029a0002c0002t0001g0030others(19): Show | 23 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.2779-55C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762077 | ||||||
| chr16:89762149
|
G | A | 1 | a0001c0034t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2779-127C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762149 | ||||||
| chr16:89762191
|
G | C | 1 | a0001c0001t0003g0040 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2779-169C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762191 | ||||||
| chr16:89762217
|
G | C | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2779-195C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762217 | ||||||
| chr16:89762218
|
C | G | 1 | a0005c0005t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2779-196G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762218 | ||||||
| chr16:89762261
|
C | G | 244 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(241): Show | 246 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.2779-239G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762261 | ||||||
| chr16:89762321
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2779-299G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762321 | ||||||
| chr16:89762378
|
GAGCCTAG others(12): Show |
G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-375_2779-357d others(21): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762378 | ||||||
| chr16:89762418
|
A | AC | 26 | a0001c0001t0001g0123a0001c0001t0001g0179a0002c0002t0001g0022others(23): Show | 26 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2779-397dupG | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762418 | ||||||
| chr16:89762454
|
T | C | 247 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(244): Show | 249 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.2779-432A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762454 | ||||||
| chr16:89762569
|
G | GA | 168 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(165): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.2779-548dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762569 | ||||||
| chr16:89762569
|
G | GAA | 28 | a0001c0001t0001g0057a0001c0001t0001g0097a0001c0001t0001g0123others(25): Show | 28 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.2779-549_2779-548d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762569 | ||||||
| chr16:89762569
|
G | GAAAA | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2779-551_2779-548d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762569 | ||||||
| chr16:89762591
|
G | C | 1 | a0001c0001t0003g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2779-569C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762591 | ||||||
| chr16:89762592
|
A | G | 1 | a0001c0001t0003g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2779-570T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762592 | ||||||
| chr16:89762641
|
C | A | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2779-619G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762641 | ||||||
| chr16:89762788
|
G | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-766C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762788 | ||||||
| chr16:89762793
|
G | C | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.2779-771C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762793 | ||||||
| chr16:89762887
|
G | C | 1 | a0006c0007t0004g0311 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2779-865C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762887 | ||||||
| chr16:89762918
|
C | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2779-896G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762918 | ||||||
| chr16:89762946
|
C | T | 4 | a0003c0003t0002g0275a0003c0003t0002g0283a0003c0003t0002g0284others(1): Show | 4 | HG02602.hp1 HG03688.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2779-924G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762946 | ||||||
| chr16:89762947
|
GA | G | 229 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(226): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2779-926delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762947 | ||||||
| chr16:89762947
|
GAAA | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-928_2779-926d others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762947 | ||||||
| chr16:89762978
|
T | G | 1 | a0004c0004t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2779-956A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89762978 | ||||||
| chr16:89763019
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-997C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763019 | ||||||
| chr16:89763022
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-1000T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763022 | ||||||
| chr16:89763047
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-1025T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763047 | ||||||
| chr16:89763110
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2779-1088C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763110 | ||||||
| chr16:89763131
|
C | T | 19 | a0001c0001t0001g0123a0001c0001t0001g0179a0002c0002t0001g0022others(16): Show | 19 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2779-1109G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763131 | ||||||
| chr16:89763162
|
C | T | 2 | a0004c0004t0002g0235a0004c0004t0002g0254 | 2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2779-1140G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763162 | ||||||
| chr16:89763247
|
CA | C | 211 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(208): Show | 213 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.2779-1226delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763247 | ||||||
| chr16:89763247
|
CAA | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-1227_2779-122 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763247 | ||||||
| chr16:89763374
|
T | G | 1 | a0004c0004t0002g0247 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2779-1352A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763374 | ||||||
| chr16:89763421
|
A | ACCTCGTG others(7): Show |
33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-1400_2779-139 others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763421 | ||||||
| chr16:89763427
|
C | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2779-1405G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763427 | ||||||
| chr16:89763441
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2779-1419C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763441 | ||||||
| chr16:89763455
|
C | T | 19 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0033others(16): Show | 19 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.2779-1433G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763455 | ||||||
| chr16:89763456
|
A | G | 19 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0033others(16): Show | 19 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.2778+1434T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763456 | ||||||
| chr16:89763469
|
C | A | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2778+1421G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763469 | ||||||
| chr16:89763487
|
C | T | 247 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(244): Show | 249 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.2778+1403G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763487 | ||||||
| chr16:89763586
|
C | G | 1 | a0035c0044t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2778+1304G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763586 | ||||||
| chr16:89763664
|
C | A | 10 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(7): Show | 10 | HG01192.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2778+1226G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763664 | ||||||
| chr16:89763678
|
C | T | 3 | a0003c0003t0002g0270a0003c0003t0002g0280a0022c0054t0002g0312 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2778+1212G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763678 | ||||||
| chr16:89763760
|
C | T | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2778+1130G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763760 | ||||||
| chr16:89763761
|
C | G | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2778+1129G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763761 | ||||||
| chr16:89763762
|
A | G | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2778+1128T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763762 | ||||||
| chr16:89763848
|
A | C | 1 | a0002c0002t0001g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2778+1042T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763848 | ||||||
| chr16:89763906
|
G | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2778+984C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763906 | ||||||
| chr16:89763920
|
G | GA | 227 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(224): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.2778+969dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763920 | ||||||
| chr16:89763920
|
G | GAA | 16 | a0001c0001t0001g0161a0006c0007t0004g0310a0006c0007t0004g0311others(13): Show | 16 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2778+968_2778+969d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763920 | ||||||
| chr16:89763931
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2778+959G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763931 | ||||||
| chr16:89763949
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2778+941T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89763949 | ||||||
| chr16:89764054
|
C | G | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.2778+836G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764054 | ||||||
| chr16:89764085
|
T | C | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.2778+805A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764085 | ||||||
| chr16:89764234
|
A | G | 1 | a0002c0038t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2778+656T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764234 | ||||||
| chr16:89764414
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2778+476A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764414 | ||||||
| chr16:89764437
|
C | G | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2778+453G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764437 | ||||||
| chr16:89764443
|
C | T | 14 | a0001c0029t0005g0103a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01167.hp1 HG03041.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.2778+447G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764443 | ||||||
| chr16:89764600
|
C | G | 1 | a0003c0003t0002g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2778+290G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764600 | ||||||
| chr16:89764778
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2778+112T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764778 | ||||||
| chr16:89764835
|
C | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2778+55G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764835 | ||||||
| chr16:89764863
|
G | A | 1 | a0005c0005t0001g0036 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2778+27C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 28/42 | chr16 | 89764863 | ||||||
| chr16:89765085
|
C | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0084 | 2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2602-19G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765085 | ||||||
| chr16:89765102
|
C | A | 29 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2602-36G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765102 | ||||||
| chr16:89765112
|
A | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2602-46T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765112 | ||||||
| chr16:89765150
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2602-84G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765150 | ||||||
| chr16:89765212
|
C | T | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2602-146G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765212 | ||||||
| chr16:89765222
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2602-156C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765222 | ||||||
| chr16:89765240
|
C | T | 1 | a0026c0036t0002g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2602-174G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765240 | ||||||
| chr16:89765284
|
T | TAGGGGAC others(44): Show |
3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2602-269_2602-219d others(53): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765284 | ||||||
| chr16:89765339
|
G | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2602-273C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765339 | ||||||
| chr16:89765385
|
T | G | 1 | a0002c0006t0011g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2602-319A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765385 | ||||||
| chr16:89765411
|
A | G | 293 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.2602-345T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765411 | ||||||
| chr16:89765433
|
A | G | 294 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.2602-367T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765433 | ||||||
| chr16:89765440
|
C | T | 1 | a0001c0001t0006g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2602-374G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765440 | ||||||
| chr16:89765532
|
G | C | 30 | a0002c0006t0005g0218a0003c0003t0002g0238a0003c0003t0002g0239others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.2602-466C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765532 | ||||||
| chr16:89765562
|
G | C | 1 | a0002c0006t0005g0218 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2602-496C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765562 | ||||||
| chr16:89765573
|
G | A | 1 | a0006c0007t0004g0311 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2602-507C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765573 | ||||||
| chr16:89765669
|
C | T | 1 | a0002c0002t0001g0091 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2602-603G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765669 | ||||||
| chr16:89765675
|
C | T | 210 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(207): Show | 212 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.2602-609G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765675 | ||||||
| chr16:89765706
|
G | A | 1 | a0031c0031t0001g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2602-640C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765706 | ||||||
| chr16:89765855
|
T | C | 4 | a0004c0004t0002g0264a0014c0015t0002g0008a0014c0015t0002g0011others(1): Show | 4 | HG00323.hp1 HG01255.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2602-789A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765855 | ||||||
| chr16:89765901
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0063others(2): Show | 5 | HG01993.hp1 HG02148.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.2602-835C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765901 | ||||||
| chr16:89765934
|
A | G | 1 | a0024c0040t0001g0017 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2602-868T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765934 | ||||||
| chr16:89765956
|
T | C | 183 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(180): Show | 185 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.2602-890A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765956 | ||||||
| chr16:89765999
|
A | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0241a0002c0006t0005g0217others(1): Show | 4 | HG02818.hp2 HG03139.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2602-933T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89765999 | ||||||
| chr16:89766002
|
T | TA | 45 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(42): Show | 45 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.2602-937_2602-936i others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766002 | ||||||
| chr16:89766003
|
T | A | 87 | a0001c0001t0001g0141a0002c0002t0001g0216a0002c0006t0005g0229others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2602-937A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766003 | ||||||
| chr16:89766065
|
C | T | 2 | a0005c0005t0001g0181a0005c0005t0001g0192 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2602-999G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766065 | ||||||
| chr16:89766136
|
A | T | 9 | a0007c0009t0001g0322a0007c0009t0001g0323a0007c0009t0001g0324others(6): Show | 10 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2601+1005T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766136 | ||||||
| chr16:89766183
|
GAC | G | 20 | a0002c0002t0001g0001a0002c0002t0001g0029a0002c0002t0001g0030others(17): Show | 21 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.2601+956_2601+957d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766183 | ||||||
| chr16:89766235
|
T | C | 1 | a0008c0008t0001g0015 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2601+906A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766235 | ||||||
| chr16:89766273
|
G | T | 1 | a0002c0002t0001g0034 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2601+868C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766273 | ||||||
| chr16:89766285
|
A | G | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.2601+856T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766285 | ||||||
| chr16:89766296
|
G | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2601+845C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766296 | ||||||
| chr16:89766343
|
G | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2601+798C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766343 | ||||||
| chr16:89766440
|
C | T | 244 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(241): Show | 246 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.2601+701G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766440 | ||||||
| chr16:89766519
|
G | A | 6 | a0003c0003t0001g0303a0012c0013t0007g0079a0012c0013t0007g0081others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2601+622C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766519 | ||||||
| chr16:89766571
|
C | T | 1 | a0002c0006t0005g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2601+570G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766571 | ||||||
| chr16:89766581
|
G | T | 2 | a0001c0001t0001g0102a0001c0034t0001g0104 | 2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2601+560C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766581 | ||||||
| chr16:89766583
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2601+558G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766583 | ||||||
| chr16:89766599
|
CAGCAACT others(5): Show |
C | 1 | a0003c0003t0002g0274 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2601+530_2601+541d others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766599 | ||||||
| chr16:89766689
|
T | C | 195 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(192): Show | 197 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.2601+452A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766689 | ||||||
| chr16:89766747
|
T | C | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2601+394A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766747 | ||||||
| chr16:89766804
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2601+337G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766804 | ||||||
| chr16:89766821
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2601+320A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766821 | ||||||
| chr16:89766835
|
T | G | 7 | a0001c0001t0006g0062a0001c0001t0006g0168a0001c0001t0006g0170others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2601+306A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766835 | ||||||
| chr16:89766947
|
G | A | 6 | a0001c0001t0001g0141a0003c0003t0002g0259a0003c0003t0002g0260others(3): Show | 6 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.2601+194C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766947 | ||||||
| chr16:89766974
|
C | G | 1 | a0002c0002t0001g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2601+167G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89766974 | ||||||
| chr16:89767048
|
C | G | 6 | a0001c0001t0001g0141a0003c0003t0002g0259a0003c0003t0002g0260others(3): Show | 6 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.2601+93G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89767048 | ||||||
| chr16:89767058
|
G | C | 3 | a0002c0002t0001g0216a0002c0006t0011g0227a0002c0006t0011g0228 | 3 | HG01081.hp1 HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2601+83C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 27/42 | chr16 | 89767058 | ||||||
| chr16:89767307
|
G | C | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2505-70C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767307 | ||||||
| chr16:89767357
|
T | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2505-120A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767357 | ||||||
| chr16:89767366
|
C | G | 243 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.2505-129G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767366 | ||||||
| chr16:89767368
|
T | G | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2505-131A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767368 | ||||||
| chr16:89767386
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2505-149C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767386 | ||||||
| chr16:89767446
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2505-209G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767446 | ||||||
| chr16:89767473
|
G | T | 243 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.2505-236C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767473 | ||||||
| chr16:89767576
|
G | C | 5 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0160others(2): Show | 5 | HG00558.hp2 HG02027.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.2505-339C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767576 | ||||||
| chr16:89767594
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2505-357C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767594 | ||||||
| chr16:89767617
|
C | G | 178 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(175): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.2505-380G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767617 | ||||||
| chr16:89767619
|
G | A | 3 | a0002c0002t0001g0118a0002c0002t0001g0122a0002c0002t0001g0124 | 3 | NA18951.hp1 NA18968.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2505-382C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767619 | ||||||
| chr16:89767668
|
T | C | 245 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(242): Show | 247 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.2505-431A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767668 | ||||||
| chr16:89767758
|
G | C | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2505-521C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767758 | ||||||
| chr16:89767770
|
G | T | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2505-533C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767770 | ||||||
| chr16:89767775
|
C | G | 1 | a0002c0002t0001g0060 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2505-538G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767775 | ||||||
| chr16:89767791
|
G | A | 1 | a0009c0010t0002g0298 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2505-554C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767791 | ||||||
| chr16:89767862
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2505-625A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767862 | ||||||
| chr16:89767870
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2505-633C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767870 | ||||||
| chr16:89767874
|
C | T | 1 | a0012c0013t0007g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2505-637G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89767874 | ||||||
| chr16:89768204
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2505-967C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768204 | ||||||
| chr16:89768224
|
G | A | 1 | a0003c0003t0002g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2505-987C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768224 | ||||||
| chr16:89768227
|
A | G | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2505-990T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768227 | ||||||
| chr16:89768253
|
A | C | 179 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(176): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.2505-1016T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768253 | ||||||
| chr16:89768323
|
T | C | 13 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2505-1086A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768323 | ||||||
| chr16:89768351
|
A | G | 3 | a0002c0002t0001g0027a0002c0002t0001g0028a0028c0043t0015g0307 | 3 | HG03041.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2505-1114T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768351 | ||||||
| chr16:89768510
|
GCTGGGCA others(13): Show |
G | 1 | a0002c0006t0005g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2505-1293_2505-127 others(24): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768510 | ||||||
| chr16:89768563
|
C | G | 179 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(176): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.2504+1274G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768563 | ||||||
| chr16:89768637
|
T | C | 1 | a0003c0003t0002g0242 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2504+1200A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768637 | ||||||
| chr16:89768640
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2504+1197T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768640 | ||||||
| chr16:89768681
|
C | CA | 15 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(12): Show | 15 | HG01109.hp1 HG01192.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2504+1155dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768681 | ||||||
| chr16:89768689
|
A | G | 179 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(176): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.2504+1148T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768689 | ||||||
| chr16:89768710
|
A | G | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2504+1127T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768710 | ||||||
| chr16:89768819
|
A | G | 16 | a0001c0001t0001g0053a0001c0029t0005g0103a0002c0002t0001g0216others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.2504+1018T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768819 | ||||||
| chr16:89768826
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2504+1011C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768826 | ||||||
| chr16:89768881
|
C | T | 71 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(68): Show | 71 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2504+956G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768881 | ||||||
| chr16:89768913
|
CCAGTACT | C | 153 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(150): Show | 155 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.2504+917_2504+923d others(9): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768913 | ||||||
| chr16:89768933
|
C | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2504+904G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768933 | ||||||
| chr16:89768943
|
G | C | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2504+894C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768943 | ||||||
| chr16:89768993
|
G | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2504+844C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89768993 | ||||||
| chr16:89769113
|
A | G | 228 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(225): Show | 230 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.2504+724T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89769113 | ||||||
| chr16:89769170
|
G | A | 2 | a0003c0003t0002g0240a0007c0009t0001g0327 | 2 | HG01123.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2504+667C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89769170 | ||||||
| chr16:89769368
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2504+469T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89769368 | ||||||
| chr16:89769676
|
A | G | 2 | a0002c0047t0001g0082a0028c0043t0015g0307 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2504+161T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 26/42 | chr16 | 89769676 | ||||||
| chr16:89770099
|
T | C | 329 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2316+67A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 25/42 | chr16 | 89770099 | ||||||
| chr16:89770101
|
G | C | 2 | a0002c0047t0001g0082a0028c0043t0015g0307 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2316+65C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 25/42 | chr16 | 89770101 | ||||||
| chr16:89770143
|
G | A | 2 | a0002c0002t0001g0027a0002c0002t0001g0028 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2316+23C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 25/42 | chr16 | 89770143 | ||||||
| chr16:89770342
|
C | T | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2223-83G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/42 | chr16 | 89770342 | ||||||
| chr16:89770373
|
G | A | 247 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(244): Show | 249 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.2223-114C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/42 | chr16 | 89770373 | ||||||
| chr16:89770407
|
T | C | 1 | a0001c0034t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2223-148A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/42 | chr16 | 89770407 | ||||||
| chr16:89770457
|
A | G | 247 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(244): Show | 249 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.2222+107T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/42 | chr16 | 89770457 | ||||||
| chr16:89770464
|
T | C | 244 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(241): Show | 246 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.2222+100A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/42 | chr16 | 89770464 | ||||||
| chr16:89770491
|
T | C | 9 | a0004c0004t0002g0237a0004c0004t0002g0264a0010c0011t0002g0004others(6): Show | 9 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.2222+73A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 24/42 | chr16 | 89770491 | ||||||
| chr16:89770673
|
G | A | 1 | a0003c0003t0002g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2152-39C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89770673 | ||||||
| chr16:89770713
|
A | G | 1 | a0009c0010t0002g0298 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2152-79T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89770713 | ||||||
| chr16:89770730
|
G | T | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2152-96C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89770730 | ||||||
| chr16:89770918
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2152-284A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89770918 | ||||||
| chr16:89770959
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2152-325T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89770959 | ||||||
| chr16:89770963
|
G | A | 1 | a0004c0004t0002g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2152-329C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89770963 | ||||||
| chr16:89771083
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2152-449A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771083 | ||||||
| chr16:89771091
|
G | T | 1 | a0005c0005t0001g0198 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2152-457C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771091 | ||||||
| chr16:89771144
|
G | A | 1 | a0001c0034t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2152-510C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771144 | ||||||
| chr16:89771155
|
C | CA | 9 | a0001c0001t0001g0116a0001c0001t0001g0179a0001c0001t0001g0201others(6): Show | 9 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.2151+522dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAA | 32 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0066others(29): Show | 32 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.2151+521_2151+522d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(3): Show |
2 | a0002c0047t0001g0082a0028c0043t0015g0307 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2151+513_2151+522d others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(4): Show |
1 | a0006c0007t0004g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2151+512_2151+522d others(13): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(16): Show |
1 | a0006c0007t0009g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2151+522_2152-521i others(25): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(17): Show |
1 | a0006c0007t0004g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2151+522_2152-521i others(26): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(18): Show |
3 | a0006c0007t0004g0313a0006c0007t0004g0317a0041c0049t0004g0207 | 3 | HG01192.hp1 HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2151+522_2152-521i others(27): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(20): Show |
1 | a0006c0007t0004g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2151+522_2152-521i others(29): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(22): Show |
1 | a0006c0007t0004g0311 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2151+522_2152-521i others(31): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(24): Show |
1 | a0006c0007t0004g0319 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2151+522_2152-521i others(33): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(29): Show |
1 | a0006c0056t0004g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2151+522_2152-521i others(38): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771155
|
C | CAAAAAAA others(30): Show |
1 | a0006c0007t0004g0318 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2151+522_2152-521i others(39): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771155 | ||||||
| chr16:89771215
|
T | C | 3 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2151+463A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771215 | ||||||
| chr16:89771246
|
C | G | 1 | a0003c0003t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2151+432G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771246 | ||||||
| chr16:89771519
|
A | G | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2151+159T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771519 | ||||||
| chr16:89771543
|
T | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2151+135A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771543 | ||||||
| chr16:89771552
|
A | T | 1 | a0002c0006t0005g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2151+126T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771552 | ||||||
| chr16:89771563
|
C | T | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2151+115G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771563 | ||||||
| chr16:89771576
|
G | A | 2 | a0013c0014t0002g0331a0013c0014t0002g0332 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2151+102C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771576 | ||||||
| chr16:89771670
|
A | G | 193 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(192): Show |
splice_region_variant&intron_variant | LOW | c.2151+8T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 23/42 | chr16 | 89771670 | ||||||
| chr16:89771838
|
G | A | 1 | a0002c0002t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2015-24C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89771838 | ||||||
| chr16:89771912
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2015-98G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89771912 | ||||||
| chr16:89771951
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2015-137C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89771951 | ||||||
| chr16:89771955
|
A | G | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2015-141T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89771955 | ||||||
| chr16:89771965
|
G | C | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2015-151C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89771965 | ||||||
| chr16:89772022
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2015-208G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772022 | ||||||
| chr16:89772024
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2015-210C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772024 | ||||||
| chr16:89772063
|
G | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2015-249C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772063 | ||||||
| chr16:89772133
|
C | T | 63 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(60): Show | 63 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2015-319G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772133 | ||||||
| chr16:89772170
|
A | T | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2015-356T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772170 | ||||||
| chr16:89772195
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2015-381G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772195 | ||||||
| chr16:89772277
|
C | G | 27 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.2015-463G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772277 | ||||||
| chr16:89772292
|
C | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2015-478G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772292 | ||||||
| chr16:89772323
|
T | A | 3 | a0007c0009t0001g0323a0007c0009t0001g0324a0015c0020t0001g0002 | 4 | HG02280.hp2 HG03195.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2015-509A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772323 | ||||||
| chr16:89772323
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2015-509A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772323 | ||||||
| chr16:89772426
|
T | C | 202 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(199): Show | 204 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.2015-612A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772426 | ||||||
| chr16:89772454
|
T | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2015-640A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772454 | ||||||
| chr16:89772712
|
G | C | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.2014+559C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772712 | ||||||
| chr16:89772732
|
T | C | 1 | a0004c0004t0002g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2014+539A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772732 | ||||||
| chr16:89772734
|
G | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2014+537C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772734 | ||||||
| chr16:89772759
|
C | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2014+512G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772759 | ||||||
| chr16:89772775
|
C | A | 3 | a0006c0055t0009g0309a0028c0043t0015g0307a0040c0050t0013g0206 | 3 | HG02451.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2014+496G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772775 | ||||||
| chr16:89772818
|
CA | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(238): Show | 243 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.2014+452delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772818 | ||||||
| chr16:89772898
|
A | G | 243 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.2014+373T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89772898 | ||||||
| chr16:89773229
|
C | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2014+42G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 22/42 | chr16 | 89773229 | ||||||
| chr16:89773446
|
T | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1901-62A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773446 | ||||||
| chr16:89773507
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1901-123C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773507 | ||||||
| chr16:89773559
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1901-175C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773559 | ||||||
| chr16:89773568
|
T | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1901-184A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773568 | ||||||
| chr16:89773589
|
G | A | 229 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(226): Show | 231 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1901-205C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773589 | ||||||
| chr16:89773599
|
A | G | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1901-215T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773599 | ||||||
| chr16:89773773
|
C | CT | 15 | a0001c0001t0001g0139a0001c0030t0001g0130a0002c0002t0001g0165others(12): Show | 15 | HG01175.hp1 HG01891.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.1901-390dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773773 | ||||||
| chr16:89773773
|
CT | C | 35 | a0002c0006t0011g0228a0005c0005t0001g0036a0005c0005t0001g0064others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1901-390delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773773 | ||||||
| chr16:89773866
|
G | A | 1 | a0032c0032t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1901-482C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773866 | ||||||
| chr16:89773873
|
A | C | 1 | a0024c0040t0001g0017 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1901-489T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773873 | ||||||
| chr16:89773876
|
C | T | 1 | a0024c0040t0001g0017 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1901-492G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773876 | ||||||
| chr16:89773877
|
A | C | 1 | a0024c0040t0001g0017 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1901-493T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773877 | ||||||
| chr16:89773963
|
A | G | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1901-579T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89773963 | ||||||
| chr16:89774045
|
G | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1901-661C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774045 | ||||||
| chr16:89774093
|
A | G | 1 | a0003c0003t0002g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1901-709T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774093 | ||||||
| chr16:89774223
|
T | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1901-839A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774223 | ||||||
| chr16:89774300
|
C | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1901-916G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774300 | ||||||
| chr16:89774316
|
AGGGGAAG others(10): Show |
A | 1 | a0002c0002t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1901-949_1901-933d others(19): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774316 | ||||||
| chr16:89774366
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1901-982G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774366 | ||||||
| chr16:89774377
|
G | A | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1901-993C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774377 | ||||||
| chr16:89774448
|
C | T | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1901-1064G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774448 | ||||||
| chr16:89774513
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1901-1129C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774513 | ||||||
| chr16:89774557
|
T | C | 244 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(241): Show | 246 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1901-1173A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774557 | ||||||
| chr16:89774603
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1900+1139C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774603 | ||||||
| chr16:89774618
|
C | T | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1900+1124G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774618 | ||||||
| chr16:89774647
|
A | G | 35 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1900+1095T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774647 | ||||||
| chr16:89774661
|
C | T | 2 | a0008c0008t0001g0019a0024c0040t0001g0017 | 2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1900+1081G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774661 | ||||||
| chr16:89774686
|
C | T | 1 | a0002c0006t0005g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1900+1056G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774686 | ||||||
| chr16:89774729
|
C | CA | 59 | a0001c0001t0001g0058a0001c0001t0001g0145a0001c0001t0003g0135others(56): Show | 61 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1900+1012dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAA | 106 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(103): Show | 106 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1900+1011_1900+101 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAA | 12 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0107others(9): Show | 12 | HG01358.hp1 HG01361.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1900+1010_1900+101 others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAA | 9 | a0003c0003t0002g0255a0003c0003t0002g0267a0003c0003t0002g0270others(6): Show | 9 | HG00639.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1900+1008_1900+101 others(9): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAA | 17 | a0003c0003t0002g0242a0003c0003t0002g0268a0005c0005t0001g0036others(14): Show | 17 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1900+1007_1900+101 others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA | 16 | a0005c0005t0001g0065a0005c0005t0001g0066a0005c0005t0001g0068others(13): Show | 16 | HG00323.hp2 HG00597.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900+1006_1900+101 others(11): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(4): Show |
20 | a0002c0006t0005g0223a0002c0006t0008g0215a0002c0006t0008g0220others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900+1002_1900+101 others(15): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(5): Show |
28 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0219others(25): Show | 28 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1900+1001_1900+101 others(16): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(6): Show |
24 | a0002c0006t0008g0225a0002c0006t0011g0228a0003c0003t0002g0238others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1900+1000_1900+101 others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(7): Show |
14 | a0002c0006t0005g0217a0003c0003t0001g0303a0003c0003t0002g0240others(11): Show | 14 | HG00733.hp2 HG01109.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1900+999_1900+1012 others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(8): Show |
2 | a0002c0006t0005g0218a0014c0015t0002g0011 | 2 | HG00323.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1900+998_1900+1012 others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(9): Show |
2 | a0003c0003t0002g0285a0014c0015t0002g0008 | 2 | HG02071.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1900+997_1900+1012 others(19): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774729
|
C | CAAAAAAA others(11): Show |
1 | a0020c0021t0002g0012 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1900+995_1900+1012 others(21): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774729 | ||||||
| chr16:89774759
|
A | G | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1900+983T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774759 | ||||||
| chr16:89774831
|
T | C | 247 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(244): Show | 249 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1900+911A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774831 | ||||||
| chr16:89774954
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1900+788G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774954 | ||||||
| chr16:89774966
|
T | C | 279 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1900+776A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774966 | ||||||
| chr16:89774994
|
T | C | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1900+748A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89774994 | ||||||
| chr16:89775016
|
C | T | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1900+726G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775016 | ||||||
| chr16:89775144
|
T | C | 279 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1900+598A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775144 | ||||||
| chr16:89775197
|
T | G | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1900+545A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775197 | ||||||
| chr16:89775219
|
T | C | 12 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1900+523A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775219 | ||||||
| chr16:89775385
|
G | C | 180 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(177): Show | 182 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1900+357C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775385 | ||||||
| chr16:89775525
|
A | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1900+217T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775525 | ||||||
| chr16:89775621
|
C | G | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1900+121G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775621 | ||||||
| chr16:89775628
|
G | C | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1900+114C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | 89775628 | ||||||
| chr16:89775834
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1827-19T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89775834 | ||||||
| chr16:89775877
|
A | T | 2 | a0008c0008t0001g0019a0024c0040t0001g0017 | 2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1827-62T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89775877 | ||||||
| chr16:89775891
|
T | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1827-76A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89775891 | ||||||
| chr16:89775939
|
C | T | 2 | a0008c0008t0001g0019a0024c0040t0001g0017 | 2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1827-124G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89775939 | ||||||
| chr16:89775966
|
T | G | 250 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(247): Show | 252 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1827-151A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89775966 | ||||||
| chr16:89776027
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1827-212T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776027 | ||||||
| chr16:89776048
|
C | A | 5 | a0002c0002t0001g0080a0002c0002t0001g0087a0002c0002t0001g0089others(2): Show | 5 | HG00423.hp1 NA18983.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1827-233G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776048 | ||||||
| chr16:89776071
|
T | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1827-256A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776071 | ||||||
| chr16:89776153
|
GTTTTTCT others(1): Show |
G | 9 | a0002c0002t0001g0216a0002c0006t0005g0219a0002c0006t0005g0223others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1827-346_1827-339d others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776153 | ||||||
| chr16:89776157
|
T | TTC | 22 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0068others(19): Show | 22 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1827-344_1827-343d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776157 | ||||||
| chr16:89776159
|
C | CT | 28 | a0001c0001t0001g0069a0001c0001t0001g0097a0001c0001t0001g0105others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1827-345dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776159 | ||||||
| chr16:89776159
|
CT | C | 12 | a0001c0001t0001g0147a0001c0001t0001g0169a0002c0002t0001g0028others(9): Show | 12 | HG00735.hp1 HG01109.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1827-345delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776159 | ||||||
| chr16:89776159
|
CTTTTTTT | C | 48 | a0001c0026t0001g0023a0002c0002t0001g0001a0002c0002t0001g0022others(45): Show | 49 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1827-351_1827-345d others(9): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776159 | ||||||
| chr16:89776160
|
T | TC | 9 | a0005c0005t0001g0065a0005c0005t0001g0066a0005c0005t0001g0181others(6): Show | 9 | HG02135.hp1 HG02165.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1827-346_1827-345i others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776160 | ||||||
| chr16:89776165
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1827-350A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776165 | ||||||
| chr16:89776166
|
T | C | 1 | a0006c0007t0004g0317 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1827-351A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776166 | ||||||
| chr16:89776168
|
T | C | 17 | a0001c0001t0001g0102a0001c0026t0001g0023a0001c0034t0001g0104others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1827-353A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776168 | ||||||
| chr16:89776341
|
G | C | 179 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(176): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1827-526C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776341 | ||||||
| chr16:89776376
|
C | T | 7 | a0010c0011t0002g0004a0010c0011t0002g0005a0010c0011t0002g0009others(4): Show | 7 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1827-561G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776376 | ||||||
| chr16:89776410
|
A | G | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1827-595T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776410 | ||||||
| chr16:89776416
|
C | T | 179 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(176): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1827-601G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776416 | ||||||
| chr16:89776473
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1827-658C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776473 | ||||||
| chr16:89776476
|
T | A | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1827-661A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776476 | ||||||
| chr16:89776495
|
T | A | 221 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(218): Show | 223 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1827-680A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776495 | ||||||
| chr16:89776553
|
C | T | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1827-738G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776553 | ||||||
| chr16:89776617
|
G | A | 1 | a0003c0003t0002g0290 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1827-802C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776617 | ||||||
| chr16:89776666
|
A | G | 13 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1827-851T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776666 | ||||||
| chr16:89776687
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1827-872G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776687 | ||||||
| chr16:89776688
|
G | A | 1 | a0011c0012t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1827-873C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776688 | ||||||
| chr16:89776728
|
G | A | 14 | a0002c0002t0001g0022a0002c0002t0001g0042a0002c0002t0001g0060others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1827-913C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776728 | ||||||
| chr16:89776781
|
A | C | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1827-966T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776781 | ||||||
| chr16:89776939
|
C | T | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1827-1124G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89776939 | ||||||
| chr16:89777027
|
C | A | 2 | a0001c0001t0001g0212a0003c0003t0002g0271 | 2 | HG02145.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1827-1212G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777027 | ||||||
| chr16:89777096
|
G | A | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1827-1281C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777096 | ||||||
| chr16:89777116
|
G | A | 1 | a0032c0032t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1827-1301C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777116 | ||||||
| chr16:89777136
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1827-1321C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777136 | ||||||
| chr16:89777142
|
C | A | 1 | a0002c0002t0001g0042 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1827-1327G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777142 | ||||||
| chr16:89777146
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1827-1331C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777146 | ||||||
| chr16:89777320
|
T | C | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826+1481A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777320 | ||||||
| chr16:89777499
|
G | C | 3 | a0006c0007t0004g0313a0006c0007t0004g0315a0006c0007t0009g0314 | 3 | HG01192.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1826+1302C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777499 | ||||||
| chr16:89777545
|
G | A | 1 | a0007c0009t0001g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1826+1256C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777545 | ||||||
| chr16:89777635
|
T | C | 208 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(205): Show | 210 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.1826+1166A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777635 | ||||||
| chr16:89777654
|
T | C | 12 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1826+1147A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777654 | ||||||
| chr16:89777712
|
G | T | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826+1089C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777712 | ||||||
| chr16:89777821
|
T | C | 180 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(177): Show | 182 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1826+980A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777821 | ||||||
| chr16:89777843
|
A | G | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1826+958T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777843 | ||||||
| chr16:89777868
|
G | C | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.1826+933C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777868 | ||||||
| chr16:89777950
|
C | T | 1 | a0003c0003t0002g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1826+851G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89777950 | ||||||
| chr16:89778034
|
C | T | 1 | a0007c0009t0001g0322 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826+767G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778034 | ||||||
| chr16:89778161
|
C | CA | 72 | a0001c0001t0001g0046a0001c0001t0001g0069a0001c0001t0001g0071others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.1826+639dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778161 | ||||||
| chr16:89778161
|
C | CAA | 10 | a0001c0001t0001g0212a0003c0003t0002g0286a0008c0008t0001g0016others(7): Show | 10 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.1826+638_1826+639d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778161 | ||||||
| chr16:89778161
|
C | CAAA | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1826+637_1826+639d others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778161 | ||||||
| chr16:89778191
|
G | A | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1826+610C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778191 | ||||||
| chr16:89778270
|
C | T | 1 | a0001c0001t0003g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1826+531G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778270 | ||||||
| chr16:89778362
|
A | C | 1 | a0003c0022t0002g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1826+439T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778362 | ||||||
| chr16:89778364
|
G | A | 1 | a0009c0010t0002g0298 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1826+437C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778364 | ||||||
| chr16:89778403
|
T | C | 1 | a0032c0032t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1826+398A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778403 | ||||||
| chr16:89778427
|
T | C | 8 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826+374A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778427 | ||||||
| chr16:89778462
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1826+339A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778462 | ||||||
| chr16:89778464
|
TA | T | 196 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(193): Show | 198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.1826+336delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778464 | ||||||
| chr16:89778626
|
C | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1826+175G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778626 | ||||||
| chr16:89778627
|
T | TA | 140 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(137): Show | 142 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1826+173dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778627
|
T | TAA | 43 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0001g0138others(40): Show | 43 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1826+172_1826+173d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778627
|
TA | T | 33 | a0002c0002t0001g0027a0002c0002t0001g0075a0002c0002t0001g0175others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1826+173delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778627
|
TAA | T | 9 | a0002c0002t0001g0031a0003c0003t0002g0242a0003c0003t0002g0267others(6): Show | 9 | HG00639.hp1 HG01169.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1826+172_1826+173d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778627
|
TAAAAAA | T | 8 | a0002c0006t0005g0025a0002c0006t0005g0219a0002c0006t0005g0223others(5): Show | 8 | HG03239.hp2 HG03704.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826+168_1826+173d others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778627
|
TAAAAAAA others(3): Show |
T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826+164_1826+173d others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778627
|
TAAAAAAA others(8): Show |
T | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1826+159_1826+173d others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778627 | ||||||
| chr16:89778638
|
A | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826+163T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778638 | ||||||
| chr16:89778661
|
A | C | 1 | a0041c0049t0004g0207 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1826+140T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778661 | ||||||
| chr16:89778702
|
A | T | 243 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1826+99T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778702 | ||||||
| chr16:89778703
|
T | C | 14 | a0005c0005t0001g0036a0005c0005t0001g0065a0005c0005t0001g0066others(11): Show | 14 | HG00323.hp2 HG00621.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1826+98A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778703 | ||||||
| chr16:89778734
|
C | T | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1826+67G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778734 | ||||||
| chr16:89778770
|
T | TAC | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1826+30_1826+31ins others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778770 | ||||||
| chr16:89778786
|
A | G | 246 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(243): Show | 248 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1826+15T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778786 | ||||||
| chr16:89778789
|
G | A | 4 | a0003c0003t0002g0293a0003c0003t0002g0294a0003c0022t0002g0295others(1): Show | 4 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+12C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 20/42 | chr16 | 89778789 | ||||||
| chr16:89778879
|
A | G | 34 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1777-29T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 19/42 | chr16 | 89778879 | ||||||
| chr16:89778887
|
GGAAA | G | 3 | a0012c0013t0007g0079a0012c0013t0007g0081a0012c0013t0007g0095 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1777-41_1777-38del others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 19/42 | chr16 | 89778887 | ||||||
| chr16:89779138
|
T | C | 1 | a0002c0035t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1716-135A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779138 | ||||||
| chr16:89779158
|
C | T | 7 | a0002c0002t0001g0029a0002c0002t0001g0080a0002c0002t0001g0087others(4): Show | 7 | HG00280.hp1 HG00423.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716-155G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779158 | ||||||
| chr16:89779207
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-204C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779207 | ||||||
| chr16:89779218
|
G | A | 16 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG02965.hp1 others(13): Show |
intron_variant | MODIFIER | c.1716-215C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779218 | ||||||
| chr16:89779263
|
C | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1716-260G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779263 | ||||||
| chr16:89779300
|
C | T | 1 | a0029c0028t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1716-297G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779300 | ||||||
| chr16:89779331
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-328C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779331 | ||||||
| chr16:89779389
|
A | G | 1 | a0004c0004t0002g0256 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1716-386T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779389 | ||||||
| chr16:89779397
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-394A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779397 | ||||||
| chr16:89779642
|
C | T | 243 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1715+227G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779642 | ||||||
| chr16:89779673
|
G | A | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1715+196C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779673 | ||||||
| chr16:89779738
|
C | T | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1715+131G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779738 | ||||||
| chr16:89779756
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1715+113G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779756 | ||||||
| chr16:89779787
|
A | G | 243 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1715+82T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 18/42 | chr16 | 89779787 | ||||||
| chr16:89779989
|
A | G | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1627-32T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89779989 | ||||||
| chr16:89780061
|
T | C | 1 | a0001c0001t0003g0051 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1627-104A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780061 | ||||||
| chr16:89780214
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1627-257C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780214 | ||||||
| chr16:89780265
|
G | A | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1627-308C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780265 | ||||||
| chr16:89780269
|
G | C | 6 | a0002c0002t0001g0042a0002c0002t0001g0060a0002c0002t0001g0128others(3): Show | 6 | HG00423.hp2 HG00597.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627-312C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780269 | ||||||
| chr16:89780282
|
A | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1627-325T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780282 | ||||||
| chr16:89780284
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1627-327T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780284 | ||||||
| chr16:89780567
|
T | A | 2 | a0001c0001t0001g0203a0030c0027t0001g0200 | 2 | HG04115.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1627-610A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780567 | ||||||
| chr16:89780579
|
A | G | 276 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1627-622T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780579 | ||||||
| chr16:89780581
|
G | A | 3 | a0002c0006t0011g0227a0002c0006t0011g0228a0021c0053t0001g0321 | 3 | HG01167.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1627-624C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780581 | ||||||
| chr16:89780602
|
C | T | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1627-645G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780602 | ||||||
| chr16:89780608
|
G | A | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1627-651C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780608 | ||||||
| chr16:89780623
|
C | CA | 6 | a0001c0001t0001g0241a0003c0003t0002g0257a0003c0003t0002g0281others(3): Show | 6 | HG00597.hp2 HG01192.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627-667dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780623 | ||||||
| chr16:89780623
|
CA | C | 214 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1627-667delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780623 | ||||||
| chr16:89780657
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1627-700C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780657 | ||||||
| chr16:89780714
|
AG | A | 4 | a0002c0006t0008g0220a0002c0006t0008g0224a0002c0006t0008g0225others(1): Show | 4 | NA18939.hp1 NA18951.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-758delC | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780714 | ||||||
| chr16:89780813
|
C | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1627-856G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780813 | ||||||
| chr16:89780814
|
C | T | 1 | a0003c0003t0002g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1627-857G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780814 | ||||||
| chr16:89780824
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627-867C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780824 | ||||||
| chr16:89780844
|
C | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1627-887G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780844 | ||||||
| chr16:89780929
|
CA | C | 61 | a0001c0001t0001g0115a0001c0001t0001g0127a0001c0001t0001g0163others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1627-973delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89780929 | ||||||
| chr16:89781012
|
T | A | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1627-1055A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781012 | ||||||
| chr16:89781094
|
G | A | 193 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(190): Show | 195 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1627-1137C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781094 | ||||||
| chr16:89781113
|
C | T | 246 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(243): Show | 248 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1627-1156G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781113 | ||||||
| chr16:89781146
|
C | T | 1 | a0006c0007t0004g0311 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1627-1189G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781146 | ||||||
| chr16:89781223
|
A | G | 244 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(241): Show | 246 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1627-1266T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781223 | ||||||
| chr16:89781343
|
A | G | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1627-1386T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781343 | ||||||
| chr16:89781345
|
T | C | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1627-1388A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781345 | ||||||
| chr16:89781349
|
A | G | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1627-1392T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781349 | ||||||
| chr16:89781356
|
T | C | 1 | a0004c0004t0002g0256 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1627-1399A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781356 | ||||||
| chr16:89781363
|
C | CA | 13 | a0003c0003t0002g0257a0003c0003t0002g0281a0004c0004t0002g0236others(10): Show | 13 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1627-1407dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781363 | ||||||
| chr16:89781363
|
C | CAA | 13 | a0001c0001t0001g0241a0002c0006t0005g0025a0002c0006t0005g0219others(10): Show | 13 | HG01167.hp1 HG01192.hp2 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.1627-1408_1627-140 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781363 | ||||||
| chr16:89781363
|
C | CAAA | 11 | a0001c0026t0001g0023a0002c0002t0001g0216a0002c0006t0005g0217others(8): Show | 11 | HG01081.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1627-1409_1627-140 others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781363 | ||||||
| chr16:89781363
|
C | CAAAA | 8 | a0002c0006t0005g0229a0006c0007t0004g0310a0006c0007t0004g0313others(5): Show | 8 | HG01109.hp1 HG01192.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1627-1410_1627-140 others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781363 | ||||||
| chr16:89781363
|
CA | C | 161 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(158): Show | 163 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1627-1407delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781363 | ||||||
| chr16:89781384
|
A | C | 1 | a0008c0008t0001g0015 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1627-1427T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781384 | ||||||
| chr16:89781395
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1627-1438A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781395 | ||||||
| chr16:89781411
|
T | C | 2 | a0001c0001t0001g0100a0028c0043t0015g0307 | 2 | HG00438.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1626+1448A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781411 | ||||||
| chr16:89781444
|
C | T | 1 | a0003c0003t0002g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1626+1415G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781444 | ||||||
| chr16:89781468
|
T | C | 4 | a0002c0051t0001g0032a0003c0003t0002g0257a0003c0003t0002g0281others(1): Show | 4 | HG02451.hp1 HG03486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+1391A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781468 | ||||||
| chr16:89781478
|
C | A | 1 | a0013c0014t0002g0330 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1626+1381G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781478 | ||||||
| chr16:89781478
|
CCTGGATA others(831): Show |
C | 1 | a0001c0001t0001g0119 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1626+543_1626+1380 others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781478 | ||||||
| chr16:89781483
|
A | C | 286 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(283): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1626+1376T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781483 | ||||||
| chr16:89781509
|
TAA | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1626+1348_1626+134 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781509 | ||||||
| chr16:89781571
|
G | C | 1 | a0036c0045t0001g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1626+1288C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781571 | ||||||
| chr16:89781577
|
G | A | 1 | a0001c0034t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1626+1282C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781577 | ||||||
| chr16:89781663
|
G | A | 9 | a0002c0002t0001g0031a0002c0002t0001g0037a0002c0002t0001g0038others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626+1196C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781663 | ||||||
| chr16:89781675
|
C | CA | 20 | a0001c0026t0001g0023a0002c0038t0001g0077a0003c0003t0002g0302others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1626+1183dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781675 | ||||||
| chr16:89781742
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1626+1117C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781742 | ||||||
| chr16:89781782
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1626+1077C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781782 | ||||||
| chr16:89781795
|
C | G | 29 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1626+1064G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781795 | ||||||
| chr16:89781795
|
C | T | 1 | a0002c0002t0001g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1626+1064G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781795 | ||||||
| chr16:89781796
|
G | A | 3 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274 | 3 | HG00140.hp2 HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1626+1063C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781796 | ||||||
| chr16:89781810
|
T | G | 1 | a0002c0002t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1626+1049A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781810 | ||||||
| chr16:89781860
|
G | C | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1626+999C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781860 | ||||||
| chr16:89781870
|
A | G | 1 | a0004c0004t0002g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1626+989T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781870 | ||||||
| chr16:89781901
|
G | GGA | 164 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(161): Show | 165 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1626+956_1626+957d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781901 | ||||||
| chr16:89781963
|
C | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1626+896G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781963 | ||||||
| chr16:89781964
|
G | T | 9 | a0003c0003t0002g0240a0003c0003t0002g0282a0004c0004t0002g0300others(6): Show | 9 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626+895C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89781964 | ||||||
| chr16:89782147
|
G | A | 1 | a0002c0006t0005g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1626+712C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782147 | ||||||
| chr16:89782151
|
A | G | 248 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(245): Show | 250 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1626+708T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782151 | ||||||
| chr16:89782157
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1626+702G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782157 | ||||||
| chr16:89782195
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1626+664C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782195 | ||||||
| chr16:89782217
|
A | C | 17 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1626+642T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782217 | ||||||
| chr16:89782285
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1626+574C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782285 | ||||||
| chr16:89782286
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0133 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1626+573G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782286 | ||||||
| chr16:89782316
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0214 | 2 | HG02015.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1626+543A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782316 | ||||||
| chr16:89782316
|
T | G | 1 | a0002c0002t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1626+543A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782316 | ||||||
| chr16:89782459
|
C | T | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1626+400G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782459 | ||||||
| chr16:89782510
|
C | CA | 35 | a0001c0001t0003g0148a0002c0002t0001g0043a0002c0006t0008g0215others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1626+348dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782510 | ||||||
| chr16:89782569
|
C | T | 1 | a0003c0003t0002g0255 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1626+290G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782569 | ||||||
| chr16:89782625
|
C | A | 2 | a0002c0002t0001g0033a0002c0002t0001g0084 | 2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1626+234G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782625 | ||||||
| chr16:89782630
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1626+229C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782630 | ||||||
| chr16:89782696
|
A | G | 54 | a0001c0026t0001g0023a0005c0005t0001g0036a0005c0005t0001g0064others(51): Show | 54 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1626+163T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782696 | ||||||
| chr16:89782773
|
AAACTC | A | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1626+81_1626+85del others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782773 | ||||||
| chr16:89782836
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1626+23G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782836 | ||||||
| chr16:89782843
|
G | A | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1626+16C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 17/42 | chr16 | 89782843 | ||||||
| chr16:89782934
|
A | C | 1 | a0029c0028t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1567-16T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 16/42 | chr16 | 89782934 | ||||||
| chr16:89783108
|
G | C | 1 | a0002c0002t0001g0060 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.1471-6C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783108 | ||||||
| chr16:89783138
|
T | A | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1471-36A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783138 | ||||||
| chr16:89783175
|
C | T | 215 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(212): Show | 217 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1471-73G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783175 | ||||||
| chr16:89783221
|
T | A | 245 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(242): Show | 247 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1471-119A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783221 | ||||||
| chr16:89783327
|
G | A | 212 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(209): Show | 214 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.1471-225C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783327 | ||||||
| chr16:89783332
|
C | T | 212 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(209): Show | 214 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.1471-230G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783332 | ||||||
| chr16:89783413
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1471-311G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783413 | ||||||
| chr16:89783506
|
G | A | 229 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(226): Show | 231 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1471-404C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783506 | ||||||
| chr16:89783510
|
C | A | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1471-408G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783510 | ||||||
| chr16:89783551
|
C | CA | 35 | a0002c0002t0001g0129a0005c0005t0001g0036a0005c0005t0001g0064others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1471-450dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783551 | ||||||
| chr16:89783551
|
CA | C | 9 | a0002c0002t0001g0031a0002c0002t0001g0037a0002c0002t0001g0038others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1471-450delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783551 | ||||||
| chr16:89783560
|
A | C | 7 | a0002c0002t0001g0029a0002c0002t0001g0080a0002c0002t0001g0087others(4): Show | 7 | HG00280.hp1 HG00423.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1471-458T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783560 | ||||||
| chr16:89783569
|
A | C | 36 | a0002c0002t0001g0072a0002c0002t0001g0073a0002c0002t0001g0114others(33): Show | 36 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1471-467T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783569 | ||||||
| chr16:89783597
|
C | G | 30 | a0001c0026t0001g0023a0002c0002t0001g0216a0002c0006t0005g0025others(27): Show | 30 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1471-495G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783597 | ||||||
| chr16:89783600
|
G | T | 13 | a0005c0005t0001g0067a0005c0005t0001g0068a0005c0005t0001g0182others(10): Show | 13 | HG00597.hp2 HG02015.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1471-498C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783600 | ||||||
| chr16:89783613
|
G | A | 1 | a0002c0041t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1471-511C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783613 | ||||||
| chr16:89783675
|
C | T | 15 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(12): Show | 15 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1471-573G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783675 | ||||||
| chr16:89783709
|
C | A | 112 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(109): Show | 113 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1471-607G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783709 | ||||||
| chr16:89783751
|
C | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1471-649G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783751 | ||||||
| chr16:89783762
|
C | T | 47 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1471-660G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783762 | ||||||
| chr16:89783904
|
C | CAG | 279 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1471-803_1471-802i others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783904 | ||||||
| chr16:89783904
|
C | G | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1471-802G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783904 | ||||||
| chr16:89783907
|
G | A | 245 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(242): Show | 247 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1471-805C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783907 | ||||||
| chr16:89783918
|
C | G | 1 | a0002c0002t0001g0085 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1471-816G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783918 | ||||||
| chr16:89783974
|
T | C | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1471-872A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783974 | ||||||
| chr16:89783981
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1470+873C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89783981 | ||||||
| chr16:89784007
|
C | G | 89 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(86): Show | 90 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1470+847G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784007 | ||||||
| chr16:89784051
|
C | T | 1 | a0002c0002t0001g0088 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1470+803G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784051 | ||||||
| chr16:89784209
|
G | C | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1470+645C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784209 | ||||||
| chr16:89784269
|
C | G | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(198): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1470+585G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784269 | ||||||
| chr16:89784368
|
CA | C | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 211 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1470+485delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784368 | ||||||
| chr16:89784398
|
C | CA | 22 | a0001c0001t0003g0040a0001c0026t0001g0023a0003c0003t0002g0302others(19): Show | 22 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1470+455dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784398 | ||||||
| chr16:89784419
|
A | AT | 3 | a0001c0001t0001g0127a0011c0012t0001g0006a0033c0025t0003g0180 | 3 | HG01243.hp2 HG02970.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1470+434dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784419 | ||||||
| chr16:89784421
|
TA | T | 6 | a0001c0001t0003g0045a0002c0002t0001g0091a0004c0004t0002g0232others(3): Show | 6 | HG01168.hp1 HG02109.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1470+432delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784421 | ||||||
| chr16:89784422
|
A | T | 206 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(203): Show | 208 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1470+432T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784422 | ||||||
| chr16:89784423
|
A | T | 2 | a0001c0001t0003g0045a0002c0002t0001g0091 | 2 | NA18994.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1470+431T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784423 | ||||||
| chr16:89784479
|
C | T | 1 | a0011c0012t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1470+375G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784479 | ||||||
| chr16:89784490
|
C | T | 1 | a0002c0002t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1470+364G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784490 | ||||||
| chr16:89784549
|
A | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1470+305T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784549 | ||||||
| chr16:89784574
|
T | C | 1 | a0002c0002t0001g0129 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1470+280A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784574 | ||||||
| chr16:89784596
|
A | G | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1470+258T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784596 | ||||||
| chr16:89784625
|
C | T | 90 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(87): Show | 91 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1470+229G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784625 | ||||||
| chr16:89784659
|
C | A | 1 | a0002c0002t0001g0085 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1470+195G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784659 | ||||||
| chr16:89784708
|
TGGGGAAG others(5): Show |
T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1470+134_1470+145d others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784708 | ||||||
| chr16:89784771
|
C | T | 33 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(30): Show | 33 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1470+83G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784771 | ||||||
| chr16:89784781
|
G | A | 1 | a0002c0002t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1470+73C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784781 | ||||||
| chr16:89784787
|
G | C | 17 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(14): Show | 17 | HG01081.hp1 HG01167.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1470+67C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 15/42 | chr16 | 89784787 | ||||||
| chr16:89784971
|
G | A | 9 | a0002c0002t0001g0031a0002c0002t0001g0037a0002c0002t0001g0038others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1360-7C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89784971 | ||||||
| chr16:89784974
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1360-10C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89784974 | ||||||
| chr16:89785007
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1360-43C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785007 | ||||||
| chr16:89785166
|
A | G | 2 | a0010c0011t0002g0005a0010c0011t0002g0010 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1360-202T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785166 | ||||||
| chr16:89785489
|
G | A | 1 | a0020c0021t0002g0012 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1360-525C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785489 | ||||||
| chr16:89785724
|
C | A | 1 | a0002c0002t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1360-760G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785724 | ||||||
| chr16:89785725
|
A | G | 248 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(245): Show | 250 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1360-761T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785725 | ||||||
| chr16:89785728
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1360-764G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785728 | ||||||
| chr16:89785841
|
G | A | 2 | a0002c0002t0001g0027a0002c0002t0001g0028 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1360-877C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785841 | ||||||
| chr16:89785853
|
G | GT | 5 | a0002c0006t0005g0217a0003c0003t0002g0242a0003c0003t0002g0292others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360-890dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785853 | ||||||
| chr16:89785853
|
G | GTT | 3 | a0006c0055t0009g0309a0028c0043t0015g0307a0040c0050t0013g0206 | 3 | HG02451.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1360-891_1360-890d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785853 | ||||||
| chr16:89785853
|
G | GTTTT | 112 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0048others(109): Show | 113 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1360-893_1360-890d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785853 | ||||||
| chr16:89785853
|
G | GTTTTT | 76 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0049others(73): Show | 77 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1360-890_1360-889i others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785853 | ||||||
| chr16:89785853
|
G | GTTTTTT | 11 | a0001c0001t0001g0115a0001c0001t0001g0212a0002c0002t0001g0026others(8): Show | 11 | HG02080.hp1 HG02145.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360-890_1360-889i others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785853 | ||||||
| chr16:89785855
|
T | G | 1 | a0004c0004t0002g0250 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1360-891A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785855 | ||||||
| chr16:89785858
|
G | T | 330 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(327): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1360-894C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785858 | ||||||
| chr16:89785899
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1360-935C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785899 | ||||||
| chr16:89785936
|
C | T | 1 | a0034c0046t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1360-972G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785936 | ||||||
| chr16:89785940
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1360-976G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89785940 | ||||||
| chr16:89786015
|
A | AT | 30 | a0001c0001t0001g0102a0001c0001t0001g0120a0001c0001t0001g0126others(27): Show | 30 | HG01175.hp1 HG01192.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1360-1052dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786015 | ||||||
| chr16:89786015
|
A | ATT | 167 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(164): Show | 169 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1360-1053_1360-105 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786015 | ||||||
| chr16:89786015
|
A | ATTT | 7 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0003g0151others(4): Show | 7 | HG00609.hp2 HG00621.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1360-1054_1360-105 others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786015 | ||||||
| chr16:89786015
|
A | ATTTT | 12 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0219others(9): Show | 12 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.1360-1055_1360-105 others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786015 | ||||||
| chr16:89786181
|
GT | G | 247 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(244): Show | 249 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1360-1218delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786181 | ||||||
| chr16:89786216
|
C | T | 13 | a0001c0026t0001g0023a0006c0007t0004g0310a0006c0007t0004g0311others(10): Show | 13 | HG01109.hp1 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1360-1252G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786216 | ||||||
| chr16:89786367
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1360-1403C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786367 | ||||||
| chr16:89786609
|
A | G | 256 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(253): Show | 258 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1360-1645T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786609 | ||||||
| chr16:89786657
|
C | T | 27 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.1360-1693G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786657 | ||||||
| chr16:89786709
|
G | C | 202 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(199): Show | 204 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1360-1745C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786709 | ||||||
| chr16:89786824
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1360-1860C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786824 | ||||||
| chr16:89786899
|
T | C | 296 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1360-1935A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786899 | ||||||
| chr16:89786920
|
C | T | 1 | a0008c0008t0001g0019 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1360-1956G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786920 | ||||||
| chr16:89786955
|
G | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1360-1991C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89786955 | ||||||
| chr16:89787010
|
G | C | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1360-2046C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787010 | ||||||
| chr16:89787015
|
G | A | 1 | a0003c0022t0002g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1360-2051C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787015 | ||||||
| chr16:89787149
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1360-2185G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787149 | ||||||
| chr16:89787212
|
T | C | 1 | a0003c0003t0002g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1360-2248A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787212 | ||||||
| chr16:89787298
|
C | T | 1 | a0002c0002t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1360-2334G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787298 | ||||||
| chr16:89787306
|
G | A | 1 | a0002c0002t0001g0129 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1360-2342C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787306 | ||||||
| chr16:89787378
|
C | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1360-2414G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787378 | ||||||
| chr16:89787380
|
G | C | 1 | a0035c0044t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1360-2416C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787380 | ||||||
| chr16:89787425
|
T | C | 226 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(223): Show | 228 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1360-2461A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787425 | ||||||
| chr16:89787446
|
C | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1360-2482G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787446 | ||||||
| chr16:89787448
|
G | A | 1 | a0002c0002t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1360-2484C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787448 | ||||||
| chr16:89787486
|
C | G | 1 | a0001c0029t0005g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1360-2522G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787486 | ||||||
| chr16:89787592
|
C | T | 1 | a0003c0003t0002g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1360-2628G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787592 | ||||||
| chr16:89787617
|
A | T | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.1360-2653T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787617 | ||||||
| chr16:89787667
|
T | C | 1 | a0004c0004t0002g0264 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1360-2703A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787667 | ||||||
| chr16:89787701
|
A | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1360-2737T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787701 | ||||||
| chr16:89787726
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1360-2762C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787726 | ||||||
| chr16:89787769
|
A | G | 1 | a0016c0019t0001g0108 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1360-2805T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787769 | ||||||
| chr16:89787869
|
T | TA | 26 | a0001c0001t0001g0214a0002c0002t0001g0129a0003c0003t0002g0242others(23): Show | 26 | HG00597.hp1 HG00639.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1360-2906dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787869 | ||||||
| chr16:89787896
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360-2932G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89787896 | ||||||
| chr16:89788093
|
G | C | 200 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(197): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1360-3129C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788093 | ||||||
| chr16:89788112
|
A | G | 2 | a0002c0002t0001g0027a0002c0002t0001g0028 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1360-3148T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788112 | ||||||
| chr16:89788238
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1359+3165C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788238 | ||||||
| chr16:89788298
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1359+3105G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788298 | ||||||
| chr16:89788337
|
T | C | 10 | a0001c0026t0001g0023a0002c0002t0001g0031a0002c0002t0001g0037others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1359+3066A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788337 | ||||||
| chr16:89788354
|
A | C | 29 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1359+3049T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788354 | ||||||
| chr16:89788421
|
C | G | 228 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(225): Show | 230 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.1359+2982G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788421 | ||||||
| chr16:89788464
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1359+2939C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788464 | ||||||
| chr16:89788485
|
C | T | 30 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(27): Show | 30 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1359+2918G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788485 | ||||||
| chr16:89788565
|
G | C | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359+2838C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788565 | ||||||
| chr16:89788569
|
C | G | 222 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(219): Show | 224 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.1359+2834G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788569 | ||||||
| chr16:89788692
|
C | A | 29 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(26): Show | 29 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1359+2711G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788692 | ||||||
| chr16:89788728
|
A | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1359+2675T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788728 | ||||||
| chr16:89788761
|
C | T | 221 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(218): Show | 223 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1359+2642G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788761 | ||||||
| chr16:89788784
|
T | C | 222 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(219): Show | 224 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.1359+2619A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89788784 | ||||||
| chr16:89789088
|
T | G | 1 | a0001c0026t0001g0023 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1359+2315A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789088 | ||||||
| chr16:89789177
|
G | A | 4 | a0006c0007t0004g0311a0006c0056t0004g0320a0022c0054t0002g0312others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359+2226C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789177 | ||||||
| chr16:89789206
|
T | C | 21 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(18): Show | 21 | HG00639.hp1 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1359+2197A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789206 | ||||||
| chr16:89789305
|
C | T | 13 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1359+2098G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789305 | ||||||
| chr16:89789306
|
T | TGG | 19 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(16): Show | 19 | HG00639.hp1 HG01109.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1359+2095_1359+209 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789306 | ||||||
| chr16:89789306
|
TG | T | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1359+2096delC | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789306 | ||||||
| chr16:89789309
|
G | GC | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1359+2093_1359+209 others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789309 | ||||||
| chr16:89789319
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1359+2084C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789319 | ||||||
| chr16:89789341
|
T | C | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1359+2062A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789341 | ||||||
| chr16:89789436
|
CT | C | 71 | a0001c0001t0001g0161a0001c0001t0010g0178a0002c0002t0001g0033others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1359+1966delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789436 | ||||||
| chr16:89789436
|
CTT | C | 177 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(174): Show | 179 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1359+1965_1359+196 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789436 | ||||||
| chr16:89789477
|
G | A | 2 | a0018c0017t0001g0244a0018c0017t0001g0277 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1359+1926C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789477 | ||||||
| chr16:89789593
|
C | T | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1359+1810G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789593 | ||||||
| chr16:89789624
|
G | C | 7 | a0010c0011t0002g0004a0010c0011t0002g0005a0010c0011t0002g0009others(4): Show | 7 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1359+1779C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789624 | ||||||
| chr16:89789781
|
CTT | C | 7 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1359+1620_1359+162 others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789781 | ||||||
| chr16:89789809
|
C | G | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1359+1594G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789809 | ||||||
| chr16:89789985
|
T | C | 255 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(252): Show | 257 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1359+1418A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89789985 | ||||||
| chr16:89790031
|
G | A | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1359+1372C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790031 | ||||||
| chr16:89790031
|
G | C | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.1359+1372C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790031 | ||||||
| chr16:89790073
|
G | C | 27 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.1359+1330C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790073 | ||||||
| chr16:89790116
|
G | A | 1 | a0001c0001t0003g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1359+1287C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790116 | ||||||
| chr16:89790131
|
G | A | 221 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(218): Show | 223 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1359+1272C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790131 | ||||||
| chr16:89790132
|
T | C | 1 | a0002c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1359+1271A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790132 | ||||||
| chr16:89790266
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1359+1137G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790266 | ||||||
| chr16:89790286
|
C | T | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359+1117G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790286 | ||||||
| chr16:89790294
|
G | A | 40 | a0002c0002t0001g0031a0002c0002t0001g0037a0002c0002t0001g0038others(37): Show | 40 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1359+1109C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790294 | ||||||
| chr16:89790298
|
G | A | 2 | a0018c0017t0001g0244a0018c0017t0001g0277 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1359+1105C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790298 | ||||||
| chr16:89790355
|
G | C | 255 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(252): Show | 257 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1359+1048C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790355 | ||||||
| chr16:89790371
|
G | C | 26 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1359+1032C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790371 | ||||||
| chr16:89790389
|
A | G | 221 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(218): Show | 223 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1359+1014T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790389 | ||||||
| chr16:89790390
|
C | G | 1 | a0003c0003t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1359+1013G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790390 | ||||||
| chr16:89790418
|
AAAAT | A | 221 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(218): Show | 223 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1359+981_1359+984d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790418 | ||||||
| chr16:89790505
|
C | T | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1359+898G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790505 | ||||||
| chr16:89790507
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1359+896C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790507 | ||||||
| chr16:89790511
|
A | ACT | 53 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1359+891_1359+892i others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790511 | ||||||
| chr16:89790512
|
T | C | 1 | a0002c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1359+891A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790512 | ||||||
| chr16:89790526
|
A | C | 53 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1359+877T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790526 | ||||||
| chr16:89790561
|
T | G | 1 | a0001c0001t0012g0125 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1359+842A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790561 | ||||||
| chr16:89790599
|
C | A | 5 | a0007c0009t0001g0325a0007c0009t0001g0327a0007c0009t0001g0329others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359+804G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790599 | ||||||
| chr16:89790600
|
A | G | 304 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(301): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1359+803T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790600 | ||||||
| chr16:89790658
|
A | G | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1359+745T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790658 | ||||||
| chr16:89790678
|
G | T | 1 | a0002c0002t0001g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1359+725C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790678 | ||||||
| chr16:89790745
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1359+658T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790745 | ||||||
| chr16:89790772
|
T | C | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1359+631A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790772 | ||||||
| chr16:89790804
|
G | A | 186 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(183): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1359+599C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790804 | ||||||
| chr16:89790842
|
C | G | 21 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(18): Show | 21 | HG00639.hp1 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1359+561G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790842 | ||||||
| chr16:89790942
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1359+461C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790942 | ||||||
| chr16:89790961
|
C | T | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1359+442G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89790961 | ||||||
| chr16:89791005
|
T | TTG | 7 | a0001c0001t0001g0127a0001c0001t0001g0163a0001c0001t0001g0212others(4): Show | 7 | HG01074.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1359+396_1359+397d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791005 | ||||||
| chr16:89791005
|
TTG | T | 16 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(13): Show | 16 | HG00639.hp1 HG01109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1359+396_1359+397d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791005 | ||||||
| chr16:89791019
|
GTGTGTTT others(3): Show |
G | 11 | a0002c0006t0005g0025a0002c0006t0005g0217a0002c0006t0005g0218others(8): Show | 11 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.1359+374_1359+383d others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791019 | ||||||
| chr16:89791021
|
GTGTTTTT others(3): Show |
G | 3 | a0002c0002t0001g0216a0002c0006t0011g0227a0002c0006t0011g0228 | 3 | HG01081.hp1 HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1359+372_1359+381d others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791021 | ||||||
| chr16:89791022
|
TG | T | 3 | a0006c0007t0004g0313a0006c0007t0004g0316a0006c0007t0009g0314 | 3 | HG01192.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1359+380delC | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791022 | ||||||
| chr16:89791023
|
G | GT | 11 | a0003c0003t0002g0259a0003c0003t0002g0263a0003c0003t0002g0272others(8): Show | 11 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1359+379dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791023 | ||||||
| chr16:89791023
|
G | T | 1 | a0006c0007t0004g0318 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1359+380C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791023 | ||||||
| chr16:89791023
|
GT | G | 150 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(147): Show | 151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1359+379delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791023 | ||||||
| chr16:89791023
|
GTT | G | 9 | a0001c0001t0001g0106a0001c0034t0001g0104a0002c0002t0001g0027others(6): Show | 9 | HG00140.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1359+378_1359+379d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791023 | ||||||
| chr16:89791024
|
T | TG | 35 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0069others(32): Show | 35 | HG00099.hp2 HG00673.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1359+378_1359+379i others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791024 | ||||||
| chr16:89791025
|
T | TG | 3 | a0005c0005t0001g0194a0034c0046t0001g0094a0036c0045t0001g0185 | 3 | HG00597.hp2 HG02080.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1359+377_1359+378i others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791025 | ||||||
| chr16:89791026
|
T | G | 30 | a0001c0001t0001g0102a0001c0029t0005g0103a0003c0003t0002g0257others(27): Show | 30 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1359+377A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791026 | ||||||
| chr16:89791027
|
T | G | 2 | a0001c0034t0001g0104a0005c0005t0001g0181 | 2 | HG02735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1359+376A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791027 | ||||||
| chr16:89791123
|
C | T | 1 | a0004c0004t0002g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1359+280G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791123 | ||||||
| chr16:89791140
|
A | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(252): Show | 257 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1359+263T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791140 | ||||||
| chr16:89791159
|
T | TGAGGCCC others(48): Show |
1 | a0002c0002t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1359+243_1359+244i others(57): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791159 | ||||||
| chr16:89791191
|
G | A | 1 | a0001c0001t0006g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1359+212C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791191 | ||||||
| chr16:89791201
|
G | T | 1 | a0004c0004t0002g0304 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1359+202C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791201 | ||||||
| chr16:89791214
|
T | C | 202 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(199): Show | 204 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1359+189A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791214 | ||||||
| chr16:89791222
|
C | T | 1 | a0005c0005t0001g0195 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1359+181G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791222 | ||||||
| chr16:89791280
|
G | C | 3 | a0011c0012t0001g0003a0011c0012t0001g0006a0011c0012t0001g0007 | 3 | HG01243.hp2 HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1359+123C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791280 | ||||||
| chr16:89791292
|
A | G | 221 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(218): Show | 223 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1359+111T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791292 | ||||||
| chr16:89791299
|
T | G | 3 | a0002c0006t0005g0217a0002c0006t0005g0218a0002c0006t0005g0229 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1359+104A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791299 | ||||||
| chr16:89791385
|
G | A | 1 | a0002c0006t0008g0215 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1359+18C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791385 | ||||||
| chr16:89791393
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1359+10C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 14/42 | chr16 | 89791393 | ||||||
| chr16:89791556
|
T | C | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(198): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1226-20A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791556 | ||||||
| chr16:89791616
|
A | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(252): Show | 257 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1226-80T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791616 | ||||||
| chr16:89791629
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1226-93C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791629 | ||||||
| chr16:89791637
|
G | A | 2 | a0002c0006t0011g0227a0002c0006t0011g0228 | 2 | HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1226-101C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791637 | ||||||
| chr16:89791651
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1226-115G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791651 | ||||||
| chr16:89791690
|
G | A | 1 | a0002c0002t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1226-154C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791690 | ||||||
| chr16:89791699
|
A | T | 3 | a0002c0002t0001g0085a0002c0002t0001g0088a0002c0002t0001g0193 | 3 | HG00609.hp2 HG02080.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1226-163T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791699 | ||||||
| chr16:89791776
|
A | G | 329 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1225+151T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791776 | ||||||
| chr16:89791813
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1225+114C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791813 | ||||||
| chr16:89791879
|
C | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1225+48G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791879 | ||||||
| chr16:89791894
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1225+33C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 13/42 | chr16 | 89791894 | ||||||
| chr16:89792097
|
T | C | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1084-29A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792097 | ||||||
| chr16:89792117
|
C | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(252): Show | 257 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1084-49G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792117 | ||||||
| chr16:89792214
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1084-146G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792214 | ||||||
| chr16:89792249
|
C | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(252): Show | 257 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1084-181G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792249 | ||||||
| chr16:89792287
|
C | T | 20 | a0003c0003t0002g0242a0003c0003t0002g0255a0003c0003t0002g0267others(17): Show | 20 | HG00639.hp1 HG01109.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1083+184G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792287 | ||||||
| chr16:89792329
|
C | T | 2 | a0004c0004t0002g0245a0004c0004t0002g0269 | 2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1083+142G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792329 | ||||||
| chr16:89792351
|
C | T | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.1083+120G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792351 | ||||||
| chr16:89792430
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+41C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 12/42 | chr16 | 89792430 | ||||||
| chr16:89792600
|
G | A | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1007-53C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792600 | ||||||
| chr16:89792605
|
T | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007-58A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792605 | ||||||
| chr16:89792607
|
GT | G | 233 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(230): Show | 235 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.1007-61delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792607 | ||||||
| chr16:89792627
|
G | A | 32 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(29): Show | 32 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1007-80C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792627 | ||||||
| chr16:89792651
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1007-104G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792651 | ||||||
| chr16:89792666
|
G | T | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1007-119C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792666 | ||||||
| chr16:89792695
|
A | G | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1007-148T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792695 | ||||||
| chr16:89792719
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007-172C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792719 | ||||||
| chr16:89792740
|
C | T | 1 | a0004c0004t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1007-193G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792740 | ||||||
| chr16:89792749
|
G | A | 1 | a0002c0002t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1007-202C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792749 | ||||||
| chr16:89792846
|
T | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1007-299A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792846 | ||||||
| chr16:89792884
|
A | C | 286 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(283): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1007-337T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792884 | ||||||
| chr16:89792891
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007-344C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792891 | ||||||
| chr16:89792976
|
A | G | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(198): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1007-429T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89792976 | ||||||
| chr16:89793027
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1007-480A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793027 | ||||||
| chr16:89793037
|
G | A | 1 | a0003c0003t0002g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1007-490C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793037 | ||||||
| chr16:89793039
|
G | A | 2 | a0001c0052t0001g0211a0002c0002t0001g0113 | 2 | HG01243.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1007-492C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793039 | ||||||
| chr16:89793054
|
C | G | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1007-507G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793054 | ||||||
| chr16:89793128
|
G | C | 2 | a0002c0006t0011g0227a0002c0006t0011g0228 | 2 | HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1007-581C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793128 | ||||||
| chr16:89793162
|
G | A | 1 | a0003c0003t0002g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1007-615C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793162 | ||||||
| chr16:89793192
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1007-645C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793192 | ||||||
| chr16:89793241
|
C | T | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1007-694G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793241 | ||||||
| chr16:89793255
|
C | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1007-708G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793255 | ||||||
| chr16:89793274
|
G | A | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1007-727C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793274 | ||||||
| chr16:89793309
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1007-762C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793309 | ||||||
| chr16:89793312
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1007-765G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793312 | ||||||
| chr16:89793345
|
T | C | 29 | a0002c0002t0001g0001a0002c0002t0001g0027a0002c0002t0001g0028others(26): Show | 30 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1007-798A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793345 | ||||||
| chr16:89793525
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1007-978C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793525 | ||||||
| chr16:89793545
|
A | G | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(198): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1007-998T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793545 | ||||||
| chr16:89793634
|
C | T | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1007-1087G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793634 | ||||||
| chr16:89793774
|
T | G | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1007-1227A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793774 | ||||||
| chr16:89793775
|
G | A | 184 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(181): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1007-1228C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793775 | ||||||
| chr16:89793896
|
G | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007-1349C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793896 | ||||||
| chr16:89793991
|
C | A | 7 | a0003c0003t0002g0282a0009c0010t0002g0287a0009c0010t0002g0288others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1444G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89793991 | ||||||
| chr16:89794055
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1007-1508C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794055 | ||||||
| chr16:89794083
|
CAGATCTT | C | 153 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(150): Show | 154 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1007-1543_1007-153 others(11): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794083 | ||||||
| chr16:89794092
|
A | C | 153 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(150): Show | 154 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1007-1545T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794092 | ||||||
| chr16:89794093
|
T | C | 1 | a0006c0007t0004g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1007-1546A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794093 | ||||||
| chr16:89794094
|
A | G | 153 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(150): Show | 154 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1007-1547T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794094 | ||||||
| chr16:89794101
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1007-1554A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794101 | ||||||
| chr16:89794140
|
C | A | 1 | a0002c0038t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1007-1593G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794140 | ||||||
| chr16:89794176
|
G | A | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1007-1629C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794176 | ||||||
| chr16:89794221
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1007-1674G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794221 | ||||||
| chr16:89794280
|
G | T | 32 | a0002c0002t0001g0022a0005c0005t0001g0036a0005c0005t0001g0064others(29): Show | 32 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1006+1626C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794280 | ||||||
| chr16:89794289
|
C | T | 31 | a0005c0005t0001g0036a0005c0005t0001g0064a0005c0005t0001g0065others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1006+1617G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794289 | ||||||
| chr16:89794315
|
G | A | 1 | a0001c0001t0003g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1006+1591C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794315 | ||||||
| chr16:89794434
|
A | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1006+1472T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794434 | ||||||
| chr16:89794438
|
T | TACTCGGG others(6): Show |
3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1006+1467_1006+146 others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794438 | ||||||
| chr16:89794439
|
T | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1006+1467A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794439 | ||||||
| chr16:89794616
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1006+1290C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794616 | ||||||
| chr16:89794652
|
C | T | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006+1254G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794652 | ||||||
| chr16:89794673
|
T | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006+1233A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794673 | ||||||
| chr16:89794819
|
C | G | 1 | a0003c0003t0002g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1006+1087G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794819 | ||||||
| chr16:89794860
|
C | A | 1 | a0025c0039t0001g0184 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1006+1046G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89794860 | ||||||
| chr16:89795022
|
C | T | 13 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(10): Show | 13 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1006+884G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795022 | ||||||
| chr16:89795083
|
G | A | 20 | a0002c0002t0001g0001a0002c0002t0001g0029a0002c0002t0001g0030others(17): Show | 21 | HG00280.hp1 HG01243.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.1006+823C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795083 | ||||||
| chr16:89795113
|
C | T | 3 | a0003c0003t0002g0302a0017c0018t0002g0305a0017c0018t0002g0306 | 3 | HG01192.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1006+793G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795113 | ||||||
| chr16:89795161
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1006+745G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795161 | ||||||
| chr16:89795162
|
G | A | 2 | a0010c0011t0002g0005a0010c0011t0002g0010 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1006+744C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795162 | ||||||
| chr16:89795242
|
G | A | 22 | a0001c0001t0001g0046a0001c0001t0001g0069a0001c0001t0001g0071others(19): Show | 22 | HG00099.hp2 HG01891.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1006+664C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795242 | ||||||
| chr16:89795265
|
C | G | 1 | a0002c0002t0001g0124 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1006+641G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795265 | ||||||
| chr16:89795284
|
C | CAATA | 66 | a0001c0001t0001g0046a0001c0001t0001g0115a0001c0001t0001g0117others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1006+618_1006+621d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795284
|
C | CAATAAAT others(1): Show |
111 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0048others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1006+614_1006+621d others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795284
|
C | CAATAAAT others(5): Show |
10 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0106others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006+610_1006+621d others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795284
|
C | CAATAAAT others(9): Show |
1 | a0002c0002t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1006+606_1006+621d others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795284
|
CAATA | C | 17 | a0001c0001t0001g0071a0001c0001t0001g0202a0001c0001t0001g0222others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1006+618_1006+621d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795284
|
CAATAAAT others(1): Show |
C | 4 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332others(1): Show | 4 | HG02109.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+614_1006+621d others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795284
|
CAATAAAT others(9): Show |
C | 1 | a0003c0003t0002g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1006+606_1006+621d others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795284 | ||||||
| chr16:89795310
|
ATAAATAA others(22): Show |
A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1006+567_1006+595d others(31): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795310 | ||||||
| chr16:89795323
|
T | TAAATAAA others(5): Show |
1 | a0011c0012t0001g0007 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1006+582_1006+583i others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795323 | ||||||
| chr16:89795356
|
C | G | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1006+550G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795356 | ||||||
| chr16:89795483
|
A | C | 13 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1006+423T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795483 | ||||||
| chr16:89795494
|
C | A | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006+412G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795494 | ||||||
| chr16:89795519
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1006+387A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795519 | ||||||
| chr16:89795724
|
G | C | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(198): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1006+182C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795724 | ||||||
| chr16:89795747
|
G | C | 2 | a0010c0011t0002g0005a0010c0011t0002g0010 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1006+159C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795747 | ||||||
| chr16:89795794
|
C | T | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.1006+112G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795794 | ||||||
| chr16:89795803
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1006+103C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 11/42 | chr16 | 89795803 | ||||||
| chr16:89796026
|
T | C | 34 | a0001c0052t0001g0211a0002c0002t0001g0022a0002c0002t0001g0193others(31): Show | 34 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.894-8A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796026 | ||||||
| chr16:89796117
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.894-99A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796117 | ||||||
| chr16:89796149
|
C | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.894-131G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796149 | ||||||
| chr16:89796163
|
T | G | 1 | a0002c0002t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.894-145A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796163 | ||||||
| chr16:89796204
|
G | C | 1 | a0006c0007t0009g0308 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.894-186C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796204 | ||||||
| chr16:89796227
|
C | T | 4 | a0002c0002t0001g0060a0002c0002t0001g0128a0002c0002t0001g0129others(1): Show | 4 | HG00597.hp1 NA18971.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.894-209G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796227 | ||||||
| chr16:89796311
|
G | A | 5 | a0001c0001t0006g0062a0001c0001t0006g0170a0001c0001t0006g0172others(2): Show | 5 | HG02451.hp2 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-293C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796311 | ||||||
| chr16:89796498
|
A | C | 19 | a0001c0001t0001g0057a0002c0002t0001g0022a0002c0002t0001g0060others(16): Show | 19 | HG00597.hp1 HG00621.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.894-480T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796498 | ||||||
| chr16:89796553
|
C | G | 200 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(197): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.894-535G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796553 | ||||||
| chr16:89796557
|
G | A | 1 | a0002c0006t0005g0223 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.894-539C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796557 | ||||||
| chr16:89796574
|
G | A | 197 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(194): Show | 199 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.894-556C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796574 | ||||||
| chr16:89796642
|
G | A | 1 | a0002c0006t0005g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.894-624C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796642 | ||||||
| chr16:89796653
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894-635G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796653 | ||||||
| chr16:89796681
|
A | G | 1 | a0002c0006t0005g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.894-663T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796681 | ||||||
| chr16:89796697
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.894-679C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796697 | ||||||
| chr16:89796702
|
A | G | 185 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(182): Show | 187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.894-684T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796702 | ||||||
| chr16:89796717
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.894-699G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796717 | ||||||
| chr16:89796766
|
T | A | 13 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.894-748A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796766 | ||||||
| chr16:89796802
|
C | G | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.894-784G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796802 | ||||||
| chr16:89796977
|
C | A | 6 | a0004c0004t0002g0235a0004c0004t0002g0254a0004c0004t0002g0265others(3): Show | 6 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.894-959G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796977 | ||||||
| chr16:89796994
|
T | TA | 87 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0048others(84): Show | 87 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.894-977dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89796994 | ||||||
| chr16:89797108
|
A | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894-1090T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797108 | ||||||
| chr16:89797178
|
A | T | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.894-1160T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797178 | ||||||
| chr16:89797264
|
T | C | 34 | a0001c0052t0001g0211a0002c0002t0001g0022a0002c0002t0001g0193others(31): Show | 34 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.894-1246A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797264 | ||||||
| chr16:89797264
|
T | G | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894-1246A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797264 | ||||||
| chr16:89797338
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894-1320A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797338 | ||||||
| chr16:89797342
|
G | T | 173 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(170): Show | 174 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.894-1324C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797342 | ||||||
| chr16:89797360
|
C | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.894-1342G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797360 | ||||||
| chr16:89797381
|
G | C | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.894-1363C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797381 | ||||||
| chr16:89797417
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.894-1399A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797417 | ||||||
| chr16:89797512
|
G | C | 1 | a0026c0036t0002g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.894-1494C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797512 | ||||||
| chr16:89797615
|
C | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0084 | 2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.893+1551G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797615 | ||||||
| chr16:89797696
|
T | C | 2 | a0001c0001t0001g0157a0003c0003t0002g0286 | 2 | HG02698.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.893+1470A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797696 | ||||||
| chr16:89797897
|
A | AAAAT | 33 | a0001c0001t0001g0057a0002c0002t0001g0022a0002c0002t0001g0042others(30): Show | 33 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.893+1265_893+1268d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89797897 | ||||||
| chr16:89798058
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.893+1108A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798058 | ||||||
| chr16:89798248
|
C | A | 1 | a0027c0037t0001g0301 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.893+918G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798248 | ||||||
| chr16:89798335
|
A | T | 1 | a0006c0007t0004g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.893+831T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798335 | ||||||
| chr16:89798425
|
G | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+741C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798425 | ||||||
| chr16:89798433
|
A | G | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.893+733T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798433 | ||||||
| chr16:89798572
|
C | T | 3 | a0014c0015t0002g0008a0014c0015t0002g0011a0020c0021t0002g0012 | 3 | HG00323.hp1 HG02300.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.893+594G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798572 | ||||||
| chr16:89798607
|
C | T | 13 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.893+559G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798607 | ||||||
| chr16:89798667
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.893+499A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798667 | ||||||
| chr16:89798695
|
T | A | 250 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(247): Show | 252 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.893+471A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798695 | ||||||
| chr16:89798746
|
C | G | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.893+420G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798746 | ||||||
| chr16:89798763
|
G | A | 1 | a0003c0003t0002g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.893+403C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798763 | ||||||
| chr16:89798834
|
T | C | 250 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(247): Show | 252 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.893+332A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798834 | ||||||
| chr16:89798903
|
T | C | 8 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.893+263A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798903 | ||||||
| chr16:89798924
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.893+242G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89798924 | ||||||
| chr16:89799026
|
G | C | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.893+140C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89799026 | ||||||
| chr16:89799082
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.893+84C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 10/42 | chr16 | 89799082 | ||||||
| chr16:89799263
|
T | C | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.827-31A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 9/42 | chr16 | 89799263 | ||||||
| chr16:89799289
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.827-57C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 9/42 | chr16 | 89799289 | ||||||
| chr16:89799752
|
A | G | 272 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.793-114T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89799752 | ||||||
| chr16:89799769
|
G | A | 3 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274 | 3 | HG00140.hp2 HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.793-131C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89799769 | ||||||
| chr16:89799793
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.793-155T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89799793 | ||||||
| chr16:89799877
|
TCAGCTAC others(1343): Show |
T | 1 | a0002c0002t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793-1589_793-240de others(1): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89799877 | ||||||
| chr16:89799887
|
G | T | 10 | a0007c0009t0001g0322a0007c0009t0001g0323a0007c0009t0001g0324others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.793-249C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89799887 | ||||||
| chr16:89799919
|
G | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.793-281C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89799919 | ||||||
| chr16:89800048
|
T | C | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.793-410A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800048 | ||||||
| chr16:89800234
|
T | C | 2 | a0002c0002t0001g0083a0002c0002t0001g0098 | 2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.793-596A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800234 | ||||||
| chr16:89800238
|
G | C | 1 | a0002c0002t0001g0030 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.793-600C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800238 | ||||||
| chr16:89800323
|
C | A | 1 | a0006c0007t0004g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793-685G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800323 | ||||||
| chr16:89800533
|
C | T | 3 | a0003c0003t0001g0303a0019c0016t0007g0276a0019c0016t0007g0291 | 3 | HG02559.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.793-895G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800533 | ||||||
| chr16:89800566
|
A | G | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.793-928T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800566 | ||||||
| chr16:89800622
|
C | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.793-984G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800622 | ||||||
| chr16:89800625
|
T | C | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.793-987A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800625 | ||||||
| chr16:89800667
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.793-1029C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800667 | ||||||
| chr16:89800702
|
T | C | 2 | a0018c0017t0001g0244a0018c0017t0001g0277 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.793-1064A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800702 | ||||||
| chr16:89800753
|
G | A | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.793-1115C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800753 | ||||||
| chr16:89800790
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.793-1152C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800790 | ||||||
| chr16:89800913
|
G | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0202a0001c0001t0001g0222 | 3 | HG02572.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.793-1275C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800913 | ||||||
| chr16:89800931
|
A | G | 294 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.793-1293T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800931 | ||||||
| chr16:89800960
|
T | G | 251 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.793-1322A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89800960 | ||||||
| chr16:89801032
|
C | CA | 42 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(39): Show | 43 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.793-1395dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801032 | ||||||
| chr16:89801032
|
C | CAAAAAAA others(306): Show |
1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.793-1395_793-1394i others(315): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801032 | ||||||
| chr16:89801210
|
G | A | 3 | a0003c0003t0001g0303a0019c0016t0007g0276a0019c0016t0007g0291 | 3 | HG02559.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.793-1572C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801210 | ||||||
| chr16:89801260
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.793-1622G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801260 | ||||||
| chr16:89801261
|
G | A | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.793-1623C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801261 | ||||||
| chr16:89801270
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0202a0001c0001t0001g0222 | 3 | HG02572.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.793-1632C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801270 | ||||||
| chr16:89801323
|
G | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.793-1685C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801323 | ||||||
| chr16:89801343
|
C | CA | 25 | a0001c0001t0001g0241a0003c0003t0002g0238a0003c0003t0002g0239others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.793-1706dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801343
|
C | CAA | 24 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(21): Show | 25 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.793-1707_793-1706d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801343
|
C | CAAAA | 16 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.793-1709_793-1706d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801343
|
C | CAAAAAAA others(4): Show |
1 | a0013c0014t0002g0331 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.793-1716_793-1706d others(13): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801343
|
C | CAAAAAAA others(5): Show |
1 | a0013c0014t0002g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.793-1717_793-1706d others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801343
|
C | CAAAAAAA others(6): Show |
1 | a0013c0014t0002g0330 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.793-1718_793-1706d others(15): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801343
|
CA | C | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(198): Show | 202 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.793-1706delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801343 | ||||||
| chr16:89801389
|
A | G | 251 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.793-1751T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801389 | ||||||
| chr16:89801467
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.792+1792G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801467 | ||||||
| chr16:89801611
|
C | T | 1 | a0003c0003t0002g0271 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.792+1648G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801611 | ||||||
| chr16:89801672
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.792+1587C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801672 | ||||||
| chr16:89801733
|
C | G | 3 | a0009c0010t0002g0287a0009c0010t0002g0296a0009c0010t0002g0298 | 3 | HG01109.hp2 HG01516.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.792+1526G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801733 | ||||||
| chr16:89801802
|
C | T | 1 | a0026c0036t0002g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.792+1457G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801802 | ||||||
| chr16:89801881
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+1378G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801881 | ||||||
| chr16:89801883
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0001g0153others(3): Show | 6 | HG00673.hp2 HG01261.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+1376C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801883 | ||||||
| chr16:89801924
|
G | A | 1 | a0001c0029t0005g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.792+1335C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89801924 | ||||||
| chr16:89802127
|
C | T | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.792+1132G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802127 | ||||||
| chr16:89802128
|
G | A | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.792+1131C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802128 | ||||||
| chr16:89802150
|
G | C | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.792+1109C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802150 | ||||||
| chr16:89802157
|
T | C | 1 | a0005c0005t0001g0190 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.792+1102A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802157 | ||||||
| chr16:89802179
|
C | T | 2 | a0002c0006t0011g0227a0002c0006t0011g0228 | 2 | HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.792+1080G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802179 | ||||||
| chr16:89802198
|
G | C | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.792+1061C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802198 | ||||||
| chr16:89802266
|
A | AT | 21 | a0001c0001t0001g0047a0001c0001t0001g0121a0001c0001t0001g0177others(18): Show | 21 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.792+992dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802266 | ||||||
| chr16:89802266
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.792+993T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802266 | ||||||
| chr16:89802266
|
AT | A | 19 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0216others(16): Show | 19 | HG01081.hp1 HG01167.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.792+992delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802266 | ||||||
| chr16:89802282
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.792+977A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802282 | ||||||
| chr16:89802295
|
G | T | 1 | a0006c0007t0004g0317 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.792+964C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802295 | ||||||
| chr16:89802358
|
C | T | 1 | a0001c0001t0006g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.792+901G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802358 | ||||||
| chr16:89802502
|
C | T | 8 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0317others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+757G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802502 | ||||||
| chr16:89802503
|
G | A | 3 | a0001c0001t0001g0121a0002c0006t0011g0227a0002c0006t0011g0228 | 3 | HG01167.hp1 HG03041.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.792+756C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802503 | ||||||
| chr16:89802522
|
C | G | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.792+737G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802522 | ||||||
| chr16:89802611
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.792+648C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802611 | ||||||
| chr16:89802639
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.792+620C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802639 | ||||||
| chr16:89802697
|
C | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.792+562G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802697 | ||||||
| chr16:89802707
|
A | G | 1 | a0026c0036t0002g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.792+552T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802707 | ||||||
| chr16:89802754
|
G | A | 5 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0047t0001g0082others(2): Show | 5 | HG01891.hp1 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+505C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802754 | ||||||
| chr16:89802771
|
T | C | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.792+488A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802771 | ||||||
| chr16:89802796
|
G | C | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+463C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802796 | ||||||
| chr16:89802856
|
G | C | 1 | a0001c0001t0003g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.792+403C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802856 | ||||||
| chr16:89802862
|
G | C | 1 | a0002c0002t0001g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.792+397C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802862 | ||||||
| chr16:89802996
|
T | C | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.792+263A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89802996 | ||||||
| chr16:89803103
|
T | A | 1 | a0007c0009t0001g0324 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.792+156A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89803103 | ||||||
| chr16:89803139
|
A | G | 1 | a0019c0016t0007g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.792+120T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89803139 | ||||||
| chr16:89803156
|
G | A | 13 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.792+103C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 8/42 | chr16 | 89803156 | ||||||
| chr16:89803353
|
T | C | 297 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.710-12A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803353 | ||||||
| chr16:89803481
|
T | TGA | 42 | a0002c0006t0005g0025a0002c0006t0005g0217a0002c0006t0005g0218others(39): Show | 43 | HG01109.hp1 HG01167.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.710-142_710-141dup others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803481 | ||||||
| chr16:89803624
|
C | CT | 157 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(154): Show | 158 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.710-284dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803624 | ||||||
| chr16:89803630
|
T | C | 2 | a0003c0003t0002g0257a0003c0003t0002g0281 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.710-289A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803630 | ||||||
| chr16:89803735
|
C | A | 28 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.710-394G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803735 | ||||||
| chr16:89803762
|
T | C | 10 | a0001c0026t0001g0023a0002c0002t0001g0031a0002c0002t0001g0037others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.710-421A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803762 | ||||||
| chr16:89803822
|
T | A | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.710-481A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803822 | ||||||
| chr16:89803960
|
C | CT | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.710-620dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803960 | ||||||
| chr16:89803982
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.710-641T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89803982 | ||||||
| chr16:89804279
|
G | A | 2 | a0005c0005t0001g0181a0005c0005t0001g0192 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.710-938C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804279 | ||||||
| chr16:89804285
|
CCAG | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.710-947_710-945del others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804285 | ||||||
| chr16:89804298
|
C | G | 1 | a0004c0004t0002g0304 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.710-957G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804298 | ||||||
| chr16:89804380
|
C | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.709+900G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804380 | ||||||
| chr16:89804424
|
G | A | 1 | a0004c0004t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.709+856C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804424 | ||||||
| chr16:89804498
|
A | C | 2 | a0003c0003t0002g0270a0003c0003t0002g0280 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.709+782T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804498 | ||||||
| chr16:89804505
|
T | C | 43 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(40): Show | 44 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.709+775A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804505 | ||||||
| chr16:89804610
|
A | G | 43 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(40): Show | 44 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.709+670T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804610 | ||||||
| chr16:89804654
|
T | C | 1 | a0002c0002t0001g0091 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.709+626A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804654 | ||||||
| chr16:89804760
|
A | G | 318 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.709+520T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804760 | ||||||
| chr16:89804877
|
C | CA | 15 | a0002c0002t0001g0165a0002c0002t0001g0216a0002c0006t0005g0025others(12): Show | 15 | HG01081.hp1 HG01167.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+402dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804877 | ||||||
| chr16:89804936
|
T | C | 93 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.709+344A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804936 | ||||||
| chr16:89804940
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.709+340C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804940 | ||||||
| chr16:89804946
|
G | T | 1 | a0002c0002t0001g0166 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.709+334C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804946 | ||||||
| chr16:89804968
|
G | A | 7 | a0004c0004t0002g0235a0004c0004t0002g0254a0004c0004t0002g0264others(4): Show | 7 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+312C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804968 | ||||||
| chr16:89804972
|
G | A | 1 | a0003c0003t0002g0255 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.709+308C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89804972 | ||||||
| chr16:89805067
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.709+213A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89805067 | ||||||
| chr16:89805199
|
G | A | 1 | a0002c0002t0001g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.709+81C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89805199 | ||||||
| chr16:89805222
|
C | T | 3 | a0009c0010t0002g0287a0009c0010t0002g0296a0009c0010t0002g0298 | 3 | HG01109.hp2 HG01516.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.709+58G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 7/42 | chr16 | 89805222 | ||||||
| chr16:89805471
|
AT | A | 14 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(11): Show | 14 | HG01081.hp1 HG01167.hp1 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.597-80delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805471 | ||||||
| chr16:89805534
|
C | G | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.597-142G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805534 | ||||||
| chr16:89805717
|
T | TGA | 29 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(26): Show | 30 | HG01109.hp1 HG01192.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.597-326_597-325ins others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805717 | ||||||
| chr16:89805719
|
G | T | 43 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(40): Show | 44 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.597-327C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805719 | ||||||
| chr16:89805762
|
C | A | 1 | a0004c0004t0002g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.597-370G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805762 | ||||||
| chr16:89805766
|
T | C | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.597-374A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805766 | ||||||
| chr16:89805779
|
G | GTTGT | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.597-388_597-387ins others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805779 | ||||||
| chr16:89805788
|
C | A | 1 | a0001c0034t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.597-396G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805788 | ||||||
| chr16:89805794
|
T | C | 1 | a0002c0002t0001g0216 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.597-402A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805794 | ||||||
| chr16:89805904
|
T | C | 3 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0092 | 3 | NA18957.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.597-512A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89805904 | ||||||
| chr16:89806007
|
A | G | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.597-615T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806007 | ||||||
| chr16:89806016
|
G | T | 1 | a0003c0003t0002g0271 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.597-624C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806016 | ||||||
| chr16:89806037
|
A | C | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.597-645T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806037 | ||||||
| chr16:89806220
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.597-828C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806220 | ||||||
| chr16:89806306
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.597-914C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806306 | ||||||
| chr16:89806347
|
C | CT | 75 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(72): Show | 76 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.597-956dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806347 | ||||||
| chr16:89806347
|
C | CTTT | 32 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0112others(29): Show | 32 | HG02165.hp2 HG02273.hp1 HG02572.hp1 others(29): Show |
intron_variant | MODIFIER | c.597-958_597-956dup others(3): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806347 | ||||||
| chr16:89806347
|
C | CTTTT | 167 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0047others(164): Show | 168 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.597-959_597-956dup others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806347 | ||||||
| chr16:89806347
|
C | CTTTTT | 9 | a0001c0001t0001g0046a0001c0001t0001g0069a0001c0001t0001g0126others(6): Show | 9 | HG00621.hp1 HG00621.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-960_597-956dup others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806347 | ||||||
| chr16:89806419
|
G | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.597-1027C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806419 | ||||||
| chr16:89806424
|
A | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0177others(3): Show | 6 | HG03492.hp1 NA18951.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1032T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806424 | ||||||
| chr16:89806434
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.597-1042C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806434 | ||||||
| chr16:89806455
|
T | C | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.597-1063A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806455 | ||||||
| chr16:89806494
|
A | C | 44 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(41): Show | 45 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.597-1102T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806494 | ||||||
| chr16:89806562
|
T | C | 210 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(207): Show | 211 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.597-1170A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806562 | ||||||
| chr16:89806754
|
TAC | T | 3 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274 | 3 | HG00140.hp2 HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.597-1364_597-1363d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806754 | ||||||
| chr16:89806765
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0121 | 2 | HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.597-1373T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806765 | ||||||
| chr16:89806805
|
C | G | 6 | a0004c0004t0001g0231a0004c0004t0002g0232a0004c0004t0002g0247others(3): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.597-1413G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806805 | ||||||
| chr16:89806819
|
T | C | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.597-1427A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806819 | ||||||
| chr16:89806838
|
A | C | 3 | a0001c0001t0001g0241a0003c0003t0002g0257a0003c0003t0002g0281 | 3 | HG03486.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.597-1446T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806838 | ||||||
| chr16:89806896
|
G | C | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596+1398C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806896 | ||||||
| chr16:89806909
|
C | T | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.596+1385G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806909 | ||||||
| chr16:89806969
|
G | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.596+1325C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89806969 | ||||||
| chr16:89807005
|
G | A | 212 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(209): Show | 213 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.596+1289C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807005 | ||||||
| chr16:89807178
|
G | GT | 19 | a0006c0007t0004g0311a0006c0007t0004g0313a0006c0007t0004g0315others(16): Show | 20 | HG01109.hp1 HG01192.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.596+1115dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807178 | ||||||
| chr16:89807178
|
G | GTT | 4 | a0006c0007t0004g0310a0006c0007t0004g0316a0007c0009t0001g0325others(1): Show | 4 | HG02145.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1114_596+1115d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807178 | ||||||
| chr16:89807184
|
C | T | 23 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(20): Show | 24 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.596+1110G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807184 | ||||||
| chr16:89807184
|
CT | C | 18 | a0001c0001t0001g0173a0001c0026t0001g0023a0001c0034t0001g0104others(15): Show | 18 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.596+1109delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807184 | ||||||
| chr16:89807224
|
C | T | 15 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(12): Show | 15 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.596+1070G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807224 | ||||||
| chr16:89807225
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.596+1069C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807225 | ||||||
| chr16:89807229
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.596+1065G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807229 | ||||||
| chr16:89807255
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.596+1039C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807255 | ||||||
| chr16:89807379
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.596+915C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807379 | ||||||
| chr16:89807409
|
T | A | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.596+885A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807409 | ||||||
| chr16:89807436
|
T | C | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.596+858A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807436 | ||||||
| chr16:89807472
|
G | A | 2 | a0005c0005t0001g0181a0005c0005t0001g0192 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.596+822C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807472 | ||||||
| chr16:89807508
|
G | C | 2 | a0006c0055t0009g0309a0040c0050t0013g0206 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.596+786C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807508 | ||||||
| chr16:89807593
|
T | C | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.596+701A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807593 | ||||||
| chr16:89807617
|
G | C | 1 | a0002c0006t0005g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.596+677C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807617 | ||||||
| chr16:89807665
|
C | A | 44 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(41): Show | 45 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.596+629G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807665 | ||||||
| chr16:89807677
|
G | A | 7 | a0002c0002t0001g0026a0002c0002t0001g0072a0002c0002t0001g0073others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.596+617C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807677 | ||||||
| chr16:89807682
|
A | T | 10 | a0007c0009t0001g0322a0007c0009t0001g0323a0007c0009t0001g0324others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.596+612T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807682 | ||||||
| chr16:89807744
|
G | A | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.596+550C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807744 | ||||||
| chr16:89807846
|
G | A | 1 | a0002c0006t0011g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.596+448C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807846 | ||||||
| chr16:89807859
|
G | A | 3 | a0001c0001t0003g0045a0001c0001t0003g0059a0016c0019t0001g0108 | 3 | HG02040.hp1 HG02071.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.596+435C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89807859 | ||||||
| chr16:89808067
|
AC | A | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.596+226delG | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808067 | ||||||
| chr16:89808068
|
C | CAACAAA | 19 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(16): Show | 19 | HG01081.hp1 HG01167.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.596+225_596+226ins others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808068 | ||||||
| chr16:89808069
|
AG | A | 286 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.596+224delC | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808069 | ||||||
| chr16:89808070
|
G | A | 45 | a0001c0001t0001g0222a0001c0001t0003g0101a0002c0002t0001g0216others(42): Show | 46 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.596+224C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808070 | ||||||
| chr16:89808071
|
A | C | 1 | a0001c0001t0003g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.596+223T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808071 | ||||||
| chr16:89808072
|
C | A | 1 | a0001c0001t0003g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.596+222G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808072 | ||||||
| chr16:89808078
|
G | A | 331 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(328): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.596+216C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808078 | ||||||
| chr16:89808082
|
ACAAAACC | A | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.596+205_596+211del others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808082 | ||||||
| chr16:89808083
|
C | A | 305 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.596+211G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808083 | ||||||
| chr16:89808086
|
A | C | 305 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.596+208T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808086 | ||||||
| chr16:89808087
|
A | C | 1 | a0002c0002t0001g0083 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.596+207T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808087 | ||||||
| chr16:89808088
|
C | A | 306 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.596+206G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808088 | ||||||
| chr16:89808089
|
C | A | 306 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.596+205G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808089 | ||||||
| chr16:89808141
|
C | A | 2 | a0002c0002t0001g0030a0002c0002t0001g0092 | 2 | NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.596+153G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808141 | ||||||
| chr16:89808151
|
A | C | 208 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(205): Show | 209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.596+143T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808151 | ||||||
| chr16:89808220
|
C | T | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.596+74G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 6/42 | chr16 | 89808220 | ||||||
| chr16:89808466
|
G | A | 5 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0011g0227others(2): Show | 5 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-99C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808466 | ||||||
| chr16:89808533
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.523-166A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808533 | ||||||
| chr16:89808581
|
A | G | 2 | a0005c0005t0001g0182a0005c0005t0001g0183 | 2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.523-214T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808581 | ||||||
| chr16:89808602
|
TTCTCTTC others(4): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.523-246_523-236del others(11): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808602 | ||||||
| chr16:89808625
|
G | T | 289 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.523-258C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808625 | ||||||
| chr16:89808646
|
C | G | 4 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0199others(1): Show | 4 | HG02040.hp2 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-279G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808646 | ||||||
| chr16:89808799
|
C | T | 2 | a0002c0002t0001g0027a0002c0002t0001g0028 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.523-432G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808799 | ||||||
| chr16:89808835
|
C | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.523-468G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808835 | ||||||
| chr16:89808838
|
T | C | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.523-471A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808838 | ||||||
| chr16:89808851
|
T | C | 283 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.523-484A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808851 | ||||||
| chr16:89808880
|
T | A | 2 | a0009c0010t0002g0288a0009c0010t0002g0299 | 2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.523-513A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808880 | ||||||
| chr16:89808884
|
C | G | 1 | a0004c0004t0002g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.523-517G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808884 | ||||||
| chr16:89808894
|
C | T | 15 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(12): Show | 15 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-527G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808894 | ||||||
| chr16:89808910
|
A | ATT | 11 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(8): Show | 11 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.523-545_523-544dup others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808910 | ||||||
| chr16:89808935
|
G | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.523-568C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808935 | ||||||
| chr16:89808937
|
G | T | 3 | a0001c0001t0001g0222a0002c0006t0011g0227a0002c0006t0011g0228 | 3 | HG01167.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.523-570C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808937 | ||||||
| chr16:89808964
|
G | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.523-597C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808964 | ||||||
| chr16:89808969
|
C | G | 295 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.523-602G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89808969 | ||||||
| chr16:89809030
|
T | C | 296 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.523-663A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809030 | ||||||
| chr16:89809031
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.523-664C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809031 | ||||||
| chr16:89809040
|
G | C | 1 | a0002c0002t0001g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.523-673C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809040 | ||||||
| chr16:89809067
|
G | A | 2 | a0012c0013t0007g0079a0012c0013t0007g0081 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.523-700C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809067 | ||||||
| chr16:89809108
|
G | A | 3 | a0002c0002t0001g0001a0002c0002t0001g0043a0002c0002t0001g0044 | 4 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-741C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809108 | ||||||
| chr16:89809128
|
G | A | 1 | a0002c0047t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.523-761C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809128 | ||||||
| chr16:89809139
|
C | G | 3 | a0006c0007t0004g0313a0006c0007t0004g0315a0006c0007t0009g0314 | 3 | HG01192.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.523-772G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809139 | ||||||
| chr16:89809213
|
C | T | 22 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(19): Show | 23 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.523-846G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809213 | ||||||
| chr16:89809230
|
G | A | 2 | a0004c0004t0002g0245a0004c0004t0002g0269 | 2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.523-863C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809230 | ||||||
| chr16:89809296
|
G | A | 1 | a0001c0001t0003g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.523-929C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809296 | ||||||
| chr16:89809302
|
A | C | 283 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.523-935T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809302 | ||||||
| chr16:89809328
|
T | C | 24 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(21): Show | 25 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.523-961A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809328 | ||||||
| chr16:89809466
|
G | A | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.523-1099C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809466 | ||||||
| chr16:89809505
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.523-1138C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809505 | ||||||
| chr16:89809578
|
G | A | 1 | a0037c0048t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.522+1129C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809578 | ||||||
| chr16:89809592
|
G | A | 1 | a0002c0006t0005g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.522+1115C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809592 | ||||||
| chr16:89809631
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+1076A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809631 | ||||||
| chr16:89809794
|
G | A | 1 | a0002c0006t0011g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.522+913C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809794 | ||||||
| chr16:89809806
|
T | A | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.522+901A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809806 | ||||||
| chr16:89809814
|
T | C | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.522+893A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809814 | ||||||
| chr16:89809841
|
A | C | 3 | a0006c0007t0004g0313a0006c0007t0004g0315a0006c0007t0009g0314 | 3 | HG01192.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.522+866T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809841 | ||||||
| chr16:89809922
|
T | G | 252 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(249): Show | 254 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.522+785A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809922 | ||||||
| chr16:89809929
|
G | C | 1 | a0030c0027t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.522+778C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809929 | ||||||
| chr16:89809936
|
C | G | 1 | a0030c0027t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.522+771G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89809936 | ||||||
| chr16:89810051
|
G | A | 1 | a0003c0003t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.522+656C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810051 | ||||||
| chr16:89810078
|
T | A | 1 | a0004c0004t0002g0256 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.522+629A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810078 | ||||||
| chr16:89810118
|
C | T | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.522+589G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810118 | ||||||
| chr16:89810201
|
T | C | 1 | a0004c0004t0002g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.522+506A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810201 | ||||||
| chr16:89810230
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.522+477C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810230 | ||||||
| chr16:89810239
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.522+468G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810239 | ||||||
| chr16:89810322
|
CA | C | 47 | a0002c0002t0001g0216a0002c0006t0005g0025a0002c0006t0005g0217others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.522+384delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810322 | ||||||
| chr16:89810350
|
G | T | 1 | a0001c0001t0003g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.522+357C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810350 | ||||||
| chr16:89810357
|
G | A | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.522+350C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810357 | ||||||
| chr16:89810393
|
AT | A | 44 | a0001c0052t0001g0211a0002c0002t0001g0022a0002c0002t0001g0060others(41): Show | 44 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.522+313delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810393 | ||||||
| chr16:89810420
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.522+287G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810420 | ||||||
| chr16:89810440
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522+267A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810440 | ||||||
| chr16:89810529
|
T | C | 1 | a0002c0002t0001g0175 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.522+178A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810529 | ||||||
| chr16:89810555
|
G | C | 3 | a0003c0003t0002g0302a0018c0017t0001g0244a0018c0017t0001g0277 | 3 | HG01192.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.522+152C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810555 | ||||||
| chr16:89810591
|
A | G | 2 | a0004c0004t0002g0245a0004c0004t0002g0269 | 2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.522+116T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 5/42 | chr16 | 89810591 | ||||||
| chr16:89810827
|
A | T | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.427-25T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 4/42 | chr16 | 89810827 | ||||||
| chr16:89810861
|
T | C | 34 | a0002c0002t0001g0022a0002c0002t0001g0193a0005c0005t0001g0036others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.427-59A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 4/42 | chr16 | 89810861 | ||||||
| chr16:89811095
|
G | A | 1 | a0002c0006t0008g0226 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.284-24C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811095 | ||||||
| chr16:89811138
|
G | C | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.284-67C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811138 | ||||||
| chr16:89811222
|
G | A | 16 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-151C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811222 | ||||||
| chr16:89811302
|
G | C | 1 | a0002c0006t0005g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-231C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811302 | ||||||
| chr16:89811312
|
C | T | 209 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(206): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.284-241G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811312 | ||||||
| chr16:89811484
|
T | C | 9 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0006g0062others(6): Show | 9 | HG02451.hp2 HG02976.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-413A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811484 | ||||||
| chr16:89811567
|
A | G | 208 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(205): Show | 209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.284-496T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811567 | ||||||
| chr16:89811690
|
G | T | 1 | a0003c0003t0002g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-619C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811690 | ||||||
| chr16:89811726
|
ATTTTT | A | 208 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(205): Show | 209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.284-660_284-656del others(5): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811726 | ||||||
| chr16:89811750
|
C | T | 1 | a0006c0055t0009g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.284-679G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811750 | ||||||
| chr16:89811769
|
C | T | 9 | a0007c0009t0001g0322a0007c0009t0001g0323a0007c0009t0001g0324others(6): Show | 10 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-698G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811769 | ||||||
| chr16:89811788
|
C | T | 1 | a0010c0011t0002g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.284-717G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811788 | ||||||
| chr16:89811917
|
A | C | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284-846T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811917 | ||||||
| chr16:89811992
|
T | A | 44 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(41): Show | 45 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-921A>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89811992 | ||||||
| chr16:89812053
|
G | A | 25 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(22): Show | 26 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.284-982C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812053 | ||||||
| chr16:89812073
|
C | G | 9 | a0007c0009t0001g0322a0007c0009t0001g0323a0007c0009t0001g0324others(6): Show | 10 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-1002G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812073 | ||||||
| chr16:89812136
|
C | A | 1 | a0001c0001t0003g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.284-1065G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812136 | ||||||
| chr16:89812144
|
G | T | 3 | a0011c0012t0001g0003a0011c0012t0001g0006a0011c0012t0001g0007 | 3 | HG01243.hp2 HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.284-1073C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812144 | ||||||
| chr16:89812279
|
A | G | 1 | a0002c0006t0005g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.284-1208T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812279 | ||||||
| chr16:89812337
|
CAAAAAAA others(8): Show |
C | 1 | a0038c0023t0002g0297 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.284-1281_284-1267d others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812337 | ||||||
| chr16:89812477
|
T | C | 1 | a0006c0056t0004g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-1406A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812477 | ||||||
| chr16:89812595
|
G | A | 1 | a0002c0002t0001g0175 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.284-1524C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812595 | ||||||
| chr16:89812642
|
G | A | 13 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-1571C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812642 | ||||||
| chr16:89812646
|
C | CA | 15 | a0003c0003t0002g0257a0003c0003t0002g0259a0003c0003t0002g0260others(12): Show | 15 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-1576dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAA | 28 | a0001c0052t0001g0211a0002c0002t0001g0193a0005c0005t0001g0036others(25): Show | 28 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.284-1579_284-1576d others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAA | 6 | a0005c0005t0001g0194a0005c0005t0001g0195a0005c0005t0001g0197others(3): Show | 6 | HG00597.hp2 HG02074.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1580_284-1576d others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(6): Show |
2 | a0006c0055t0009g0309a0040c0050t0013g0206 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-1588_284-1576d others(15): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(8): Show |
3 | a0003c0003t0002g0284a0003c0003t0002g0293a0003c0003t0002g0294 | 3 | HG01167.hp2 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.284-1590_284-1576d others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(9): Show |
6 | a0003c0003t0002g0238a0003c0003t0002g0274a0003c0003t0002g0283others(3): Show | 6 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-1591_284-1576d others(18): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(10): Show |
7 | a0003c0003t0002g0239a0003c0003t0002g0275a0003c0003t0002g0286others(4): Show | 7 | HG00733.hp2 HG01516.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-1592_284-1576d others(19): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(11): Show |
5 | a0009c0010t0002g0287a0009c0010t0002g0288a0009c0010t0002g0298others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-1593_284-1576d others(20): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(12): Show |
4 | a0004c0004t0002g0300a0009c0010t0002g0289a0014c0015t0002g0008others(1): Show | 4 | HG00735.hp1 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-1594_284-1576d others(21): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(16): Show |
1 | a0010c0011t0002g0010 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.284-1598_284-1576d others(25): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
C | CAAAAAAA others(22): Show |
1 | a0003c0003t0002g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-1576_284-1575i others(31): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812646
|
CAAAAA | C | 24 | a0003c0003t0002g0292a0006c0007t0004g0310a0006c0007t0004g0311others(21): Show | 25 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.284-1580_284-1576d others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812646 | ||||||
| chr16:89812648
|
A | AAAAC | 169 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(166): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.284-1578_284-1577i others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812648 | ||||||
| chr16:89812654
|
A | C | 1 | a0001c0001t0001g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-1583T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812654 | ||||||
| chr16:89812655
|
A | C | 169 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(166): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.284-1584T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812655 | ||||||
| chr16:89812656
|
A | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0119a0002c0002t0001g0074others(1): Show | 4 | HG01106.hp2 NA18968.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1585T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812656 | ||||||
| chr16:89812659
|
A | C | 15 | a0001c0001t0001g0024a0001c0001t0001g0115a0001c0001t0001g0116others(12): Show | 15 | HG01884.hp2 HG02109.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-1588T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812659 | ||||||
| chr16:89812660
|
A | C | 34 | a0001c0001t0001g0071a0001c0001t0001g0097a0002c0002t0001g0001others(31): Show | 35 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.284-1589T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812660 | ||||||
| chr16:89812664
|
A | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.284-1593T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812664 | ||||||
| chr16:89812666
|
A | AAAAAAAA others(3): Show |
1 | a0002c0006t0011g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.284-1596_284-1595i others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812666 | ||||||
| chr16:89812666
|
A | AAAAAAAA others(1): Show |
10 | a0002c0002t0001g0216a0002c0006t0005g0217a0002c0006t0005g0219others(7): Show | 10 | HG01081.hp1 HG03239.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-1596_284-1595i others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812666 | ||||||
| chr16:89812670
|
A | C | 1 | a0002c0051t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284-1599T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812670 | ||||||
| chr16:89812715
|
A | G | 1 | a0029c0028t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.284-1644T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812715 | ||||||
| chr16:89812887
|
G | C | 1 | a0004c0004t0002g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.283+1633C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812887 | ||||||
| chr16:89812910
|
A | G | 45 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(42): Show | 46 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.283+1610T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812910 | ||||||
| chr16:89812923
|
T | C | 45 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(42): Show | 46 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.283+1597A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812923 | ||||||
| chr16:89812924
|
T | G | 45 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(42): Show | 46 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.283+1596A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812924 | ||||||
| chr16:89812973
|
T | C | 1 | a0002c0002t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.283+1547A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89812973 | ||||||
| chr16:89813032
|
CA | C | 220 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.283+1487delT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813032 | ||||||
| chr16:89813032
|
CAA | C | 56 | a0001c0001t0001g0112a0001c0001t0001g0222a0001c0001t0003g0040others(53): Show | 57 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.283+1486_283+1487d others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813032 | ||||||
| chr16:89813057
|
A | C | 8 | a0002c0006t0005g0025a0002c0006t0005g0219a0002c0006t0005g0223others(5): Show | 8 | HG03239.hp2 HG03704.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+1463T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813057 | ||||||
| chr16:89813064
|
C | T | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283+1456G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813064 | ||||||
| chr16:89813285
|
G | A | 4 | a0001c0001t0001g0222a0002c0006t0011g0227a0002c0006t0011g0228others(1): Show | 4 | HG01167.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+1235C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813285 | ||||||
| chr16:89813290
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283+1230G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813290 | ||||||
| chr16:89813305
|
T | G | 249 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(246): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.283+1215A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813305 | ||||||
| chr16:89813361
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.283+1159A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813361 | ||||||
| chr16:89813377
|
C | T | 1 | a0011c0012t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.283+1143G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813377 | ||||||
| chr16:89813391
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.283+1129C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813391 | ||||||
| chr16:89813409
|
T | TA | 216 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(213): Show | 217 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.283+1110dupT | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813409 | ||||||
| chr16:89813429
|
G | C | 32 | a0002c0002t0001g0193a0005c0005t0001g0036a0005c0005t0001g0064others(29): Show | 32 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.283+1091C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813429 | ||||||
| chr16:89813488
|
A | C | 1 | a0002c0006t0005g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+1032T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813488 | ||||||
| chr16:89813508
|
A | C | 280 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(277): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.283+1012T>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813508 | ||||||
| chr16:89813669
|
G | C | 1 | a0003c0003t0002g0271 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.283+851C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813669 | ||||||
| chr16:89813712
|
C | T | 3 | a0001c0001t0001g0102a0001c0029t0005g0103a0001c0034t0001g0104 | 3 | HG02735.hp2 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.283+808G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813712 | ||||||
| chr16:89813713
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.283+807C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813713 | ||||||
| chr16:89813732
|
C | G | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.283+788G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813732 | ||||||
| chr16:89813782
|
G | GT | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.283+737dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813782 | ||||||
| chr16:89813806
|
C | CTG | 54 | a0001c0001t0001g0069a0001c0001t0001g0201a0001c0001t0001g0202others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.283+712_283+713dup others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
C | CTGTG | 170 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(167): Show | 171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.283+710_283+713dup others(4): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
C | CTGTGTG | 23 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0241others(20): Show | 24 | HG00438.hp2 HG00621.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.283+708_283+713dup others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
C | CTGTGTGT others(1): Show |
17 | a0002c0002t0001g0030a0002c0002t0001g0083a0002c0002t0001g0084others(14): Show | 17 | HG00423.hp1 HG02080.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+706_283+713dup others(8): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
C | CTGTGTGT others(3): Show |
4 | a0002c0002t0001g0029a0002c0002t0001g0080a0002c0047t0001g0082others(1): Show | 4 | HG00280.hp1 HG02970.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+704_283+713dup others(10): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
C | CTGTGTGT others(5): Show |
1 | a0012c0013t0007g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.283+702_283+713dup others(12): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
C | CTGTGTGT others(7): Show |
2 | a0002c0002t0001g0027a0002c0002t0001g0028 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.283+700_283+713dup others(14): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813806
|
CTG | C | 3 | a0003c0003t0002g0272a0028c0043t0015g0307a0040c0050t0013g0206 | 3 | HG02451.hp1 HG03139.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.283+712_283+713del others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813806 | ||||||
| chr16:89813841
|
C | T | 31 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.283+679G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813841 | ||||||
| chr16:89813850
|
G | C | 203 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(200): Show | 204 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.283+670C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813850 | ||||||
| chr16:89813870
|
T | C | 16 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+650A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813870 | ||||||
| chr16:89813976
|
T | C | 16 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0025others(13): Show | 16 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+544A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89813976 | ||||||
| chr16:89814034
|
G | C | 1 | a0008c0008t0001g0021 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.283+486C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814034 | ||||||
| chr16:89814047
|
G | C | 1 | a0004c0004t0002g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.283+473C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814047 | ||||||
| chr16:89814070
|
G | A | 3 | a0003c0003t0001g0303a0019c0016t0007g0276a0019c0016t0007g0291 | 3 | HG02559.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.283+450C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814070 | ||||||
| chr16:89814085
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+435G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814085 | ||||||
| chr16:89814126
|
C | G | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283+394G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814126 | ||||||
| chr16:89814129
|
A | T | 248 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(245): Show | 250 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.283+391T>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814129 | ||||||
| chr16:89814162
|
G | T | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283+358C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814162 | ||||||
| chr16:89814163
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283+357C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814163 | ||||||
| chr16:89814188
|
G | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283+332C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814188 | ||||||
| chr16:89814226
|
T | C | 31 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0274others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.283+294A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814226 | ||||||
| chr16:89814385
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283+135C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814385 | ||||||
| chr16:89814388
|
T | C | 1 | a0003c0003t0002g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.283+132A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814388 | ||||||
| chr16:89814414
|
C | G | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.283+106G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814414 | ||||||
| chr16:89814436
|
A | G | 7 | a0002c0002t0001g0026a0002c0002t0001g0072a0002c0002t0001g0073others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+84T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | 89814436 | ||||||
| chr16:89814668
|
C | A | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.190-55G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89814668 | ||||||
| chr16:89814785
|
AC | A | 26 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(23): Show | 27 | HG01109.hp1 HG01192.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.190-173delG | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89814785 | ||||||
| chr16:89814805
|
G | C | 1 | a0003c0003t0002g0290 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.190-192C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89814805 | ||||||
| chr16:89814848
|
G | C | 1 | a0002c0002t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190-235C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89814848 | ||||||
| chr16:89814900
|
C | T | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.190-287G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89814900 | ||||||
| chr16:89815035
|
C | A | 3 | a0003c0003t0001g0303a0019c0016t0007g0276a0019c0016t0007g0291 | 3 | HG02559.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.190-422G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815035 | ||||||
| chr16:89815078
|
T | C | 233 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(230): Show | 235 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.190-465A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815078 | ||||||
| chr16:89815115
|
C | G | 1 | a0002c0002t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.190-502G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815115 | ||||||
| chr16:89815171
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.190-558C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815171 | ||||||
| chr16:89815204
|
T | C | 203 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(200): Show | 204 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.190-591A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815204 | ||||||
| chr16:89815288
|
C | A | 1 | a0002c0006t0005g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.189+589G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815288 | ||||||
| chr16:89815333
|
G | A | 1 | a0003c0003t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.189+544C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815333 | ||||||
| chr16:89815335
|
C | CT | 14 | a0001c0001t0001g0241a0002c0006t0008g0215a0003c0003t0002g0238others(11): Show | 14 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.189+541dupA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CT | C | 30 | a0002c0006t0005g0025a0002c0006t0005g0223a0002c0006t0005g0229others(27): Show | 30 | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.189+541delA | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CTT | C | 16 | a0003c0003t0002g0292a0003c0003t0002g0293a0003c0003t0002g0294others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.189+540_189+541del others(2): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CTTTTTT | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0047others(51): Show | 55 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.189+536_189+541del others(6): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CTTTTTTT | C | 147 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0102others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.189+535_189+541del others(7): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CTTTTTTT others(8): Show |
C | 2 | a0006c0007t0004g0310a0006c0007t0004g0311 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.189+527_189+541del others(15): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CTTTTTTT others(9): Show |
C | 10 | a0006c0007t0004g0313a0006c0007t0004g0315a0006c0007t0004g0316others(7): Show | 10 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.189+526_189+541del others(16): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815335
|
CTTTTTTT others(10): Show |
C | 13 | a0006c0007t0009g0308a0006c0055t0009g0309a0007c0009t0001g0322others(10): Show | 14 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.189+525_189+541del others(17): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815335 | ||||||
| chr16:89815365
|
T | G | 1 | a0040c0050t0013g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.189+512A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815365 | ||||||
| chr16:89815403
|
C | G | 1 | a0002c0002t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.189+474G>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815403 | ||||||
| chr16:89815414
|
A | G | 7 | a0008c0008t0001g0015a0008c0008t0001g0016a0008c0008t0001g0018others(4): Show | 7 | HG00323.hp2 HG01175.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+463T>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815414 | ||||||
| chr16:89815445
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.189+432C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815445 | ||||||
| chr16:89815503
|
G | C | 12 | a0006c0007t0004g0310a0006c0007t0004g0311a0006c0007t0004g0313others(9): Show | 12 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+374C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815503 | ||||||
| chr16:89815519
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.189+358G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815519 | ||||||
| chr16:89815524
|
T | C | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.189+353A>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815524 | ||||||
| chr16:89815535
|
C | T | 1 | a0001c0001t0010g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.189+342G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815535 | ||||||
| chr16:89815694
|
G | C | 1 | a0003c0003t0002g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189+183C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815694 | ||||||
| chr16:89815710
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189+167C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815710 | ||||||
| chr16:89815775
|
C | A | 2 | a0001c0001t0001g0208a0001c0001t0003g0209 | 2 | NA18971.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.189+102G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815775 | ||||||
| chr16:89815818
|
C | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189+59G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815818 | ||||||
| chr16:89815846
|
T | G | 1 | a0001c0001t0006g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.189+31A>C | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 2/42 | chr16 | 89815846 | ||||||
| chr16:89816121
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.80-135C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816121 | ||||||
| chr16:89816150
|
G | A | 10 | a0007c0009t0001g0322a0007c0009t0001g0323a0007c0009t0001g0324others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-164C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816150 | ||||||
| chr16:89816164
|
C | A | 1 | a0003c0003t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80-178G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816164 | ||||||
| chr16:89816201
|
G | T | 15 | a0001c0001t0001g0222a0002c0002t0001g0216a0002c0006t0005g0217others(12): Show | 15 | HG01081.hp1 HG01167.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.80-215C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816201 | ||||||
| chr16:89816275
|
G | C | 1 | a0004c0004t0002g0304 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79+262C>G | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816275 | ||||||
| chr16:89816280
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.79+257C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816280 | ||||||
| chr16:89816285
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.79+252G>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816285 | ||||||
| chr16:89816309
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.79+228C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816309 | ||||||
| chr16:89816314
|
G | A | 3 | a0013c0014t0002g0330a0013c0014t0002g0331a0013c0014t0002g0332 | 3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.79+223C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816314 | ||||||
| chr16:89816399
|
G | T | 205 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(202): Show | 206 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.79+138C>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816399 | ||||||
| chr16:89816418
|
C | T | 205 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0046others(202): Show | 206 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.79+119G>A | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816418 | ||||||
| chr16:89816458
|
G | A | 2 | a0017c0018t0002g0305a0017c0018t0002g0306 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.79+79C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816458 | ||||||
| chr16:89816502
|
G | A | 1 | a0028c0043t0015g0307 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.79+35C>T | FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 1/42 | chr16 | 89816502 |