Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2177 |
|---|---|
| ensemblid | ENSG00000144554.13 |
| hgncid | 3585 |
| symbol | FANCD2 |
| name | FA complementation group D2 |
| refseq_nuc | NM_001018115.3 |
| refseq_prot | NP_001018125.1 |
| ensembl_nuc | ENST00000675286.1 |
| ensembl_prot | ENSP00000502379.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 10026437 |
| end | 10101932 |
| strand | + |
| ver | v1.2 |
| region | chr3:10026437-10101932 |
| region5000 | chr3:10021437-10106932 |
| regionname0 | FANCD2_chr3_10026437_10101932 |
| regionname5000 | FANCD2_chr3_10021437_10106932 |
| 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 | 1/1 | 1451 | 145 | 39 | 36 | 40 | 6 | 22 | 30 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002 | 0/0 | 1451 | 59 | 30 | 13 | 11 | 1 | 4 | 9 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0003 | 0/0 | 1451 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0004 | 0/0 | 1451 | 7 | 1 | 2 | 3 | 0 | 1 | 3 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0005 | 0/0 | 1451 | 5 | 0 | 0 | 2 | 0 | 3 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0006 | 0/0 | 1451 | 4 | 2 | 1 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0007 | 0/0 | 1451 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0008 | 0/0 | 1451 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0009 | 0/0 | 1451 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0010 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0011 | 0/0 | 1451 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0012 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0013 | 0/0 | 1451 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0014 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0015 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| 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 | 1/1 | 4356 | 128 | 27 | 32 | 40 | 6 | 21 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0002 | 0/0 | 4356 | 56 | 30 | 10 | 11 | 1 | 4 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0003 | 0/0 | 4356 | 12 | 9 | 3 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0004 | 0/0 | 4356 | 9 | 9 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0005 | 0/0 | 4356 | 7 | 1 | 2 | 3 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0006 | 0/0 | 4356 | 4 | 2 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0007 | 0/0 | 4356 | 3 | 3 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0008 | 0/0 | 4356 | 3 | 0 | 0 | 2 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0009 | 0/0 | 4356 | 2 | 0 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0010 | 0/0 | 4356 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0011 | 0/0 | 4356 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0012 | 0/0 | 4356 | 2 | 0 | 2 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0013 | 0/0 | 4356 | 2 | 0 | 0 | 0 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0014 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0015 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0016 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0017 | 0/0 | 4356 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0018 | 0/0 | 4356 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0019 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0020 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0021 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0022 | 0/0 | 4356 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| c0023 | 0/0 | 4356 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| 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 | 1/0 | 741 | 77 | 9 | 21 | 26 | 4 | 16 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0002 | 0/0 | 741 | 54 | 36 | 14 | 2 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0003 | 0/0 | 740 | 41 | 33 | 3 | 4 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0004 | 0/1 | 741 | 32 | 1 | 11 | 8 | 3 | 8 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0005 | 0/0 | 742 | 12 | 0 | 3 | 7 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0006 | 0/0 | 740 | 6 | 4 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0007 | 0/0 | 742 | 5 | 0 | 1 | 3 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0008 | 0/0 | 741 | 3 | 0 | 0 | 3 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0009 | 0/0 | 741 | 2 | 0 | 0 | 2 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0010 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0011 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0012 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0013 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0014 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0015 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0016 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0017 | 0/0 | 742 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0018 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| t0019 | 0/0 | 742 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| 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 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| 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 | 1/1 | 4356 | 128 | 27 | 32 | 40 | 6 | 21 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0003 | 0/0 | 4356 | 12 | 9 | 3 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0011 | 0/0 | 4356 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0016 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0019 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0023 | 0/0 | 4356 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0002 | 0/0 | 4356 | 56 | 30 | 10 | 11 | 1 | 4 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0012 | 0/0 | 4356 | 2 | 0 | 2 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0020 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0003c0004 | 0/0 | 4356 | 9 | 9 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0004c0005 | 0/0 | 4356 | 7 | 1 | 2 | 3 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0005c0008 | 0/0 | 4356 | 3 | 0 | 0 | 2 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0005c0013 | 0/0 | 4356 | 2 | 0 | 0 | 0 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0006c0006 | 0/0 | 4356 | 4 | 2 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0007c0007 | 0/0 | 4356 | 3 | 3 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0008c0009 | 0/0 | 4356 | 2 | 0 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0009c0010 | 0/0 | 4356 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0010c0022 | 0/0 | 4356 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0011c0021 | 0/0 | 4356 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0012c0018 | 0/0 | 4356 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0013c0017 | 0/0 | 4356 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0014c0015 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0015c0014 | 0/0 | 4356 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5096 | 65 | 7 | 18 | 23 | 4 | 12 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0003 | 0/0 | 5095 | 25 | 17 | 3 | 4 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0004 | 0/1 | 5096 | 28 | 1 | 10 | 7 | 2 | 7 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0007 | 0/0 | 5097 | 2 | 0 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0008 | 0/0 | 5096 | 3 | 0 | 0 | 3 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0010 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0011 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0012 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0018 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0001t0019 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0003t0002 | 0/0 | 5096 | 11 | 8 | 3 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0003t0006 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0011t0002 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0011t0003 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0016t0003 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0019t0001 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0001c0023t0001 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0002t0002 | 0/0 | 5096 | 39 | 27 | 9 | 2 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0002t0005 | 0/0 | 5097 | 9 | 0 | 0 | 7 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0002t0006 | 0/0 | 5095 | 5 | 3 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0002t0009 | 0/0 | 5096 | 2 | 0 | 0 | 2 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0002t0017 | 0/0 | 5097 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0012t0005 | 0/0 | 5097 | 2 | 0 | 2 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0002c0020t0002 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0003c0004t0003 | 0/0 | 5095 | 9 | 9 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0004c0005t0001 | 0/0 | 5096 | 6 | 1 | 2 | 3 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0004c0005t0016 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0005c0008t0001 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0005c0008t0007 | 0/0 | 5097 | 2 | 0 | 0 | 2 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0005c0013t0001 | 0/0 | 5096 | 2 | 0 | 0 | 0 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0006c0006t0002 | 0/0 | 5096 | 2 | 0 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0006c0006t0014 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0006c0006t0015 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0007c0007t0003 | 0/0 | 5095 | 3 | 3 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0008c0009t0004 | 0/0 | 5096 | 2 | 0 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0009c0010t0003 | 0/0 | 5095 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0010c0022t0007 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0011c0021t0005 | 0/0 | 5097 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0012c0018t0004 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0013c0017t0004 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0014c0015t0001 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| a0015c0014t0013 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | copy fasta | chr3 | 10021437 | 10106932 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0008g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0011t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0011t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0016t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0019t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0023t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0017g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0012t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0012t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0020t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0016g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0008t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0008t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0008t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0013t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0013t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0015g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0007c0007t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0007c0007t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0007c0007t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0008c0009t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0008c0009t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0009c0010t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0009c0010t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0010c0022t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0011c0021t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0012c0018t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0013c0017t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0014c0015t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0015c0014t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0040 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00408 | hp1 | a0002 | c0002 | t0005 | g0219 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00558 | hp1 | a0001 | c0001 | t0008 | g0025 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00558 | hp2 | a0005 | c0008 | t0007 | g0020 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00639 | hp2 | a0006 | c0006 | t0002 | g0223 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00741 | hp2 | a0011 | c0021 | t0005 | g0182 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0128 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01069 | hp2 | a0002 | c0002 | t0006 | g0202 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0133 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0028 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0196 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01081 | hp2 | a0008 | c0009 | t0004 | g0001 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0118 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0123 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0229 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0183 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01257 | hp2 | a0002 | c0012 | t0005 | g0193 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01258 | hp2 | a0002 | c0012 | t0005 | g0194 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01358 | hp2 | a0002 | c0020 | t0002 | g0227 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01516 | hp2 | a0008 | c0009 | t0004 | g0032 | EUR | IBS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01884 | hp2 | a0002 | c0002 | t0006 | g0176 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01891 | hp1 | a0003 | c0004 | t0003 | g0164 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0241 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0228 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01934 | hp2 | a0001 | c0019 | t0001 | g0094 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01952 | hp1 | a0004 | c0005 | t0001 | g0169 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01975 | hp1 | a0004 | c0005 | t0001 | g0173 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0225 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02080 | hp1 | a0001 | c0001 | t0011 | g0045 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0124 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0240 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0238 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02257 | hp2 | a0003 | c0004 | t0003 | g0165 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02258 | hp2 | a0009 | c0010 | t0003 | g0158 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0212 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0200 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0185 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02572 | hp1 | a0001 | c0011 | t0002 | g0199 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02602 | hp2 | a0002 | c0002 | t0017 | g0178 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02615 | hp2 | a0003 | c0004 | t0003 | g0166 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02622 | hp1 | a0003 | c0004 | t0003 | g0160 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0209 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0189 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02683 | hp2 | a0005 | c0013 | t0001 | g0115 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02698 | hp1 | a0013 | c0017 | t0004 | g0054 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02698 | hp2 | a0001 | c0023 | t0001 | g0066 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0203 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02717 | hp2 | a0006 | c0006 | t0014 | g0222 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0232 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02738 | hp2 | a0005 | c0008 | t0001 | g0019 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02809 | hp1 | a0003 | c0004 | t0003 | g0167 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02818 | hp1 | a0015 | c0014 | t0013 | g0154 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0205 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0134 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02896 | hp1 | a0002 | c0002 | t0006 | g0204 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0179 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0144 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02970 | hp1 | a0014 | c0015 | t0001 | g0027 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02976 | hp1 | a0003 | c0004 | t0003 | g0168 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0197 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0186 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03098 | hp1 | a0003 | c0004 | t0003 | g0161 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03098 | hp2 | a0007 | c0007 | t0003 | g0156 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0130 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0235 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03195 | hp1 | a0007 | c0007 | t0003 | g0157 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0129 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03209 | hp2 | a0001 | c0016 | t0003 | g0122 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03239 | hp1 | a0004 | c0005 | t0016 | g0174 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0126 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03516 | hp1 | a0003 | c0004 | t0003 | g0162 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0237 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0070 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03579 | hp2 | a0001 | c0011 | t0003 | g0239 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0113 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03654 | hp2 | a0002 | c0002 | t0005 | g0231 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03688 | hp2 | a0005 | c0013 | t0001 | g0116 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | BEB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04115 | hp1 | a0006 | c0006 | t0002 | g0221 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04184 | hp1 | a0002 | c0002 | t0005 | g0230 | SAS | BEB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0074 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18522 | hp1 | a0006 | c0006 | t0015 | g0220 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0210 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18747 | hp1 | a0010 | c0022 | t0007 | g0018 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18906 | hp1 | a0007 | c0007 | t0003 | g0155 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18940 | hp1 | a0002 | c0002 | t0005 | g0177 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18948 | hp1 | a0002 | c0002 | t0005 | g0213 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18953 | hp1 | a0002 | c0002 | t0005 | g0181 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18956 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18957 | hp2 | a0002 | c0002 | t0009 | g0180 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18967 | hp1 | a0005 | c0008 | t0007 | g0021 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18971 | hp2 | a0004 | c0005 | t0001 | g0171 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0218 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18985 | hp1 | a0002 | c0002 | t0005 | g0215 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18986 | hp1 | a0004 | c0005 | t0001 | g0172 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18988 | hp1 | a0004 | c0005 | t0001 | g0175 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19004 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19007 | hp2 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19012 | hp1 | a0012 | c0018 | t0004 | g0079 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19056 | hp1 | a0002 | c0002 | t0009 | g0216 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19080 | hp1 | a0002 | c0002 | t0005 | g0217 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20129 | hp2 | a0009 | c0010 | t0003 | g0159 | AFR | ASW | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20805 | hp1 | a0002 | c0002 | t0006 | g0201 | EUR | TSI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | TSI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | GIH | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0135 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0153 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0143 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03471 | hp2 | a0003 | c0004 | t0003 | g0163 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | USA | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0234 | AFR | USA | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0170 | AFR | USA | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0137 | AFR | USA | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0037 | REF | REF | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0016 | REF | REF | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10032962
|
G | C | 1 | a0006 | 4 | HG00639.hp2 HG02717.hp2 HG04115.hp1 others(1): Show |
missense_variant | MODERATE | c.195G>C | p.Gln65His | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/44 | 265/5096 | 195/4356 | 65/1451 | chr3 | 10032962 | ||
| chr3:10034732
|
T | C | 1 | a0015 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.311T>C | p.Ile104Thr | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 5/44 | 381/5096 | 311/4356 | 104/1451 | chr3 | 10034732 | ||
| chr3:10039303
|
A | G | 1 | a0003 | 9 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
missense_variant | MODERATE | c.516A>G | p.Ile172Met | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 8/44 | 586/5096 | 516/4356 | 172/1451 | chr3 | 10039303 | ||
| chr3:10039727
|
A | G | 2 | a0005a0010 | 6 | HG00558.hp2 HG02683.hp2 HG02738.hp2 others(3): Show |
missense_variant | MODERATE | c.577A>G | p.Thr193Ala | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/44 | 647/5096 | 577/4356 | 193/1451 | chr3 | 10039727 | ||
| chr3:10043144
|
G | A | 1 | a0004 | 7 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(4): Show |
missense_variant | MODERATE | c.983G>A | p.Arg328Gln | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 12/44 | 1053/5096 | 983/4356 | 328/1451 | chr3 | 10043144 | ||
| chr3:10043147
|
C | G | 1 | a0015 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.986C>G | p.Ala329Gly | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 12/44 | 1056/5096 | 986/4356 | 329/1451 | chr3 | 10043147 | ||
| chr3:10047974
|
C | G | 1 | a0007 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1336C>G | p.Leu446Val | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/44 | 1406/5096 | 1336/4356 | 446/1451 | chr3 | 10047974 | ||
| chr3:10048005
|
T | G | 4 | a0003a0007a0009others(1): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
missense_variant | MODERATE | c.1367T>G | p.Leu456Arg | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/44 | 1437/5096 | 1367/4356 | 456/1451 | chr3 | 10048005 | ||
| chr3:10052442
|
A | G | 1 | a0011 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.1601A>G | p.Tyr534Cys | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/44 | 1671/5096 | 1601/4356 | 534/1451 | chr3 | 10052442 | ||
| chr3:10063832
|
A | C | 2 | a0003a0007 | 12 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(9): Show |
missense_variant | MODERATE | c.1868A>C | p.Gln623Pro | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 21/44 | 1938/5096 | 1868/4356 | 623/1451 | chr3 | 10063832 | ||
| chr3:10064775
|
G | A | 1 | a0010 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.2068G>A | p.Asp690Asn | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/44 | 2138/5096 | 2068/4356 | 690/1451 | chr3 | 10064775 | ||
| chr3:10064848
|
C | T | 3 | a0002a0006a0011 | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
missense_variant | MODERATE | c.2141C>T | p.Pro714Leu | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/44 | 2211/5096 | 2141/4356 | 714/1451 | chr3 | 10064848 | ||
| chr3:10067303
|
A | C | 1 | a0012 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.2480A>C | p.Glu827Ala | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/44 | 2550/5096 | 2480/4356 | 827/1451 | chr3 | 10067303 | ||
| chr3:10073256
|
G | T | 1 | a0013 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2609G>T | p.Arg870Met | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/44 | 2679/5096 | 2609/4356 | 870/1451 | chr3 | 10073256 | ||
| chr3:10073260
|
A | C | 1 | a0014 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2613A>C | p.Lys871Asn | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/44 | 2683/5096 | 2613/4356 | 871/1451 | chr3 | 10073260 | ||
| chr3:10073349
|
G | T | 1 | a0008 | 2 | HG01081.hp2 HG01516.hp2 |
missense_variant | MODERATE | c.2702G>T | p.Gly901Val | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/44 | 2772/5096 | 2702/4356 | 901/1451 | chr3 | 10073349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10032932
|
A | G | 1 | a0001c0023 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.165A>G | p.Ser55Ser | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/44 | 235/5096 | 165/4356 | 55/1451 | chr3 | 10032932 | ||
| chr3:10043562
|
T | C | 1 | a0014c0015 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1068T>C | p.Tyr356Tyr | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 13/44 | 1138/5096 | 1068/4356 | 356/1451 | chr3 | 10043562 | ||
| chr3:10043852
|
A | G | 10 | a0001c0011a0002c0002a0002c0012others(7): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
synonymous_variant | LOW | c.1122A>G | p.Val374Val | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/44 | 1192/5096 | 1122/4356 | 374/1451 | chr3 | 10043852 | ||
| chr3:10049469
|
C | T | 6 | a0001c0011a0002c0002a0002c0012others(3): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
synonymous_variant | LOW | c.1509C>T | p.Asn503Asn | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/44 | 1579/5096 | 1509/4356 | 503/1451 | chr3 | 10049469 | ||
| chr3:10064831
|
T | C | 3 | a0003c0004a0007c0007a0009c0010 | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
synonymous_variant | LOW | c.2124T>C | p.Phe708Phe | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/44 | 2194/5096 | 2124/4356 | 708/1451 | chr3 | 10064831 | ||
| chr3:10065406
|
G | A | 1 | a0002c0020 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.2181G>A | p.Pro727Pro | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/44 | 2251/5096 | 2181/4356 | 727/1451 | chr3 | 10065406 | ||
| chr3:10065439
|
A | G | 1 | a0001c0019 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.2214A>G | p.Arg738Arg | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/44 | 2284/5096 | 2214/4356 | 738/1451 | chr3 | 10065439 | ||
| chr3:10067307
|
G | A | 1 | a0001c0016 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2484G>A | p.Lys828Lys | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/44 | 2554/5096 | 2484/4356 | 828/1451 | chr3 | 10067307 | ||
| chr3:10073359
|
C | T | 4 | a0003c0004a0007c0007a0009c0010others(1): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
synonymous_variant | LOW | c.2712C>T | p.Asn904Asn | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/44 | 2782/5096 | 2712/4356 | 904/1451 | chr3 | 10073359 | ||
| chr3:10087239
|
T | C | 1 | a0002c0012 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.3441T>C | p.Ala1147Ala | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/44 | 3511/5096 | 3441/4356 | 1147/1451 | chr3 | 10087239 | ||
| chr3:10087257
|
A | G | 1 | a0002c0012 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.3459A>G | p.Glu1153Glu | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/44 | 3529/5096 | 3459/4356 | 1153/1451 | chr3 | 10087257 | ||
| chr3:10096385
|
T | G | 14 | a0001c0003a0001c0011a0002c0002others(11): Show | 104 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
synonymous_variant | LOW | c.4098T>G | p.Leu1366Leu | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/44 | 4168/5096 | 4098/4356 | 1366/1451 | chr3 | 10096385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10028652
|
G | C | 3 | a0001c0001t0008a0001c0001t0010a0001c0001t0011 | 5 | HG00558.hp1 HG02080.hp1 NA19004.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/44 | 6 | chr3 | 10028652 | |||||
| chr3:10101265
|
C | T | 8 | a0001c0001t0004a0001c0001t0008a0001c0001t0011others(5): Show | 38 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 3 | chr3 | 10101265 | |||||
| chr3:10101374
|
C | A | 1 | a0001c0001t0012 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 112 | chr3 | 10101374 | |||||
| chr3:10101377
|
C | CT | 7 | a0001c0001t0007a0001c0001t0011a0001c0001t0018others(4): Show | 9 | HG00558.hp2 HG01071.hp2 HG02080.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*140dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 141 | INFO_REALIGN_3_PRIME | chr3 | 10101377 | ||||
| chr3:10101377
|
CT | C | 9 | a0001c0001t0003a0001c0001t0012a0001c0003t0006others(6): Show | 48 | HG01069.hp2 HG01099.hp1 HG01109.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*140delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 140 | INFO_REALIGN_3_PRIME | chr3 | 10101377 | ||||
| chr3:10101402
|
T | A | 1 | a0002c0002t0009 | 2 | NA18957.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 140 | chr3 | 10101402 | |||||
| chr3:10101402
|
T | TA | 3 | a0002c0002t0005a0002c0012t0005a0011c0021t0005 | 12 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*143dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 144 | INFO_REALIGN_3_PRIME | chr3 | 10101402 | ||||
| chr3:10101417
|
G | T | 1 | a0004c0005t0016 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 155 | chr3 | 10101417 | |||||
| chr3:10101466
|
A | C | 1 | a0006c0006t0015 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 204 | chr3 | 10101466 | |||||
| chr3:10101590
|
C | T | 14 | a0001c0003t0002a0001c0003t0006a0001c0011t0002others(11): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*328C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 328 | chr3 | 10101590 | |||||
| chr3:10101644
|
A | T | 15 | a0001c0003t0002a0001c0003t0006a0001c0011t0002others(12): Show | 78 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*382A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 382 | chr3 | 10101644 | |||||
| chr3:10101693
|
C | T | 1 | a0001c0001t0019 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 431 | chr3 | 10101693 | |||||
| chr3:10101702
|
G | A | 1 | a0006c0006t0014 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 44/44 | 440 | chr3 | 10101702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10026687
|
C | G | 1 | a0002c0002t0002g0241 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-34+214C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10026687 | ||||||
| chr3:10026743
|
GCCAGATG others(3): Show |
G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.-34+271_-34+280del others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10026743 | ||||||
| chr3:10026842
|
C | T | 7 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(4): Show | 7 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+369C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10026842 | ||||||
| chr3:10026888
|
G | T | 80 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.-34+415G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10026888 | ||||||
| chr3:10026978
|
C | CTG | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.-34+506_-34+507ins others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10026978 | |||||
| chr3:10027096
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-34+623G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027096 | ||||||
| chr3:10027255
|
T | C | 1 | a0007c0007t0003g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-34+782T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027255 | ||||||
| chr3:10027305
|
A | T | 9 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+832A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027305 | ||||||
| chr3:10027473
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-34+1000A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027473 | ||||||
| chr3:10027474
|
C | G | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-34+1001C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027474 | ||||||
| chr3:10027480
|
C | T | 32 | a0001c0001t0003g0002a0001c0001t0003g0125a0001c0001t0003g0127others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.-34+1007C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027480 | ||||||
| chr3:10027483
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-34+1010C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027483 | ||||||
| chr3:10027490
|
T | C | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-34+1017T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027490 | ||||||
| chr3:10027614
|
A | C | 1 | a0001c0001t0004g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-33-1011A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027614 | ||||||
| chr3:10027778
|
G | A | 1 | a0003c0004t0003g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-33-847G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027778 | ||||||
| chr3:10027803
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-33-822G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027803 | ||||||
| chr3:10027821
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.-33-804T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027821 | ||||||
| chr3:10027829
|
C | T | 8 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0147others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-796C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027829 | ||||||
| chr3:10027904
|
C | CA | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG00140.hp2 HG00642.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-701dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10027904 | |||||
| chr3:10027904
|
C | CAAAA | 11 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(8): Show | 11 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-704_-33-701dup others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10027904 | |||||
| chr3:10027904
|
C | CAAAAA | 42 | a0001c0011t0002g0199a0002c0002t0002g0196a0002c0002t0002g0198others(39): Show | 42 | HG00408.hp1 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-33-705_-33-701dup others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10027904 | |||||
| chr3:10027904
|
C | CAAAAAA | 22 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(19): Show | 22 | HG00741.hp2 HG01257.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-33-706_-33-701dup others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10027904 | |||||
| chr3:10027978
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-33-647C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10027978 | ||||||
| chr3:10028050
|
TA | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-33-556delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10028050 | |||||
| chr3:10028050
|
TAA | T | 82 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0004g0118others(79): Show | 82 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.-33-557_-33-556del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr3 | 10028050 | |||||
| chr3:10028271
|
G | C | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-354G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028271 | ||||||
| chr3:10028274
|
A | T | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-351A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028274 | ||||||
| chr3:10028275
|
C | A | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-350C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028275 | ||||||
| chr3:10028277
|
C | A | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-348C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028277 | ||||||
| chr3:10028278
|
C | T | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-347C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028278 | ||||||
| chr3:10028286
|
A | G | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-339A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028286 | ||||||
| chr3:10028287
|
G | A | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-338G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028287 | ||||||
| chr3:10028288
|
C | T | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-337C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028288 | ||||||
| chr3:10028289
|
A | G | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-336A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028289 | ||||||
| chr3:10028290
|
C | T | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-335C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028290 | ||||||
| chr3:10028291
|
A | T | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-33-334A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 1/43 | chr3 | 10028291 | ||||||
| chr3:10028733
|
G | C | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+12G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10028733 | ||||||
| chr3:10028868
|
G | C | 3 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0006g0197 | 3 | HG01081.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.64+147G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10028868 | ||||||
| chr3:10028869
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+148G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10028869 | ||||||
| chr3:10028913
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.64+192C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10028913 | ||||||
| chr3:10029187
|
A | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64+466A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029187 | ||||||
| chr3:10029231
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0119 | 3 | HG00642.hp1 HG01070.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.64+510C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029231 | ||||||
| chr3:10029372
|
G | T | 1 | a0003c0004t0003g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64+651G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029372 | ||||||
| chr3:10029608
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.64+887T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029608 | ||||||
| chr3:10029678
|
G | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+957G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029678 | ||||||
| chr3:10029689
|
A | C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64+968A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029689 | ||||||
| chr3:10029824
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.64+1103C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029824 | ||||||
| chr3:10029974
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64+1253C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10029974 | ||||||
| chr3:10030035
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+1314T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030035 | ||||||
| chr3:10030095
|
CAT | C | 3 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0006g0197 | 3 | HG01081.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.64+1375_64+1376del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030095 | ||||||
| chr3:10030096
|
AT | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(95): Show | 98 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.64+1392delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr3 | 10030096 | |||||
| chr3:10030096
|
ATT | A | 76 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(73): Show | 76 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.64+1391_64+1392del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr3 | 10030096 | |||||
| chr3:10030180
|
T | C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64+1459T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030180 | ||||||
| chr3:10030258
|
G | A | 1 | a0001c0023t0001g0066 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+1537G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030258 | ||||||
| chr3:10030263
|
A | T | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64+1542A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030263 | ||||||
| chr3:10030264
|
T | A | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64+1543T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030264 | ||||||
| chr3:10030265
|
T | C | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64+1544T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030265 | ||||||
| chr3:10030271
|
A | G | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64+1550A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030271 | ||||||
| chr3:10030272
|
T | A | 1 | a0002c0002t0005g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64+1551T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030272 | ||||||
| chr3:10030774
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+2053T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030774 | ||||||
| chr3:10030793
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-2039G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030793 | ||||||
| chr3:10030825
|
C | T | 2 | a0001c0003t0002g0143a0001c0003t0006g0144 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-2007C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030825 | ||||||
| chr3:10030826
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-2006G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030826 | ||||||
| chr3:10030900
|
C | CA | 80 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.65-1922dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr3 | 10030900 | |||||
| chr3:10030951
|
C | A | 95 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.65-1881C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10030951 | ||||||
| chr3:10031130
|
A | T | 80 | a0001c0011t0003g0239a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.65-1702A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031130 | ||||||
| chr3:10031230
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-1602A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031230 | ||||||
| chr3:10031241
|
C | T | 1 | a0002c0002t0005g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-1591C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031241 | ||||||
| chr3:10031265
|
T | A | 1 | a0002c0002t0002g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.65-1567T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031265 | ||||||
| chr3:10031285
|
C | T | 2 | a0005c0008t0007g0020a0005c0008t0007g0021 | 2 | HG00558.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.65-1547C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031285 | ||||||
| chr3:10031309
|
T | C | 19 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0003g0125others(16): Show | 19 | HG01169.hp2 HG01891.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.65-1523T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031309 | ||||||
| chr3:10031314
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-1518T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031314 | ||||||
| chr3:10031316
|
A | G | 1 | a0001c0001t0003g0111 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.65-1516A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031316 | ||||||
| chr3:10031319
|
T | C | 142 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0031others(139): Show | 142 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.65-1513T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031319 | ||||||
| chr3:10031320
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.65-1512G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031320 | ||||||
| chr3:10031320
|
G | T | 137 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0044others(134): Show | 137 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.65-1512G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031320 | ||||||
| chr3:10031330
|
C | T | 1 | a0005c0008t0001g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.65-1502C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031330 | ||||||
| chr3:10031344
|
A | C | 162 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0044others(159): Show | 162 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.65-1488A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031344 | ||||||
| chr3:10031360
|
G | A | 32 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0196others(29): Show | 32 | HG00408.hp1 HG01069.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.65-1472G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031360 | ||||||
| chr3:10031371
|
T | C | 1 | a0001c0001t0008g0026 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.65-1461T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031371 | ||||||
| chr3:10031373
|
T | G | 1 | a0001c0001t0008g0026 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.65-1459T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031373 | ||||||
| chr3:10031427
|
G | A | 1 | a0003c0004t0003g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-1405G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031427 | ||||||
| chr3:10031449
|
C | T | 2 | a0002c0002t0005g0177a0002c0002t0005g0219 | 2 | HG00408.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.65-1383C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031449 | ||||||
| chr3:10031450
|
C | G | 2 | a0002c0002t0005g0177a0002c0002t0005g0219 | 2 | HG00408.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.65-1382C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031450 | ||||||
| chr3:10031451
|
A | G | 2 | a0002c0002t0005g0177a0002c0002t0005g0219 | 2 | HG00408.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.65-1381A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031451 | ||||||
| chr3:10031459
|
G | A | 14 | a0001c0016t0003g0122a0004c0005t0001g0169a0004c0005t0001g0170others(11): Show | 14 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-1373G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031459 | ||||||
| chr3:10031489
|
A | G | 53 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0183others(50): Show | 53 | HG00408.hp1 HG00741.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.65-1343A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031489 | ||||||
| chr3:10031497
|
A | G | 53 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0183others(50): Show | 53 | HG00408.hp1 HG00741.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.65-1335A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031497 | ||||||
| chr3:10031499
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.65-1333T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031499 | ||||||
| chr3:10031501
|
CA | C | 64 | a0001c0001t0001g0059a0001c0001t0001g0119a0001c0011t0002g0199others(61): Show | 64 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.65-1315delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr3 | 10031501 | |||||
| chr3:10031627
|
C | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-1205C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031627 | ||||||
| chr3:10031786
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.65-1046C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031786 | ||||||
| chr3:10031860
|
C | T | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.65-972C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10031860 | ||||||
| chr3:10032014
|
T | C | 1 | a0001c0023t0001g0066 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.65-818T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032014 | ||||||
| chr3:10032105
|
A | C | 1 | a0002c0002t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-727A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032105 | ||||||
| chr3:10032140
|
G | C | 95 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.65-692G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032140 | ||||||
| chr3:10032202
|
C | A | 1 | a0002c0002t0002g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.65-630C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032202 | ||||||
| chr3:10032281
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.65-551T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032281 | ||||||
| chr3:10032461
|
G | T | 59 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(56): Show | 59 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.65-371G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032461 | ||||||
| chr3:10032469
|
T | G | 83 | a0001c0001t0001g0003a0001c0011t0002g0199a0001c0011t0003g0239others(80): Show | 83 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.65-363T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032469 | ||||||
| chr3:10032474
|
G | A | 13 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(10): Show | 13 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-358G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032474 | ||||||
| chr3:10032493
|
G | T | 16 | a0002c0002t0002g0214a0002c0002t0002g0232a0002c0002t0005g0177others(13): Show | 16 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-339G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032493 | ||||||
| chr3:10032569
|
T | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.65-263T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032569 | ||||||
| chr3:10032657
|
A | ATTTG | 134 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(131): Show | 134 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.65-167_65-164dupGT others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr3 | 10032657 | |||||
| chr3:10032759
|
T | G | 1 | a0001c0001t0003g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.65-73T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 2/43 | chr3 | 10032759 | ||||||
| chr3:10032981
|
T | G | 4 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(1): Show | 4 | HG00558.hp2 HG02738.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.205+9T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10032981 | ||||||
| chr3:10033222
|
G | A | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.205+250G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033222 | ||||||
| chr3:10033229
|
C | T | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.205+257C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033229 | ||||||
| chr3:10033528
|
G | A | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.205+556G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033528 | ||||||
| chr3:10033559
|
C | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.205+587C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033559 | ||||||
| chr3:10033563
|
G | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+591G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033563 | ||||||
| chr3:10033566
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+594A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033566 | ||||||
| chr3:10033568
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+596A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033568 | ||||||
| chr3:10033572
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+600A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033572 | ||||||
| chr3:10033574
|
T | TATTTTTT others(3): Show |
1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+602_205+603ins others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033574 | ||||||
| chr3:10033581
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+609G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033581 | ||||||
| chr3:10033587
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+615T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033587 | ||||||
| chr3:10033588
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+616T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033588 | ||||||
| chr3:10033591
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+619A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033591 | ||||||
| chr3:10033595
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+623C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033595 | ||||||
| chr3:10033609
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+637G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033609 | ||||||
| chr3:10033613
|
TGGGGGAG others(7): Show |
T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+642_205+655del others(14): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033613 | ||||||
| chr3:10033633
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+661T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033633 | ||||||
| chr3:10033639
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+667T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033639 | ||||||
| chr3:10033645
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+673T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033645 | ||||||
| chr3:10033650
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+678C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033650 | ||||||
| chr3:10033652
|
G | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+680G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033652 | ||||||
| chr3:10033654
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+682T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033654 | ||||||
| chr3:10033655
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+683C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033655 | ||||||
| chr3:10033658
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+686T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033658 | ||||||
| chr3:10033659
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+687T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033659 | ||||||
| chr3:10033663
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+691G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033663 | ||||||
| chr3:10033664
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+692A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033664 | ||||||
| chr3:10033674
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+702G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033674 | ||||||
| chr3:10033683
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+711C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033683 | ||||||
| chr3:10033684
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+712T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033684 | ||||||
| chr3:10033685
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+713A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033685 | ||||||
| chr3:10033686
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+714T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033686 | ||||||
| chr3:10033695
|
A | G | 1 | a0001c0001t0004g0058 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.205+723A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033695 | ||||||
| chr3:10033698
|
C | CT | 98 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.205+746dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033698
|
C | CTT | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0060others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.205+745_205+746dup others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033698
|
C | CTTTT | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+743_205+746dup others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033698
|
C | CTTTTT | 24 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0002g0210others(21): Show | 24 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.205+742_205+746dup others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033698
|
C | CTTTTTT | 39 | a0001c0011t0003g0239a0002c0002t0002g0179a0002c0002t0002g0183others(36): Show | 39 | HG00639.hp2 HG01069.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.205+741_205+746dup others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033698
|
C | CTTTTTTT | 14 | a0001c0011t0002g0199a0002c0002t0002g0184a0002c0002t0002g0214others(11): Show | 14 | HG00741.hp2 HG01258.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.205+740_205+746dup others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033698
|
C | CTTTTTTT others(1): Show |
6 | a0002c0002t0005g0177a0002c0002t0005g0181a0002c0002t0005g0218others(3): Show | 6 | HG00408.hp1 HG03654.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+739_205+746dup others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033698 | |||||
| chr3:10033703
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+731T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033703 | ||||||
| chr3:10033711
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+739T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033711 | ||||||
| chr3:10033718
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205+746T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033718 | ||||||
| chr3:10033721
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-748G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033721 | ||||||
| chr3:10033723
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0107 | 2 | HG02602.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.206-746C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033723 | ||||||
| chr3:10033731
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-738T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033731 | ||||||
| chr3:10033732
|
G | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-737G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033732 | ||||||
| chr3:10033756
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-713A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033756 | ||||||
| chr3:10033782
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-687G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033782 | ||||||
| chr3:10033783
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-686C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033783 | ||||||
| chr3:10033785
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-684C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033785 | ||||||
| chr3:10033794
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-675A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033794 | ||||||
| chr3:10033803
|
C | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-666C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033803 | ||||||
| chr3:10033807
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-662T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033807 | ||||||
| chr3:10033807
|
T | TCTC | 234 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.206-660_206-659ins others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10033807 | |||||
| chr3:10033811
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-658C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033811 | ||||||
| chr3:10033817
|
C | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-652C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033817 | ||||||
| chr3:10033818
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-651T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033818 | ||||||
| chr3:10033819
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-650T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033819 | ||||||
| chr3:10033826
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-643T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033826 | ||||||
| chr3:10033843
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-626G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033843 | ||||||
| chr3:10033845
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-624C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033845 | ||||||
| chr3:10033846
|
C | T | 2 | a0001c0001t0001g0008a0006c0006t0002g0223 | 2 | HG00639.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.206-623C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033846 | ||||||
| chr3:10033854
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.206-615T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033854 | ||||||
| chr3:10033858
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-611T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033858 | ||||||
| chr3:10033871
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-598G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033871 | ||||||
| chr3:10033982
|
C | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.206-487C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033982 | ||||||
| chr3:10033990
|
C | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.206-479C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10033990 | ||||||
| chr3:10034196
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.206-273T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10034196 | ||||||
| chr3:10034216
|
TG | T | 82 | a0001c0001t0001g0008a0001c0011t0002g0199a0001c0011t0003g0239others(79): Show | 82 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.206-246delG | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10034216 | |||||
| chr3:10034299
|
T | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.206-170T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10034299 | ||||||
| chr3:10034305
|
A | G | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.206-164A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10034305 | ||||||
| chr3:10034307
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.206-162A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10034307 | ||||||
| chr3:10034324
|
C | CAAA | 18 | a0002c0002t0002g0179a0002c0002t0002g0208a0002c0002t0002g0234others(15): Show | 18 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.206-126_206-124dup others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10034324 | |||||
| chr3:10034324
|
C | CAAAA | 60 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0183others(57): Show | 60 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.206-127_206-124dup others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10034324 | |||||
| chr3:10034324
|
CA | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0112a0001c0001t0004g0055others(3): Show | 6 | HG01099.hp2 HG01975.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-124delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr3 | 10034324 | |||||
| chr3:10034352
|
T | C | 1 | a0002c0002t0002g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.206-117T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10034352 | ||||||
| chr3:10034421
|
A | C | 2 | a0006c0006t0002g0223a0006c0006t0014g0222 | 2 | HG00639.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.206-48A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 3/43 | chr3 | 10034421 | ||||||
| chr3:10034641
|
A | G | 1 | a0001c0001t0018g0005 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.274-54A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 4/43 | chr3 | 10034641 | ||||||
| chr3:10034962
|
G | A | 14 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.377+164G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 5/43 | chr3 | 10034962 | ||||||
| chr3:10035158
|
CTT | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.378-6_378-5delTT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr3 | 10035158 | |||||
| chr3:10035291
|
A | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.438+58A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10035291 | ||||||
| chr3:10035339
|
T | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.438+106T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10035339 | ||||||
| chr3:10035461
|
A | G | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.438+228A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10035461 | ||||||
| chr3:10035626
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.438+393T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10035626 | ||||||
| chr3:10035920
|
C | G | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-367C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10035920 | ||||||
| chr3:10035993
|
A | G | 3 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0006g0197 | 3 | HG01081.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.439-294A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10035993 | ||||||
| chr3:10036002
|
C | T | 1 | a0001c0001t0004g0053 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.439-285C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10036002 | ||||||
| chr3:10036086
|
C | CTTTTTTT others(5): Show |
2 | a0002c0002t0002g0210a0002c0002t0002g0211 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439-193_439-182dup others(12): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(10): Show |
6 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.439-198_439-182dup others(17): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(11): Show |
7 | a0002c0002t0002g0188a0002c0002t0002g0189a0002c0002t0002g0190others(4): Show | 7 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-199_439-182dup others(18): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(12): Show |
5 | a0002c0002t0002g0179a0002c0002t0002g0191a0002c0002t0002g0192others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-200_439-182dup others(19): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(13): Show |
10 | a0002c0002t0002g0195a0002c0002t0002g0200a0002c0002t0002g0205others(7): Show | 10 | HG01975.hp2 HG02451.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.439-182_439-181ins others(20): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(14): Show |
12 | a0002c0002t0002g0183a0002c0002t0002g0226a0002c0002t0005g0177others(9): Show | 12 | HG00408.hp1 HG00639.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-182_439-181ins others(21): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(15): Show |
6 | a0002c0002t0002g0212a0002c0002t0002g0224a0002c0002t0002g0228others(3): Show | 6 | HG01358.hp2 HG01928.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-182_439-181ins others(22): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(16): Show |
3 | a0002c0002t0002g0184a0002c0002t0002g0196a0002c0002t0005g0181 | 3 | HG01081.hp1 NA18953.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.439-182_439-181ins others(23): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(17): Show |
7 | a0001c0011t0002g0199a0002c0002t0002g0198a0002c0002t0002g0241others(4): Show | 7 | HG00741.hp2 HG01257.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-182_439-181ins others(24): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(18): Show |
3 | a0002c0002t0002g0229a0002c0002t0002g0232a0002c0012t0005g0194 | 3 | HG01255.hp1 HG01258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.439-182_439-181ins others(25): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(19): Show |
2 | a0002c0002t0002g0233a0002c0002t0005g0231 | 2 | HG02965.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.439-182_439-181ins others(26): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(20): Show |
1 | a0002c0002t0002g0234 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439-182_439-181ins others(27): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(21): Show |
2 | a0002c0002t0002g0236a0002c0002t0005g0230 | 2 | HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.439-182_439-181ins others(28): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
C | CTTTTTTT others(31): Show |
1 | a0002c0002t0002g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.439-182_439-181ins others(38): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036086
|
CT | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0062a0001c0001t0003g0125others(30): Show | 33 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.439-182delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | 10036086 | |||||
| chr3:10036107
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.439-180A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10036107 | ||||||
| chr3:10036271
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.439-16A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | chr3 | 10036271 | ||||||
| chr3:10036418
|
T | A | 2 | a0002c0002t0002g0179a0002c0002t0006g0204 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.491+79T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036418 | ||||||
| chr3:10036563
|
A | G | 95 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.491+224A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036563 | ||||||
| chr3:10036572
|
C | T | 3 | a0004c0005t0001g0171a0004c0005t0001g0172a0004c0005t0001g0175 | 3 | NA18971.hp2 NA18986.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.491+233C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036572 | ||||||
| chr3:10036605
|
G | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.491+266G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036605 | ||||||
| chr3:10036683
|
A | AT | 10 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0004g0049others(7): Show | 10 | HG00621.hp2 HG03654.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.491+360dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10036683 | |||||
| chr3:10036683
|
AT | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0112others(17): Show | 20 | HG01099.hp2 HG01516.hp1 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.491+360delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10036683 | |||||
| chr3:10036788
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.491+449C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036788 | ||||||
| chr3:10036834
|
T | C | 3 | a0002c0002t0002g0179a0002c0002t0002g0205a0002c0002t0006g0204 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.491+495T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036834 | ||||||
| chr3:10036842
|
G | A | 65 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.491+503G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10036842 | ||||||
| chr3:10037010
|
G | GT | 59 | a0001c0011t0003g0239a0002c0002t0002g0183a0002c0002t0002g0184others(56): Show | 59 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.491+671_491+672ins others(1): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037010 | ||||||
| chr3:10037010
|
G | GTT | 3 | a0002c0002t0002g0190a0002c0002t0002g0192a0002c0002t0002g0240 | 3 | HG02145.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.491+671_491+672ins others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037010 | ||||||
| chr3:10037011
|
G | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.491+672G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037011 | ||||||
| chr3:10037132
|
T | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.491+793T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037132 | ||||||
| chr3:10037140
|
T | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.491+801T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037140 | ||||||
| chr3:10037330
|
A | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0109 | 2 | NA18979.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.491+991A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037330 | ||||||
| chr3:10037423
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.491+1084G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037423 | ||||||
| chr3:10037571
|
G | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.491+1232G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037571 | ||||||
| chr3:10037736
|
T | A | 1 | a0001c0001t0004g0074 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.491+1397T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10037736 | ||||||
| chr3:10038193
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.492-1086T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10038193 | ||||||
| chr3:10038579
|
C | CT | 5 | a0001c0001t0001g0008a0001c0001t0004g0121a0002c0002t0002g0184others(2): Show | 5 | HG01928.hp1 HG01981.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.492-682dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10038579 | |||||
| chr3:10038579
|
C | CTTTTT | 10 | a0003c0004t0003g0160a0003c0004t0003g0162a0003c0004t0003g0163others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.492-686_492-682dup others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10038579 | |||||
| chr3:10038579
|
C | CTTTTTT | 5 | a0003c0004t0003g0161a0003c0004t0003g0165a0007c0007t0003g0156others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.492-687_492-682dup others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10038579 | |||||
| chr3:10038579
|
CT | C | 44 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(41): Show | 44 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.492-682delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10038579 | |||||
| chr3:10038579
|
CTT | C | 13 | a0001c0016t0003g0122a0004c0005t0001g0169a0004c0005t0001g0170others(10): Show | 13 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-683_492-682del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr3 | 10038579 | |||||
| chr3:10038780
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.492-499C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10038780 | ||||||
| chr3:10038922
|
G | A | 1 | a0013c0017t0004g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.492-357G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10038922 | ||||||
| chr3:10039038
|
T | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.492-241T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10039038 | ||||||
| chr3:10039073
|
T | C | 1 | a0001c0001t0007g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.492-206T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10039073 | ||||||
| chr3:10039206
|
G | T | 1 | a0001c0001t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.492-73G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 7/43 | chr3 | 10039206 | ||||||
| chr3:10039690
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-31G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 8/43 | chr3 | 10039690 | ||||||
| chr3:10039692
|
T | A | 1 | a0001c0001t0003g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.571-29T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 8/43 | chr3 | 10039692 | ||||||
| chr3:10039861
|
G | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.695+16G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10039861 | ||||||
| chr3:10039906
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.695+61G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10039906 | ||||||
| chr3:10039947
|
A | G | 16 | a0002c0002t0002g0214a0002c0002t0002g0232a0002c0002t0005g0177others(13): Show | 16 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.695+102A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10039947 | ||||||
| chr3:10039992
|
TA | T | 7 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(4): Show | 7 | HG00558.hp2 HG02683.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+157delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr3 | 10039992 | |||||
| chr3:10040033
|
C | CT | 6 | a0001c0001t0001g0009a0001c0001t0004g0033a0001c0001t0004g0048others(3): Show | 6 | HG01109.hp1 HG01123.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+207dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr3 | 10040033 | |||||
| chr3:10040033
|
CT | C | 16 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0076others(13): Show | 16 | HG00558.hp2 HG00639.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.695+207delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr3 | 10040033 | |||||
| chr3:10040033
|
CTT | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.695+206_695+207del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr3 | 10040033 | |||||
| chr3:10040033
|
CTTT | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.695+205_695+207del others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr3 | 10040033 | |||||
| chr3:10040257
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.695+412C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040257 | ||||||
| chr3:10040272
|
G | C | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.695+427G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040272 | ||||||
| chr3:10040541
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0077 | 2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.695+696T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040541 | ||||||
| chr3:10040651
|
A | G | 6 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(3): Show | 6 | HG00558.hp2 HG02683.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+806A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040651 | ||||||
| chr3:10040685
|
A | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.695+840A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040685 | ||||||
| chr3:10040715
|
T | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.695+870T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040715 | ||||||
| chr3:10040882
|
CT | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-728delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr3 | 10040882 | |||||
| chr3:10040908
|
C | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.696-715C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040908 | ||||||
| chr3:10040930
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.696-693A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040930 | ||||||
| chr3:10040948
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.696-675T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040948 | ||||||
| chr3:10040956
|
G | A | 1 | a0006c0006t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.696-667G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040956 | ||||||
| chr3:10040963
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.696-660G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10040963 | ||||||
| chr3:10041143
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-480G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10041143 | ||||||
| chr3:10041189
|
G | C | 1 | a0001c0003t0002g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.696-434G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10041189 | ||||||
| chr3:10041218
|
A | C | 2 | a0002c0002t0002g0210a0002c0002t0002g0211 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.696-405A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10041218 | ||||||
| chr3:10041281
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-342G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10041281 | ||||||
| chr3:10041485
|
C | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.696-138C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 9/43 | chr3 | 10041485 | ||||||
| chr3:10041837
|
T | C | 2 | a0001c0001t0004g0034a0001c0001t0004g0055 | 2 | HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.783+127T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041837 | ||||||
| chr3:10041842
|
C | CT | 19 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.783+147dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr3 | 10041842 | |||||
| chr3:10041842
|
CT | C | 17 | a0001c0003t0002g0128a0002c0002t0002g0240a0003c0004t0003g0160others(14): Show | 17 | HG01069.hp1 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.783+147delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr3 | 10041842 | |||||
| chr3:10041842
|
CTT | C | 65 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.783+146_783+147del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr3 | 10041842 | |||||
| chr3:10041854
|
T | C | 1 | a0002c0002t0005g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.783+144T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041854 | ||||||
| chr3:10041857
|
T | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.783+147T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041857 | ||||||
| chr3:10041861
|
C | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.783+151C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041861 | ||||||
| chr3:10041865
|
A | G | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.783+155A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041865 | ||||||
| chr3:10041905
|
G | GT | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.783+206dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr3 | 10041905 | |||||
| chr3:10041905
|
GT | G | 37 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(34): Show | 37 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.783+206delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr3 | 10041905 | |||||
| chr3:10041987
|
C | T | 2 | a0001c0001t0003g0105a0001c0001t0003g0106 | 2 | NA18978.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.783+277C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041987 | ||||||
| chr3:10042064
|
A | G | 1 | a0001c0001t0007g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.783+354A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042064 | ||||||
| chr3:10042108
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.783+398G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042108 | ||||||
| chr3:10042148
|
G | A | 1 | a0012c0018t0004g0079 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.784-411G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042148 | ||||||
| chr3:10042186
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.784-373G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042186 | ||||||
| chr3:10042191
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.784-368T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042191 | ||||||
| chr3:10042192
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.784-367G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042192 | ||||||
| chr3:10042251
|
G | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.784-308G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042251 | ||||||
| chr3:10042352
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.784-207T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042352 | ||||||
| chr3:10042540
|
C | T | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.784-19C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10042540 | ||||||
| chr3:10042712
|
A | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.888+49A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 11/43 | chr3 | 10042712 | ||||||
| chr3:10043223
|
A | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.989+73A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 12/43 | chr3 | 10043223 | ||||||
| chr3:10043351
|
G | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.990-133G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 12/43 | chr3 | 10043351 | ||||||
| chr3:10043446
|
C | G | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.990-38C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 12/43 | chr3 | 10043446 | ||||||
| chr3:10043665
|
G | A | 1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1098+73G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 13/43 | chr3 | 10043665 | ||||||
| chr3:10043667
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1098+75C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 13/43 | chr3 | 10043667 | ||||||
| chr3:10043881
|
A | G | 3 | a0002c0002t0002g0179a0002c0002t0002g0205a0002c0002t0006g0204 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1134+17A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10043881 | ||||||
| chr3:10043940
|
G | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1134+76G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10043940 | ||||||
| chr3:10043954
|
C | T | 5 | a0001c0001t0001g0007a0005c0008t0001g0019a0005c0008t0007g0020others(2): Show | 5 | HG00558.hp2 HG02738.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+90C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10043954 | ||||||
| chr3:10044132
|
G | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0062others(15): Show | 18 | HG00099.hp1 HG01123.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1134+268G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044132 | ||||||
| chr3:10044302
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1134+438A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044302 | ||||||
| chr3:10044329
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1134+465T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044329 | ||||||
| chr3:10044373
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1134+509A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044373 | ||||||
| chr3:10044394
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1134+530G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044394 | ||||||
| chr3:10044399
|
A | G | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1134+535A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044399 | ||||||
| chr3:10044476
|
T | C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1134+612T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044476 | ||||||
| chr3:10044602
|
G | A | 84 | a0001c0001t0004g0118a0001c0001t0007g0113a0001c0011t0002g0199others(81): Show | 84 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.1134+738G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044602 | ||||||
| chr3:10044652
|
T | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1134+788T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044652 | ||||||
| chr3:10044697
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1134+833A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044697 | ||||||
| chr3:10044710
|
T | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1134+846T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044710 | ||||||
| chr3:10044996
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1134+1132G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10044996 | ||||||
| chr3:10045088
|
G | GTTTTTTT others(3): Show |
12 | a0002c0002t0002g0214a0002c0002t0002g0229a0002c0002t0005g0177others(9): Show | 12 | HG01255.hp1 HG01258.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1134+1228_1134+123 others(14): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045088 | |||||
| chr3:10045088
|
G | GTTTTTTT others(4): Show |
44 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(41): Show | 44 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1134+1227_1134+123 others(15): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045088 | |||||
| chr3:10045088
|
G | GTTTTTTT others(5): Show |
9 | a0001c0011t0003g0239a0002c0002t0002g0184a0002c0002t0002g0187others(6): Show | 9 | HG01358.hp2 HG01884.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+1226_1134+123 others(16): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045088 | |||||
| chr3:10045088
|
GT | G | 16 | a0001c0001t0001g0022a0001c0001t0004g0035a0001c0016t0003g0122others(13): Show | 16 | HG00558.hp2 HG01192.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1134+1237delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045088 | |||||
| chr3:10045101
|
T | TTTTTTTT others(6): Show |
1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1134+1237_1134+123 others(17): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045101 | ||||||
| chr3:10045101
|
T | TTTTTTTT others(8): Show |
1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1134+1237_1134+123 others(19): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045101 | ||||||
| chr3:10045101
|
T | TTTTTTTT others(8): Show |
7 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0163others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1134+1237_1134+123 others(19): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045101 | ||||||
| chr3:10045101
|
T | TTTTTTTT others(9): Show |
1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1134+1237_1134+123 others(20): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045101 | ||||||
| chr3:10045101
|
T | TTTTTTTT others(9): Show |
5 | a0003c0004t0003g0162a0003c0004t0003g0164a0003c0004t0003g0167others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+1237_1134+123 others(20): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045101 | ||||||
| chr3:10045110
|
C | T | 13 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1134+1246C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045110 | ||||||
| chr3:10045136
|
C | T | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(36): Show | 39 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1134+1272C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045136 | ||||||
| chr3:10045137
|
G | A | 1 | a0001c0001t0003g0105 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1134+1273G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045137 | ||||||
| chr3:10045142
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1134+1278A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045142 | ||||||
| chr3:10045164
|
G | GTTTTGTT others(5): Show |
66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1134+1312_1134+132 others(16): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045164 | |||||
| chr3:10045227
|
G | C | 13 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(10): Show | 13 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135-1353G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045227 | ||||||
| chr3:10045229
|
C | T | 3 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0006g0197 | 3 | HG01081.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1135-1351C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045229 | ||||||
| chr3:10045270
|
G | A | 8 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0002g0210others(5): Show | 8 | HG01081.hp1 HG01928.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135-1310G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045270 | ||||||
| chr3:10045396
|
C | T | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1135-1184C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045396 | ||||||
| chr3:10045542
|
CTGTATTG others(1): Show |
C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1135-1027_1135-102 others(12): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045542 | |||||
| chr3:10045601
|
C | CT | 63 | a0001c0001t0001g0114a0001c0001t0004g0121a0001c0003t0002g0137others(60): Show | 63 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1135-961dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045601 | |||||
| chr3:10045601
|
C | CTT | 5 | a0001c0011t0002g0199a0002c0002t0002g0189a0002c0002t0002g0228others(2): Show | 5 | HG01928.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135-962_1135-961d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10045601 | |||||
| chr3:10045694
|
C | T | 38 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(35): Show | 38 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1135-886C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045694 | ||||||
| chr3:10045833
|
G | C | 82 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(79): Show | 82 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.1135-747G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045833 | ||||||
| chr3:10045852
|
G | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1135-728G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045852 | ||||||
| chr3:10045954
|
C | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1135-626C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045954 | ||||||
| chr3:10045977
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1135-603A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10045977 | ||||||
| chr3:10046055
|
C | CTTTTTTT others(2): Show |
10 | a0003c0004t0003g0160a0003c0004t0003g0162a0003c0004t0003g0163others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-518_1135-510d others(11): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10046055 | |||||
| chr3:10046055
|
C | CTTTTTTT others(3): Show |
3 | a0002c0002t0006g0202a0003c0004t0003g0161a0009c0010t0003g0158 | 3 | HG01069.hp2 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1135-519_1135-510d others(12): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10046055 | |||||
| chr3:10046055
|
C | CTTTTTTT others(4): Show |
7 | a0002c0002t0002g0206a0002c0002t0002g0209a0002c0002t0002g0214others(4): Show | 7 | HG02523.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-520_1135-510d others(13): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10046055 | |||||
| chr3:10046055
|
C | CTTTTTTT others(5): Show |
49 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(46): Show | 49 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1135-521_1135-510d others(14): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10046055 | |||||
| chr3:10046055
|
C | CTTTTTTT others(6): Show |
9 | a0002c0002t0002g0191a0002c0002t0002g0203a0002c0002t0002g0205others(6): Show | 9 | HG01928.hp2 HG02257.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1135-522_1135-510d others(15): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr3 | 10046055 | |||||
| chr3:10046147
|
G | A | 3 | a0002c0002t0002g0179a0002c0002t0002g0205a0002c0002t0006g0204 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1135-433G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046147 | ||||||
| chr3:10046157
|
C | T | 16 | a0001c0003t0002g0134a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1135-423C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046157 | ||||||
| chr3:10046275
|
G | C | 55 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(52): Show | 55 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1135-305G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046275 | ||||||
| chr3:10046288
|
T | C | 10 | a0002c0002t0002g0214a0002c0002t0005g0177a0002c0002t0005g0181others(7): Show | 10 | HG00408.hp1 HG02523.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135-292T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046288 | ||||||
| chr3:10046327
|
A | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1135-253A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046327 | ||||||
| chr3:10046331
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1135-249A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046331 | ||||||
| chr3:10046332
|
T | C | 69 | a0001c0001t0003g0136a0001c0001t0003g0138a0001c0001t0003g0139others(66): Show | 69 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1135-248T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046332 | ||||||
| chr3:10046516
|
T | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1135-64T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 14/43 | chr3 | 10046516 | ||||||
| chr3:10046838
|
G | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1278+115G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10046838 | ||||||
| chr3:10046872
|
A | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1278+149A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10046872 | ||||||
| chr3:10046904
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1278+181C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10046904 | ||||||
| chr3:10047041
|
C | A | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1278+318C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047041 | ||||||
| chr3:10047168
|
G | T | 13 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(10): Show | 13 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1278+445G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047168 | ||||||
| chr3:10047230
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0062others(15): Show | 18 | HG00099.hp1 HG01123.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1278+507C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047230 | ||||||
| chr3:10047231
|
G | A | 1 | a0001c0001t0003g0029 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1278+508G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047231 | ||||||
| chr3:10047361
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1279-556A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047361 | ||||||
| chr3:10047464
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1279-453A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047464 | ||||||
| chr3:10047786
|
T | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1279-131T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 15/43 | chr3 | 10047786 | ||||||
| chr3:10048089
|
A | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1413+38A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048089 | ||||||
| chr3:10048460
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1413+409C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048460 | ||||||
| chr3:10048490
|
A | T | 1 | a0001c0001t0003g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1413+439A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048490 | ||||||
| chr3:10048548
|
G | A | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1413+497G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048548 | ||||||
| chr3:10048565
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1413+514A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048565 | ||||||
| chr3:10048590
|
C | T | 1 | a0006c0006t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1413+539C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048590 | ||||||
| chr3:10048673
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1413+622A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048673 | ||||||
| chr3:10048685
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1413+634T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048685 | ||||||
| chr3:10048803
|
A | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1414-571A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048803 | ||||||
| chr3:10048869
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1414-505G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048869 | ||||||
| chr3:10048940
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-434A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048940 | ||||||
| chr3:10048967
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-407G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048967 | ||||||
| chr3:10048985
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-389G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10048985 | ||||||
| chr3:10049020
|
C | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-354C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049020 | ||||||
| chr3:10049033
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1414-341G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049033 | ||||||
| chr3:10049063
|
C | T | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1414-311C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049063 | ||||||
| chr3:10049069
|
G | C | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1414-305G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049069 | ||||||
| chr3:10049115
|
A | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-259A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049115 | ||||||
| chr3:10049137
|
T | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-237T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049137 | ||||||
| chr3:10049174
|
A | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1414-200A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049174 | ||||||
| chr3:10049178
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1414-196T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049178 | ||||||
| chr3:10049225
|
A | G | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-149A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049225 | ||||||
| chr3:10049249
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-125G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049249 | ||||||
| chr3:10049257
|
T | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-117T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049257 | ||||||
| chr3:10049284
|
T | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-90T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049284 | ||||||
| chr3:10049351
|
T | C | 135 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(132): Show | 135 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.1414-23T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049351 | ||||||
| chr3:10049365
|
C | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-9C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 16/43 | chr3 | 10049365 | ||||||
| chr3:10049715
|
C | G | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1545+210C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10049715 | ||||||
| chr3:10050056
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1545+551G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050056 | ||||||
| chr3:10050101
|
C | T | 2 | a0003c0004t0003g0162a0003c0004t0003g0163 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1545+596C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050101 | ||||||
| chr3:10050165
|
G | A | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1545+660G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050165 | ||||||
| chr3:10050172
|
G | C | 1 | a0002c0002t0002g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1545+667G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050172 | ||||||
| chr3:10050350
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1545+845T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050350 | ||||||
| chr3:10050351
|
G | A | 1 | a0006c0006t0015g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1545+846G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050351 | ||||||
| chr3:10050362
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+857T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050362 | ||||||
| chr3:10050365
|
T | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+860T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050365 | ||||||
| chr3:10050421
|
A | G | 2 | a0002c0002t0002g0206a0002c0002t0002g0209 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1545+916A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050421 | ||||||
| chr3:10050438
|
CACGGTGA others(749): Show |
C | 1 | a0003c0004t0003g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1545+969_1546-1158 others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10050438 | |||||
| chr3:10050487
|
G | A | 7 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(4): Show | 7 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+982G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050487 | ||||||
| chr3:10050495
|
C | T | 40 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0183others(37): Show | 40 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1545+990C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050495 | ||||||
| chr3:10050539
|
C | T | 22 | a0001c0011t0003g0239a0002c0002t0002g0179a0002c0002t0002g0185others(19): Show | 22 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1545+1034C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050539 | ||||||
| chr3:10050572
|
A | C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1545+1067A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050572 | ||||||
| chr3:10050591
|
C | G | 1 | a0002c0002t0017g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1545+1086C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050591 | ||||||
| chr3:10050622
|
C | CA | 25 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0062others(22): Show | 25 | HG00558.hp2 HG01175.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1545+1138dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10050622 | |||||
| chr3:10050622
|
CA | C | 60 | a0001c0001t0004g0074a0001c0011t0002g0199a0001c0011t0003g0239others(57): Show | 60 | HG00408.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1545+1138delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10050622 | |||||
| chr3:10050853
|
G | A | 57 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(54): Show | 57 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1545+1348G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050853 | ||||||
| chr3:10050885
|
G | A | 31 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0183others(28): Show | 31 | HG00741.hp2 HG01081.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1545+1380G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10050885 | ||||||
| chr3:10051041
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1546-1346A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051041 | ||||||
| chr3:10051082
|
CA | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1546-1295delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051082 | |||||
| chr3:10051146
|
C | T | 1 | a0003c0004t0003g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1546-1241C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051146 | ||||||
| chr3:10051151
|
T | C | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1546-1236T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051151 | ||||||
| chr3:10051197
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1546-1190G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051197 | ||||||
| chr3:10051223
|
A | G | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-1164A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051223 | ||||||
| chr3:10051249
|
T | C | 95 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1546-1138T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051249 | ||||||
| chr3:10051258
|
G | T | 1 | a0003c0004t0003g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1546-1129G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051258 | ||||||
| chr3:10051298
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1546-1089G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051298 | ||||||
| chr3:10051330
|
G | A | 38 | a0001c0001t0001g0044a0001c0001t0004g0001a0001c0001t0004g0004others(35): Show | 38 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1546-1057G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051330 | ||||||
| chr3:10051368
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546-1019G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051368 | ||||||
| chr3:10051380
|
C | CA | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(4): Show | 7 | HG02698.hp2 HG03139.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-980dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051380 | |||||
| chr3:10051380
|
C | CAAA | 8 | a0001c0001t0001g0006a0001c0001t0001g0108a0004c0005t0001g0171others(5): Show | 8 | HG00558.hp2 HG01975.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1546-982_1546-980d others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051380 | |||||
| chr3:10051394
|
AAAAAAAA others(17): Show |
A | 4 | a0006c0006t0002g0221a0006c0006t0002g0223a0006c0006t0014g0222others(1): Show | 4 | HG00639.hp2 HG02717.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-992_1546-969d others(26): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051394 | ||||||
| chr3:10051398
|
AAAAAAAA others(9): Show |
A | 40 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0060others(37): Show | 40 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1546-988_1546-973d others(18): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051398 | ||||||
| chr3:10051399
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1546-987_1546-973d others(17): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051399 | ||||||
| chr3:10051401
|
AAAAAAAC others(6): Show |
A | 1 | a0001c0001t0004g0004 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1546-985_1546-973d others(15): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051401 | ||||||
| chr3:10051402
|
AAAAAACA others(5): Show |
A | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1546-984_1546-973d others(14): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051402 | ||||||
| chr3:10051403
|
AAAAAC | A | 11 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0163others(8): Show | 11 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1546-979_1546-975d others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051403 | |||||
| chr3:10051406
|
AAC | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0068others(24): Show | 27 | HG00558.hp1 HG00639.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1546-979_1546-978d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051406 | |||||
| chr3:10051407
|
AC | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.1546-979delC | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051407 | ||||||
| chr3:10051407
|
ACAAAAAG others(3): Show |
A | 2 | a0002c0002t0005g0181a0002c0012t0005g0193 | 2 | HG01257.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1546-979_1546-970d others(12): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051407 | ||||||
| chr3:10051408
|
C | A | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(100): Show | 103 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-979C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051408 | ||||||
| chr3:10051409
|
AAAAAGGA others(2): Show |
A | 27 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0185others(24): Show | 27 | HG00408.hp1 HG01255.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.1546-977_1546-969d others(11): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051409 | ||||||
| chr3:10051410
|
AAAAGGAG others(1): Show |
A | 17 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(14): Show | 17 | HG00741.hp2 HG01258.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-976_1546-969d others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051410 | ||||||
| chr3:10051411
|
AAAGGAGT | A | 9 | a0001c0016t0003g0122a0002c0002t0002g0203a0002c0002t0002g0205others(6): Show | 9 | HG01069.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-975_1546-969d others(9): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051411 | ||||||
| chr3:10051414
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1546-973G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051414 | ||||||
| chr3:10051415
|
G | A | 1 | a0002c0002t0002g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1546-972G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051415 | ||||||
| chr3:10051417
|
G | A | 4 | a0002c0002t0002g0210a0002c0002t0002g0211a0002c0002t0002g0212others(1): Show | 4 | HG01928.hp1 HG02273.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546-970G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051417 | ||||||
| chr3:10051418
|
T | A | 8 | a0002c0002t0002g0210a0002c0002t0002g0211a0002c0002t0002g0212others(5): Show | 8 | HG01257.hp2 HG01928.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-969T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051418 | ||||||
| chr3:10051431
|
TC | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1546-953delC | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051431 | |||||
| chr3:10051449
|
A | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1546-938A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051449 | ||||||
| chr3:10051451
|
A | G | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1546-936A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051451 | ||||||
| chr3:10051465
|
AG | A | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1546-920delG | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | INFO_REALIGN_3_PRIME | chr3 | 10051465 | |||||
| chr3:10051473
|
G | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1546-914G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051473 | ||||||
| chr3:10051602
|
C | T | 10 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0200others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546-785C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051602 | ||||||
| chr3:10051603
|
A | G | 10 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0200others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546-784A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051603 | ||||||
| chr3:10051604
|
A | T | 10 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0200others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546-783A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051604 | ||||||
| chr3:10051605
|
G | C | 10 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0200others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546-782G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051605 | ||||||
| chr3:10051672
|
G | T | 5 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0086others(2): Show | 5 | HG00639.hp1 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-715G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10051672 | ||||||
| chr3:10052049
|
C | T | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-338C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10052049 | ||||||
| chr3:10052121
|
T | G | 2 | a0002c0002t0002g0210a0002c0002t0002g0211 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1546-266T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10052121 | ||||||
| chr3:10052140
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1546-247G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10052140 | ||||||
| chr3:10052306
|
T | C | 2 | a0003c0004t0003g0162a0003c0004t0003g0163 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1546-81T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10052306 | ||||||
| chr3:10052329
|
A | T | 1 | a0001c0001t0004g0074 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546-58A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10052329 | ||||||
| chr3:10052379
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00639.hp1 | splice_region_variant&intron_variant | LOW | c.1546-8T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 17/43 | chr3 | 10052379 | ||||||
| chr3:10052508
|
A | G | 1 | a0001c0003t0002g0134 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1656+11A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052508 | ||||||
| chr3:10052522
|
A | AT | 54 | a0001c0001t0001g0067a0001c0001t0001g0114a0001c0011t0002g0199others(51): Show | 54 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1656+38dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10052522 | |||||
| chr3:10052666
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1656+169G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052666 | ||||||
| chr3:10052734
|
T | C | 45 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0183others(42): Show | 45 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1656+237T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052734 | ||||||
| chr3:10052808
|
C | A | 1 | a0001c0003t0002g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1656+311C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052808 | ||||||
| chr3:10052872
|
G | T | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1656+375G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052872 | ||||||
| chr3:10052883
|
T | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+386T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052883 | ||||||
| chr3:10052917
|
TA | T | 13 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1656+421delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10052917 | ||||||
| chr3:10053250
|
T | C | 1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1656+753T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053250 | ||||||
| chr3:10053287
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+790C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053287 | ||||||
| chr3:10053306
|
G | C | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1656+809G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053306 | ||||||
| chr3:10053361
|
C | T | 16 | a0001c0001t0001g0067a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01433.hp1 HG01891.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1656+864C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053361 | ||||||
| chr3:10053392
|
C | T | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1656+895C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053392 | ||||||
| chr3:10053401
|
T | C | 28 | a0001c0011t0002g0199a0002c0002t0002g0183a0002c0002t0002g0184others(25): Show | 28 | HG00639.hp2 HG01081.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1656+904T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053401 | ||||||
| chr3:10053467
|
T | G | 12 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(9): Show | 12 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1656+970T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053467 | ||||||
| chr3:10053494
|
T | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1656+997T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053494 | ||||||
| chr3:10053534
|
AAAAAT | A | 5 | a0001c0001t0008g0025a0001c0001t0008g0026a0001c0001t0008g0046others(2): Show | 5 | HG00558.hp1 HG02080.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1656+1049_1656+105 others(9): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10053534 | |||||
| chr3:10053536
|
AAAT | A | 64 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1656+1042_1656+104 others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10053536 | |||||
| chr3:10053544
|
T | A | 2 | a0002c0002t0002g0207a0002c0002t0002g0208 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1656+1047T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053544 | ||||||
| chr3:10053568
|
A | T | 12 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(9): Show | 12 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1656+1071A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053568 | ||||||
| chr3:10053570
|
T | G | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1656+1073T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053570 | ||||||
| chr3:10053676
|
GAGTACAT others(6): Show |
G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+1185_1656+119 others(17): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10053676 | |||||
| chr3:10053798
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+1301A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10053798 | ||||||
| chr3:10054112
|
G | A | 12 | a0001c0001t0003g0136a0001c0001t0003g0138a0001c0001t0003g0139others(9): Show | 12 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1656+1615G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054112 | ||||||
| chr3:10054211
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1656+1714C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054211 | ||||||
| chr3:10054238
|
G | A | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+1741G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054238 | ||||||
| chr3:10054271
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1656+1774C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054271 | ||||||
| chr3:10054336
|
C | CAT | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1656+1853_1656+185 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054336 | |||||
| chr3:10054336
|
CAT | C | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.1656+1853_1656+185 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054336 | |||||
| chr3:10054345
|
ATATATAC others(19): Show |
A | 1 | a0001c0001t0001g0010 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1656+1856_1656+188 others(30): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054345 | |||||
| chr3:10054358
|
TATATATA others(13): Show |
T | 13 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1656+1871_1656+189 others(24): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054358 | |||||
| chr3:10054360
|
TATATATA others(11): Show |
T | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1656+1871_1656+188 others(22): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054360 | |||||
| chr3:10054361
|
A | G | 69 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(66): Show | 69 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1656+1864A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054361 | ||||||
| chr3:10054363
|
ATATACGT others(33): Show |
A | 1 | a0001c0001t0003g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1656+1871_1656+191 others(44): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054363 | |||||
| chr3:10054366
|
T | C | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1656+1869T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054366 | ||||||
| chr3:10054368
|
CGT | C | 46 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(43): Show | 46 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1656+1874_1656+187 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054368 | |||||
| chr3:10054368
|
CGTGTATA others(13): Show |
C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+1874_1656+189 others(24): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054368 | |||||
| chr3:10054369
|
G | A | 15 | a0001c0001t0004g0065a0001c0016t0003g0122a0004c0005t0001g0169others(12): Show | 15 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1656+1872G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054369 | ||||||
| chr3:10054370
|
TGTATATA others(33): Show |
T | 3 | a0001c0001t0010g0023a0001c0003t0002g0123a0001c0003t0002g0128 | 3 | HG01069.hp1 HG01175.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1656+1889_1656+192 others(44): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054370 | |||||
| chr3:10054371
|
G | A | 3 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0236 | 3 | HG02647.hp1 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1656+1874G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054371 | ||||||
| chr3:10054376
|
TAC | T | 16 | a0002c0002t0002g0214a0002c0002t0002g0232a0002c0002t0005g0177others(13): Show | 16 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1656+1881_1656+188 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054376 | |||||
| chr3:10054378
|
C | T | 50 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(47): Show | 50 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.1656+1881C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054378 | ||||||
| chr3:10054381
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0090others(7): Show | 10 | HG00140.hp2 HG01433.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1656+1884A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054381 | ||||||
| chr3:10054382
|
TATATATG others(57): Show |
T | 1 | a0001c0001t0004g0058 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1656+1892_1656+195 others(68): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054382 | |||||
| chr3:10054383
|
ATATATGT others(7): Show |
A | 4 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0087others(1): Show | 4 | HG03710.hp2 NA18969.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+1906_1656+191 others(18): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054383 | |||||
| chr3:10054386
|
T | C | 36 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(33): Show | 36 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1656+1889T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054386 | ||||||
| chr3:10054388
|
T | C | 1 | a0002c0002t0006g0201 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1656+1891T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054388 | ||||||
| chr3:10054389
|
GTATATAC others(23): Show |
G | 26 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(23): Show | 26 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1656+1900_1656+192 others(34): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054389 | |||||
| chr3:10054396
|
C | CATGTATA others(13): Show |
1 | a0001c0001t0003g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1656+1899_1656+190 others(24): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054396 | ||||||
| chr3:10054396
|
CGTAT | C | 9 | a0001c0001t0003g0002a0001c0001t0003g0029a0001c0001t0003g0136others(6): Show | 9 | HG01099.hp1 HG01109.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1656+1900_1656+190 others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054396 | ||||||
| chr3:10054397
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1656+1900G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054397 | ||||||
| chr3:10054403
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1656+1906G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054403 | ||||||
| chr3:10054410
|
C | T | 1 | a0001c0001t0008g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1656+1913C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054410 | ||||||
| chr3:10054410
|
CGTATATA others(13): Show |
C | 2 | a0001c0001t0003g0150a0001c0001t0012g0153 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1656+1914_1656+193 others(24): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054410 | ||||||
| chr3:10054411
|
G | A | 6 | a0001c0001t0003g0002a0001c0001t0003g0029a0001c0001t0003g0136others(3): Show | 6 | HG01099.hp1 HG01109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+1914G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054411 | ||||||
| chr3:10054415
|
ATACATAT others(17): Show |
A | 1 | a0001c0001t0003g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1656+1921_1656+194 others(28): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054415 | |||||
| chr3:10054417
|
ACATATAT others(15): Show |
A | 4 | a0001c0001t0003g0029a0001c0001t0003g0136a0001c0001t0003g0138others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+1921_1656+194 others(26): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054417 | ||||||
| chr3:10054425
|
ACATGTAT others(7): Show |
A | 1 | a0001c0001t0003g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1656+1929_1656+194 others(18): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054425 | ||||||
| chr3:10054428
|
T | TGTATATA others(1): Show |
34 | a0001c0011t0003g0239a0002c0002t0002g0179a0002c0002t0002g0185others(31): Show | 34 | HG00408.hp1 HG00639.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1656+1932_1656+193 others(12): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054428 | |||||
| chr3:10054436
|
C | T | 2 | a0001c0001t0003g0150a0001c0001t0012g0153 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1656+1939C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054436 | ||||||
| chr3:10054436
|
CAT | C | 29 | a0001c0011t0002g0199a0002c0002t0002g0183a0002c0002t0002g0184others(26): Show | 29 | HG00741.hp2 HG01069.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1656+1940_1656+194 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054436 | ||||||
| chr3:10054436
|
CATGTATA others(7): Show |
C | 7 | a0001c0001t0001g0077a0003c0004t0003g0161a0003c0004t0003g0163others(4): Show | 7 | HG00099.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656+1942_1656+195 others(18): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054436 | |||||
| chr3:10054436
|
CATGTATA others(9): Show |
C | 3 | a0003c0004t0003g0162a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1656+1942_1656+195 others(20): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054436 | |||||
| chr3:10054436
|
CATGTATA others(11): Show |
C | 4 | a0003c0004t0003g0160a0003c0004t0003g0166a0003c0004t0003g0167others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+1942_1656+195 others(22): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054436 | |||||
| chr3:10054436
|
CATGTATA others(15): Show |
C | 1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1656+1942_1656+196 others(26): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054436 | |||||
| chr3:10054437
|
A | G | 2 | a0002c0002t0002g0210a0002c0002t0006g0197 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1656+1940A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054437 | ||||||
| chr3:10054438
|
T | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0003g0024others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+1941T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054438 | ||||||
| chr3:10054439
|
G | A | 31 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1656+1942G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054439 | ||||||
| chr3:10054444
|
T | C | 1 | a0002c0002t0002g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1656+1947T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054444 | ||||||
| chr3:10054446
|
C | CATATATA others(5): Show |
1 | a0004c0005t0016g0174 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1656+1966_1656+197 others(16): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054446 | |||||
| chr3:10054446
|
C | T | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(36): Show | 39 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1656+1949C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054446 | ||||||
| chr3:10054446
|
CAT | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0047others(40): Show | 43 | HG00621.hp1 HG00639.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.1656+1976_1656+197 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054446 | |||||
| chr3:10054446
|
CATAT | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0062others(9): Show | 12 | HG01192.hp2 HG01516.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1656+1974_1656+197 others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054446 | |||||
| chr3:10054447
|
A | G | 1 | a0002c0002t0002g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1656+1950A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054447 | ||||||
| chr3:10054449
|
A | G | 28 | a0001c0011t0002g0199a0002c0002t0002g0183a0002c0002t0002g0184others(25): Show | 28 | HG00741.hp2 HG01069.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1656+1952A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054449 | ||||||
| chr3:10054450
|
T | C | 2 | a0002c0002t0002g0210a0002c0002t0006g0197 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1656+1953T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054450 | ||||||
| chr3:10054451
|
A | G | 6 | a0003c0004t0003g0161a0003c0004t0003g0163a0003c0004t0003g0164others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+1954A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054451 | ||||||
| chr3:10054453
|
A | G | 3 | a0003c0004t0003g0162a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1656+1956A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054453 | ||||||
| chr3:10054454
|
T | C | 1 | a0002c0002t0002g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1656+1957T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054454 | ||||||
| chr3:10054455
|
A | G | 4 | a0003c0004t0003g0160a0003c0004t0003g0166a0003c0004t0003g0167others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+1958A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054455 | ||||||
| chr3:10054456
|
T | C | 28 | a0001c0011t0002g0199a0002c0002t0002g0183a0002c0002t0002g0184others(25): Show | 28 | HG00741.hp2 HG01069.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1656+1959T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054456 | ||||||
| chr3:10054457
|
ATATATAT others(15): Show |
A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+1962_1656+198 others(26): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054457 | |||||
| chr3:10054459
|
A | G | 1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1656+1962A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054459 | ||||||
| chr3:10054466
|
TA | T | 6 | a0001c0001t0001g0063a0002c0002t0002g0232a0002c0002t0005g0217others(3): Show | 6 | HG02738.hp1 HG03453.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+1970delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054466 | ||||||
| chr3:10054467
|
A | T | 1 | a0002c0002t0002g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1656+1970A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054467 | ||||||
| chr3:10054468
|
TA | T | 7 | a0001c0001t0001g0006a0001c0001t0004g0052a0001c0001t0004g0058others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1656+1972delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054468 | ||||||
| chr3:10054468
|
TATA | T | 4 | a0001c0001t0003g0131a0002c0002t0002g0195a0002c0002t0002g0196others(1): Show | 4 | HG01081.hp1 HG02559.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+1972_1656+197 others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054468 | ||||||
| chr3:10054469
|
A | AT | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0003g0125others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+1973dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054469 | |||||
| chr3:10054469
|
A | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0063a0001c0001t0003g0132others(10): Show | 13 | HG00408.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1656+1972A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054469 | ||||||
| chr3:10054469
|
ATATATTT others(11): Show |
A | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1656+1974_1656+199 others(22): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054469 | |||||
| chr3:10054470
|
TA | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(4): Show | 7 | HG02080.hp2 HG02523.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656+1974delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054470 | ||||||
| chr3:10054471
|
A | AT | 5 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0003g0029others(2): Show | 5 | HG00408.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1656+1975dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054471 | |||||
| chr3:10054471
|
A | ATT | 4 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0151others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+1975_1656+197 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054471 | |||||
| chr3:10054471
|
A | ATTT | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0044others(4): Show | 7 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656+1975_1656+197 others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054471 | |||||
| chr3:10054471
|
A | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0059others(53): Show | 56 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1656+1974A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054471 | ||||||
| chr3:10054472
|
TA | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0120others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1656+1976delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054472 | ||||||
| chr3:10054473
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1656+1977_1656+197 others(14): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054473
|
A | ATATATAT others(3): Show |
1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1656+1977_1656+197 others(14): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054473
|
A | ATATATT | 6 | a0001c0001t0004g0041a0001c0001t0008g0026a0004c0005t0001g0169others(3): Show | 6 | HG00741.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+1977_1656+197 others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054473
|
A | ATATTTT | 5 | a0001c0001t0011g0045a0002c0002t0002g0184a0002c0002t0002g0211others(2): Show | 5 | HG02080.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1656+1977_1656+197 others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054473
|
A | ATATTTTT | 6 | a0001c0011t0002g0199a0002c0002t0002g0198a0002c0002t0002g0229others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+1977_1656+197 others(11): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054473
|
A | ATATTTTT others(1): Show |
6 | a0002c0002t0002g0206a0002c0002t0005g0213a0002c0002t0005g0230others(3): Show | 6 | HG00741.hp2 HG01069.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+1977_1656+197 others(12): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054473
|
A | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 128 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1656+1976A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054473 | ||||||
| chr3:10054473
|
ATTTT | A | 6 | a0003c0004t0003g0161a0003c0004t0003g0162a0003c0004t0003g0164others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+2001_1656+200 others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054473 | |||||
| chr3:10054475
|
T | A | 7 | a0001c0001t0001g0076a0001c0001t0004g0038a0003c0004t0003g0160others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656+1978T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054475 | ||||||
| chr3:10054514
|
C | T | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1656+2017C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054514 | ||||||
| chr3:10054585
|
G | A | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1656+2088G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054585 | ||||||
| chr3:10054635
|
C | CA | 6 | a0002c0002t0002g0183a0002c0002t0002g0224a0002c0002t0002g0225others(3): Show | 6 | HG01257.hp1 HG01358.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+2139dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054635 | |||||
| chr3:10054673
|
T | C | 82 | a0001c0001t0003g0125a0001c0011t0002g0199a0001c0011t0003g0239others(79): Show | 82 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.1656+2176T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054673 | ||||||
| chr3:10054684
|
C | T | 14 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1656+2187C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054684 | ||||||
| chr3:10054815
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1656+2318C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054815 | ||||||
| chr3:10054854
|
A | T | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1656+2357A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054854 | ||||||
| chr3:10055017
|
A | T | 1 | a0005c0008t0001g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1656+2520A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055017 | ||||||
| chr3:10055043
|
T | A | 4 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+2546T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055043 | ||||||
| chr3:10055128
|
A | G | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1656+2631A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055128 | ||||||
| chr3:10055291
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1656+2794A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055291 | ||||||
| chr3:10055429
|
G | C | 13 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(10): Show | 13 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1656+2932G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055429 | ||||||
| chr3:10055583
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1656+3086C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055583 | ||||||
| chr3:10055595
|
G | T | 1 | a0002c0002t0002g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1656+3098G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055595 | ||||||
| chr3:10055701
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0109 | 2 | NA18979.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1656+3204A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055701 | ||||||
| chr3:10055721
|
G | A | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1656+3224G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055721 | ||||||
| chr3:10055770
|
T | C | 95 | a0001c0011t0002g0199a0001c0011t0003g0239a0001c0016t0003g0122others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1656+3273T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055770 | ||||||
| chr3:10055819
|
A | T | 1 | a0012c0018t0004g0079 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1656+3322A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055819 | ||||||
| chr3:10055822
|
T | A | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1656+3325T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055822 | ||||||
| chr3:10055912
|
T | A | 28 | a0001c0011t0002g0199a0002c0002t0002g0183a0002c0002t0002g0184others(25): Show | 28 | HG00639.hp2 HG01081.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1656+3415T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055912 | ||||||
| chr3:10055913
|
C | G | 81 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1656+3416C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10055913 | ||||||
| chr3:10056068
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1656+3571G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056068 | ||||||
| chr3:10056116
|
T | G | 2 | a0002c0002t0002g0206a0002c0002t0002g0209 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1656+3619T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056116 | ||||||
| chr3:10056171
|
G | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1656+3674G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056171 | ||||||
| chr3:10056182
|
A | G | 1 | a0001c0011t0002g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1656+3685A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056182 | ||||||
| chr3:10056212
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1656+3715C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056212 | ||||||
| chr3:10056284
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1656+3787G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056284 | ||||||
| chr3:10056313
|
T | C | 1 | a0001c0001t0003g0029 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1656+3816T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056313 | ||||||
| chr3:10056573
|
C | G | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1657-3721C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056573 | ||||||
| chr3:10056583
|
G | A | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1657-3711G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056583 | ||||||
| chr3:10056592
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1657-3702C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056592 | ||||||
| chr3:10056603
|
T | G | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1657-3691T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056603 | ||||||
| chr3:10056726
|
G | A | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1657-3568G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056726 | ||||||
| chr3:10056893
|
C | T | 1 | a0001c0001t0004g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1657-3401C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056893 | ||||||
| chr3:10056994
|
A | G | 5 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0043others(2): Show | 5 | HG01243.hp1 HG01255.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-3300A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10056994 | ||||||
| chr3:10057016
|
A | C | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1657-3278A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057016 | ||||||
| chr3:10057064
|
C | T | 10 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0200others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1657-3230C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057064 | ||||||
| chr3:10057371
|
C | CT | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1657-2911dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10057371 | |||||
| chr3:10057537
|
G | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1657-2757G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057537 | ||||||
| chr3:10057582
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0108 | 3 | NA18956.hp1 NA18985.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1657-2712C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057582 | ||||||
| chr3:10057639
|
A | G | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1657-2655A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057639 | ||||||
| chr3:10057791
|
A | T | 4 | a0001c0001t0003g0145a0001c0001t0003g0148a0001c0001t0003g0150others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1657-2503A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057791 | ||||||
| chr3:10057979
|
A | G | 1 | a0002c0002t0002g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1657-2315A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10057979 | ||||||
| chr3:10058288
|
A | G | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1657-2006A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10058288 | ||||||
| chr3:10058378
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1657-1916C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10058378 | ||||||
| chr3:10058427
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1657-1867C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10058427 | ||||||
| chr3:10058461
|
G | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1657-1833G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10058461 | ||||||
| chr3:10058647
|
A | G | 4 | a0001c0001t0008g0025a0001c0001t0008g0026a0001c0001t0008g0046others(1): Show | 4 | HG00558.hp1 HG02080.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-1647A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10058647 | ||||||
| chr3:10058686
|
T | G | 1 | a0001c0001t0004g0004 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1657-1608T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10058686 | ||||||
| chr3:10059151
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0109 | 2 | NA18979.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1657-1143C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10059151 | ||||||
| chr3:10059573
|
C | G | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1657-721C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10059573 | ||||||
| chr3:10059584
|
C | T | 1 | a0001c0011t0002g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1657-710C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10059584 | ||||||
| chr3:10059809
|
G | GA | 18 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0005g0218others(15): Show | 18 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1657-472dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10059809 | |||||
| chr3:10059903
|
G | A | 16 | a0002c0002t0002g0214a0002c0002t0002g0232a0002c0002t0005g0177others(13): Show | 16 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1657-391G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10059903 | ||||||
| chr3:10059968
|
C | T | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1657-326C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10059968 | ||||||
| chr3:10060075
|
G | A | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1657-219G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10060075 | ||||||
| chr3:10060163
|
G | A | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1657-131G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10060163 | ||||||
| chr3:10060167
|
C | CA | 55 | a0001c0001t0001g0120a0001c0001t0004g0039a0001c0011t0002g0199others(52): Show | 55 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1657-112dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10060167 | |||||
| chr3:10060167
|
C | CAA | 29 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(26): Show | 29 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1657-113_1657-112d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10060167 | |||||
| chr3:10060212
|
T | A | 1 | a0002c0002t0002g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1657-82T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10060212 | ||||||
| chr3:10060693
|
T | A | 66 | a0001c0011t0002g0199a0001c0011t0003g0239a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1766+290T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10060693 | ||||||
| chr3:10060733
|
A | C | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1766+330A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10060733 | ||||||
| chr3:10060985
|
G | A | 13 | a0001c0011t0003g0239a0002c0002t0002g0185a0002c0002t0002g0186others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1766+582G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10060985 | ||||||
| chr3:10061080
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1766+677C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10061080 | ||||||
| chr3:10061582
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1767-569A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10061582 | ||||||
| chr3:10061709
|
G | T | 8 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0002g0210others(5): Show | 8 | HG01081.hp1 HG01928.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767-442G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10061709 | ||||||
| chr3:10061779
|
C | G | 1 | a0005c0013t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1767-372C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10061779 | ||||||
| chr3:10061891
|
G | A | 8 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0002g0210others(5): Show | 8 | HG01081.hp1 HG01928.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767-260G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10061891 | ||||||
| chr3:10061999
|
T | C | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1767-152T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10061999 | ||||||
| chr3:10062014
|
A | G | 16 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1767-137A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10062014 | ||||||
| chr3:10062127
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1767-24T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | chr3 | 10062127 | ||||||
| chr3:10062127
|
TA | T | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(37): Show | 40 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1767-15delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr3 | 10062127 | |||||
| chr3:10062325
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1827+114C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062325 | ||||||
| chr3:10062350
|
C | T | 81 | a0001c0011t0003g0239a0002c0002t0002g0179a0002c0002t0002g0183others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1827+139C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062350 | ||||||
| chr3:10062493
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1827+282C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062493 | ||||||
| chr3:10062502
|
A | T | 65 | a0001c0011t0003g0239a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1827+291A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062502 | ||||||
| chr3:10062512
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0104 | 2 | HG01123.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1827+301G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062512 | ||||||
| chr3:10062518
|
A | G | 1 | a0001c0001t0004g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1827+307A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062518 | ||||||
| chr3:10062701
|
T | C | 16 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1827+490T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062701 | ||||||
| chr3:10062869
|
G | C | 64 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1827+658G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062869 | ||||||
| chr3:10062901
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1827+690A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10062901 | ||||||
| chr3:10063466
|
G | A | 64 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1828-326G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10063466 | ||||||
| chr3:10063499
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1828-293C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10063499 | ||||||
| chr3:10063503
|
T | G | 1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1828-289T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10063503 | ||||||
| chr3:10063715
|
C | T | 16 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1828-77C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10063715 | ||||||
| chr3:10063786
|
C | T | 1 | a0004c0005t0001g0170 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.1828-6C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 20/43 | chr3 | 10063786 | ||||||
| chr3:10064163
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1948-193A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 21/43 | chr3 | 10064163 | ||||||
| chr3:10064512
|
C | T | 1 | a0002c0002t0002g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2021+83C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 22/43 | chr3 | 10064512 | ||||||
| chr3:10065104
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2168+229C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/43 | chr3 | 10065104 | ||||||
| chr3:10065122
|
C | G | 1 | a0001c0001t0003g0029 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2168+247C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/43 | chr3 | 10065122 | ||||||
| chr3:10065240
|
G | A | 64 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.2169-154G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/43 | chr3 | 10065240 | ||||||
| chr3:10065268
|
G | A | 2 | a0002c0002t0002g0190a0002c0002t0002g0192 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2169-126G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/43 | chr3 | 10065268 | ||||||
| chr3:10065319
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2169-75G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 23/43 | chr3 | 10065319 | ||||||
| chr3:10065506
|
A | G | 1 | a0009c0010t0003g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2269+12A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/43 | chr3 | 10065506 | ||||||
| chr3:10065531
|
A | G | 16 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2269+37A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/43 | chr3 | 10065531 | ||||||
| chr3:10065677
|
T | C | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2269+183T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/43 | chr3 | 10065677 | ||||||
| chr3:10065808
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2270-56C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/43 | chr3 | 10065808 | ||||||
| chr3:10065836
|
G | T | 64 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.2270-28G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 24/43 | chr3 | 10065836 | ||||||
| chr3:10066087
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2385+108C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10066087 | ||||||
| chr3:10066182
|
C | T | 4 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2385+203C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10066182 | ||||||
| chr3:10066282
|
T | C | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2385+303T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10066282 | ||||||
| chr3:10066494
|
C | T | 64 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.2385+515C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10066494 | ||||||
| chr3:10066794
|
G | A | 3 | a0002c0002t0002g0184a0002c0002t0002g0229a0002c0002t0006g0201 | 3 | HG01255.hp1 NA18961.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2386-415G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10066794 | ||||||
| chr3:10067034
|
A | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2386-175A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10067034 | ||||||
| chr3:10067061
|
G | C | 79 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(76): Show | 79 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.2386-148G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 25/43 | chr3 | 10067061 | ||||||
| chr3:10067417
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0076a0001c0001t0001g0083others(5): Show | 8 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2494+100A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10067417 | ||||||
| chr3:10067659
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2494+342G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10067659 | ||||||
| chr3:10067766
|
C | T | 4 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(1): Show | 4 | HG00558.hp2 HG02738.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+449C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10067766 | ||||||
| chr3:10067827
|
C | T | 3 | a0002c0002t0002g0184a0002c0002t0002g0229a0002c0002t0006g0201 | 3 | HG01255.hp1 NA18961.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2494+510C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10067827 | ||||||
| chr3:10068141
|
C | A | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(37): Show | 40 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+824C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10068141 | ||||||
| chr3:10068279
|
A | C | 16 | a0002c0002t0002g0214a0002c0002t0002g0232a0002c0002t0005g0177others(13): Show | 16 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2494+962A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10068279 | ||||||
| chr3:10068308
|
A | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2494+991A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10068308 | ||||||
| chr3:10068490
|
A | G | 79 | a0002c0002t0002g0179a0002c0002t0002g0183a0002c0002t0002g0184others(76): Show | 79 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.2494+1173A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10068490 | ||||||
| chr3:10069029
|
A | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2494+1712A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069029 | ||||||
| chr3:10069036
|
TAAC | T | 2 | a0002c0002t0002g0210a0002c0002t0002g0211 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2494+1731_2494+173 others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10069036 | |||||
| chr3:10069048
|
C | A | 1 | a0001c0001t0004g0074 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2494+1731C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069048 | ||||||
| chr3:10069156
|
T | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2494+1839T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069156 | ||||||
| chr3:10069194
|
A | C | 4 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(1): Show | 4 | HG00558.hp2 HG02738.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+1877A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069194 | ||||||
| chr3:10069197
|
G | A | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2494+1880G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069197 | ||||||
| chr3:10069243
|
T | C | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2494+1926T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069243 | ||||||
| chr3:10069260
|
A | ACAAGGGA others(10): Show |
16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2494+1944_2494+196 others(21): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10069260 | |||||
| chr3:10069296
|
A | C | 1 | a0001c0001t0001g0101 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2494+1979A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069296 | ||||||
| chr3:10069321
|
G | T | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2494+2004G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069321 | ||||||
| chr3:10069325
|
A | G | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2494+2008A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069325 | ||||||
| chr3:10069459
|
G | GGCCCTCG others(311): Show |
1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2494+2142_2494+214 others(322): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069459 | ||||||
| chr3:10069459
|
G | GGCTC | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2494+2142_2494+214 others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069459 | ||||||
| chr3:10069459
|
G | GGCTCTCC others(30): Show |
1 | a0003c0004t0003g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2494+2142_2494+214 others(41): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069459 | ||||||
| chr3:10069460
|
C | G | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2494+2143C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069460 | ||||||
| chr3:10069462
|
T | C | 66 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.2494+2145T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069462 | ||||||
| chr3:10069462
|
T | TCTCCCC | 45 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0060others(42): Show | 45 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.2494+2167_2494+217 others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10069462 | |||||
| chr3:10069468
|
C | T | 14 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2494+2151C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069468 | ||||||
| chr3:10069474
|
C | T | 2 | a0001c0016t0003g0122a0015c0014t0013g0154 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2494+2157C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069474 | ||||||
| chr3:10069478
|
C | CCTCTCCC others(291): Show |
1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2494+2162_2494+216 others(302): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10069478 | |||||
| chr3:10069480
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2494+2163C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069480 | ||||||
| chr3:10069482
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2494+2165T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069482 | ||||||
| chr3:10069484
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2494+2167C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069484 | ||||||
| chr3:10069486
|
C | T | 66 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.2494+2169C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069486 | ||||||
| chr3:10069490
|
T | C | 79 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(76): Show | 79 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.2494+2173T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069490 | ||||||
| chr3:10069491
|
C | A | 66 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.2494+2174C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069491 | ||||||
| chr3:10069493
|
C | CCTCCCCC others(38): Show |
1 | a0003c0004t0003g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2494+2176_2494+217 others(49): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | CTCCCCCT others(61): Show |
1 | a0007c0007t0003g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2494+2176_2494+217 others(72): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | CTCCCCCT others(55): Show |
1 | a0007c0007t0003g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2494+2176_2494+217 others(66): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | CTCCCCCT others(37): Show |
6 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494+2176_2494+217 others(48): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | CTCCCCCT others(31): Show |
2 | a0003c0004t0003g0166a0009c0010t0003g0158 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2494+2176_2494+217 others(42): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | CTCCCCCT others(25): Show |
1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2494+2176_2494+217 others(36): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | CTCCCCCT others(103): Show |
1 | a0007c0007t0003g0156 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2494+2176_2494+217 others(114): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069493
|
C | G | 67 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(64): Show | 67 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.2494+2176C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069493 | ||||||
| chr3:10069495
|
T | TCTCCCTC | 7 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(4): Show | 7 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.2494+2179_2494+218 others(11): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10069495 | |||||
| chr3:10069610
|
C | T | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2494+2293C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069610 | ||||||
| chr3:10069618
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2494+2301C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069618 | ||||||
| chr3:10069625
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2494+2308C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069625 | ||||||
| chr3:10069634
|
G | A | 1 | a0002c0002t0002g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2494+2317G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069634 | ||||||
| chr3:10069667
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0108 | 3 | NA18956.hp1 NA18985.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2494+2350T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069667 | ||||||
| chr3:10069677
|
C | T | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.2494+2360C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069677 | ||||||
| chr3:10069698
|
G | A | 1 | a0007c0007t0003g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2494+2381G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069698 | ||||||
| chr3:10069709
|
T | C | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2494+2392T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069709 | ||||||
| chr3:10069719
|
C | T | 1 | a0001c0001t0004g0043 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2494+2402C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069719 | ||||||
| chr3:10069807
|
C | T | 2 | a0001c0001t0004g0050a0001c0001t0004g0051 | 2 | HG00621.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2494+2490C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069807 | ||||||
| chr3:10069855
|
C | G | 1 | a0002c0002t0002g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2494+2538C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069855 | ||||||
| chr3:10069879
|
G | A | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2494+2562G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069879 | ||||||
| chr3:10069882
|
A | AC | 4 | a0001c0001t0004g0074a0001c0003t0002g0123a0002c0002t0017g0178others(1): Show | 4 | HG01175.hp2 HG02602.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+2569dupC | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10069882 | |||||
| chr3:10069887
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2494+2570G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069887 | ||||||
| chr3:10069980
|
C | A | 2 | a0002c0002t0005g0217a0002c0002t0009g0216 | 2 | NA19056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2494+2663C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10069980 | ||||||
| chr3:10070033
|
C | T | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(37): Show | 40 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+2716C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070033 | ||||||
| chr3:10070119
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2495-2752G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070119 | ||||||
| chr3:10070145
|
C | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2495-2726C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070145 | ||||||
| chr3:10070155
|
C | T | 12 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(9): Show | 12 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495-2716C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070155 | ||||||
| chr3:10070180
|
G | A | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-2691G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070180 | ||||||
| chr3:10070196
|
G | A | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2495-2675G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070196 | ||||||
| chr3:10070230
|
C | T | 17 | a0001c0001t0001g0063a0001c0016t0003g0122a0003c0004t0003g0160others(14): Show | 17 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2495-2641C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070230 | ||||||
| chr3:10070242
|
G | C | 1 | a0005c0013t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2495-2629G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070242 | ||||||
| chr3:10070264
|
G | A | 1 | a0002c0002t0002g0212 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2495-2607G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070264 | ||||||
| chr3:10070275
|
T | C | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2495-2596T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070275 | ||||||
| chr3:10070319
|
C | A | 2 | a0001c0001t0003g0105a0001c0001t0003g0106 | 2 | NA18978.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2495-2552C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070319 | ||||||
| chr3:10070356
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2495-2515C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070356 | ||||||
| chr3:10070360
|
C | T | 8 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(5): Show | 8 | HG01952.hp1 HG01975.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-2511C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070360 | ||||||
| chr3:10070369
|
A | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-2502A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070369 | ||||||
| chr3:10070387
|
G | GC | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-2478dupC | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070387 | |||||
| chr3:10070411
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2495-2460G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070411 | ||||||
| chr3:10070475
|
G | GGGCCAGC others(169): Show |
1 | a0001c0001t0001g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2495-2388_2495-238 others(180): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070475 | |||||
| chr3:10070476
|
G | GGCCAGCC others(206): Show |
1 | a0001c0001t0004g0037 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2495-2388_2495-238 others(217): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070476 | |||||
| chr3:10070476
|
G | GGCCAGCC others(207): Show |
1 | a0001c0001t0001g0097 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2495-2388_2495-238 others(218): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070476 | |||||
| chr3:10070476
|
G | GGCCAGCC others(207): Show |
3 | a0001c0001t0001g0107a0001c0001t0003g0140a0005c0008t0001g0019 | 3 | HG02572.hp2 HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2495-2388_2495-238 others(218): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070476 | |||||
| chr3:10070476
|
G | GGCCAGCC others(207): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0003g0148others(1): Show | 4 | HG01261.hp2 HG02145.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495-2388_2495-238 others(218): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070476 | |||||
| chr3:10070476
|
G | GGCCAGCC others(206): Show |
145 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.2495-2388_2495-238 others(217): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070476 | |||||
| chr3:10070476
|
G | GGCCAGCC others(293): Show |
2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2495-2388_2495-238 others(304): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070476 | |||||
| chr3:10070484
|
T | A | 84 | a0001c0001t0004g0036a0001c0001t0004g0048a0001c0001t0004g0121others(81): Show | 84 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.2495-2387T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070484 | ||||||
| chr3:10070484
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2495-2387T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070484 | ||||||
| chr3:10070488
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2495-2383G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070488 | ||||||
| chr3:10070488
|
G | T | 84 | a0001c0001t0004g0036a0001c0001t0004g0048a0001c0001t0004g0121others(81): Show | 84 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.2495-2383G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070488 | ||||||
| chr3:10070493
|
G | A | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-2378G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070493 | ||||||
| chr3:10070503
|
TG | T | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-2360delG | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070503 | |||||
| chr3:10070504
|
G | GGGGGGCT others(168): Show |
3 | a0001c0001t0004g0036a0001c0001t0004g0048a0001c0001t0004g0121 | 3 | HG01123.hp1 HG01981.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2495-2362_2495-236 others(179): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070504 | |||||
| chr3:10070504
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2495-2367G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070504 | ||||||
| chr3:10070509
|
G | GCTCAGCC others(219): Show |
2 | a0002c0002t0002g0207a0002c0002t0002g0208 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2495-2362_2495-236 others(230): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070509 | ||||||
| chr3:10070509
|
G | GCTCAGCC others(220): Show |
1 | a0002c0002t0017g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2495-2362_2495-236 others(231): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070509 | ||||||
| chr3:10070509
|
G | GCTCAGCC others(219): Show |
62 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(59): Show | 62 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.2495-2362_2495-236 others(230): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070509 | ||||||
| chr3:10070511
|
G | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-2360G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070511 | ||||||
| chr3:10070521
|
T | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-2350T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070521 | ||||||
| chr3:10070523
|
T | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-2348T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070523 | ||||||
| chr3:10070538
|
C | CGTCCGGG others(103): Show |
14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495-2301_2495-230 others(114): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070538 | |||||
| chr3:10070538
|
C | CGTCCGGG others(104): Show |
1 | a0003c0004t0003g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2495-2301_2495-230 others(115): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070538 | |||||
| chr3:10070538
|
C | CGTCCGGG others(140): Show |
1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2495-2263_2495-226 others(151): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10070538 | |||||
| chr3:10070594
|
C | T | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-2277C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070594 | ||||||
| chr3:10070603
|
C | T | 5 | a0001c0001t0003g0125a0001c0001t0003g0127a0001c0001t0003g0131others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-2268C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070603 | ||||||
| chr3:10070745
|
G | A | 1 | a0001c0001t0004g0037 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2495-2126G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070745 | ||||||
| chr3:10070762
|
C | G | 4 | a0006c0006t0002g0221a0006c0006t0002g0223a0006c0006t0014g0222others(1): Show | 4 | HG00639.hp2 HG02717.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495-2109C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070762 | ||||||
| chr3:10070831
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0003g0024 | 3 | HG02615.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2495-2040C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070831 | ||||||
| chr3:10070974
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2495-1897C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10070974 | ||||||
| chr3:10071022
|
A | C | 1 | a0012c0018t0004g0079 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2495-1849A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071022 | ||||||
| chr3:10071125
|
TA | T | 80 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2495-1733delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10071125 | |||||
| chr3:10071126
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2495-1745A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071126 | ||||||
| chr3:10071127
|
A | G | 15 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2495-1744A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071127 | ||||||
| chr3:10071147
|
GA | G | 19 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0003g0024others(16): Show | 19 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.2495-1711delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10071147 | |||||
| chr3:10071155
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2495-1716A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071155 | ||||||
| chr3:10071176
|
A | G | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2495-1695A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071176 | ||||||
| chr3:10071178
|
G | A | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2495-1693G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071178 | ||||||
| chr3:10071187
|
A | G | 1 | a0002c0002t0017g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2495-1684A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071187 | ||||||
| chr3:10071301
|
A | G | 5 | a0001c0001t0008g0025a0001c0001t0008g0026a0001c0001t0008g0046others(2): Show | 5 | HG00558.hp1 HG02080.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-1570A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071301 | ||||||
| chr3:10071366
|
G | A | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-1505G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071366 | ||||||
| chr3:10071387
|
A | C | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-1484A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071387 | ||||||
| chr3:10071516
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2495-1355A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071516 | ||||||
| chr3:10071724
|
C | G | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2495-1147C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071724 | ||||||
| chr3:10071784
|
G | T | 2 | a0001c0001t0001g0075a0012c0018t0004g0079 | 2 | NA19012.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2495-1087G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071784 | ||||||
| chr3:10071851
|
C | T | 3 | a0002c0002t0002g0184a0002c0002t0002g0229a0002c0002t0006g0201 | 3 | HG01255.hp1 NA18961.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2495-1020C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071851 | ||||||
| chr3:10071884
|
T | C | 94 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(91): Show | 94 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2495-987T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071884 | ||||||
| chr3:10071885
|
G | C | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-986G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071885 | ||||||
| chr3:10071945
|
AGAT | A | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-924_2495-922d others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10071945 | |||||
| chr3:10071960
|
G | A | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-911G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10071960 | ||||||
| chr3:10072084
|
C | T | 16 | a0002c0002t0002g0214a0002c0002t0002g0232a0002c0002t0005g0177others(13): Show | 16 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-787C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10072084 | ||||||
| chr3:10072118
|
A | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-753A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10072118 | ||||||
| chr3:10072280
|
CT | C | 54 | a0001c0001t0001g0093a0001c0001t0003g0125a0001c0001t0003g0127others(51): Show | 54 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.2495-575delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10072280 | |||||
| chr3:10072280
|
CTT | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495-576_2495-575d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr3 | 10072280 | |||||
| chr3:10072342
|
G | A | 8 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0002g0210others(5): Show | 8 | HG01081.hp1 HG01928.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-529G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10072342 | ||||||
| chr3:10072521
|
C | T | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2495-350C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10072521 | ||||||
| chr3:10072670
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0007g0028 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2495-201C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10072670 | ||||||
| chr3:10072847
|
G | A | 7 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(4): Show | 7 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-24G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 26/43 | chr3 | 10072847 | ||||||
| chr3:10073112
|
T | A | 1 | a0006c0006t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2605+131T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 27/43 | chr3 | 10073112 | ||||||
| chr3:10073118
|
T | C | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2606-135T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 27/43 | chr3 | 10073118 | ||||||
| chr3:10073150
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2606-103C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 27/43 | chr3 | 10073150 | ||||||
| chr3:10073213
|
A | T | 3 | a0001c0001t0004g0038a0001c0001t0004g0043a0001c0001t0004g0056 | 3 | HG01243.hp1 HG01255.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2606-40A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 27/43 | chr3 | 10073213 | ||||||
| chr3:10073470
|
C | T | 1 | a0002c0002t0002g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2715+108C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10073470 | ||||||
| chr3:10073475
|
C | G | 9 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2715+113C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10073475 | ||||||
| chr3:10073541
|
A | G | 1 | a0006c0006t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2715+179A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10073541 | ||||||
| chr3:10073757
|
CATTTATT others(4): Show |
C | 1 | a0001c0001t0004g0004 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2715+403_2715+413d others(13): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr3 | 10073757 | |||||
| chr3:10073866
|
C | G | 1 | a0013c0017t0004g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2715+504C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10073866 | ||||||
| chr3:10073935
|
C | T | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2715+573C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10073935 | ||||||
| chr3:10074006
|
C | T | 1 | a0002c0002t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2716-524C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10074006 | ||||||
| chr3:10074462
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2716-68G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 28/43 | chr3 | 10074462 | ||||||
| chr3:10074857
|
G | T | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2859+184G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10074857 | ||||||
| chr3:10074916
|
T | TTAC | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2859+261_2859+263d others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10074916 | |||||
| chr3:10074916
|
TTACTAC | T | 12 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2859+258_2859+263d others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10074916 | |||||
| chr3:10074937
|
A | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2859+264A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10074937 | ||||||
| chr3:10075028
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2859+355C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075028 | ||||||
| chr3:10075188
|
C | CT | 66 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(63): Show | 66 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.2859+527dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10075188 | |||||
| chr3:10075253
|
C | A | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2859+580C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075253 | ||||||
| chr3:10075254
|
A | G | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2859+581A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075254 | ||||||
| chr3:10075255
|
C | T | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2859+582C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075255 | ||||||
| chr3:10075284
|
C | T | 1 | a0002c0002t0002g0238 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2859+611C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075284 | ||||||
| chr3:10075285
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2859+612G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075285 | ||||||
| chr3:10075432
|
C | G | 1 | a0001c0001t0004g0052 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2859+759C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075432 | ||||||
| chr3:10075463
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2859+790C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075463 | ||||||
| chr3:10075521
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2859+848C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075521 | ||||||
| chr3:10075566
|
A | G | 4 | a0001c0001t0003g0145a0001c0001t0003g0148a0001c0001t0003g0150others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2859+893A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075566 | ||||||
| chr3:10075728
|
C | CT | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.2859+1075dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10075728 | |||||
| chr3:10075728
|
C | CTT | 45 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 45 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.2859+1074_2859+107 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10075728 | |||||
| chr3:10075728
|
C | CTTTT | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2859+1072_2859+107 others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10075728 | |||||
| chr3:10075728
|
CT | C | 10 | a0002c0002t0002g0214a0002c0002t0005g0177a0002c0002t0005g0181others(7): Show | 10 | HG00408.hp1 HG02523.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.2859+1075delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10075728 | |||||
| chr3:10075786
|
G | A | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2859+1113G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075786 | ||||||
| chr3:10076035
|
CT | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0080a0001c0011t0002g0199others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2859+1378delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10076035 | |||||
| chr3:10076092
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2859+1419A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076092 | ||||||
| chr3:10076148
|
A | G | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2859+1475A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076148 | ||||||
| chr3:10076153
|
T | TATGCTTC others(7): Show |
4 | a0002c0002t0002g0188a0002c0002t0002g0190a0002c0002t0002g0192others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2859+1480_2859+148 others(18): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076153 | ||||||
| chr3:10076228
|
C | G | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2859+1555C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076228 | ||||||
| chr3:10076284
|
C | CT | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2859+1623dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10076284 | |||||
| chr3:10076284
|
C | CTT | 64 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(61): Show | 64 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.2859+1622_2859+162 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10076284 | |||||
| chr3:10076320
|
A | G | 1 | a0001c0001t0004g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2859+1647A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076320 | ||||||
| chr3:10076391
|
G | C | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2860-1690G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076391 | ||||||
| chr3:10076492
|
A | T | 1 | a0001c0001t0004g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2860-1589A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076492 | ||||||
| chr3:10076618
|
C | T | 1 | a0002c0002t0002g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2860-1463C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076618 | ||||||
| chr3:10076695
|
A | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2860-1386A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076695 | ||||||
| chr3:10076954
|
T | C | 1 | a0006c0006t0015g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2860-1127T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076954 | ||||||
| chr3:10077023
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2860-1058G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077023 | ||||||
| chr3:10077062
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2860-1019T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077062 | ||||||
| chr3:10077126
|
GGGCGGCT others(25): Show |
G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2860-952_2860-921d others(34): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10077126 | |||||
| chr3:10077140
|
G | A | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2860-941G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077140 | ||||||
| chr3:10077163
|
G | A | 1 | a0001c0001t0019g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2860-918G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077163 | ||||||
| chr3:10077205
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2860-876C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077205 | ||||||
| chr3:10077278
|
T | C | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2860-803T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077278 | ||||||
| chr3:10077278
|
T | G | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(37): Show | 40 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.2860-803T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077278 | ||||||
| chr3:10077299
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2860-782C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077299 | ||||||
| chr3:10077332
|
GT | G | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2860-747delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10077332 | |||||
| chr3:10077564
|
A | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2860-517A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077564 | ||||||
| chr3:10077564
|
AT | A | 63 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(60): Show | 63 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.2860-508delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr3 | 10077564 | |||||
| chr3:10077565
|
T | A | 1 | a0002c0002t0005g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2860-516T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077565 | ||||||
| chr3:10077717
|
G | A | 3 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0006g0197 | 3 | HG01081.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2860-364G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077717 | ||||||
| chr3:10077919
|
C | A | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2860-162C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077919 | ||||||
| chr3:10077931
|
G | A | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2860-150G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10077931 | ||||||
| chr3:10078233
|
T | C | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2976+36T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078233 | ||||||
| chr3:10078244
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2976+47A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078244 | ||||||
| chr3:10078332
|
GA | G | 4 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(1): Show | 4 | HG00558.hp2 HG02738.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2976+136delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078332 | ||||||
| chr3:10078348
|
C | CTTTA | 4 | a0002c0002t0002g0196a0002c0002t0002g0198a0002c0002t0005g0219others(1): Show | 4 | HG00408.hp1 HG01081.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2976+172_2976+175d others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr3 | 10078348 | |||||
| chr3:10078630
|
G | A | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2976+433G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078630 | ||||||
| chr3:10078643
|
C | T | 1 | a0006c0006t0002g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2976+446C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078643 | ||||||
| chr3:10078646
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2976+449G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078646 | ||||||
| chr3:10078647
|
C | A | 1 | a0001c0001t0012g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2976+450C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078647 | ||||||
| chr3:10078649
|
C | T | 10 | a0002c0002t0002g0214a0002c0002t0005g0177a0002c0002t0005g0181others(7): Show | 10 | HG00408.hp1 HG02523.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.2976+452C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078649 | ||||||
| chr3:10078721
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2976+524T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078721 | ||||||
| chr3:10078847
|
T | C | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.2976+650T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078847 | ||||||
| chr3:10078946
|
CA | C | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2976+759delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr3 | 10078946 | |||||
| chr3:10078963
|
C | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2976+766C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10078963 | ||||||
| chr3:10079094
|
A | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2976+897A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079094 | ||||||
| chr3:10079105
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0087 | 2 | HG03710.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2976+908A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079105 | ||||||
| chr3:10079186
|
G | A | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2976+989G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079186 | ||||||
| chr3:10079249
|
T | C | 4 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2976+1052T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079249 | ||||||
| chr3:10079345
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2976+1148C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079345 | ||||||
| chr3:10079420
|
G | T | 134 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(131): Show | 134 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.2976+1223G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079420 | ||||||
| chr3:10079452
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2976+1255C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079452 | ||||||
| chr3:10079569
|
G | A | 15 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2976+1372G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079569 | ||||||
| chr3:10079630
|
A | C | 1 | a0002c0002t0002g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2976+1433A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10079630 | ||||||
| chr3:10079921
|
C | CT | 9 | a0002c0002t0002g0179a0002c0002t0002g0203a0002c0002t0002g0206others(6): Show | 9 | HG01069.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2977-1167dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr3 | 10079921 | |||||
| chr3:10080131
|
T | C | 16 | a0001c0016t0003g0122a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2977-969T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10080131 | ||||||
| chr3:10080238
|
C | T | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.2977-862C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10080238 | ||||||
| chr3:10080408
|
A | G | 7 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(4): Show | 7 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.2977-692A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10080408 | ||||||
| chr3:10080506
|
C | T | 2 | a0001c0001t0004g0004a0013c0017t0004g0054 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2977-594C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10080506 | ||||||
| chr3:10080693
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2977-407C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10080693 | ||||||
| chr3:10080891
|
T | C | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2977-209T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10080891 | ||||||
| chr3:10081018
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2977-82T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10081018 | ||||||
| chr3:10081035
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2977-65C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 30/43 | chr3 | 10081035 | ||||||
| chr3:10081243
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0077 | 2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3105+15C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 31/43 | chr3 | 10081243 | ||||||
| chr3:10081627
|
A | C | 2 | a0002c0002t0002g0190a0002c0002t0002g0192 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3224+163A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10081627 | ||||||
| chr3:10081635
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3224+171C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10081635 | ||||||
| chr3:10082121
|
A | G | 65 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(62): Show | 65 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.3224+657A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082121 | ||||||
| chr3:10082149
|
C | T | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3224+685C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082149 | ||||||
| chr3:10082239
|
T | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3224+775T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082239 | ||||||
| chr3:10082249
|
C | G | 1 | a0001c0011t0002g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3224+785C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082249 | ||||||
| chr3:10082382
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3224+918C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082382 | ||||||
| chr3:10082436
|
G | A | 94 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(91): Show | 94 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.3224+972G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082436 | ||||||
| chr3:10082642
|
C | T | 1 | a0003c0004t0003g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3224+1178C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082642 | ||||||
| chr3:10082760
|
C | T | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.3224+1296C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082760 | ||||||
| chr3:10082907
|
CAA | C | 3 | a0001c0001t0004g0033a0001c0001t0004g0058a0001c0001t0004g0118 | 3 | HG01109.hp1 HG01168.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3224+1445_3224+144 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10082907 | |||||
| chr3:10082942
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3224+1478A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10082942 | ||||||
| chr3:10083187
|
A | C | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3224+1723A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083187 | ||||||
| chr3:10083205
|
C | A | 2 | a0009c0010t0003g0158a0009c0010t0003g0159 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3224+1741C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083205 | ||||||
| chr3:10083240
|
T | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3224+1776T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083240 | ||||||
| chr3:10083599
|
C | T | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.3224+2135C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083599 | ||||||
| chr3:10083658
|
G | A | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.3225-2154G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083658 | ||||||
| chr3:10083713
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3225-2099T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083713 | ||||||
| chr3:10083720
|
G | C | 81 | a0001c0011t0002g0199a0001c0016t0003g0122a0002c0002t0002g0179others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.3225-2092G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083720 | ||||||
| chr3:10083866
|
C | A | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.3225-1946C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083866 | ||||||
| chr3:10083887
|
C | CA | 21 | a0001c0001t0001g0008a0001c0001t0001g0104a0001c0001t0001g0107others(18): Show | 21 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3225-1905dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10083887 | |||||
| chr3:10083908
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3225-1904G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083908 | ||||||
| chr3:10083992
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3225-1820A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10083992 | ||||||
| chr3:10084000
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3225-1812G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084000 | ||||||
| chr3:10084001
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3225-1811T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084001 | ||||||
| chr3:10084002
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3225-1810G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084002 | ||||||
| chr3:10084013
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3225-1799A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084013 | ||||||
| chr3:10084052
|
G | T | 1 | a0002c0002t0005g0230 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3225-1760G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084052 | ||||||
| chr3:10084087
|
G | A | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3225-1725G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084087 | ||||||
| chr3:10084097
|
G | A | 2 | a0002c0002t0002g0183a0002c0020t0002g0227 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3225-1715G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084097 | ||||||
| chr3:10084290
|
C | CT | 18 | a0001c0001t0001g0008a0001c0016t0003g0122a0003c0004t0003g0160others(15): Show | 18 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.3225-1510dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10084290 | |||||
| chr3:10084290
|
C | CTT | 76 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(73): Show | 76 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.3225-1511_3225-151 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10084290 | |||||
| chr3:10084399
|
C | G | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.3225-1413C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084399 | ||||||
| chr3:10084469
|
T | G | 77 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.3225-1343T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084469 | ||||||
| chr3:10084628
|
G | T | 80 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(77): Show | 80 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.3225-1184G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084628 | ||||||
| chr3:10084682
|
C | T | 3 | a0007c0007t0003g0155a0007c0007t0003g0156a0007c0007t0003g0157 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3225-1130C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084682 | ||||||
| chr3:10084718
|
G | A | 3 | a0002c0002t0002g0179a0002c0002t0002g0205a0002c0002t0006g0204 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3225-1094G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084718 | ||||||
| chr3:10084739
|
A | C | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3225-1073A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084739 | ||||||
| chr3:10084795
|
G | A | 2 | a0002c0002t0005g0217a0002c0002t0009g0216 | 2 | NA19056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3225-1017G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10084795 | ||||||
| chr3:10085083
|
G | A | 2 | a0001c0001t0003g0105a0001c0001t0003g0106 | 2 | NA18978.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3225-729G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10085083 | ||||||
| chr3:10085225
|
C | T | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3225-587C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10085225 | ||||||
| chr3:10085373
|
ATTCTTTT | A | 10 | a0002c0002t0002g0214a0002c0002t0005g0177a0002c0002t0005g0181others(7): Show | 10 | HG00408.hp1 HG02523.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.3225-425_3225-419d others(9): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10085373 | |||||
| chr3:10085394
|
C | CT | 7 | a0001c0001t0001g0047a0001c0001t0001g0081a0007c0007t0003g0155others(4): Show | 7 | HG00621.hp1 HG02258.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3225-402dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10085394 | |||||
| chr3:10085394
|
C | CTT | 10 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3225-403_3225-402d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr3 | 10085394 | |||||
| chr3:10085398
|
T | C | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00621.hp2 NA18612.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.3225-414T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10085398 | ||||||
| chr3:10085541
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3225-271G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10085541 | ||||||
| chr3:10085626
|
G | A | 2 | a0002c0012t0005g0193a0002c0012t0005g0194 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3225-186G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10085626 | ||||||
| chr3:10085734
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0104 | 2 | HG01123.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3225-78T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 32/43 | chr3 | 10085734 | ||||||
| chr3:10086145
|
C | G | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3335+223C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086145 | ||||||
| chr3:10086146
|
A | G | 13 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(10): Show | 13 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.3335+224A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086146 | ||||||
| chr3:10086319
|
A | G | 77 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.3335+397A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086319 | ||||||
| chr3:10086468
|
T | C | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3335+546T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086468 | ||||||
| chr3:10086641
|
C | T | 3 | a0001c0003t0002g0123a0001c0003t0002g0128a0001c0003t0002g0133 | 3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3336-493C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086641 | ||||||
| chr3:10086675
|
C | T | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3336-459C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086675 | ||||||
| chr3:10086951
|
A | G | 11 | a0001c0011t0002g0199a0002c0002t0002g0183a0002c0002t0002g0184others(8): Show | 11 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.3336-183A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10086951 | ||||||
| chr3:10087060
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3336-74G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10087060 | ||||||
| chr3:10087116
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3336-18T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 33/43 | chr3 | 10087116 | ||||||
| chr3:10087281
|
C | CT | 9 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0085others(6): Show | 9 | HG00099.hp2 HG00558.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3466+36dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr3 | 10087281 | |||||
| chr3:10087281
|
C | CTT | 16 | a0002c0002t0002g0185a0002c0002t0002g0186a0002c0002t0002g0233others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3466+35_3466+36dup others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr3 | 10087281 | |||||
| chr3:10087281
|
C | CTTT | 70 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(67): Show | 70 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.3466+34_3466+36dup others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr3 | 10087281 | |||||
| chr3:10087281
|
C | CTTTT | 5 | a0001c0011t0002g0199a0002c0002t0002g0232a0002c0002t0005g0177others(2): Show | 5 | HG02572.hp1 HG02738.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.3466+33_3466+36dup others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr3 | 10087281 | |||||
| chr3:10087426
|
A | G | 1 | a0001c0001t0004g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3466+162A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10087426 | ||||||
| chr3:10087434
|
G | A | 4 | a0002c0002t0002g0210a0002c0002t0002g0211a0002c0002t0002g0212others(1): Show | 4 | HG01928.hp1 HG02273.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3466+170G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10087434 | ||||||
| chr3:10087457
|
C | A | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3466+193C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10087457 | ||||||
| chr3:10087527
|
C | CA | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.3466+275dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr3 | 10087527 | |||||
| chr3:10087678
|
C | T | 7 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(4): Show | 7 | HG00639.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3466+414C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10087678 | ||||||
| chr3:10087869
|
G | A | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3467-580G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10087869 | ||||||
| chr3:10087901
|
C | T | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3467-548C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10087901 | ||||||
| chr3:10088044
|
A | C | 10 | a0002c0002t0002g0214a0002c0002t0005g0177a0002c0002t0005g0181others(7): Show | 10 | HG00408.hp1 HG02523.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.3467-405A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10088044 | ||||||
| chr3:10088151
|
C | G | 15 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3467-298C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10088151 | ||||||
| chr3:10088167
|
T | C | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3467-282T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10088167 | ||||||
| chr3:10088235
|
C | T | 1 | a0001c0001t0003g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3467-214C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10088235 | ||||||
| chr3:10088294
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3467-155G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 34/43 | chr3 | 10088294 | ||||||
| chr3:10088687
|
T | C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3561-141T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 35/43 | chr3 | 10088687 | ||||||
| chr3:10088704
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3561-124T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 35/43 | chr3 | 10088704 | ||||||
| chr3:10089116
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0067 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3683+166C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089116 | ||||||
| chr3:10089141
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3683+191C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089141 | ||||||
| chr3:10089285
|
C | CA | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.3683+346dupA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr3 | 10089285 | |||||
| chr3:10089347
|
C | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3683+397C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089347 | ||||||
| chr3:10089420
|
C | T | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.3683+470C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089420 | ||||||
| chr3:10089438
|
C | G | 1 | a0002c0002t0006g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3683+488C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089438 | ||||||
| chr3:10089454
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3683+504G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089454 | ||||||
| chr3:10089631
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3684-661G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10089631 | ||||||
| chr3:10090117
|
A | G | 1 | a0002c0002t0002g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3684-175A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10090117 | ||||||
| chr3:10090127
|
G | T | 1 | a0002c0002t0005g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3684-165G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10090127 | ||||||
| chr3:10090147
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0089 | 2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3684-145C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10090147 | ||||||
| chr3:10090201
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3684-91G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10090201 | ||||||
| chr3:10090270
|
G | A | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3684-22G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 36/43 | chr3 | 10090270 | ||||||
| chr3:10090443
|
A | AT | 36 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(33): Show | 36 | HG00741.hp1 HG01109.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.3777+86dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090443
|
A | ATT | 8 | a0001c0001t0001g0081a0001c0001t0012g0153a0004c0005t0001g0169others(5): Show | 8 | HG00621.hp1 HG01952.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3777+85_3777+86dup others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090443
|
A | ATTT | 8 | a0003c0004t0003g0161a0003c0004t0003g0163a0003c0004t0003g0164others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3777+84_3777+86dup others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090443
|
ATT | A | 12 | a0002c0002t0002g0191a0002c0002t0002g0196a0002c0002t0002g0210others(9): Show | 12 | HG01081.hp1 HG02273.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.3777+85_3777+86del others(2): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090443
|
ATTT | A | 41 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0135others(38): Show | 41 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.3777+84_3777+86del others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090443
|
ATTTT | A | 18 | a0001c0001t0003g0029a0001c0003t0002g0126a0001c0003t0002g0128others(15): Show | 18 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.3777+83_3777+86del others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090443
|
ATTTTTTT others(3): Show |
A | 1 | a0006c0006t0014g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3777+77_3777+86del others(10): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr3 | 10090443 | |||||
| chr3:10090529
|
G | A | 1 | a0002c0002t0002g0229 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3777+144G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090529 | ||||||
| chr3:10090619
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3777+234C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090619 | ||||||
| chr3:10090620
|
G | A | 2 | a0001c0001t0007g0113a0003c0004t0003g0166 | 2 | HG02615.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3777+235G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090620 | ||||||
| chr3:10090709
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3777+324C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090709 | ||||||
| chr3:10090744
|
C | T | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3777+359C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090744 | ||||||
| chr3:10090776
|
A | G | 77 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.3777+391A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090776 | ||||||
| chr3:10090960
|
G | T | 3 | a0005c0008t0007g0020a0005c0008t0007g0021a0010c0022t0007g0018 | 3 | HG00558.hp2 NA18747.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.3777+575G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10090960 | ||||||
| chr3:10091117
|
G | T | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3777+732G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091117 | ||||||
| chr3:10091165
|
T | G | 10 | a0002c0002t0002g0183a0002c0002t0002g0184a0002c0002t0002g0200others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.3777+780T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091165 | ||||||
| chr3:10091327
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3778-854C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091327 | ||||||
| chr3:10091385
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0088others(1): Show | 4 | HG00099.hp2 HG01258.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3778-796C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091385 | ||||||
| chr3:10091478
|
A | G | 22 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(19): Show | 22 | HG01891.hp1 HG01952.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.3778-703A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091478 | ||||||
| chr3:10091502
|
C | T | 6 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(3): Show | 6 | HG00558.hp2 HG02683.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.3778-679C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091502 | ||||||
| chr3:10091595
|
A | G | 1 | a0001c0001t0004g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3778-586A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091595 | ||||||
| chr3:10091610
|
C | A | 4 | a0005c0008t0001g0019a0005c0008t0007g0020a0005c0008t0007g0021others(1): Show | 4 | HG00558.hp2 HG02738.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.3778-571C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091610 | ||||||
| chr3:10091656
|
A | G | 1 | a0001c0001t0003g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3778-525A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091656 | ||||||
| chr3:10091701
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3778-480C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091701 | ||||||
| chr3:10091794
|
T | C | 77 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.3778-387T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091794 | ||||||
| chr3:10091797
|
A | C | 1 | a0001c0001t0003g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3778-384A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091797 | ||||||
| chr3:10091820
|
T | C | 12 | a0001c0001t0001g0098a0004c0005t0001g0169a0004c0005t0001g0170others(9): Show | 12 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.3778-361T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091820 | ||||||
| chr3:10091890
|
C | T | 92 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(89): Show | 92 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.3778-291C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091890 | ||||||
| chr3:10091907
|
A | C | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3778-274A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091907 | ||||||
| chr3:10091907
|
A | G | 2 | a0003c0004t0003g0162a0003c0004t0003g0163 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3778-274A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10091907 | ||||||
| chr3:10092026
|
G | A | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.3778-155G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 37/43 | chr3 | 10092026 | ||||||
| chr3:10092265
|
A | G | 105 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(102): Show | 105 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.3849+13A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092265 | ||||||
| chr3:10092416
|
C | G | 1 | a0001c0001t0003g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3849+164C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092416 | ||||||
| chr3:10092431
|
A | AT | 62 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(59): Show | 62 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.3849+190dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092431 | |||||
| chr3:10092431
|
AT | A | 41 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(38): Show | 41 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.3849+190delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092431 | |||||
| chr3:10092471
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3849+219C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092471 | ||||||
| chr3:10092482
|
T | C | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3849+230T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092482 | ||||||
| chr3:10092621
|
C | T | 2 | a0005c0013t0001g0115a0005c0013t0001g0116 | 2 | HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3849+369C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092621 | ||||||
| chr3:10092622
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3849+370G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092622 | ||||||
| chr3:10092636
|
C | G | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(25): Show | 28 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.3849+384C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092636 | ||||||
| chr3:10092684
|
C | CT | 6 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0096others(3): Show | 6 | HG01123.hp2 HG02683.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.3849+458dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092684 | |||||
| chr3:10092684
|
CT | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0047others(21): Show | 24 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.3849+458delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092684 | |||||
| chr3:10092684
|
CTT | C | 109 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0059others(106): Show | 109 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.3849+457_3849+458d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092684 | |||||
| chr3:10092684
|
CTTT | C | 7 | a0001c0016t0003g0122a0002c0002t0002g0233a0002c0002t0002g0234others(4): Show | 7 | HG02683.hp2 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.3849+456_3849+458d others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092684 | |||||
| chr3:10092684
|
CTTTTT | C | 6 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(3): Show | 6 | HG01952.hp1 HG01975.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.3849+454_3849+458d others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr3 | 10092684 | |||||
| chr3:10092807
|
G | T | 91 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(88): Show | 91 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.3850-478G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10092807 | ||||||
| chr3:10093082
|
C | T | 77 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.3850-203C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10093082 | ||||||
| chr3:10093109
|
A | G | 7 | a0002c0002t0002g0233a0002c0002t0002g0234a0002c0002t0002g0235others(4): Show | 7 | HG00639.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3850-176A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10093109 | ||||||
| chr3:10093213
|
G | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3850-72G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 38/43 | chr3 | 10093213 | ||||||
| chr3:10093350
|
A | C | 1 | a0001c0001t0001g0101 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3888+27A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10093350 | ||||||
| chr3:10093480
|
C | A | 1 | a0007c0007t0003g0156 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3888+157C>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10093480 | ||||||
| chr3:10093634
|
GAGT | G | 6 | a0002c0002t0002g0232a0002c0002t0005g0230a0002c0002t0005g0231others(3): Show | 6 | HG00741.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3888+314_3888+316d others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr3 | 10093634 | |||||
| chr3:10093658
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3888+335C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10093658 | ||||||
| chr3:10093791
|
G | T | 1 | a0006c0006t0014g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3888+468G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10093791 | ||||||
| chr3:10093886
|
G | C | 13 | a0001c0011t0003g0239a0003c0004t0003g0160a0003c0004t0003g0161others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3889-403G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10093886 | ||||||
| chr3:10093893
|
A | G | 107 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(104): Show | 107 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.3889-396A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10093893 | ||||||
| chr3:10094112
|
A | G | 1 | a0011c0021t0005g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3889-177A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 39/43 | chr3 | 10094112 | ||||||
| chr3:10094389
|
G | A | 2 | a0001c0001t0004g0049a0001c0001t0004g0052 | 2 | NA18612.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.3963+26G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094389 | ||||||
| chr3:10094466
|
C | T | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.3963+103C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094466 | ||||||
| chr3:10094472
|
G | A | 13 | a0002c0002t0002g0185a0002c0002t0002g0186a0002c0002t0002g0187others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3963+109G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094472 | ||||||
| chr3:10094504
|
T | A | 1 | a0002c0002t0002g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3963+141T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094504 | ||||||
| chr3:10094518
|
C | T | 1 | a0001c0001t0004g0037 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3963+155C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094518 | ||||||
| chr3:10094641
|
C | T | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.3963+278C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094641 | ||||||
| chr3:10094705
|
T | A | 1 | a0007c0007t0003g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3963+342T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094705 | ||||||
| chr3:10094706
|
T | A | 106 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(103): Show | 106 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.3963+343T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094706 | ||||||
| chr3:10094707
|
A | T | 1 | a0001c0001t0003g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3963+344A>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094707 | ||||||
| chr3:10095072
|
G | A | 1 | a0002c0002t0002g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3964-128G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10095072 | ||||||
| chr3:10095133
|
A | G | 1 | a0001c0001t0004g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3964-67A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10095133 | ||||||
| chr3:10095454
|
G | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4038+180G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | chr3 | 10095454 | ||||||
| chr3:10095548
|
C | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4038+274C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | chr3 | 10095548 | ||||||
| chr3:10095878
|
A | AT | 18 | a0001c0001t0001g0073a0001c0001t0001g0107a0001c0001t0003g0106others(15): Show | 18 | HG00558.hp2 HG01192.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.4039-427dupT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr3 | 10095878 | |||||
| chr3:10095878
|
A | ATT | 56 | a0001c0003t0002g0124a0001c0003t0002g0126a0001c0003t0002g0128others(53): Show | 56 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.4039-428_4039-427d others(4): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr3 | 10095878 | |||||
| chr3:10095878
|
A | ATTT | 23 | a0001c0003t0002g0123a0001c0003t0002g0129a0002c0002t0002g0185others(20): Show | 23 | HG01175.hp2 HG01358.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.4039-429_4039-427d others(5): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr3 | 10095878 | |||||
| chr3:10095878
|
AT | A | 10 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0086others(7): Show | 10 | HG00639.hp1 HG01070.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.4039-427delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr3 | 10095878 | |||||
| chr3:10096003
|
T | C | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4039-323T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | chr3 | 10096003 | ||||||
| chr3:10096082
|
G | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4039-244G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 41/43 | chr3 | 10096082 | ||||||
| chr3:10096505
|
T | C | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4185+33T>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096505 | ||||||
| chr3:10096525
|
G | A | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4185+53G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096525 | ||||||
| chr3:10096614
|
A | C | 2 | a0002c0002t0002g0210a0002c0002t0002g0211 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4185+142A>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096614 | ||||||
| chr3:10096705
|
A | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4185+233A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096705 | ||||||
| chr3:10096942
|
A | G | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4185+470A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096942 | ||||||
| chr3:10096963
|
G | C | 1 | a0002c0002t0002g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4185+491G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096963 | ||||||
| chr3:10096999
|
G | T | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4185+527G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10096999 | ||||||
| chr3:10097093
|
G | T | 91 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(88): Show | 91 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.4185+621G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097093 | ||||||
| chr3:10097196
|
G | A | 2 | a0009c0010t0003g0158a0009c0010t0003g0159 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4185+724G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097196 | ||||||
| chr3:10097330
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4185+858T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097330 | ||||||
| chr3:10097398
|
C | T | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4185+926C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097398 | ||||||
| chr3:10097401
|
G | C | 3 | a0006c0006t0002g0223a0006c0006t0014g0222a0006c0006t0015g0220 | 3 | HG00639.hp2 HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4185+929G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097401 | ||||||
| chr3:10097530
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.4185+1058G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097530 | ||||||
| chr3:10097534
|
G | A | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4185+1062G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097534 | ||||||
| chr3:10097552
|
G | A | 1 | a0002c0002t0002g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4185+1080G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097552 | ||||||
| chr3:10097610
|
G | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4186-1110G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097610 | ||||||
| chr3:10097624
|
A | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4186-1096A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097624 | ||||||
| chr3:10097818
|
C | T | 14 | a0003c0004t0003g0160a0003c0004t0003g0161a0003c0004t0003g0162others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.4186-902C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097818 | ||||||
| chr3:10097950
|
G | T | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4186-770G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10097950 | ||||||
| chr3:10097988
|
GT | G | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4186-724delT | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | INFO_REALIGN_3_PRIME | chr3 | 10097988 | |||||
| chr3:10098042
|
T | G | 1 | a0015c0014t0013g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4186-678T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098042 | ||||||
| chr3:10098141
|
C | T | 103 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4186-579C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098141 | ||||||
| chr3:10098149
|
C | T | 102 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(99): Show | 102 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.4186-571C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098149 | ||||||
| chr3:10098158
|
A | G | 1 | a0001c0016t0003g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4186-562A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098158 | ||||||
| chr3:10098333
|
A | G | 104 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.4186-387A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098333 | ||||||
| chr3:10098431
|
G | A | 77 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.4186-289G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098431 | ||||||
| chr3:10098451
|
G | C | 1 | a0001c0003t0002g0134 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4186-269G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098451 | ||||||
| chr3:10098573
|
G | C | 32 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(29): Show | 32 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.4186-147G>C | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 42/43 | chr3 | 10098573 | ||||||
| chr3:10098976
|
G | T | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4281+161G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10098976 | ||||||
| chr3:10098977
|
G | A | 1 | a0014c0015t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4281+162G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10098977 | ||||||
| chr3:10098987
|
G | A | 129 | a0001c0001t0003g0002a0001c0001t0003g0029a0001c0001t0003g0125others(126): Show | 129 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4281+172G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10098987 | ||||||
| chr3:10099012
|
A | G | 104 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.4281+197A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10099012 | ||||||
| chr3:10099085
|
A | G | 16 | a0001c0011t0003g0239a0003c0004t0003g0160a0003c0004t0003g0161others(13): Show | 16 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.4281+270A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10099085 | ||||||
| chr3:10099381
|
T | G | 104 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.4281+566T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10099381 | ||||||
| chr3:10099488
|
G | A | 20 | a0001c0001t0003g0002a0001c0001t0003g0029a0001c0001t0003g0125others(17): Show | 20 | HG01099.hp1 HG01109.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.4281+673G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10099488 | ||||||
| chr3:10099500
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0033others(35): Show | 38 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.4281+685C>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10099500 | ||||||
| chr3:10099864
|
G | A | 11 | a0004c0005t0001g0169a0004c0005t0001g0170a0004c0005t0001g0171others(8): Show | 11 | HG00558.hp2 HG01952.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.4281+1049G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10099864 | ||||||
| chr3:10100029
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0104 | 2 | HG01123.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.4282-1159T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100029 | ||||||
| chr3:10100408
|
C | G | 1 | a0002c0002t0017g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4282-780C>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100408 | ||||||
| chr3:10100418
|
G | T | 91 | a0001c0011t0002g0199a0002c0002t0002g0179a0002c0002t0002g0183others(88): Show | 91 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.4282-770G>T | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100418 | ||||||
| chr3:10100421
|
T | G | 1 | a0002c0002t0002g0229 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4282-767T>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100421 | ||||||
| chr3:10100768
|
A | G | 171 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0064others(168): Show | 171 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.4282-420A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100768 | ||||||
| chr3:10100926
|
G | A | 1 | a0009c0010t0003g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4282-262G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100926 | ||||||
| chr3:10100930
|
G | A | 1 | a0002c0002t0005g0230 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4282-258G>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | chr3 | 10100930 | ||||||
| chr3:10101065
|
TA | T | 81 | a0001c0003t0002g0123a0001c0003t0002g0124a0001c0003t0002g0126others(78): Show | 81 | HG00408.hp1 HG00639.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.4282-109delA | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr3 | 10101065 |